N. Kondo

发表

BLM (the causative gene of Bloom syndrome) protein translocation into the nucleus by a nuclear localization signal.

N. Shimozawa, H. Kaneko, K. Orii, 1997, Biochemical and biophysical research communications.

Acute disseminated encephalomyelitis associated with enterovirus 71

N. Kondo, Z. Kato, K. Omoya, 2015 .

Reversion to the Neurovilurent Genome Sequence of Polio Vaccine VirusIsolated from Community-Acquired Meningitis

N. Kondo, Z. Kato, Y. Shimada, 2009 .

Site‐directed mutagenesis of the ATM promoter: Consequences for response to proliferation and ionizing radiation

N. Gueven, H. Rodemann, M. Lavin, 2003, Genes, chromosomes & cancer.

Inhibition of interferon-gamma production from lymphocytes stimulated with food antigens by a beta 2-agonist, procaterol, in patients with food-sensitive atopic dermatitis.

H. Kaneko, T. Fukao, N. Kondo, 1997, Journal of investigational allergology & clinical immunology.

Roles of anti-hemagglutinin IgA and IgG antibodies in different sites of the respiratory tract of vaccinated mice in preventing lethal influenza pneumonia.

N. Kondo, T. Sata, Yuko Sato, 2003, Vaccine.

Congenital myotonic dystrophy: report of paternal transmission

E. Nanba, N. Shimozawa, Yasuyuki Suzuki, 2000, Brain and Development.

Temperature-sensitive phenotype of Chinese hamster ovary cells defective in PEX5 gene.

T. Imanaka, R. Ito, M. Ito, 2001, Biochemical and biophysical research communications.

Improvement of food‐sensitive atopic dermatitis accompanied by reduced lymphocyte responses to food antigen following natural measles virus infection

N. Kondo, T. Orii, O. Fukutomi, 1993, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Risk factors for infantile atopic dermatitis and recurrent wheezing.

M. Takemura, M. Seishima, H. Kaneko, 2012, Journal of investigational allergology & clinical immunology.

Pharmacogenetics of asthma in children

H. Kaneko, E. Matsui, N. Kondo, 2009, Allergy, asthma & immunology research.

Genetics of Pediatric Asthma

H. Kaneko, E. Matsui, T. Fukao, 2009 .

Atopy and mutations of IL-12 receptor beta 2 chain gene.

H. Kaneko, E. Matsui, T. Fukao, 2001, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Genetic and molecular bases of peroxisome biogenesis disorders

T. Tsukamoto, N. Shimozawa, T. Osumi, 2001, Genetics in Medicine.

A novel polymorphism, E254K, in the 5-lipoxygenase gene associated with bronchial asthma.

H. Kaneko, E. Matsui, T. Fukao, 2008, International journal of molecular medicine.

D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.

T. Hashimoto, S. Miyazawa, Y. Suzuki, 1997, American journal of human genetics.

Vaccination and Infection as Causative Factors in Japanese Patients With Rasmussen Syndrome: Molecular Mimicry and HLA Class I

H. Osaka, A. Imamura, N. Kondo, 2006, Clinical & developmental immunology.

Identification of monocyte chemotactic factors in supernatants of ovalbumin‐stimulated lymphocytes from patients with atopic dermatitis who are sensitive to hen's egg

N. Kondo, M. Shinbara, T. Orii, 1994, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures.

K. Ghaedi, A. Imamura, Y. Suzuki, 2000, Human molecular genetics.

Genes for the Human Mitochondrial Trifunctional Protein α- and β-Subunits Are Divergently Transcribed from a Common Promoter Region*

T. Hashimoto, T. Aoyama, K. Orii, 1999, The Journal of Biological Chemistry.

Thyroid cancer in a case with the Alagille syndrome

N. Kondo, Z. Kato, S. Yamaguchi, 1994, Clinical genetics.

Identification of β‐lactoglobulin‐derived peptides and class II HLA molecules recognized by T cells from patients with milk allergy

S. Matsushita, Y. Nishimura, H. Kaneko, 2001, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Inosiplex Affects the Spectra of Proton Magnetic Resonance Spectroscopy in Subacute Sclerosing Panencephalitis

T. Asano, N. Kondo, Z. Kato, 2006, Journal of child neurology.

Proton Magnetic Resonance Spectroscopy in a Case of Subacute Sclerosing Panencephalitis

T. Asano, N. Kondo, Z. Kato, 2002, Journal of child neurology.

M. Takemura, M. Seishima, H. Kaneko, 2006, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Molluscum contagiosum prevents progression of staphylococcal scalded skin syndrome

N. Kondo, Z. Kato, K. Tsubouchi, 2005, European Journal of Pediatrics.

to human and mouse β-glucuronidase

W. Sly, J. Grubb, K. Orii, 2006 .

Production of MPS VII mouse (Gustm(hE540A.mE536A)Sly) doubly tolerant to human and mouse β-glucuronidase

W. Sly, J. Grubb, K. Orii, 2003 .

human and mouse b-glucuronidase

W. Sly, J. Grubb, K. Orii, 2003 .

The structural basis for receptor recognition of human interleukin-18

M. Shirakawa, X. Zuo, E. Park, 2014, Nature Communications.

Urinary leukotriene E4 and 11-dehydro-thromboxane B2 excretion in children with bronchial asthma

H. Kaneko, E. Matsui, K. Kasahara, 2004 .

Urinary leukotriene E 4 and 11-dehydro-thromboxane B 2 excretion in children with bronchial asthma

H. Kaneko, E. Matsui, K. Kasahara, 2004 .

[Diagnostic approach for the autoinflammatory syndromes based on the molecular mechanism of innate immunity].

H. Kaneko, T. Fukao, N. Kondo, 2009, Arerugi = [Allergy].

Timing of onset of allergic symptoms as a response to a double-blind, placebo-controlled food challenge in patients with food allergy combined with a radioallergosorbent test and the evaluation of proliferative lymphocyte responses.

N. Kondo, M. Shinbara, T. Orii, 1994, International archives of allergy and immunology.

Comparison of the MAST chemiluminescent assay system with RAST and skin tests in allergic children.

N. Kondo, T. Orii, H. Agata, 1993, Annals of allergy.

Proliferative responses of lymphocytes to food antigens are useful for detection of allergens in nonimmediate types of food allergy.

N. Kondo, O. Fukutomi, H. Agata, 1997, Journal of investigational allergology & clinical immunology.

Effect of elimination diets on food-specific IgE antibodies and lymphocyte proliferative responses to food antigens in atopic dermatitis patients exhibiting sensitivity to food allergens.

N. Kondo, T. Orii, O. Fukutomi, 1993, The Journal of allergy and clinical immunology.

Lymphocyte responses to food antigens in patients with atopic dermatitis who are sensitive to foods.

N. Kondo, T. Orii, O. Fukutomi, 1990, The Journal of allergy and clinical immunology.

Evaluation of lymphocyte proliferative responses to food antigens with regard to age and food-specific IgE antibodies in food-sensitive atopic dermatitis.

N. Kondo, T. Orii, O. Fukutomi, 1993, Journal of investigational allergology & clinical immunology.

Combinations of IgE values and lymphocyte proliferative responses for consideration of the clinical course of infantile hen's-egg-sensitive atopic dermatitis.

N. Kondo, O. Fukutomi, H. Agata, 1997, International archives of allergy and immunology.

Mononuclear Cells ATM Is Upregulated During the Mitogenic Response in Peripheral Blood

M. Lavin, G. Birrell, D. Watters, 2013 .

ATM is upregulated during the mitogenic response in peripheral blood mononuclear cells.

M. Gatei, M. Lavin, G. Birrell, 1999, Blood.

Duplications and deletions of the human IGHC locus: evolutionary implications

L. Hammarström, N. Kondo, C. I. Smith, 1996, Immunogenetics.

T‐cell epitope‐containing hypoallergenic β‐lactoglobulin for oral immunotherapy in milk allergy

H. Kaneko, N. Kondo, H. Ohnishi, 2016, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

In Vitro Analysis of the Functional Effects of an NLRP3 G809S Variant with the co-Existence of MEFV Haplotype Variants in Atypical Autoinflammatory Syndrome

H. Kaneko, E. Matsui, N. Kondo, 2013, Journal of Clinical Immunology.

Reduced Interferon-γ Production and Mutations of the Interleukin-12 Receptor β2 Chain Gene in Atopic Subjects

H. Kaneko, E. Matsui, T. Fukao, 2001, International Archives of Allergy and Immunology.

FcεRI-induced mast cell cytokine production critically involves an aspartic acid residue (D234) in the C-terminal intracellular domain of the FcεRIβ chain.

C. Ra, N. Kondo, S. Era, 2011, Biochemical and biophysical research communications.

Asparagine-linked sugar chains of membrane glycoproteins from healthy and Wiskott-Aldrich syndrome patient's erythrocytes

N. Kondo, T. Orii, Y. Hirano, 1986 .

Identification of the D-enantiomer of 2-hydroxyglutaric acid in glutaric aciduria type II.

N. Kondo, S. Yamaguchi, N. Shimizu, 1995, Clinica chimica acta; international journal of clinical chemistry.

Bone marrow transplantation for the treatment of X-linked adrenoleukodystrophy

N. Shimozawa, N. Kondo, S. Kato, 2000, Journal of Inherited Metabolic Disease.

Diabetes mellitus in a young man with Bloom's syndrome

H. Kaneko, N. Kondo, S. Yamaguchi, 1990, Clinical genetics.

The clinical phenotype and outcome of mitochondrial acetoacetyl-CoA thiolase deficiency (beta-ketothiolase or T2 deficiency) in 26 enzymatically proved and mutation-defined patients.

T. Fukao, N. Kondo, C. Scriver, 2001, Molecular genetics and metabolism.

Parameters that govern the regulation of immunoglobulin delta heavy-chain gene expression

R. Tisch, N. Kondo, N. Hozumi, 1990, Molecular and cellular biology.

Mass screening test for mucopolysaccharidoses using the 1,9-dimethylmethylene blue method: positive interference from paper diapers.

N. Kondo, T. Sasaki, A. Noma, 1997, Clinica chimica acta; international journal of clinical chemistry.

Regulation of the Atm promoter in vivo

G. Kay, C. Paterson, N. Gueven, 2006, Genes, chromosomes & cancer.

Spinal muscular atrophy type 1 with anti-acetylcholine receptor antibody

Kayoko Saito, N. Kondo, Z. Kato, 2002, European Journal of Pediatrics.

Purification and properties of rat liver peroxisomal very-long-chain acyl-CoA synthetase.

T. Hashimoto, N. Kondo, Y. Uchida, 1996, Journal of biochemistry.

Expression of immunoglobulin genes in common variable immunodeficiency

H. Kaneko, N. Kondo, T. Orii, 1991, Journal of Clinical Immunology.

Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders

R. Wanders, N. Shimozawa, Yasuyuki Suzuki, 2003, Brain and Development.

Two novel missense mutations in the ATP‐binding domain of the adrenoleukodystrophy gene: immunoblotting and immunocytological study of two patients

T. Hashimoto, K. Kamijo, A. Imamura, 1997, Clinical genetics.

Reduced Expression of the Interferon‐Gamma Messenger RNA in IgG2 Deficiency

H. Kaneko, T. Fukao, K. Kasahara, 1997, Scandinavian journal of immunology.

IgG2 Deficiency Associated with Defects in Production of Interferon‐Gamma; Comparison with Common Variable Immunodeficiency

N. Kondo, R. Inoue, T. Orii, 1995, Scandinavian journal of immunology.

The role of dendritic cells in the generation of CD4(+) CD25(HI) Foxp3(+) T cells induced by amino acid copolymers.

J. Strominger, N. Kondo, H. Ohnishi, 2013, International immunology.

The mitochondrial acetoacetyl-CoA thiolase (T2) deficiency in Japanese patients: urinary organic acid and blood acylcarnitine profiles under stable conditions have subtle abnormalities in T2-deficient patients with some residual T2 activity

T. Fukao, N. Kondo, S. Yamaguchi, 2003, Journal of Inherited Metabolic Disease.

IL-10 plays an important role as an immune-modulator in the pathogenesis of atopic diseases.

H. Kaneko, E. Matsui, T. Fukao, 2008, Molecular medicine reports.

Population pharmacokinetics of pranlukast hydrate dry syrup in children with bronchial asthma

E. Yukawa, S. Higuchi, N. Kondo, 2003 .

Association between Fc ɛ RIβ and atopic disorder in Japanese population?

H. Kaneko, T. Fukao, N. Kondo, 1996, The Lancet.

Predictive values of cord blood IgE and cord blood lymphocyte responses to food antigens in allergic disorders during infancy.

N. Kondo, T. Orii, O. Fukutomi, 1994, The Journal of allergy and clinical immunology.

Predominant expression of 950delCAG of IL-18R α chain cDNA is associated with reduced IFN-γ production and high serum IgE levels in atopic Japanese children

H. Kaneko, E. Matsui, K. Kasahara, 2002 .

Predominant expression of 950delCAG of IL-18R alpha chain cDNA is associated with reduced IFN-gamma production and high serum IgE levels in atopic Japanese children.

H. Kaneko, E. Matsui, K. Kasahara, 2002, The Journal of allergy and clinical immunology.

Differences of genetic effects for the development of allergic diseases in two cities of Japan.

N. Kondo, H. Shimizu, N. Kawakami, 1999, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Generation of highly stable IL-18 based on a ligand-receptor complex structure.

N. Kondo, H. Ohnishi, Z. Kato, 2004, Biochemical and biophysical research communications.

Formation of the enzyme complex in mitochondria is required for function of trifunctional beta-oxidation protein.

S. Hayashi, T. Hashimoto, T. Aoyama, 1996, Biochemical and biophysical research communications.

Defining the pathway for Tat-mediated delivery of beta-glucuronidase in cultured cells and MPS VII mice.

W. Sly, Q. Mao, B. Davidson, 2005, Molecular therapy : the journal of the American Society of Gene Therapy.

Accelerated expression of secreted α-chain gene in anaphylactoid purpura

K. Kasahara, N. Kondo, T. Orii, 1992, Journal of Clinical Immunology.

Expression of Secreted Immunoglobulin Heavy Chain Genes and Immunoglobulin‐Secreting Cells in Human Lymphocytes

Y. Suzuki, N. Shimozawa, N. Kondo, 1993, Scandinavian journal of immunology.

Reduced secreted μ mRNA synthesis in selective IgM deficiency of Bloom's syndrome

K. Kasahara, N. Kondo, T. Orii, 1992 .

Epilepsy in Peroxisomal Diseases

T. Nishiguchi, Y. Suzuki, N. Shimozawa, 1997, Epilepsia.

Augmented cell death with Bloom syndrome helicase deficiency.

H. Kaneko, T. Fukao, K. Kasahara, 2011, Molecular medicine reports.

Molecular analysis of B‐cell differentiation in selective or partial IgA deficiency

H. Kaneko, T. Fukao, K. Kasahara, 2004, Clinical and experimental immunology.

Disruption of the BLM gene in ATM-null DT40 cells does not exacerbate either phenotype

M. Lavin, Philip Chen, Ken‐ichi Yamamoto, 2004, Oncogene.

The function of RecQ helicase gene family (especially BLM) in DNA recombination and joining.

H. Kaneko, T. Fukao, N. Kondo, 2004, Advances in biophysics.

The N-terminal internal region of BLM is required for the formation of dots/rod-like structures which are associated with SUMO-1.

T. Kobayashi, T. Masuko, H. Kaneko, 2001, Biochemical and biophysical research communications.

Telomerase Activity in Cell Lines and Lymphoma Originating from Bloom Syndrome

H. Kaneko, T. Fukao, K. Kasahara, 2001, Leukemia & lymphoma.

Two Japanese siblings with Bloom syndrome gene mutation and B-cell lymphoma.

H. Kaneko, T. Fukao, K. Kasahara, 1997, Leukemia & lymphoma.

New Gaucher disease mutations in exon 10: a novel L444R mutation produces a new NciI site the same as L444P.

Y. Suzuki, N. Shimozawa, N. Kondo, 1994, Human molecular genetics.

Enzymes of Ketone Body Utilization in Human Tissues: Protein and Messenger RNA Levels of Succinyl-Coenzyme A (CoA):3-Ketoacid CoA Transferase and Mitochondrial and Cytosolic Acetoacetyl-CoA Thiolases

G. Mitchell, T. Fukao, N. Kondo, 1997, Pediatric Research.

An extremely severe case of cutaneous calcinosis with juvenile dermatomyositis, and successful treatment with diltiazem

Y. Suzuki, N. Shimozawa, N. Kondo, 2001, The British journal of dermatology.

Development and Testing of New Screening Method for Keratan Sulfate in Mucopolysaccharidosis IVA

T. Taketani, J. Grubb, R. Giugliani, 2004, Pediatric Research.

Mucopolysaccharidosis type II (Hunter disease): 13 gene mutations in 52 Japanese patients and carrier detection in four families

Yasuyuki Suzuki, N. Kondo, J. Hopwood, 1993, Human Genetics.

[Peroxisomal disorders].

A. Imamura, Y. Suzuki, N. Shimozawa, 2000, Ryoikibetsu shokogun shirizu.

Intravenous Immunoglobulins Suppress Immunoglobulin Productions by Suppressing Ca2+ ‐Dependent Signal Transduction Through Fc γ Receptors in B Lymphocytes

Y. Suzuki, N. Shimozawa, K. Kasahara, 1994, Scandinavian journal of immunology.

Clinical and Genetic Characterization of Japanese Sporadic Cases of Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis Syndrome from a Single Medical Center in Japan

O. Ohara, K. Kasahara, N. Kondo, 2014, Journal of Clinical Immunology.

Suppression of proliferative responses of lymphocytes to food antigens by an anti-allergic drug, ketotifen fumarate, in patients with food-sensitive atopic dermatitis.

N. Kondo, M. Shinbara, T. Orii, 1994, International archives of allergy and immunology.

Development of Fluorescence-linked Immunosorbent Assay for High Throughput Screening of Interferon-γ.

N. Kondo, H. Ohnishi, Z. Kato, 2006, Allergology international : official journal of the Japanese Society of Allergology.

Systematic optimization of active protein expression using GFP as a folding reporter.

N. Kondo, H. Ohnishi, Z. Kato, 2004, Protein expression and purification.

Prevalence of and risk factors for allergic diseases: comparison of two cities in Japan.

N. Kondo, H. Shimizu, N. Kawakami, 1995, Annals of Allergy, Asthma & Immunology.

Comparison of allergic diseases and specific IgE antibodies in different parts of Japan.

Y. Suzuki, N. Shimozawa, N. Kondo, 1994, Annals of allergy.

Pediatric allergy and immunology in Japan

M. Ebisawa, N. Kondo, H. Ohnishi, 2013, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

The effect of photosensitive dye Platonin on juvenile rheumatoid arthritis

N. Kondo, T. Orii, F. Motoyoshi, 1991, Biotherapy.

Mutations of the IL-12 receptor beta2 chain gene in atopic subjects.

H. Kaneko, E. Matsui, T. Fukao, 1999, Biochemical and biophysical research communications.

Suppression of IFN‐gamma production in atopic group at the acute phase of RSV infection

H. Kaneko, E. Matsui, K. Kasahara, 2006, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Questionnaire-based Study on the Relationship between Pet-keeping and Allergic Diseases in Young Children in Japan

H. Kaneko, E. Matsui, T. Fukao, 2005 .

Glycogen storage disease type Ib without neutropenia.

M. Hiratsuka, Y. Matsubara, Y. Suzuki, 2000, The Journal of pediatrics.

Cord blood lymphocyte responses to food antigens for the prediction of allergic disorders.

K. Kasahara, N. Kondo, T. Orii, 1992, Archives of disease in childhood.

Purification, crystallization and preliminary X-ray crystallographic analysis of human IL-18 and its extracellular complexes.

M. Shirakawa, N. Kondo, H. Ohnishi, 2014, Acta crystallographica. Section F, Structural biology communications.

Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.

R. Wanders, R. Wanders, T. Tsukamoto, 1999, Human molecular genetics.

Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.

R. Wanders, A. Imamura, Y. Suzuki, 1998, Biochemical and biophysical research communications.

Treatment of MPS VII (Sly disease) by allogeneic BMT in a female with homozygous A619V mutation

W. Sly, S. Kojima, N. Kondo, 1998, Bone Marrow Transplantation.

A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome.

H. Kaneko, N. Kondo, H. Ohnishi, 2012, The Journal of allergy and clinical immunology.

Sweet’s syndrome in a neonate with non-B54 types of human leukocyte antigen

N. Kondo, Z. Kato, K. Omoya, 2012, World Journal of Pediatrics.

DNA MUTATION INDUCED IN THE SEQUENCE UPSTREAM OF THE SECRETED MYU C‐TERMINAL CODING SEQUENCE BY ULTRAVIOLET IRRADIATION IN THE CELL LINE OF BLOOM'S SYNDROME

K. Kasahara, N. Kondo, T. Orii, 1995, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

[IgA subclass and IgA deficiency].

H. Kaneko, N. Kondo, Hiroko Suzuki, 2009, Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology.

The response of bovine beta‐lactoglobulin‐specific T‐cell clones to single amino acid substitution of T‐cell core epitope

H. Kaneko, E. Matsui, T. Fukao, 2008, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

TRAM Is Involved in IL-18 Signaling and Functions as a Sorting Adaptor for MyD88

M. Shirakawa, N. Kondo, H. Ohnishi, 2012, PloS one.

Structural basis for the multiple interactions of the MyD88 TIR domain in TLR4 signaling

M. Shirakawa, N. Kondo, H. Ohnishi, 2009, Proceedings of the National Academy of Sciences.

Progressive Multifocal Leukoencephalopathy in a Patient with X-linked Agammaglobulinemia

Y. Hirose, H. Kaneko, N. Kondo, 2003, Scandinavian journal of infectious diseases.

UvA-DARE ( Digital Academic Repository ) Defective PEX gene products correlate with the protein import , biochemical abnormalities , and phenotypic heterogeneity in peroxisome biogenesis disorders

R. Wanders, G. Besley, T. Tsukamoto, 1999 .

Genetic analysis of IgE and the IGHE, IGHEP1 and IGHEP2 genes in atopic families.

N. Kondo, S. Tomatsu, T. Orii, 1995, International archives of allergy and immunology.

Propranolol for intractable diffuse lymphangiomatosis.

T. Fukao, N. Kondo, M. Ozeki, 2011, The New England journal of medicine.

IL-12B Promoter Polymorphism Associated with Asthma and IL-12B Transcriptional Activity

H. Kaneko, E. Matsui, T. Fukao, 2005 .

Leaky phenotype of X‐linked agammaglobulinaemia in a Japanese family

H. Kaneko, E. Matsui, T. Fukao, 2005, Clinical and experimental immunology.

H. Kaneko, E. Matsui, T. Fukao, 2009 .

H. Kaneko, E. Matsui, T. Fukao, 2009, Allergology international : official journal of the Japanese Society of Allergology.

Single base substitutions at the initiator codon in the mitochondrial acetoacetyl‐CoA thiolase (ACAT1/T2) gene result in production of varying amounts of wild‐type T2 polypeptide

Naomi Kondo, T. Fukao, N. Kondo, 2003, Human mutation.

A novel mutation (c.951C>T) in an exonic splicing enhancer results in exon 10 skipping in the human mitochondrial acetoacetyl-CoA thiolase gene.

T. Fukao, N. Kondo, Y. Naiki, 2010, Molecular genetics and metabolism.

A common mutation, R208X, identified in Vietnamese patients with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency.

R. Wanders, T. Fukao, N. Kondo, 2010, Molecular genetics and metabolism.

A novel single-base substitution (c.1124A>G) that activates a 5-base upstream cryptic splice donor site within exon 11 in the human mitochondrial acetoacetyl-CoA thiolase gene.

T. Fukao, N. Kondo, A. Boneh, 2008, Molecular genetics and metabolism.

A novel single-base substitution (380C>T) that activates a 5-base downstream cryptic splice-acceptor site within exon 5 in almost all transcripts in the human mitochondrial acetoacetyl-CoA thiolase gene.

C. Pérez-Cerdá, M. Ugarte, T. Fukao, 2001, Molecular genetics and metabolism.

Immunotitration Analysis of Cytosolic Acetoacetyl-Coenzyme A Thiolase Activity in Human Fibroblasts

T. Hashimoto, T. Fukao, N. Kondo, 1996, Pediatric Research.

Psychological status of patients with mucopolysaccharidosis type II and their parents

I. Kuratsubo, Yasuyuki Suzuki, K. Orii, 2009, Pediatrics international : official journal of the Japan Pediatric Society.

Epileptic seizures and structural abnormalities in a patient with holoprosencephaly

N. Kondo, Yukitoshi Takahashi, T. Orii, 2001, Brain and Development.

Relationship between the benefits of suplatast tosilate, a Th2 cytokine inhibitor, and gene polymorphisms in children with bronchial asthma.

H. Kaneko, E. Matsui, T. Fukao, 2010, Experimental and therapeutic medicine.

Structural property of soybean protein P34 and specific IgE response to recombinant P34 in patients with soybean allergy.

H. Kaneko, E. Matsui, T. Fukao, 2011, International journal of molecular medicine.

Hypothermia augments NF-kappaB activity and the production of IL-12 and IFN-gamma.

H. Kaneko, E. Matsui, T. Fukao, 2008, Allergology international : official journal of the Japanese Society of Allergology.

IFN‐γ production in response to IL‐18 or IL‐12 stimulation by peripheral blood mononuclear cells of atopic patients

M. Takemura, H. Kaneko, K. Kasahara, 2001, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Total IgE at 6 months predicts remittance or persistence of atopic dermatitis at 14 months.

M. Takemura, M. Seishima, H. Kaneko, 2013, Allergy and asthma proceedings.

A Complement Factor B Mutation in a Large Kindred with Atypical Hemolytic Uremic Syndrome

O. Ohara, H. Kaneko, N. Kondo, 2014, Journal of Clinical Immunology.

Toll-like receptor signaling is impaired in dendritic cells from patients with X-linked agammaglobulinemia.

H. Kanegane, T. Kaisho, T. Miyawaki, 2008, Clinical immunology.

Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.

R. Wanders, R. Wanders, T. Tsukamoto, 1999, Biochemical and biophysical research communications.

Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient.

C. Pérez-Cerdá, M. Ugarte, A. Duncan, 1996, American journal of human genetics.

Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).

N. Kondo, Z. Kato, Takeshi Kimura, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Translocation (1;10)(p34;p15) in infant acute myeloid leukemia with extramedullary infiltration in multiple sites.

H. Kaneko, T. Fukao, N. Kondo, 2009, Cancer genetics and cytogenetics.

Fate of the mutated IgG2 heavy chain: lack of expression of mutated membrane-bound IgG2 on the B cell surface in selective IgG2 deficiency.

M. Takemura, H. Kaneko, T. Fukao, 2001, International immunology.

Fate of the mutated IgG 2 heavy chain : lack of expression of mutated membrane-bound IgG 2 on the B cell surface in selective IgG 2 deficiency

M. Takemura, H. Kaneko, T. Fukao, 2001 .

Identification of Alu-mediated, large deletion-spanning exons 2-4 in a patient with mitochondrial acetoacetyl-CoA thiolase deficiency.

Keitaro Yamada, Naomi Kondo, T. Fukao, 2006, Molecular genetics and metabolism.

Three Japanese Patients with Beta-Ketothiolase Deficiency Who Share a Mutation, c.431A>C (H144P) in ACAT1 : Subtle Abnormality in Urinary Organic Acid Analysis and Blood Acylcarnitine Analysis Using Tandem Mass Spectrometry.

R. Wierenga, A. Haapalainen, T. Fukao, 2012, JIMD reports.

Two novel mutations in mitochondrial acetoacetyl-CoA thiolase deficiency

T. Fukao, N. Kondo, E. Pospíšilová, 2005, Journal of Inherited Metabolic Disease.

Mitochondrial Acetoacetyl-CoA Thiolase (T2) Deficiency: T2-Deficient Patients with “Mild” Mutation(s) Were Previously Misinterpreted as Normal by the Coupled Assay with Tiglyl-CoA

M. Rolland, T. Fukao, N. Kondo, 2004, Pediatric Research.

Characterization of six mutations in five Spanish patients with mitochondrial acetoacetyl-CoA thiolase deficiency: effects of amino acid substitutions on tertiary structure.

Haruki Nakamura, C. Pérez-Cerdá, M. Ugarte, 2002, Molecular genetics and metabolism.

Epidemiology of X-linked adrenoleukodystrophy in Japan

S. Tsuji, A. Tamakoshi, T. Hashimoto, 2002, Journal of Human Genetics.

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.

T. Hashimoto, Y. Suzuki, N. Shimozawa, 1994, American journal of human genetics.

Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.

R. Wanders, Y. Suzuki, N. Shimozawa, 1999, Human molecular genetics.

Characterization of T-cell clones specific to ovomucoid from patients with egg-white allergy.

H. Kaneko, T. Fukao, N. Kondo, 2005, Journal of investigational allergology & clinical immunology.

High Sensitivity and Specificity of Proliferative Responses of Lymphocytes to Food Antigens for Detection of the Offending Food in Patients with Food-Sensitive Atopic Dermatitis

H. Kaneko, T. Fukao, N. Kondo, 1996 .

Inhibition of interferon- γ and interleukin-2 production from lymphocytes stimulated with food antigens by an anti-allergic drug, Tranilast, in patients with food-sensitive atopic dermatitis

N. Kondo, M. Shinbara, T. Orii, 1994, Biotherapy.

The role of T lymphocytes in patients with food-sensitive atopic dermatitis.

N. Kondo, T. Orii, O. Fukutomi, 1993, The Journal of allergy and clinical immunology.

Interleukin-2 production of lymphocytes in food sensitive atopic dermatitis.

N. Kondo, T. Orii, O. Fukutomi, 1992, Archives of disease in childhood.

[New knowledge of Li-Fraumeni syndrome].

N. Kondo, M. Funato, 2013, Gan to kagaku ryoho. Cancer & chemotherapy.

Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivation

T. Fukao, N. Kondo, S. Fukuda, 1998, Clinical genetics.

Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency.

J. Sass, T. Fukao, N. Kondo, 2011, Biochimica et biophysica acta.

A neonatal-onset succinyl-CoA:3-ketoacid CoA transferase (SCOT)-deficient patient with T435N and c.658-666dupAACGTGATT p.N220_I222dup mutations in the OXCT1 gene

T. Fukao, N. Kondo, P. Kursula, 2010, Journal of Inherited Metabolic Disease.

Neonatal hypoglycaemia in severe succinyl-CoA:3-oxoacid CoA-transferase deficiency

G. Mitchell, T. Fukao, N. Kondo, 2001, Journal of Inherited Metabolic Disease.

A common variable immunodeficient patient who developed acute disseminated encephalomyelitis followed by the Lennox‐Gastaut syndrome

H. Kaneko, T. Fukao, N. Kondo, 2005, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Selective pontine hypoplasia: A possible common feature in 5p monosomy syndrome

H. Kato, K. Shimizu, K. Miyamoto, 2011, Brain and Development.

Transformation of Bloom syndrome T-lymphocytes by cocultivation with a lethally irradiated human T-cell line carrying type C virus particles.

N. Kondo, I. Miyoshi, M. Fujishita, 1983, Gan.

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.

R. Wanders, R. Wanders, K. Ghaedi, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Y. Suzuki, N. Shimozawa, S. Tamura, 1998, American journal of human genetics.

Computed Tomographic Findings of Kawasaki Disease With Cervical Lymphadenopathy

M. Kanematsu, H. Hoshi, H. Kato, 2012, Journal of computer assisted tomography.

Carnitine palmitoyltransferase 2 deficiency: the time-course of blood and urinary acylcarnitine levels during initial L-carnitine supplementation.

T. Fukao, N. Kondo, Y. Hasegawa, 2010, The Tohoku journal of experimental medicine.

The influence of gene deletions and duplications within the IGHC locus on serum immunoglobulin subclass levels.

L. Hammarström, N. Kondo, C. I. Smith, 1995, Clinical immunology and immunopathology.

Urinary Oligosaccharide Excretion in Nephrotic Syndrome

N. Kondo, Yukitoshi Takahashi, T. Orii, 1993, Pediatric Research.

Immunoglobulin Production in Kawasaki Disease

N. Kondo, Geng Li, T. Orii, 1995 .

Correlations Between Serum Immunoglobulin Concentrations and Immunoglobulin Secreting Cells in Healthy Peripheral Blood

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1993 .

Lymphocyte Responses to Chymotrypsin- or Trypsin V-Digested β-Lactoglobulin in Patients with Cow's Milk Allergy

H. Kaneko, E. Matsui, T. Fukao, 2007, Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology.

H. Kaneko, T. Fukao, N. Kondo, 2008, International journal of molecular medicine.

Case report: Immunoglobulin A deficiency in patients with juvenile rheumatoid arthritis treated with aspirin

N. Kondo, T. Orii, A. Takao, 1993, Biotherapy.

Mucopolysaccharidosis IVA: polymorphic haplotypes and informative RFLPs in the Japanese population

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1995, Human Genetics.

RNA editing of interleukin‐12 receptor β2, 2451 C‐to‐U (Ala 604 Val) conversion, associated with atopy

H. Kaneko, E. Matsui, T. Fukao, 2004, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Herpes gestationis in a mother and newborn: immunoclinical perspectives based on a weekly follow-up of the enzyme-linked immunosorbent assay index of a bullous pemphigoid antigen noncollagenous domain.

N. Kondo, Y. Aoyama, Y. Kitajima, 2007, Archives of dermatology.

Mitochondrial acetoacetyl-CoA thiolase (β-ketothiolase) deficiency and pregnancy

A. Sewell, T. Fukao, N. Kondo, 1998, Journal of Inherited Metabolic Disease.

Adenovirus infection mimics the cerebellitis caused by rotavirus infection

N. Kondo, Z. Kato, Takahide Teramoto, 2011, European Journal of Pediatrics.

Acute cerebellitis in primary human herpesvirus-6 infection

N. Kondo, Z. Kato, S. Shinoda, 2003, European Journal of Pediatrics.

Autosomal-Dominant Chronic Mucocutaneous Candidiasis with STAT1-Mutation can be Complicated with Chronic Active Hepatitis and Hypothyroidism

Y. Hirose, H. Kaneko, T. Fukao, 2012, Journal of Clinical Immunology.

Effect of Hunter disease (mucopolysaccharidosis type II) mutations on molecular phenotypes of iduronate-2-sulfatase: Enzymatic activity, protein processing and structural analysis

T. Fukao, N. Kondo, K. Kuwata, 2006, Journal of Inherited Metabolic Disease.

Mucopolysaccharidosis IVA (Morquio A): Identification of novel common mutations in the N‐acetylgalactosamine‐6‐sulfate sulfatase (GALNS) gene in Italian patients

W. Sly, M. Filocamo, K. Orii, 2004, Human mutation.

Mucopolysaccharidosis IVA: characterization of a common mutation found in Finnish patients with attenuated phenotype

I. Kaitila, N. Kondo, Z. Kato, 2003, Human Genetics.

Genomic and mutational analysis of the mitochondrial trifunctional protein beta-subunit (HADHB) gene in patients with trifunctional protein deficiency.

N. Kondo, K. Orii, S. Yamaguchi, 1997, Human molecular genetics.

Dimorphism of sister chromatid exchange in Bloom's syndrome B- and T-cell lines transformed with Epstein-Barr and adult T-cell leukemia viruses.

A. Sandberg, N. Kondo, I. Miyoshi, 1983, Cancer research.

Asparagine-linked sugar chains of plasma membrane glycoproteins from lymphoblastoid cells and acute lymphocytic leukemia cells

N. Kondo, T. Orii, Fumiaki Motoyosi, 1986 .

Interferon-gamma and interleukin-4 production of ovalbumin-stimulated lymphocytes in egg-sensitive children.

N. Kondo, M. Shinbara, T. Orii, 1996, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Impaired B-cell differentiation and T-cell regulatory function in four patients with Bloom's syndrome.

T. Miyawaki, N. Kondo, H. Takahashi, 1982, Clinical immunology and immunopathology.

Bisected N-acetylglucosamine residue of biantennary sugar chains and high-molecular-weight oligosaccharides of neuroblastoma cell membranes.

N. Kondo, T. Orii, F. Motoyoshi, 1993, Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine.

Appearance of bisected N-acetylglucosamine residue of biantennary sugar chains and decrease of high molecular weight oligosaccharides of human lymphocytic cell membranes during differentiation.

N. Kondo, T. Orii, F. Motoyoshi, 1990, Clinical immunology and immunopathology.

Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene

R. Wanders, T. Tsukamoto, N. Shimozawa, 2004, Human mutation.

Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.

H. Moser, A. Moser, N. Shimozawa, 2003, American journal of human genetics.

Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.

Y. Kuroki, T. Tsukamoto, Y. Suzuki, 1996, American journal of human genetics.

Prenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells

Y. Suzuki, N. Shimozawa, N. Kondo, 1999, Clinical genetics.

PRENATAL DIAGNOSIS OF ADRENOLEUKODYSTROPHY BY MEANS OF MUTATION ANALYSIS

A. Imamura, N. Shimozawa, Yasuyuki Suzuki, 1996, Prenatal diagnosis.

Temperature sensitivity in peroxisome assembly processes characterizes milder forms of peroxisome biogenesis disorders

T. Tsukamoto, A. Imamura, N. Shimozawa, 2000, Cell Biochemistry and Biophysics.

Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders.

T. Imanaka, T. Tsukamoto, A. Imamura, 1998, American journal of human genetics.

Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders

A. Imamura, Y. Suzuki, N. Shimozawa, 2001, Journal of Inherited Metabolic Disease.

Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein.

K. Ghaedi, Y. Suzuki, N. Shimozawa, 1999, Experimental cell research.

Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts.

R. Wanders, R. Wanders, T. Imanaka, 1998, American journal of human genetics.

Genetic basis of peroxisomes-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts (letter)

R. Wanders, T. Imanaka, F. Beemer, 1998 .

Hyper-IgM syndrome with putative dominant negative mutation in activation-induced cytidine deaminase.

H. Kaneko, T. Fukao, K. Kasahara, 2003, The Journal of allergy and clinical immunology.

Very long chain fatty acid analysis of dried blood spots on filter paper to screen for adrenoleukodystrophy.

Y. Suzuki, N. Shimozawa, N. Kondo, 1997, Clinical chemistry.

Effects of erucic acid therapy on Japanese patients with X-linked adrenoleukodystrophy

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1994, Brain and Development.

Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development.

Naomi Kondo, N. Kondo, K. Orii, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Mucopolysaccharidosis IVA: Submicroscopic deletion of 16q24.3 and a novel R386C mutation of n‐acetylgalactosamine‐6‐sulfate sulfatase gene in a classical Morquio disease

Y. Kuroki, N. Shimozawa, Yasuyuki Suzuki, 1996, Human mutation.

STXBP1 mutations in early infantile epileptic encephalopathy with suppression‐burst pattern

H. Arai, M. Kubota, N. Matsumoto, 2010, Epilepsia.

Molecular characterization of the mouse very-long-chain acyl-CoA dehydrogenase gene

T. Hashimoto, T. Aoyama, K. Orii, 1997, Mammalian Genome.

A novel common missense mutation G301C in the N-acetylgalactosamine-6-sulfate sulfatase gene in mucopolysaccharidosis IVA

T. Yasunaga, N. Kondo, Z. Kato, 1997, Human Genetics.

The correlation between ovomucoid‐derived peptides, human leucocyte antigen class II molecules and T cell receptor‐complementarity determining region 3 compositions in patients with egg‐white allergy

S. Matsushita, H. Kaneko, N. Kondo, 2002, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Molecular Basis of Two‐Exon Skipping (Exons 12 and 13) by c.1248+5g>a in OXCT1 Gene: Study on Intermediates of OXCT1 Transcripts in Fibroblasts

C. Harding, T. Fukao, N. Kondo, 2013, Human mutation.

Ataxia telangiectasia syndrome with B cell lymphoma

H. Kaneko, K. Kasahara, N. Kondo, 1996, Clinical genetics.

Chediak‐Higashi syndrome: report of a case with an ovarian tumor

N. Kondo, R. Inoue, T. Orii, 1991, Clinical genetics.

Methylation patterns of the human β-glucuronidase gene locus: Boundaries of methylation and general implications for frequent point mutations at CpG dinucleotides

W. Sly, G. Shah, J. Grubb, 2002 .

Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophy.

A. Imamura, Y. Suzuki, N. Shimozawa, 1994, Biochemical and biophysical research communications.

The common phospholipid‐binding activity of the N‐terminal domains of PEX1 and VCP/p97

K. Mizuguchi, M. Shirakawa, Toshiyuki Shimizu, 2006, The FEBS journal.

Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease)

T. Fukao, N. Kondo, S. Fukuda, 1998, Journal of Inherited Metabolic Disease.

Temperature sensitive acyl-CoA oxidase import in group A peroxisome biogenesis disorders

A. Imamura, Y. Suzuki, N. Shimozawa, 2001, Journal of medical genetics.

Temperature-Sensitive Mutation of PEX6 in Peroxisome Biogenesis Disorders in Complementation Group C (CG-C): Comparative Study of PEX6 and PEX1

R. Wanders, T. Tsukamoto, A. Imamura, 2000, Pediatric Research.

Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans

T. Tsukamoto, A. Imamura, N. Shimozawa, 2000, Brain and Development.

Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals.

K. Ghaedi, Y. Suzuki, N. Shimozawa, 1999, Experimental cell research.

Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.

T. Tsukamoto, A. Imamura, Y. Suzuki, 1998, Human molecular genetics.

Newly Identified Chinese Hamster Ovary Cell Mutants Are Defective in Biogenesis of Peroxisomal Membrane Vesicles (Peroxisomal Ghosts), Representing a Novel Complementation Group in Mammals*

R. Wanders, K. Ghaedi, N. Shimozawa, 1998, The Journal of Biological Chemistry.

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.

Y. Suzuki, N. Shimozawa, K. Okumoto, 1998, Human molecular genetics.

Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.

T. Tsukamoto, Y. Suzuki, N. Shimozawa, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Functional Link between BLM Defective in Bloom's Syndrome and the Ataxia-telangiectasia-mutated Protein, ATM*

N. Ellis, D. Purdie, N. Gueven, 2002, The Journal of Biological Chemistry.

Effect of ‘attenuated’ mutations in mucopolysaccharidosis IVA on molecular phenotypes of N-acetylgalactosamine-6-sulfate sulfatase

R. Carrozzo, E. Christensen, K. Orii, 2007, Journal of Inherited Metabolic Disease.

Biochemical and structural analysis of missense mutations in N-acetylgalactosamine-6-sulfate sulfatase causing mucopolysaccharidosis IVA phenotypes.

T. Fukao, N. Kondo, P. Tortora, 2000, Human molecular genetics.

Mucopolysaccharidosis IVA: A novel splice acceptor site mutation in intron 4 of the N-acetylgalactosamine-6-sulfate sulfatase gene in an afghanistan girl with classical morquio disease

N. Kondo, J. Hopwood, S. Fukuda, 1997, Japanese Journal of Human Genetics.

Mucopolysaccharidosis IVA: screening and identification of mutations of the N-acetylgalactosamine-6-sulfate sulfatase gene.

Y. Suzuki, N. Shimozawa, N. Kondo, 1995, Human molecular genetics.

Erratum: A randomized study of pomalidomide vs placebo in persons with myeloproliferative neoplasm-associated myelofibrosis and RBC-transfusion dependence

Y. Okuno, S. Kojima, T. Fukao, 2017, Leukemia.

Various cells retrovirally transduced with N-acetylgalactosoamine-6-sulfate sulfatase correct Morquio skin fibroblasts in vitro.

N. Kondo, C. Bordignon, P. Tortora, 2001, Human gene therapy.

Recurrent genomic alterations characterize medulloblastoma arising from DNA double-strand break repair deficiency

S. Baker, N. Chalhoub, Yong-Dong Wang, 2009, Proceedings of the National Academy of Sciences.

Suppression of immunoglobulin production of lymphocytes by intravenous immunoglobulin

H. Kaneko, K. Kasahara, N. Kondo, 1991, Journal of Clinical Immunology.

Clinical features of Bloom syndrome and function of the causative gene, BLM helicase

Hideo Kaneko, Naomi Kondo, H. Kaneko, 2004, Expert review of molecular diagnostics.

Semiquantitative Evaluation of mRNAs for the Membranous Form of Immunoglobulin Heavy Chain is Useful for Investigating the Etiology in CVID

H. Kaneko, T. Fukao, K. Kasahara, 2003, Scandinavian journal of immunology.

Analysis of Ig subclass deficiency: First reported case of IgG2, IgG4, and IgA deficiency caused by deletion of Cα1, ψCγ, Cγ2, Cγ4, and Cε in a Mongoloid patient☆☆☆

H. Kaneko, K. Kasahara, N. Kondo, 2001 .

Molecular basis of selective IgG2 deficiency. The mutated membrane-bound form of gamma2 heavy chain caused complete IGG2 deficiency in two Japanese siblings.

H. Kaneko, T. Fukao, K. Kasahara, 1998, The Journal of clinical investigation.

DIVERSITY IN DNA REARRANGEMENTS AND IN RNA EXPRESSIONS OF IMMUNOGLOBULIN GENE ON COMMON VARIABLE IMMUNODEFICIENCY

H. Kaneko, N. Kondo, T. Orii, 1992, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

METHYLATION PATTERNS OF I ε REGION IN B CELLS STIMULATED WITH INTERLEUKIN 4 AND EPSTEIN‐BARR VIRUS IN PATIENTS WITH A HIGH LEVEL OF SERUM IgE

N. Kondo, T. Orii, O. Fukutomi, 1995, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

A WILD‐TYPE μs C‐TERMINAL GENE IS EXPRESSED IN BLOOM'S SYNDROME CELLS

Y. Suzuki, N. Shimozawa, N. Kondo, 1994, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

Molecular Mechanism of a Temperature-Sensitive Phenotype in Peroxisomal Biogenesis Disorder

R. Wanders, M. Shirakawa, N. Shimozawa, 2005, Pediatric Research.

PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

K. Ghaedi, Y. Suzuki, N. Shimozawa, 2000, American journal of human genetics.

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6

H. Moser, A. Moser, N. Braverman, 2001, Journal of Human Genetics.

Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.

Y. Suzuki, N. Shimozawa, K. Okumoto, 1997, European journal of cell biology.

A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.

R. Wanders, N. Shimozawa, Yasuyuki Suzuki, 2002, Biochemical and biophysical research communications.

Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.

Y Fujiki, A. Imamura, Y. Suzuki, 2001, The Biochemical journal.

A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.

H. Waterham, R. Wanders, S. Korman, 2002, American journal of human genetics.

A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctata

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1999, Journal of Human Genetics.

A Case of Bloom's Syndrome with Malignant Lymphoma

N. Kondo, T. Takami, T. Orii, 1994 .

Defective Calcium‐Dependent Signal Transduction in T Lymphocytes of Ataxia‐Telangiectasia

S. Nishimura, K. Kasahara, N. Kondo, 1993, Scandinavian journal of immunology.

Competence of B cells for T-cell help in pokeweed mitogen-induced immunoglobulin production.

N. Kondo, H. Uetake, T. Orii, 1983, Clinical immunology and immunopathology.

Literature abstracts

N. Kondo, Yukitoshi Takahashi, P. Wantzin, 2004, Pediatric nephrology (Berlin, West).

Propranolol as an alternative treatment option for pediatric lymphatic malformation.

T. Fukao, N. Kondo, H. Ohnishi, 2013, The Tohoku journal of experimental medicine.

Treatment with OK-432 for persistent congenital chylothorax in newborn infants resistant to octreotide.

N. Kondo, I. Kawabata, N. Kawamoto, 2009, Journal of pediatric surgery.

Aberrant Patterns of Immunoglobulin Levels in Wiskott‐Aldrich Syndrome

N. Kondo, R. Inoue, T. Orii, 1995, Scandinavian journal of immunology.

Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity.

T. Morio, H. Ochs, H. Takada, 2006, Immunity.

Functional assessment of the mutational effects of human IRAK4 and MyD88 genes.

M. Shirakawa, N. Kondo, H. Ohnishi, 2014, Molecular immunology.

[Primary immunodeficiency diseases caused by defects in innate immunity: update].

H. Kaneko, N. Kondo, H. Ohnishi, 2009, Arerugi = [Allergy].

Chediak‐Higashi syndrome with cerebellar cortical atrophy detected by MRI

A. Imamura, N. Shimozawa, N. Kondo, 1994, Clinical genetics.

Autologous peripheral blood stem cell transplantation in a patient with relapsed pleuropulmonary blastoma.

H. Kaneko, N. Kondo, M. Kondo, 2006, Journal of pediatric hematology/oncology.

Magnetic resonance imaging for early detection of bronchial foreign bodies

N. Kondo, R. Inoue, H. Tashita, 1998, European Journal of Pediatrics.

Congenital inner ear malformations without sensorineural hearing loss in children.

H. Kaneko, T. Fukao, N. Kondo, 2009, International journal of pediatric otorhinolaryngology.

Optimized gene synthesis and high expression of human interleukin-18.

Hidenori Ohnishi, Naomi Kondo, N. Kondo, 2003, Protein expression and purification.

Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: Evidence for a founder haplotype for the most common PEX10 gene mutation

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 2003, American journal of medical genetics. Part A.

CLINICAL IMPROVEMENT OF DIFFUSE LYMPHANGIOMATOSIS WITH PEGYLATED INTERFERON ALFA-2B THERAPY: Case Report and Review of the Literature

H. Kaneko, T. Fukao, N. Kondo, 2007, Pediatric hematology and oncology.

Acute mumps cerebellitis with abnormal findings in MRI diffusion-weighted images

T. Asano, H. Kaneko, E. Matsui, 2008, European Journal of Pediatrics.

Interstitial deletion of the short arm of chromosome 10: Report of a case and review of the literature

Naomi Kondo, N. Kondo, Z. Kato, 1996, Japanese Journal of Human Genetics.

Evaluation of Accumulated Mucopolysaccharides in the Brain of Patients with Mucopolysaccharidoses by 1H-Magnetic Resonance Spectroscopy before and after Bone Marrow Transplantation

H. Hoshi, N. Kondo, S. Kato, 2001, Pediatric Research.

Renal Failure and Long-Term Survival in Wiskott-Aldrich Syndrome

N. Kondo, T. Orii, T. Kato, 1994 .

Long-term Study of the IgM Deficiency of Wiskott-Aldrich Syndrome

N. Kondo, Z. Kato, R. Inoue, 1993 .

Facial palsy as an unusual presenting symptom associated with acute myeloid leukemia

T. Asano, T. Fukao, N. Kondo, 2014, Pediatrics international : official journal of the Japan Pediatric Society.

Autosomal-Dominant Chronic Mucocutaneous Candidiasis with STAT1-Mutation can be Complicated with Chronic Active Hepatitis and Hypothyroidism

O. Ohara, Y. Hirose, H. Kaneko, 2012, Journal of Clinical Immunology.

Interleukin‐17 expression in the urticarial rash of familial cold autoinflammatory syndrome: a case report

M. Seishima, N. Kondo, H. Ohnishi, 2010, The British journal of dermatology.

Mutation in the Q28SDD31SD site, but not in the two SQ sites of the survival of motor neuron protein, affects its foci formation.

T. Fukao, N. Kondo, H. Ohnishi, 2010, International journal of molecular medicine.

Failure of IgG production due to a defect in the opening of the chromatin structure of Iγ1 region in a patient with IgG and IgA deficiency

H. Kaneko, K. Kasahara, N. Kondo, 1995, Clinical and experimental immunology.

Relationship between interferon-gamma, interleukin-4 and IgE production of lymphocytes from hen's egg-sensitive patients.

N. Kondo, T. Orii, O. Fukutomi, 1995, Journal of investigational allergology & clinical immunology.

Suppressive effects of elimination diets on T cell responses to ovalbumin in hen's egg‐sensitive atopic dermatitis patients

M. Takemura, Y. Suzuki, N. Shimozawa, 1993, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Molecular analysis of the binding mode of Toll/interleukin-1 receptor (TIR) domain proteins during TLR2 signaling.

M. Shirakawa, N. Kondo, H. Ohnishi, 2012, Molecular immunology.

Paclitaxel‐based chemotherapy for aggressive kaposiform hemangioendothelioma of the temporomastoid region: Case report and review of the literature

Y. Hirose, H. Kaneko, T. Fukao, 2013, Head & neck.

A transient lesion in the corpus callosum during rotavirus infection.

N. Kondo, Z. Kato, K. Orii, 2009, Pediatric neurology.

CpG islands around exon 1 in the succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene are hypomethylated even in human and mouse hepatic tissues where SCOT gene expression is completely suppressed.

T. Fukao, N. Kondo, N. Matsuo, 2010, Molecular medicine reports.

General implications for CpG hot spot mutations: Methylation patterns of the human iduronate‐2‐sulfatase gene locus

W. Sly, K. Orii, N. Kondo, 2004, Human mutation.

Liver-specific silencing of the human gene encoding succinyl-CoA: 3-ketoacid CoA transferase.

G. Mitchell, T. Fukao, N. Kondo, 2008, The Tohoku journal of experimental medicine.

Identification and characterization of a temperature-sensitive R268H mutation in the human succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene.

T. Fukao, N. Kondo, P. Kursula, 2007, Molecular genetics and metabolism.

Single-base substitution at the last nucleotide of exon 6 (c.671G>A), resulting in the skipping of exon 6, and exons 6 and 7 in human succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene.

R. Wanders, T. Fukao, N. Kondo, 2007, Molecular genetics and metabolism.

A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency.

M. Rolland, T. Fukao, N. Kondo, 2006, Molecular genetics and metabolism.

Patients Homozygous for the T435N Mutation of Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Do Not Show Permanent Ketosis

T. Fukao, N. Kondo, H. Shintaku, 2004, Pediatric Research.

Succinyl-CoA:3-ketoacid CoA transferase (SCOT): cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations.

R. Wanders, R. Wanders, G. Besley, 2000, Genomics.

Characterization of infiltrating CD4+ cells in atopic dermatitis using CD45R and CD29 monoclonal antibodies.

N. Kondo, T. Takami, T. Orii, 1994, Annals of allergy.

Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency.

R. Wanders, M. Ugarte, G. Mitchell, 1997, Biochimica et biophysica acta.

PRENATAL DIAGNOSIS OF SUCCINYL‐COENZYME A:3‐KETOACID COENZYME A TRANSFERASE DEFICIENCY

T. Fukao, N. Kondo, H. Shintaku, 1996, Prenatal diagnosis.

Succinyl-CoA:3-ketoacid transferase (SCOT) deficiency in a new patient homozygous for an R217X mutation

N. Longo, K. Gibson, M. Pasquali, 2004, Journal of Inherited Metabolic Disease.

Expression, purification and structural analysis of human IL-18 binding protein: a potent therapeutic molecule for allergy.

M. Shirakawa, N. Kondo, H. Ohnishi, 2008, Allergology international : official journal of the Japanese Society of Allergology.

The structure and binding mode of interleukin-18

Masaki Mishima, Hidenori Ohnishi, Masahiro Shirakawa, 2003, Nature Structural Biology.

Vitamin K-deficient intracranial hemorrhage as the first symptom of cytomegalovirus hepatitis with cholestasis.

T. Fukao, N. Kondo, R. Inoue, 2007, The Tohoku journal of experimental medicine.

MR imaging findings of cervical lymphadenopathy in patients with Kikuchi disease.

M. Kanematsu, H. Hoshi, H. Kato, 2011, European journal of radiology.

Pediatric acute lymphoblastic leukemia mimicking Henoch–Schönlein purpura

H. Kaneko, T. Fukao, N. Kondo, 2011, Pediatrics international : official journal of the Japan Pediatric Society.

Mucopolysaccharidosis IVA: structural gene alterations identified by Southern blot analysis and identification of racial differences

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1995, Human Genetics.

Mucopolysaccharidosis IVA: a comparative study of polymorphic DNA haplotypes in the Caucasian and Japanese populations

Y. Suzuki, N. Shimozawa, N. Kondo, 1996, Journal of Inherited Metabolic Disease.

Mucopolysaccharidosis IVA: four new exonic mutations in patients with N-acetylgalactosamine-6-sulfate sulfatase deficiency.

Y. Suzuki, N. Shimozawa, N. Kondo, 1996, American journal of human genetics.

Mucopolysaccharidosis type IVA: common double deletion in the N-acetylgalactosamine-6-sulfatase gene (GALNS).

Y. Suzuki, N. Shimozawa, N. Kondo, 1995, Genomics.

Lymphocyte responses to food antigens in food sensitive patients with allergic tension-fatigue syndrome

N. Kondo, H. Fujii, T. Orii, 1992, Biotherapy.

Suppression of IgA production by lymphocytes induced by diphenylhydantoin.

Y. Suzuki, N. Shimozawa, N. Kondo, 1994, Journal of investigational allergology & clinical immunology.

Missense models [Gustm(E536A)Sly, Gustm(E536Q)Sly, and Gustm(L175F)Sly] of murine mucopolysaccharidosis type VII produced by targeted mutagenesis

W. Sly, J. Grubb, K. Orii, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Reversible cerebrospinal fluid edema and porencephalic cyst, a rare complication of ventricular catheter

T. Asano, H. Kaneko, T. Fukao, 2010, Journal of Clinical Neuroscience.

The mouse N-acetylgalactosamine-6-sulfate sulfatase (Galns) gene: cDNA isolation, genomic characterization, chromosomal assignment and analysis of the 5'-flanking region.

N. Copeland, D. Gilbert, N. Jenkins, 2000, Biochimica et biophysica acta.

Molecular analysis by Southern blot for theN-acetylgalactosamine-6-sulphate sulphatase gene causing mucopolysaccharidosis IVA in the Japanese population

Y. Suzuki, N. Shimozawa, N. Kondo, 1994, Journal of Inherited Metabolic Disease.

Two new mutations, Q473X and N487S, in a caucasian patient with mucopolysaccharidosis IVA (Morquio disease)

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1995, Human mutation.

A novel splice site mutation in intron 1 of the GALNS gene in a Japanese patient with mucopolysaccharidosis IVA.

Y. Suzuki, N. Shimozawa, N. Kondo, 1994, Human molecular genetics.

Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region.

Y. Suzuki, N. Shimozawa, N. Kondo, 1994, Genomics.

Mouse model of N-acetylgalactosamine-6-sulfate sulfatase deficiency (Galns-/-) produced by targeted disruption of the gene defective in Morquio A disease.

W. Sly, J. Grubb, K. Orii, 2003, Human molecular genetics.

Mouse model of N -acetylgalactosamine-6-sulfate sulfatase deﬁciency ( Galns (cid:1) / (cid:1) ) produced by targeted disruption of the gene defective in Morquio A disease

W. Sly, J. Nakayama, K. Orii, 2003 .

Polymerase chain reaction detection of two novel human N-acetylgalactosamine-6-sulfate sulfatase gene polymorphisms by single-strand conformation polymorphism analysis or by StyI and StuI cleavages

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1995, Human Genetics.

Mucopolysaccharidosis type I: Identification of common mutations that cause Hurler and Scheie syndromes in Japanese populations

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1996, Human mutation.

[Mucopolysaccharidosis type II (Hunter syndrome)].

N. Kondo, S. Tomatsu, T. Orii, 1998, Ryoikibetsu shokogun shirizu.

Keratan sulphate levels in mucopolysaccharidoses and mucolipidoses

T. Taketani, J. Grubb, R. Giugliani, 2005, Journal of Inherited Metabolic Disease.

Transient Lesion in the Splenium of the Corpus Callosum in Acute Cerebellitis

N. Kondo, Z. Kato, Kazuyuki Hashimoto, 2003, Journal of child neurology.

Acute cerebellitis associated with rotavirus infection

T. Asano, N. Kondo, Z. Kato, 2013, World Journal of Pediatrics.

Interaction among human leucocyte antigen–peptide–T cell receptor complexes in cow's milk allergy: the significance of human leucocyte antigen and T cell receptor–complementarity determining region 3 loops

S. Matsushita, H. Kaneko, N. Kondo, 2002, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Expression of the Alpha‐Chain Gene in Heterogeneous IgA Immunodeficiency

H. Kaneko, N. Kondo, T. Orii, 1990, Scandinavian journal of immunology.

Lipocalin-type prostaglandin D synthase and egg white cystatin react with IgE antibodies from children with egg allergy.

M. Seishima, Kuniaki Saito, M. Kimoto, 2010, Allergology international : official journal of the Japanese Society of Allergology.

An alternative form of nucleolysin binds to a T-cluster DNA in the silencer element of platelet factor 4 gene.

H. Aburatani, T. Kodama, N. Kondo, 1997, Biochemical and biophysical research communications.

Various Expression Patterns of α1 and α2 Genes in IgA Deficiency.

H. Kaneko, E. Matsui, T. Fukao, 2009, Allergology international : official journal of the Japanese Society of Allergology.

A Complement Factor B Mutation in a Large Kindred with Atypical Hemolytic Uremic Syndrome

O. Ohara, H. Kaneko, N. Kondo, 2014, Journal of Clinical Immunology.

Accelerated expression of secreted alpha-chain gene in anaphylactoid purpura.

K. Kasahara, N. Kondo, T. Orii, 1992, Journal of Clinical Immunology.

In Vitro Analysis of the Functional Effects of an NLRP3 G809S Variant with the co-Existence of MEFV Haplotype Variants in Atypical Autoinflammatory Syndrome

H. Kaneko, E. Matsui, N. Kondo, 2013, Journal of Clinical Immunology.

Pulmonary hemosiderosis with hypersensitivity to buckwheat.

M. Takemura, N. Kondo, M. Shinbara, 1997, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Escherichia coli O‐157‐induced hemolytic uremic syndrome: Usefulness of SCWP score for the prediction of neurological complication

T. Fukao, N. Kondo, Takahide Teramoto, 2009, Pediatrics international : official journal of the Japan Pediatric Society.

Reduced secreted mu mRNA synthesis in selective IgM deficiency of Bloom's syndrome.

K. Kasahara, N. Kondo, T. Orii, 1992, Clinical and experimental immunology.

Development of MLPA for human ACAT1 gene and identification of a heterozygous Alu-mediated deletion of exons 3 and 4 in a patient with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency.

R. Wierenga, T. Fukao, N. Kondo, 2013, Molecular genetics and metabolism.

Interstitial deletion of the long arm of chromosome 11: Report of a case and review of the literature

N. Kondo, S. Yamaguchi, M. Masuno, 1992, Japanese Journal of Human Genetics.

Neuroradiologic Findings in Sotos Syndrome

T. Asano, N. Matsumoto, N. Kondo, 2006, Journal of child neurology.

Common Variable Immunodeficiency with Increased Surface igM‐Positive Double‐Bearing B Cells

M. Takemura, N. Kondo, A. Noma, 1992, Scandinavian journal of immunology.

Successful treatment of pediatric immune thrombocytopenic purpura associated with ulcerative colitis

H. Kaneko, T. Fukao, N. Kondo, 2011, Pediatrics international : official journal of the Japan Pediatric Society.

A novel single-nucleotide substitution, Glu 4 Lys, in the leukotriene C4 synthase gene associated with allergic diseases.

H. Kaneko, E. Matsui, T. Fukao, 2005, International journal of molecular medicine.

Prediction of the pathogenesis of the mutation in MeCP2 C-terminal domain

N. Kondo, H. Ohnishi, Z. Kato, 2010, Brain and Development.

New Methods for Clinical Proteomics in Allergy

N. Kondo, Z. Kato, Zenichiro Kato, 2005 .

Microsatellite instability in B‐cell lymphoma originating from Bloom syndrome

H. Kaneko, T. Fukao, K. Kasahara, 1996, International journal of cancer.

Impaired natural killer cell activity in Bloom's syndrome could be restored by human recombinant IL-2 in vitro.

T. Miyawaki, N. Kondo, H. Takahashi, 1985, Clinical immunology and immunopathology.

The clinical course of childhood and adolescent adrenoleukodystrophy before and after Lorenzo's oil

A. Imamura, N. Shimozawa, N. Kondo, 2001, Brain and Development.

Protein-losing enteropathy associated with egg allergy in a 5-month-old boy.

H. Kaneko, T. Fukao, N. Kondo, 2008, Journal of investigational allergology & clinical immunology.

Inhibition of proliferative responses of lymphocytes to food antigens by an anti‐allergic drug, N(3′,4′‐dimethoxycinnamoyl) anthranilic acid (Tranilast) in children with atopic dermatitis

N. Kondo, T. Orii, O. Fukutomi, 1992, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Abnormal responses of the autonomic nervous system in food-dependent exercise-induced anaphylaxis.

N. Kondo, M. Shinbara, T. Orii, 1992, Annals of allergy.

D-bifunctional protein deficiency with fetal ascites, polyhydramnios, and contractures of hands and toes.

S. Takashima, Y. Suzuki, N. Shimozawa, 2001, The Journal of pediatrics.

Biochemical and immunocytochemical properties of peroxisomes and mitochondria in bovine chromaffin cells.

Y. Suzuki, N. Shimozawa, N. Kondo, 1997, Cell structure and function.

Characterization of N93S, I312T, and A333P missense mutations in two Japanese families with mitochondrial acetoacetyl‐CoA thiolase deficiency

T. Hashimoto, T. Fukao, N. Kondo, 1998, Human mutation.

Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase / D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency

S. Toda, T. Hashimoto, S. Takashima, 1999, Journal of Human Genetics.

Kinetic and expression analyses of seven novel mutations in mitochondrial acetoacetyl-CoA thiolase (T2): identification of a Km mutant and an analysis of the mutational sites in the structure.

R. Wierenga, R. Wanders, G. Mitchell, 2007, Molecular genetics and metabolism.

Production of MPS VII mouse (Gus(tm(hE540A x mE536A)Sly)) doubly tolerant to human and mouse beta-glucuronidase.

W. Sly, J. Grubb, K. Orii, 2003, Human molecular genetics.

Short latency somatosensory evoked potentials and 99mTc-HMPAO SPECT in a case of flunarizine-effective alternating hemiplegia in infancy

A. Imamura, N. Shimozawa, Yasuyuki Suzuki, 1994, Brain and Development.

Preferential Damage to IgM Production by Ultraviolet B in the Cells of Patients with Bloom's Syndrome

N. Kondo, T. Orii, T. Ozawa, 1993, Scandinavian journal of immunology.

Suppressive Effects of an Anti-allergic Drug: Azelastine Hydrochloride on Interferon-γ Production of Lymphocytes to Food Antigens in Patients with Food-sensitive Atopic Dermatitis

N. Kondo, T. Orii, O. Fukutomi, 1993 .

A novel single-nucleotide substitution, Leu 467 Pro, in the interferon-gamma receptor 1 gene associated with allergic diseases.

Yasuyuki Suzuki, H. Kaneko, E. Matsui, 2003, International journal of molecular medicine.

Urinary organic acids in peroxisomal disorders: a simple screening method.

Y. Suzuki, N. Shimozawa, T. Fukao, 2001, Journal of chromatography. B, Biomedical sciences and applications.

Genomic DNA organization of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis.

T. Hashimoto, T. Aoyama, N. Kondo, 1995, Biochemical and biophysical research communications.

Genetic defects in downregulation of IgE production and a new genetic classification of atopy

H. Kaneko, E. Matsui, T. Fukao, 2004 .

Proliferative responses towards native, heat-denatured and pepsin-treated ovalbumin by peripheral blood mononuclear cells from patients with hen's egg-sensitive atopic dermatitis

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1994, Biotherapy.

Ataxia telangiectasia associated with B-cell lymphoma: the effect of a half-dose of the drugs administered according to the acute lymphoblastic leukemia standard risk protocol.

Y. Suzuki, N. Shimozawa, H. Kaneko, 1998, Pediatric hematology and oncology.

High regression rate of coronary aneurysms developed in patients with immune globulin-resistant Kawasaki disease treated with steroid pulse therapy.

T. Fukao, N. Kondo, T. Kuwahara, 2010, The Tohoku journal of experimental medicine.

Interleukin-18 is associated with the severity of atopic dermatitis

N. Kondo, H. Ohnishi, Z. Kato, 2003 .

Theophylline-associated status epilepticus in an infant: pharmacokinetics and the risk of suppository use

N. Kondo, Z. Kato, Mitsuhiro Nakamura, 2009, World Journal of Pediatrics.

Intrinsic factors for unbound theophylline.

N. Kondo, Z. Kato, O. Fukutomi, 2002, Journal of investigational allergology & clinical immunology.

Developmental changes of unbound theophylline.

N. Kondo, O. Fukutomi, Z. Kato, 1998, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Prediction of steady-state serum theophylline concentration in children by first-order and zero-order absorption models.

N. Kondo, N. Imaeda, T. Orii, 1994, International journal of clinical pharmacology and therapeutics.

Frontometaphyseal dysplasia: patient with ruptured aneurysm of the aortic sinus of Valsalva and cerebral aneurysms.

N. Kondo, Kazuhiro Takahashi, T. Kuwahara, 2002, American journal of medical genetics.

Induction of α1 and α2 gene expression in selective immunoglobulin A deficiency.

H. Kaneko, E. Matsui, T. Fukao, 2008, Molecular medicine reports.

[Newly identified peroxisomal disorders].

A. Imamura, Y. Suzuki, N. Shimozawa, 1999, No to shinkei = Brain and nerve.

Peroxisomal acyl CoA oxidase deficiency.

Yasuhiko Takemoto, Atsushi Kamei, Naomi Kondo, 2020, The Journal of pediatrics.

Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies

T. Tsukamoto, N. Shimozawa, T. Osumi, 2006, Brain and Development.

Crystallographic and kinetic studies of human mitochondrial acetoacetyl-CoA thiolase: the importance of potassium and chloride ions for its structure and function.

R. Wierenga, A. Haapalainen, T. Fukao, 2007, Biochemistry.

Assignment of the human cytosolic acetoacetyl-coenzyme A thiolase (ACAT2) gene to chromosome 6q25.3-q26.

M. Masuno, Y. Kuroki, N. Kondo, 1996, Genomics.

Characterization of NLRP3 Variants in Japanese Cryopyrin-Associated Periodic Syndrome Patients

H. Kaneko, N. Kondo, H. Ohnishi, 2012, Journal of Clinical Immunology.

Long-Term Study of a Female Hyper-IgM Immunodeficiency

H. Kaneko, E. Matsui, T. Fukao, 2000, Experimental and Clinical Immunogenetics.

Abnormal B cell response of protein kinase C in some common variable immunodeficiency.

H. Kaneko, N. Kondo, T. Teramoto, 1996, Experimental and clinical immunogenetics.

Incidence of peroxisomal disorders in Japan

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1996, The Japanese Journal of Human Genetics.

Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case

H. Kaneko, E. Matsui, T. Fukao, 2004, Clinical genetics.

Analysis of Ig subclass deficiency: First reported case of IgG2, IgG4, and IgA deficiency caused by deletion of C alpha 1, psi C gamma, C gamma 2, C gamma 4, and C epsilon in a Mongoloid patient.

H. Kaneko, K. Kasahara, N. Kondo, 2001, The Journal of allergy and clinical immunology.

Topical Review: Molecular and Neurologic Findings of Peroxisome Biogenesis Disorders

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 2004, Journal of child neurology.

Refractory Chronic Pleurisy Caused by Helicobacter equorum-Like Bacterium in a Patient with X-Linked Agammaglobulinemia

H. Kaneko, T. Fukao, N. Kondo, 2011, Journal of Clinical Microbiology.

Myopathic Form of Very-Long Chain Acyl-CoA Dehydrogenase Deficiency: Evidence for Temperature-Sensitive Mild Mutations in Both Mutant Alleles in a Japanese Girl

T. Aoyama, T. Fukao, N. Kondo, 2001, Pediatric Research.

Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes.

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 2004, Biochimica et biophysica acta.

Clinical and bacteriological evaluation of the efficacy of piperacillin in children with pneumonia

M. Seishima, H. Kaneko, T. Fukao, 2007, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient.

R. Wanders, A. Imamura, Y. Suzuki, 2000, Biochemical and biophysical research communications.

A family having type 2B von Willebrand disease with an R1306W mutation: Severe thrombocytopenia leads to the normalization of high molecular weight multimers.

H. Kaneko, T. Fukao, K. Kasahara, 2010, Thrombosis research.

Various responses of lymphocytes to Epstein-Barr virus in patients with common variable immunodeficiency.

N. Kondo, T. Orii, R. Inoue, 1992, Journal of clinical & laboratory immunology.

Accidental Etizolam Ingestion in a Child

N. Kondo, Z. Kato, Mitsuhiro Nakamura, 2007, Pediatric emergency care.

Changes of Autonomic Nervous System Function in Patients With Breath-Holding Spells Treated With Iron

N. Shimozawa, N. Kondo, Z. Kato, 2002, Journal of child neurology.

Efficacy of the slow dose-up method for specific oral tolerance induction in children with cow's milk allergy: comparison with reported protocols.

H. Kaneko, E. Matsui, N. Kondo, 2010, Journal of investigational allergology & clinical immunology.

Lysinuric protein intolerance in siblings: complication of systemic lupus erythematosus in the elder sister

Yasuyuki Suzuki, T. Fukao, N. Kondo, 2001, European Journal of Pediatrics.

Portal hypertension in a patient with Hunter disease

I. Kuratsubo, Yasuyuki Suzuki, K. Orii, 2006, Journal of Inherited Metabolic Disease.

Correction by Gene Expression of Biochemical Abnormalities in Fibroblasts from Zellweger Patients

T. Tsukamoto, T. Hashimoto, K. Kamijo, 1996, Pediatric Research.

Improvement of neurological symptoms by enzyme replacement therapy for Gaucher disease type IIIb

N. Kondo, Yukitoshi Takahashi, T. Orii, 2001, European Journal of Pediatrics.

Prenatal diagnosis of peroxisomal disorders Biochemical and immunocytochemical studies on peroxisomes in human amniocytes

N. Shimozawa, Yasuyuki Suzuki, N. Kondo, 1994, Brain & development (Tokyo. 1979).

Pediatric synovial sarcoma of the right masseter muscle: A case report

H. Kaneko, T. Fukao, N. Kondo, 2008 .

Use of buccal smears for rapid detection of peroxisomes.

Y. Suzuki, N. Shimozawa, N. Kondo, 1997, European journal of pediatrics.

Peripheral blood stem cell transplantation in a significant body weight difference between a smaller donor and a larger recipient: a case report.

H. Kaneko, N. Kondo, Kazuo Kubota, 2013, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Parents of childhood X-linked adrenoleukodystrophy: High risk for depression and neurosis

I. Kuratsubo, N. Shimozawa, Yasuyuki Suzuki, 2008, Brain and Development.

Apparition of iodinated contrast agents in twin neonatal gastrointestinal tracts after maternal contrast-enhanced computed tomography

M. Kanematsu, H. Kato, N. Kondo, 2011, Japanese Journal of Radiology.

Glycosaminoglycans in neonatal urine

N. Kondo, S. Tomatsu, T. Orii, 2000, Archives of Disease in Childhood: Fetal and Neonatal Edition.

Bacterial meningitis and septicemia of neonate due to Lactococcus lactis

N. Kondo, H. Morita, T. Taga, 2011, Pediatrics international : official journal of the Japan Pediatric Society.

Long-term duration of reduced serum complement level following burn injury.

H. Kaneko, N. Kondo, K. Orii, 2001, Journal of investigational allergology & clinical immunology.

Hypoallergenic casein hydrolysate for peptide-based oral immunotherapy in cow's milk allergy.

H. Kaneko, N. Kondo, H. Ohnishi, 2018, The Journal of allergy and clinical immunology.

Oral immunotherapy with antigenicity‐modified casein induces desensitization in cow’s milk allergy

H. Kaneko, E. Matsui, T. Fukao, 2020, Allergy. European Journal of Allergy and Clinical Immunology.

Identification of an Alu-mediated tandem duplication of exons 8 and 9 in a patient with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency.

M. Rolland, T. Fukao, N. Kondo, 2007, Molecular genetics and metabolism.

Evaluation of patch test with dimethylsulfoxide in association with lymphocyte proliferation in food-sensitive atopic dermatitis

N. Kondo, T. Orii, O. Fukutomi, 1993 .

T cell proliferation restricted by HLA class II molecules in patients with hen's egg allergy.

N. Kondo, M. Shinbara, T. Orii, 1995, Experimental and Clinical Immunogenetics.

High resolution crystal structures of human cytosolic thiolase (CT): a comparison of the active sites of human CT, bacterial thiolase, and bacterial KAS I.

R. Wierenga, T. Fukao, N. Kondo, 2005, Journal of molecular biology.

Autonomic regulation after exercise evidenced by spectral analysis of heart rate variability in asthmatic children.

M. Seishima, N. Kondo, K. Saito, 2000, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Vaccination and Infection as Causative Factors in Japanese Patients With Rasmussen Syndrome: Molecular Mimicry and HLA Class I

H. Osaka, A. Imamura, N. Kondo, 2006, Clinical & developmental immunology.

The autoimmune TCR-Ob.2F3 can bind to MBP85-99/HLA-DR2 having an unconventional mode as in TCR-Ob.1A12.

Hironori K. Nakamura, J. Strominger, N. Kondo, 2010, Molecular immunology.

1H, 13C, and 15N resonance assignment of the TIR domain of human MyD88

M. Shirakawa, N. Kondo, H. Ohnishi, 2010, Biomolecular NMR assignments.

TRAM Is Involved in IL-18 Signaling and Functions as a Sorting Adaptor for MyD88

M. Shirakawa, N. Kondo, H. Ohnishi, 2012, PloS one.

A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome.

H. Kaneko, N. Kondo, H. Ohnishi, 2012, The Journal of allergy and clinical immunology.

Functions of T cells and B cells of a (hypo)-gammaglobulinemia patients in pokeweed mitogen induced immunoglobulin production system

N. Kondo, T. Orii, Y. Kuno, 1982 .

N. Kondo, Y. Aoyama, Y. Kitajima, 2007, Archives of dermatology.