Zenichiro Kato

发表

Proton Magnetic Resonance Spectroscopy in a Case of Subacute Sclerosing Panencephalitis

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

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

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

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.

Trial of intraventricular ribavirin therapy for subacute sclerosing panencephalitis in Japan

M. Hosoya, A. Tomoda, T. Miike, 2003, Brain and Development.

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

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

Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: Nine novel mutations including T312S, a common allele that confers a mild phenotype

J. Hopwood, Z. Kato, S. Fukuda, 1998, Human mutation.

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

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

Established Stem Cell Model of Spinal Muscular Atrophy Is Applicable in the Evaluation of the Efficacy of Thyrotropin‐Releasing Hormone Analog

H. Hara, Z. Kato, M. Shimazawa, 2016, Stem cells translational medicine.

Clinical and Radiological Features of Rotavirus Cerebellitis

A. Barkovich, J. Takanashi, M. Kikuchi, 2010, American Journal of Neuroradiology.

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.

Thyroid cancer in a case with the Alagille syndrome

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

Alanine‐scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss‐ or gain‐of‐function variants

J. Casanova, O. Ohara, A. Bousfiha, 2017, The Journal of allergy and clinical immunology.

Gain-of-function IKBKB mutation causes human combined immune deficiency

T. Andrews, S. Miyano, M. Field, 2018, The Journal of experimental medicine.

Fifty microdeletions among 112 cases of Sotos syndrome: Low copy repeats possibly mediate the common deletion

Jan-Fang Cheng, Naomichi Matsumoto, Kenji Kurosawa, 2003, Human mutation.

IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation

J. Casanova, O. Ohara, C. Picard, 2020, Journal of clinical immunology.

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].

Human anti-human IL-18 antibody recognizing the IL-18-binding site 3 with IL-18 signaling blocking activity.

Kenji Nakanishi, Yuji Ito, K. Sugimura, 2005, Journal of biochemistry.

Acute cerebellitis in primary human herpesvirus-6 infection

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

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 .

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

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

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.

Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency.

O. Ohara, S. Miyano, Y. Shiraishi, 2016, The Journal of allergy and clinical immunology.

Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan

M. V. van Zelm, H. Kanegane, T. Morio, 2022, Journal of Clinical Immunology.

Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases

H. Kanegane, S. Okada, M. Tsumura, 2022, Journal of Clinical Immunology.

Glucose metabolism evaluated by positron emission tomography in Lafora disease

K. Ishii, N. Shimozawa, Shinji Mizuno, 1999, Pediatrics international : official journal of the Japan Pediatric Society.

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.

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.

ADA‐SCID with ‘WAZA‐ARI’ mutations that synergistically abolished ADA protein stability

O. Ohara, M. Yamada, I. Kobayashi, 2011, British journal of haematology.

Molluscum contagiosum prevents progression of staphylococcal scalded skin syndrome

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

Amino acid copolymer-specific IL-10-secreting regulatory T cells that ameliorate autoimmune diseases in mice

D. Keskin, J. Strominger, Hong Zhang, 2008, Proceedings of the National Academy of Sciences.

Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L

S. Tsujino, M. Kaga, A. Imamura, 2003, Brain and Development.

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.

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.

Mucopolysaccharidosis IVA: identification of a common missense mutation I113F in the N-Acetylgalactosamine-6-sulfate sulfatase gene.

S. Fukuda, S. Tomatsu, K. Isogai, 1995, American journal of human genetics.

Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS gene

W. Sly, N. Shimozawa, Yasuyuki Suzuki, 1997, Human mutation.

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.

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.

HLA-DQ and RBFOX1 as susceptibility genes for an outbreak of hydrolyzed wheat allergy.

R. Kishikawa, Y. Kamatani, Y. Okada, 2019, The Journal of allergy and clinical immunology.

Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3

O. Ohara, H. Kanegane, T. Morio, 2021, Journal of Clinical Immunology.

A case of selective IgG subclass deficiency with STAT3 mutation.

O. Ohara, H. Kaneko, T. Fukao, 2016, Allergology international : official journal of the Japanese Society of Allergology.

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.

A transient lesion in the corpus callosum during rotavirus infection.

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

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

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

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.

The structural basis for receptor recognition of human interleukin-18

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

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

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

Promoting tolerance to proteolipid protein-induced experimental autoimmune encephalomyelitis through targeting dendritic cells

D. Keskin, J. Strominger, K. Kretschmer, 2010, Proceedings of the National Academy of Sciences.

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.

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.

The structure and binding mode of interleukin-18

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

Analysis of Neuropsychiatric Adverse Events in Patients Treated with Oseltamivir in Spontaneous Adverse Event Reports.

Y. Kinosada, Z. Kato, Ryogo Umetsu, 2015, Biological & pharmaceutical bulletin.

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.

Outbreak of immediate‐type hydrolyzed wheat protein allergy due to a facial soap in Japan

R. Kishikawa, R. Teshima, Z. Ikezawa, 2017, 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.

Analysis of the Association between Neuraminidase Inhibitors and Neuropsychiatric Adverse Events Using Japanese Adverse Drug Event Report (JADER)

Y. Kinosada, Z. Kato, Yumi Motooka, 2016 .

Interleukin-18 is associated with the severity of atopic dermatitis

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

Analysis of Stevens-Johnson syndrome and toxic epidermal necrolysis using the Japanese Adverse Drug Event Report database

Y. Kinosada, H. Hara, Z. Kato, 2016, Journal of Pharmaceutical Health Care and Sciences.

An innate interaction between IL-18 and the propeptide that inactivates its precursor form

M. Shirakawa, T. Fukao, H. Ohnishi, 2019, Scientific Reports.

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.

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

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

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.

New quantitative method for evaluation of motor functions applicable to spinal muscular atrophy

T. Ichinomiya, N. Matsumaru, K. Tsukamoto, 2018, Brain and Development.

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.

A Novel Homozygous Mutation Destabilizes IKKβ and Leads to Human Combined Immunodeficiency

H. Kanegane, S. Okada, M. Tsumura, 2021, Frontiers in Immunology.

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.

Fifteen polymorphisms in the N‐acetylgalactosamine‐6‐sulfate sulfatase (GALNS) gene: Diagnostic implications in morquio disease

N. Shimozawa, Yasuyuki Suzuki, Z. Kato, 1998, Human mutation.

Mucopolysaccharidosis IVA (Morquio A): Three novel small deletions in the N‐acetylgalactosamine‐6‐sulfate sulfatase gene

S. Fukuda, S. Tomatsu, T. Orii, 1996, Human mutation.

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

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

Amino acid copolymer-specific IL-10-secreting regulatory T cells that ameliorate autoimmune diseases in mice

D. Keskin, J. Strominger, Hong Zhang, 2008, Proceedings of the National Academy of Sciences.

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.

New Methods for Clinical Proteomics in Allergy

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

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.

Genetics of Pediatric Asthma

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

Computed Tomographic Findings of Kawasaki Disease With Cervical Lymphadenopathy

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

Neuroradiologic Findings in Sotos Syndrome

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

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.

Magnetic resonance spectroscopy of tubers in patients with tuberous sclerosis

H. Hoshi, N. Kondo, Shinji Mizuno, 2000, Acta neurologica Scandinavica.

Pediatric acute lymphoblastic leukemia mimicking Henoch–Schönlein purpura

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

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.

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.