S. Fukuda

发表

Essential Role of Signal Transducer and Activator of Transcription (Stat)5a but Not Stat5b for Flt3-Dependent Signaling

W. Leonard, H. Broxmeyer, Younghee Lee, 2000, The Journal of experimental medicine.

Study of deep intronic sequence exonization in a Japanese neonate with a mitochondrial trifunctional protein deficiency.

T. Fukao, S. Fukuda, J. Purevsuren, 2008, Molecular genetics and metabolism.

Metabolic disease in 10 patients with sudden unexpected death in infancy or acute life‐threatening events

T. Taketani, S. Fukuda, Y. Hasegawa, 2015, Pediatrics international : official journal of the Japan Pediatric Society.

Stromal cell-derived factor-1alpha/CXCL12-induced chemotaxis of T cells involves activation of the RasGAP-associated docking protein p62Dok-1.

Seiji Fukuda, Pier Paolo Pandolfi, P. Pandolfi, 2005, Blood.

The Human Immunodeficiency Virus Protease Inhibitor Ritonavir Inhibits Lung Cancer Cells, in Part, by Inhibition of Survivin

A. Srirangam, A. Rizzardi, D. Potter, 2011, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Neutrophil-derived MMP-9 mediates synergistic mobilization of hematopoietic stem and progenitor cells by the combination of G-CSF and the chemokines GRObeta/CXCL2 and GRObetaT/CXCL2delta4.

S. Fukuda, L. Pelus, H. Bian, 2004, Blood.

Neutrophil-derived MMP-9 mediates synergistic mobilization of hematopoietic stem and progenitor cells by the combination of G-CSF and the chemokines GROβ/CXCL2 and GROβT /CXCL2Δ4

S. Fukuda, L. Pelus, H. Bian, 2004 .

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.

Transmigration of human CD34+ cells.

S. Fukuda, L. Pelus, 2008, Methods in molecular biology.

a functionally distinct subunit in human hematopoietic progenitors c-kit associated with the transmembrane 4 superfamily proteins constitutes

H. Broxmeyer, C. Mantel, Young‐June Kim, 2013 .

C-kit associated with the transmembrane 4 superfamily proteins constitutes a functionally distinct subunit in human hematopoietic progenitors.

M. Akashi, H. Broxmeyer, C. Mantel, 2002, Blood.

implication of survivin expression in normal hematopoiesis blood and bone marrow CD34+ cells by hematopoietic growth factors: Regulation of the inhibitor-of-apoptosis family member survivin in normal cord

S. Fukuda, L. Pelus, 2013 .

Regulation of the inhibitor-of-apoptosis family member survivin in normal cord blood and bone marrow CD34(+) cells by hematopoietic growth factors: implication of survivin expression in normal hematopoiesis.

S. Fukuda, L. Pelus, 2001, Blood.

Flt3 ligand and the Flt3 receptor regulate hematopoietic cell migration by modulating the SDF-1alpha(CXCL12)/CXCR4 axis.

H. Broxmeyer, S. Fukuda, L. Pelus, 2005, Blood.

Survivin Is Required for Mouse and Human Bone Marrow Mesenchymal Stromal Cell Function

S. Fukuda, Pratibha Singh, Liqiong Liu, 2018, Stem cells.

cells: a source of karyotpic instability Checkpoint-apoptosis uncoupling in human and mouse embryonic stem

H. Broxmeyer, Ying Guo, C. Mantel, 2013 .

Checkpoint-apoptosis uncoupling in human and mouse embryonic stem cells: a source of karyotpic instability.

H. Broxmeyer, Ying Guo, C. Mantel, 2007, Blood.

Trafficking of Acute Leukemia Cells – Chemokine Receptor Pathways that Modulate Leukemia Cell Dissemination

S. Fukuda, L. Pelus, Chie Onishi, 2011 .

Activated H-Ras regulates hematopoietic cell survival by modulating Survivin.

S. Fukuda, L. Pelus, 2004, Biochemical and biophysical research communications.

Disruption of the inhibitor of apoptosis protein survivin sensitizes Bcr-abl-positive cells to STI571-induced apoptosis.

J. Sampath, S. Fukuda, Zhanxiang Wang, 2005, Cancer research.

Sulfated disaccharide inhibitors of L-selectin: deriving structural leads from a physiological selectin ligand.

C. Bertozzi, S. Fukuda, S. Rosen, 1995, Biochemistry.

Src kinase, but not the src kinase family member p56lck, mediates stromal cell-derived factor 1alpha/CXCL12-induced chemotaxis of a T cell line.

H. Broxmeyer, S. Okabe, S. Fukuda, 2002, Journal of hematotherapy & stem cell research.

Effect of plasmapheresis on familial type III hyperlipoproteinemia associated with glomerular lipidosis, nephrotic syndrome and diabetes mellitus

M. Shichiri, Kiyoshi Takahashi, S. Fukuda, 1990 .

Mucopolysaccharidosis type VII: characterization of mutations and molecular heterogeneity.

T. Sasaki, S. Fukuda, S. Yamaguchi, 1991, American journal of human genetics.

Efficacy of bezafibrate on fibroblasts of glutaric acidemia type II patients evaluated using an in vitro probe acylcarnitine assay

T. Taketani, S. Fukuda, J. Purevsuren, 2017, Brain and Development.

Clinical and molecular aspects of Japanese children with medium chain acyl-CoA dehydrogenase deficiency.

T. Fukao, S. Fukuda, J. Purevsuren, 2012, Molecular genetics and metabolism.

Effect of heat stress and bezafibrate on mitochondrial β-oxidation: Comparison between cultured cells from normal and mitochondrial fatty acid oxidation disorder children using in vitro probe acylcarnitine profiling assay

S. Fukuda, J. Purevsuren, Y. Hasegawa, 2010, Brain and Development.

Heat stress deteriorates mitochondrial beta-oxidation of long-chain fatty acids in cultured fibroblasts with fatty acid beta-oxidation disorders.

S. Fukuda, J. Purevsuren, Y. Hasegawa, 2010, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Blockade of prostaglandin E2 signaling through EP1 and EP3 receptors attenuates Flt3L-dependent dendritic cell development from hematopoietic progenitor cells.

R. Breyer, J. Speth, S. Fukuda, 2012, Blood.

The chemokine GRObeta mobilizes early hematopoietic stem cells characterized by enhanced homing and engraftment.

S. Fukuda, L. Pelus, H. Bian, 2007, Blood.

Acetylated low-density lipoprotein is endocytosed through coated pits by rat peritoneal macrophages

Y. Morino, S. Horiuchi, Kiyoshi Takahashi, 1986, Virchows Archiv. B, Cell pathology including molecular pathology.

Peripheral blood stem cell mobilization: the CXCR2 ligand GRObeta rapidly mobilizes hematopoietic stem cells with enhanced engraftment properties.

S. Fukuda, L. Pelus, 2006, Experimental hematology.

Internal tandem duplication of Flt3 modulates chemotaxis and survival of hematopoietic cells by SDF1alpha but negatively regulates marrow homing in vivo.

S. Fukuda, L. Pelus, 2006, Experimental hematology.

Fatal pulmonary arterial hypertension in an infant girl with incontinentia pigmenti

T. Taketani, S. Fukuda, S. Yamaguchi, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

ENDOCYTIC PATHWAY OF ACETYLATED LOW-DENSITY LIPOPROTEIN IN RAT PERITONEAL MACROPHAGES

S. Horiuchi, Kiyoshi Takahashi, S. Fukuda, 1986 .

Clinical Features of Carnitine Deficiency Secondary to Pivalate-Conjugated Antibiotic Therapy.

S. Fukuda, J. Purevsuren, Y. Hasegawa, 2016, The Journal of pediatrics.

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.

Blockade of prostaglandin E 2 signaling through EP1 and EP3 receptors attenuates Flt3L-dependent dendritic cell development from hematopoietic progenitor cells

R. Breyer, J. Speth, S. Fukuda, 2012 .

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.

Induced Integrin Activation - H-Ras Is Involved in the Inside-out Signaling Pathway of Interleukin-3

S. Braun, C. Mantel, S. Fukuda, 2013 .

H-Ras is involved in the inside-out signaling pathway of interleukin-3-induced integrin activation.

S. Braun, H. Broxmeyer, C. Mantel, 1999, Blood.

Mucopolysaccharidosis type IVA. N-acetylgalactosamine-6-sulfate sulfatase exonic point mutations in classical Morquio and mild cases.

S. Fukuda, S. Tomatsu, K. Sukegawa, 1992, The Journal of clinical investigation.

The CXCR4 agonist peptide, CTCE-0021, rapidly mobilizes polymorphonuclear neutrophils and hematopoietic progenitor cells into peripheral blood and synergizes with granulocyte colony-stimulating factor.

D. Wong, S. Fukuda, L. Pelus, 2005, Experimental hematology.

[Stem cell transplantation in multiple myeloma].

S. Fukuda, K. Sunami, T. Sezaki, 1999, Gan to kagaku ryoho. Cancer & chemotherapy.

characterized by enhanced homing and engraftment mobilizes early hematopoietic stem cells β The chemokine GRO

S. Fukuda, L. Pelus, H. Bian, 2013 .

Clinical and molecular aspects of Japanese patients with mitochondrial trifunctional protein deficiency.

T. Fukao, S. Fukuda, J. Purevsuren, 2009, Molecular genetics and metabolism.

Activation of Wiskott-Aldrich syndrome protein and its association with other proteins by stromal cell-derived factor-1alpha is associated with cell migration in a T-lymphocyte line.

H. Broxmeyer, S. Okabe, S. Fukuda, 2002, Experimental hematology.

Inhibition of caspase-3 by Survivin prevents Wee1 Kinase degradation and promotes cell survival by maintaining phosphorylation of p34Cdc2.

J. Guzman, S. Fukuda, L. Pelus, 2009, Gene therapy & molecular biology.

Polyclonal B-cell lymphocytosis with features resembling hairy cell leukemia-Japanese variant.

O. Yamada, H. Nagai, S. Fukuda, 1997, Blood.

Bezafibrate can be a new treatment option for mitochondrial fatty acid oxidation disorders: evaluation by in vitro probe acylcarnitine assay.

T. Taketani, T. Fukao, S. Fukuda, 2012, Molecular genetics and metabolism.

In vitro probe acylcarnitine profiling assay using cultured fibroblasts and electrospray ionization tandem mass spectrometry predicts severity of patients with glutaric aciduria type 2.

S. Fukuda, J. Purevsuren, Y. Hasegawa, 2010, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Immunohistochemical demonstration of acid α-glucosidase in muscle in Pompe's disease

I. Matsuda, S. Fukuda, M. Osame, 1983, The Histochemical Journal.

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

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

The magnitude of CXCR4 signaling regulates resistance to quizartinib in FLT3/ITD+ cells via RUNX1.

T. Taketani, S. Fukuda, L. Pelus, 2022, Leukemia research.

Adenovirus serotype 31 infection in a newborn girl and review of the literature

S. Fukuda, S. Yamaguchi, K. Yasuda, 2011, Pediatrics International.

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

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

Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases

T. Taketani, H. Mizusawa, A. Tamaoka, 2016, Brain and Development.

Clinical and molecular investigations of Japanese cases of glutaric acidemia type 2.

T. Fukao, S. Fukuda, Y. Hasegawa, 2008, Molecular genetics and metabolism.

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

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

Survivin, a cancer target with an emerging role in normal adult tissues

S. Fukuda, L. Pelus, 2006, Molecular Cancer Therapeutics.

Survivin Modulates Genes with Divergent Molecular Functions and Regulates Proliferation of Hematopoietic Stem Cells through Evi-1

G. Nucifora, J. Speth, E. Conway, 2014, Leukemia.

Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: a comparison with Caucasian cases

T. Taketani, Y. Niida, S. Fukuda, 2017, Journal of Human Genetics.

High frequencies of simultaneous FLT3-ITD, WT1 and KIT mutations in hematological malignancies with NUP98-fusion genes

T. Taki, T. Taketani, Y. Hayashi, 2010, Leukemia.

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.

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

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

Validation of Liquid Chromatography-Tandem Mass Spectrometry-Based 5-Plex Assay for Mucopolysaccharidoses

M. Gelb, T. Taketani, A. Nagai, 2020, International journal of molecular sciences.

Endocytic pathway of high density lipoprotein via trans-Golgi system in rat resident peritoneal macrophages.

Y. Morino, S. Horiuchi, M. Naito, 1989, Laboratory investigation; a journal of technical methods and pathology.

Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report

T. Taketani, S. Fukuda, Y. Hasegawa, 2019, Brain and Development.

[Prevention of hepatitis B flare-up using lamivudine in a patient with non-Hodgkin's lymphoma after allogeneic bone marrow transplantation].

S. Fukuda, T. Fujiwara, S. Fujii, 2000, [Rinsho ketsueki] The Japanese journal of clinical hematology.

Heteroallelic missense mutations of the galactosamine-6-sulfate sulfatase (GALNS) gene in a mild form of Morquio disease (MPS IVA).

D. Cole, S. Fukuda, S. Tomatsu, 1996, American journal of medical genetics.

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.

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.

Survivin mediates aberrant hematopoietic progenitor cell proliferation and acute leukemia in mice induced by internal tandem duplication of Flt3.

Xin-Yuan Fu, H. Boswell, E. Conway, 2009, Blood.

Ectopic neuroblastoma in monozygotic twins with different ages of onset: possible twin-to-twin metastasis in utero with distinct genetic alterations after birth.

S. Ogawa, T. Taketani, K. Hayashi, 2014, Journal of pediatric hematology/oncology.

The Protein Tyrosine Phosphatase, Shp2, Positively Contributes to FLT3-ITD-Induced Hematopoietic Progenitor Hyperproliferation and Malignant Disease In Vivo

Menggang Yu, G. Sandusky, H. Boswell, 2012, Leukemia.

Identification and Characterization of Novel Survivin Splice Variants with Anti-Apoptotic Activities

J. Sampath, S. Fukuda, M. Louis, 2017 .

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.

Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor‐2) gene in patients with peroxisome biogenesis disorders

H. Moser, R. Wanders, G. Besley, 1999, Human mutation.

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.

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.

Identification of 31 novel mutations in the N‐acetylgalactosamine‐6‐sulfatase gene reveals excessive allelic heterogeneity among patients with Morquio A syndrome

B. Poorthuis, W. Kleijer, A. Tylki-Szymańska, 1997, Human mutation.

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.

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.

Morquio disease: isolation, characterization and expression of full-length cDNA for human N-acetylgalactosamine-6-sulfate sulfatase.

K. Titani, T. Fukao, Y. Hayashi, 1991, Biochemical and biophysical research communications.

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.

Survivin: Identification of Selective Functional Signaling Pathways inTransformed Cells and Identification of a New Splice Variant with Growth Survival Activity

S. Fukuda, L. Pelus, 2011 .

The antiapoptosis protein survivin is associated with cell cycle entry of normal cord blood CD34(+) cells and modulates cell cycle and proliferation of mouse hematopoietic progenitor cells.

S. Fukuda, L. Pelus, S. B. Porter, 2002, Blood.

Survivin regulates the p53 tumor suppressor gene family

S. Fukuda, Zhanxiang Wang, L. Pelus, 2004, Oncogene.

Survivin regulates hematopoietic progenitor cell proliferation through p21WAF1/Cip1-dependent and -independent pathways.

C. Mantel, S. Fukuda, L. Pelus, 2004, Blood.

Elevation of Survivin Levels by Hematopoietic Growth Factors Occurs in Quiescent CD34+ Hematopoietic Stem and Progenitor Cells Before Cell Cycle Entry

S. Fukuda, L. Pelus, 2002, Cell cycle.

Stromal cell – derived factor-1 / CXCL 12 – induced chemotaxis of T cells involves activation of the RasGAP-associated docking protein p 62 Dok-1

P. Pandolfi, H. Broxmeyer, Young‐June Kim, 2004 .

Internal tandem duplication of FLT3 deregulates proliferation and differentiation and confers resistance to the FLT3 inhibitor AC220 by Up-regulating RUNX1 expression in hematopoietic cells

T. Taketani, S. Fukuda, S. Yamaguchi, 2015, International Journal of Hematology.

A novel ALL-L3 cell line, BALM-16, lacking expression of immunoglobulin chains derived from a patient with hypercalcemia

K. Orita, Y. Matsuo, K. Kojima, 1997, Leukemia.

Survivin Selectively Modulates Genes Deregulated in Human Leukemia Stem Cells

T. Taketani, E. Conway, S. Fukuda, 2010, Journal of oncology.

Cloning and characterization of a proliferation-associated cytokine-inducible protein, CIP29.

S. Fukuda, L. Pelus, D. W. Wu, 2002, Biochemical and biophysical research communications.

Chemokine-mobilized adult stem cells; defining a better hematopoietic graft

S. Fukuda, L. Pelus, 2008, Leukemia.

Improvement with disodium cromoglycate of neutrophil phagocytosis and respiratory burst activity in a patient with hyperimmunoglobulin E syndrome

K. Kojima, M. Harada, S. Fukuda, 1998, Allergy.

Immunohistochemical localization of acid alpha-glucosidase in rat liver.

S. Fukuda, T. Hamada, T. Iwamasa, 1982, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Glycogen storage disease. Studies related to the mechanism of glycogenosome formation.

S. Fukuda, M. Osame, T. Hamada, 1983, Pathology, research and practice.

Acute osteomyelitis of the acetabulum induced by Staphylococcus capitis in a young athlete

J. Iwasa, S. Fukuda, S. Yamaguchi, 2010, Pediatric reports.

Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening

Dong Hwan Lee, Nguyen Ngoc Khanh, T. Taketani, 2018, Molecular genetics and metabolism reports.

Hunter disease in a girl caused by R468Q mutation in the iduronate‐2‐sulfatase gene and skewed inactivation of the X chromosome carrying the normal allele

H. Nishio, M. Matsuo, N. Shimozawa, 1997, Human mutation.

Rapid Mobilization Reveals a Highly Engraftable Hematopoietic Stem Cell

P. Kharchenko, D. Scadden, A. Schajnovitz, 2016, Cell.

Intracellular in vitro probe acylcarnitine assay for identifying deficiencies of carnitine transporter and carnitine palmitoyltransferase-1

T. Fukao, S. Fukuda, J. Purevsuren, 2013, Analytical and Bioanalytical Chemistry.

Enzymatic evaluation of glutaric acidemia type 1 by an in vitro probe assay of acylcarnitine profiling using fibroblasts and electrospray ionization/tandem mass spectrometry (MS/MS).

T. Taketani, S. Fukuda, J. Purevsuren, 2009, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Pure red cell precursor toxicity by linezolid in a pediatric case.

T. Taketani, S. Mishima, S. Fukuda, 2009, Journal of pediatric hematology/oncology.

Mucopolysaccharidosis type II (Hunter disease): Identification and characterization of eight point mutations in the iduronate‐2‐sulfatase gene in Japanese patients

T. Fukao, S. Fukuda, S. Tomatsu, 1995, Human mutation.

Intermediate form of mucopolysaccharidosis type II (Hunter disease): a C1327 to T substitution in the iduronate sulfatase gene.

K. Tamai, T. Sasaki, S. Fukuda, 1992, Biochemical and biophysical research communications.

Overexpression rescues the mutant phenotype of L176F mutation causing beta-glucuronidase deficiency mucopolysaccharidosis in two Mennonite siblings.

W. Sly, S. Fukuda, S. Tomatsu, 1994, The Journal of biological chemistry.

Amino acid sequences of lysozymes newly purified from invertebrates imply wide distribution of a novel class in the lysozyme family.

T. Imoto, K. Sugimura, S. Fukuda, 1999, European journal of biochemistry.

Rotavirus-associated encephalopathy with a reversible splenial lesion.

S. Fukuda, S. Yamaguchi, K. Yasuda, 2009, Pediatric neurology.

Internal Tandem Duplication in FLT3 Attenuates Proliferation and Regulates Resistance to the FLT3 Inhibitor AC220 by Modulating p21Cdkn1a and Pbx1 in Hematopoietic Cells

T. Taketani, S. Fukuda, J. Purevsuren, 2016, PloS one.

Molecular Interaction Between the Microenvironment and FLT3/ITD+ AML Cells Leading to the Refractory Phenotype

T. Taketani, S. Fukuda, Chie Onishi, 2017 .

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.

Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS gene

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

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.

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.

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

Z. Kato, S. Fukuda, S. Tomatsu, 1996, Human mutation.

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.

Four novel mutations in mucopolysaccharidosis type VII including a unique base substitution in exon 10 of the beta-glucuronidase gene that creates a novel 5'-splice site.

W. Sly, S. Fukuda, S. Tomatsu, 1995, Human molecular genetics.

Mucopolysaccharidosis type IVA: identification of six novel mutations among non-Japanese patients

N. Shimozawa, Yasuyuki Suzuki, S. Fukuda, 1995 .

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.

Mucopolysaccharidosis IV A: assignment of the human N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene to chromosome 16q24.

S. Fukuda, S. Tomatsu, M. Masuno, 1993, Genomics.

Molecular basis of mucopolysaccharidosis type VII: replacement of Ala619 in beta-glucuronidase with Val.

T. Sasaki, S. Fukuda, S. Tomatsu, 1990, Gene.

XhoI and SphI RFLPs in the GALNS gene.

S. Fukuda, S. Tomatsu, T. Orii, 1994, Human molecular genetics.

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.

Polymorphism in the GALNS gene.

S. Fukuda, S. Tomatsu, T. Orii, 1994, Human molecular genetics.

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.

Molecular analysis of mucopolysaccharidosis type VII

T. Sasaki, S. Fukuda, S. Yamaguchi, 1991, Journal of Inherited Metabolic Disease.

Serum C14:1/C12:1 ratio is a useful marker for differentiating affected patients with very long-chain acyl-CoA dehydrogenase deficiency from heterozygous carriers

T. Taketani, S. Fukuda, Y. Hasegawa, 2019, Molecular genetics and metabolism reports.

A newborn case with carnitine palmitoyltransferase II deficiency initially judged as unaffected by acylcarnitine analysis soon after birth

T. Taketani, S. Fukuda, Y. Hasegawa, 2017, Molecular genetics and metabolism reports.

Mad2 is required for optimal hematopoiesis: Mad2 associates with c-Kit in MO7e cells.

H. Broxmeyer, C. Mantel, S. Ito, 2007, Blood.

The CXCR4 Antagonist AMD3100 and the CXCR2 Agonist GROβ Synergistically Mobilize Hematopoetic Stem Cells (HSC) with Short and Long Term Repopulating Activity.

G. Bridger, S. Fukuda, L. Pelus, 2006 .

Internal Tandem Duplication Mutations in FLT3 Gene Augment Chemotaxis to Cxcl12 Protein by Blocking the Down-regulation of the Rho-associated Kinase via the Cxcl12/Cxcr4 Signaling Axis*

T. Taketani, T. Sugimoto, S. Fukuda, 2014, The Journal of Biological Chemistry.

Clinical course in a patient with myopathic VLCAD deficiency during pregnancy with an affected baby

T. Taketani, Y. Matsubara, S. Fukuda, 2019, JIMD reports.

A novel molecular aspect of Japanese patients with medium-chain acyl-CoA dehydrogenase deficiency (MCADD): c.449-452delCTGA is a common mutation in Japanese patients with MCADD.

T. Fukao, S. Fukuda, J. Purevsuren, 2009, Molecular genetics and metabolism.

Clinical and molecular investigation of 19 Japanese cases of glutaric acidemia type 1.

T. Taketani, S. Fukuda, J. Purevsuren, 2011, Molecular genetics and metabolism.

Clinical and genetic aspects of hypophosphatasia in Japanese patients

T. Taketani, S. Fukuda, Hironori Kobayashi, 2013, Archives of Disease in Childhood.

Idiopathic testicular infarction in a boy initially suspected to have acute epididymo-orchitis associated with mycoplasma infection and Henoch-Schönlein purpura.

S. Fukuda, S. Yamaguchi, K. Yasuda, 2009, Journal of pediatric urology.

Acute Myositis Associated with Concurrent Infection of Rotavirus and Norovirus in a 2-Year-Old Girl

S. Fukuda, S. Yamaguchi, Kei Yamamoto, 2015, Pediatric reports.

Survivin Regulates Proliferation of Normal Hematopoietic Stem and Progenitor Cells In Vivo.

E. Conway, S. Fukuda, L. Pelus, 2006 .

ULTRASTRUCTURAL AND PHYSICOCHEMICAL STUDIES ON GLYCOGEN MAGROMOLECULES FROM ASCITES HEPATOMA AH 13 CELLS

S. Fukuda, T. Hamada, T. Takeuchi, 1982 .

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.

Chromosomal instability in Marinesco‐Sjögren Syndrome associated with acute myeloblastic leukemia

T. Terada, N. Kondo, S. Fukuda, 1998, Clinical Genetics.

Myopathy due to glycogen storage disease: pathological and biochemical studies in relation to glycogenosome formation.

I. Matsuda, S. Fukuda, M. Osame, 1983, Experimental and molecular pathology.

Rational Design of Chemokine SDF-1 Analogs with Agonist Activity for the CXCR4 Receptor and the Capacity to Rapidly Mobilize PMN and Hematopoietic Progenitor Cells in Mice

D. Wong, S. Fukuda, L. Pelus, 2004 .

The frequencies of very long-chain acyl-CoA dehydrogenase deficiency genetic variants in Japan have changed since the implementation of expanded newborn screening.

T. Taketani, T. Takizawa, S. Okada, 2022, Molecular genetics and metabolism.

Immunohistochemical demonstration of acid alpha-glucosidase in fetal rat hepatocytes and glycogenosomes of newborn rat hepatocytes.

S. Fukuda, T. Hamada, T. Iwamasa, 1982, Pathology, research and practice.

Inhibition of hematopoietic progenitor cell growth by Tyr-MIF, an endogenous opiate modulator, and its degradation products.

S. Fukuda, J. Callahan, L. Pelus, 2002, International immunopharmacology.

A fetus with mitochondrial trifunctional protein deficiency: Elevation of 3-OH-acylcarnitines in amniotic fluid functionally assured the genetic diagnosis

T. Taketani, S. Fukuda, Y. Hasegawa, 2015, Molecular genetics and metabolism reports.

Trisomy 12 and t(14;18) in B-cell chronic lymphocytic leukemia.

M. Taniwaki, T. Yoshino, K. Kojima, 1998, International journal of hematology.

Effects of plasmapheresis on familial type III hyperlipoproteinemia associated with glomerular lipidosis, nephrotic syndrome and diabetes mellitus.

S. Fukuda, N. Nakamura, H. Uzawa, 1990, Atherosclerosis.

T. Taketani, S. Mishima, S. Yuba, 2013, Pediatrics international : official journal of the Japan Pediatric Society.

Purification and Partial Characterization of α-N-Acetylglucosaminidase from Human Liver

T. Sasaki, S. Fukuda, S. Tomatsu, 1991 .

Mad 2 is required for optimal hematopoiesis : Mad 2 associates with c-Kit in MO 7 e cells

H. Broxmeyer, C. Mantel, S. Ito, 2006 .

[Detection of circulating activated platelets by anti-GMP-140 monoclonal antibodies].

S. Fukuda, Y. Katagiri, N. Akamatsu, 1992, Nihon rinsho. Japanese journal of clinical medicine.

Fighting against the CNS Invasion of Pediatric Leukemia

S. Fukuda, 2012 .

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.

in MO7e cells Mad2 is required for optimal hematopoiesis: Mad2 associates with c-Kit

C. Mantel, S. Ito, S. Cooper, 2013 .

Mad 2 is required for optimal hematopoiesis : Mad 2 associates with c-Kit in MO 7 e cells

H. Broxmeyer, C. Mantel, S. Ito, 2007 .

Survivin Is Required for Mouse and Human Bone Marrow Mesenchymal Stromal Cell Function

S. Fukuda, Pratibha Singh, Liqiong Liu, 2018, Stem cells.

Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase : 3-hydroxyacyl-CoA dehydrogenase cDNA

T. Hashimoto, T. Aoyama, Y. Suzuki, 1998, Journal of Inherited Metabolic Disease.