H. Fujii

发表

Graphitization behavior of Kapton-derived carbon film related to structure, microtexture and transport properties

A. Yoshida, T. Koidesawa, Y. Hishiyama, 1997 .

Molecular analysis of glucose phosphate isomerase deficiency associated with hereditary hemolytic anemia.

S. Ohga, S. Miwa, H. Kanno, 1996, Blood.

Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by nonradioisotopic single-strand conformation polymorphism analysis.

S. Miwa, F. Ishida, K. Yamada, 1994, Blood.

Structure and function of normal and variant human phosphoglycerate kinase.

A. Yoshida, I. Huang, H. Fujii, 1980, Hemoglobin.

Abscess-Forming Neutrophilic Dermatosis: Report of Three Cases Associated with Hemopathies

S. Imamura, N. Arima, H. Fujii, 1998, Dermatology.

cDNA cloning of human R-type pyruvate kinase and identification of a single amino acid substitution (Thr384----Met) affecting enzymatic stability in a pyruvate kinase variant (PK Tokyo) associated with hereditary hemolytic anemia.

H. Fujii, S. Miwa, H. Kanno, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Purification and properties of adenosine deaminase in normal and hereditary hemolytic anemia with increased red cell activity.

S. Miwa, K. Suzuki, H. Fujii, 1980, Hemoglobin.

hereditary hemolytic anemia by a single amino acid substitution (426 Arg-->Gln) associated with Low substrate affinity of pyruvate kinase variant (PK Sapporo) caused

S. Miwa, H. Kanno, H. Fujii, 2011 .

Three Cases of Hereditary Nonspherocytic Hemolytic Anemia Associated With Red Blood Cell Glutathione Deficiency

S. Miwa, H. Kanno, I. Sekine, 1996 .

Membrane abnormality in red blood cells with weak type B expression

A. Yoshida, P. Morel, V. Dave, 1980 .

Membrane abnormality in red blood cells with weak type B expression.

A. Yoshida, P. Morel, V. Dave, 1980, Blood.

Multiple components of blood group A and B antigens in human erythrocyte membranes and their difference between A1 and A2 status.

A. Yoshida, H. Fujii, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Other erythrocyte enzyme deficiencies associated with non-haematological symptoms: phosphoglycerate kinase and phosphofructokinase deficiency.

S. Miwa, H. Fujii, 2000, Bailliere's best practice & research. Clinical haematology.

Molecular abnormality of phosphoglycerate kinase-Uppsala associated with chronic nonspherocytic hemolytic anemia.

A. Yoshida, H. Fujii, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Use of cultured lymphoblastoid cells for the study of abnormal enzymes: molecular abnormality of a phosphoglycerate kinase variant associated with hemolytic anemia.

A. Yoshida, S. Miwa, S. H. Chen, 1981, Proceedings of the National Academy of Sciences of the United States of America.

A single amino acid substitution (Asp leads to Asn) in a phosphoglycerate kinase variant (PGK München) associated with enzyme deficiency.

A. Yoshida, W. Krietsch, H. Fujii, 1980, The Journal of biological chemistry.

Structural analysis of human pyruvate kinase L-gene and identification of the promoter activity in erythroid cells.

S. Miwa, H. Kanno, H. Fujii, 1992, Biochemical and biophysical research communications.

A unique electrophoretic slow-moving glucose 6-phosphate dehydrogenase variant (G6PD Asahikawa) with a markedly acidic pH optimum

T. Morisaki, S. Miwa, H. Kanno, 2004, Human Genetics.

Human adenylate kinase deficiency associated with hemolytic anemia. A single base substitution affecting solubility and catalytic activity of the cytosolic adenylate kinase.

M. Yamada, F. Kishi, A. Nakazawa, 1989, The Journal of biological chemistry.

Isozymes of human erythrocyte pyrimidine 5'-nucleotidase--chromatographic separation and their properties.

S. Miwa, A. Hirono, H. Fujii, 1985, The Japanese journal of experimental medicine.

Identical point mutations of the R-type pyruvate kinase (PK) cDNA found in unrelated PK variants associated with hereditary hemolytic anemia.

H. Fujii, S. Miwa, H. Kanno, 1992, Blood.

A single nucleotide substitution in the phosphoglycerate kinase (PGK)-1 gene occurred after the separation of PGK-1 and PGK-2

S. Miwa, H. Kanno, A. Hirono, 1992, Human Genetics.

A new glucose-6-phosphate dehydrogenase variant (G6PD Tsukui) associated with congenital hemolytic anemia

T. Morisaki, S. Miwa, H. Kanno, 2004, Human Genetics.

A new glucose-6-phosphate dehydrogenase variant (G6PD Nagano) associated with congenital hemolytic anemia

S. Miwa, K. Tani, A. Hirono, 2004, Human Genetics.

Gd(-) Gifu and Gd(-) Fukuoka. Two new variants of glucose-6-phosphate dehydrogenase found in Japan

T. Morisaki, S. Miwa, H. Kanno, 2004, Human Genetics.

Molecular abnormality of erythrocyte pyruvate kinase deficiency in the Amish.

S. Miwa, S. Ballas, H. Kanno, 1994, Blood.

Hereditary hemolytic anemia caused by diverse point mutations of pyruvate kinase gene found in Japan and Hong Kong.

H. Mizoguchi, T. Nakahata, K. Narisawa, 1994, Blood.

Primary structure of murine red blood cell-type pyruvate kinase (PK) and molecular characterization of PK deficiency identified in the CBA strain.

Y. Kitamura, M. Morimoto, T. Tsujimura, 1995, Blood.

Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation.

T. Mukai, K. Hori, S. Miwa, 1987, Proceedings of the National Academy of Sciences of the United States of America.

A novel human catalase mutation (358 T-->del) causing Japanese-type acatalasemia.

H. Fujii, S. Miwa, H. Kanno, 1995, Blood cells, molecules & diseases.

Hereditary hemolytic anemia caused by diverse point mutations of pyruvate kinase gene found in Japan and Hong Kong

H. Mizoguchi, T. Nakahata, K. Narisawa, 1994 .

Frame shift mutation, exon skipping, and a two-codon deletion caused by splice site mutations account for pyruvate kinase deficiency.

I. Tsukimoto, L. Chan, H. Fujii, 1997, Blood.

Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological symptoms

H. Fujii, S. Miwa, Susan Hollán, 1993, Human Genetics.

In ̄uence of the CYP2D6*10 allele on the metabolism of mexiletine by human liver microsomes

K. Chiba, K. Kobayashi, H. Fujii, 2022 .

Expression and enzymatic characterization of human glucose phosphate isomerase (GPI) variants accounting for GPI deficiency.

S. Miwa, H. Kanno, H. Fujii, 1998, Blood cells, molecules & diseases.

Molecular analysis of eight biochemically unique glucose-6-phosphate dehydrogenase variants found in Japan.

T. Takano, S. Miwa, A. Hirono, 1997, Blood.

Low substrate affinity of pyruvate kinase variant (PK Sapporo) caused by a single amino acid substitution (426 Arg-->Gln) associated with hereditary hemolytic anemia.

S. Miwa, H. Kanno, H. Fujii, 1993, Blood.

Hematologically important mutations: molecular abnormalities of glucose phosphate isomerase deficiency.

S. Miwa, H. Kanno, A. Hirono, 1996, Blood cells, molecules & diseases.

Identification of two novel deletion mutations in glucose-6-phosphate dehydrogenase gene causing hemolytic anemia.

S. Miwa, A. Hirono, H. Fujii, 1995, Blood.

A new simple screening method for glucose 6-phosphate dehydrogenase deficiency.

S. Miwa, H. Fujii, K. Takahashi, 1984, Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society.

Molecular analysis of glucose-6-phosphate dehydrogenase variants in the Solomon Islands.

S. Miwa, A. Ishii, A. Hirono, 1995, American journal of human genetics.

Three families with hereditary hemolytic anemia and pyrimidine 5'-nucleotidase deficiency: electrophoretic and kinetic studies.

S. Miwa, A. Hirono, H. Fujii, 1983, Clinica chimica acta; international journal of clinical chemistry.

Evaluation of the blue formazan spot test for screening glucose 6 phosphate dehydrogenase deficiency.

S. Miwa, J. L. Corrons, A. Salvati, 1999, International journal of hematology.

Molecular basis of impaired pyruvate kinase isozyme conversion in erythroid cells: a single amino acid substitution near the active site and decreased mRNA content of the R-type PK.

S. Miwa, H. Kanno, H. Fujii, 1993, Biochemical and biophysical research communications.