H. Fujii

发表

Recent progress in the molecular genetic analysis of erythroenzymopathy

H. Fujii, S. Miwa, 1990, American journal of hematology.

Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: Tabulation of mutant enzymes

H. Fujii, S. Miwa, 1996 .

Red blood cell enzymes and their clinical application.

H. Fujii, S. Miwa, 1998, Advances in clinical chemistry.

Human liver type pyruvate kinase: complete amino acid sequence and the expression in mammalian cells.

S. Nagata, H. Fujii, S. Miwa, 1988, Proceedings of the National Academy of Sciences of the United States of America.

High-dose chemotherapy followed by autologous and allogeneic peripheral blood stem cell transplantation for recurrent disseminated trilateral retinoblastoma

M. Ōsawa, H. Fujii, Y. Okada, 2011, Child's Nervous System.

PYRUVATE SUPPLEMENTATION ENHANCES VASCULAR ENDOTHELIAL GROWTH FACTOR PRODUCTION BY BONE MARROW-DERIVED MONONUCLEAR CELLS

H. Fujii, H. Kanno, H. Ogura, 2012 .

Expression of L- and M-type pyruvate kinase in human tissues.

H. Fujii, S. Miwa, K. Tani, 1988, Genomics.

Elevated erythrocyte adenosine deaminase activity in a patient with primary acquired sideroblastic anemia

T. Morisaki, M. Kizaki, H. Fujii, 1988, American journal of hematology.

Genetic analysis of adenosine deaminase expression in adult T‐cell leukemia

T. Morisaki, H. Fujii, S. Miwa, 1988, American journal of hematology.

Molecular analysis of Lesch-Nyhan syndrome found in Japan.

T. Morisaki, H. Fujii, S. Miwa, 1988, The Tohoku journal of experimental medicine.

Molecular basis of Japanese variants of pyrimidine 5′‐nucleotidase deficiency

H. Fujii, S. Miwa, H. Kanno, 2004, British journal of haematology.

An SNP in CYP39A1 is associated with severe neutropenia induced by docetaxel

N. Kamatani, Kayoko Saito, H. Fujii, 2012, Cancer Chemotherapy and Pharmacology.

Three glucose 6-phosphate dehydrogenase variants found in Japan

H. Fujii, S. Miwa, K. Nakashima, 1977, Human Genetics.

An Improved Single-step Screening Method for Glucose-6-Phosphate Dehydrogenase Deficiency.

H. Fujii, S. Miwa, A. Hirono, 1998 .

GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS IN JAPAN

H. Fujii, S. Miwa, 1986 .

A case of congenital dyserythropoietic anemia type 1 in a Japanese adult with a CDAN1 gene mutation and an inappropriately low serum hepcidin-25 level.

K. Nakao, K. Hosoda, S. Kojima, 2012, Internal medicine.

The human liver-type pyruvate kinase (PKL) gene is on chromosome 1 at band q21.

H. Satoh, M. Yoshida, H. Fujii, 1988, Cytogenetics and cell genetics.

Human liver type pyruvate kinase: cDNA cloning and chromosomal assignment.

T. Tanaka, M. Yoshida, K. Toyoshima, 1987, Biochemical and biophysical research communications.

Characterization of purine nucleoside phosphorylase in leukemia

T. Morisaki, H. Fujii, S. Miwa, 1986, American journal of hematology.

Adenosine deaminase (ADA) in leukemia: Clinical value of plasma ADA activity and characterization of leukemic cell ADA

T. Morisaki, H. Fujii, S. Miwa, 1985, American journal of hematology.

Overproduction of structurally normal enzyme in man: hereditary haemolytic anaemia with increased red cell adenosine deaminase activity

H. Fujii, S. Miwa, K. Tani, 1982, British journal of haematology.

A case of red‐cell adenosine deaminase overproduction associated with hereditary hemolytic anemia found in Japan

H. Fujii, S. Miwa, N. Matsumoto, 1978, American journal of hematology.

A single mutation 202G>A in the human glucose-6-phosphate dehydrogenase gene (G6PD) can cause acute hemolysis by itself.

H. Fujii, S. Miwa, A. Hirono, 2002, Blood.

Biochemical Basis of Senescence and Premature Death of Red Blood Cells: Phosphatidylserine on Red Cell Membrane as a Marker of Phagocytosis

H. Fujii, H. Kanno, 2007 .

Three cases of hereditary nonspherocytic hemolytic anemia associated with red blood cell glutathione deficiency.

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

Fulminant varicella hepatitis following bone marrow transplantation.

S. Asano, K. Morishita, H. Fujii, 1985, JAMA.

Gene Expression and Biological Significance of Hexokinase in Erythroid Cells

H. Fujii, H. Kanno, J. Tancabelic, 2002, Acta Haematologica.

Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia

H. Fujii, S. Miwa, 1985, American journal of hematology.

Change of pyruvate kinase isozymes from M2‐ to L‐type during development of the red cell

H. Fujii, S. Miwa, S. Takegawa, 1983, British journal of haematology.

associated with red blood cell glutathione deficiency Three cases of hereditary nonspherocytic hemolytic anemia

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

Enhanced expression of myogenic differentiation factors and skeletal muscle proteins in human amnion-derived cells via the forced expression of MYOD1

Kayoko Saito, H. Fujii, Y. Matsuda, 2013, Brain and Development.

Human M2-type pyruvate kinase: cDNA cloning, chromosomal assignment and expression in hepatoma.

T. Tanaka, H. Satoh, M. Yoshida, 1988, Gene.

Seven Pyruvate Kinase Variants Characterized by the ICSH Recommended Methods

H. Fujii, S. Miwa, Y. Ishida, 1980, British journal of haematology.

without host irradiation hemolytic anemia and cure of the anemia by marrow transplantation Pyruvate kinase deficiency of mice associated with nonspherocytic

M. Morimoto, T. Tsujimura, H. Fujii, 2011 .

An example of Hb Christchurch in Japan. Identification by high-performance liquid chromatography.

T. Morisaki, H. Fujii, S. Miwa, 1985, Hemoglobin.

A novel missense mutation (1060G → C) in the phosphoglycerate kinase gene in a Japanese boy with chronic haemolytic anaemia, developmental delay and rhabdomyolysis

T. Sugimoto, H. Fujii, A. Morimoto, 2003, British journal of haematology.

A single amino acid substitution (157 Gly----Val) in a phosphoglycerate kinase variant (PGK Shizuoka) associated with chronic hemolysis and myoglobinuria.

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

Physiological significance and molecular genetics of red cell enzymes involved in the ribonucleotide metabolism

H. Fujii, S. Miwa, H. Kanno, 2002 .

Chromatographic analysis of human erythrocyte pyrimidine 5′‐nucleotidase from five patients with pyrimidine 5′‐nucleotidase deficiency

H. Fujii, S. Miwa, A. Hirono, 1987, British journal of haematology.

Red cell adenylate kinase deficiency associated with hereditary nonspherocytic hemolytic anemia: Clinical and biochemical studies

H. Fujii, S. Miwa, Keisuke Takahashi, 1983, American journal of hematology.

Transgenic rescue of hemolytic anemia due to red blood cell pyruvate kinase deficiency.

S. Aizawa, T. Koizumi, H. Fujii, 2007, Haematologica.

Pyruvate kinase deficiency of mice associated with nonspherocytic hemolytic anemia and cure of the anemia by marrow transplantation without host irradiation.

Y. Kitamura, M. Morimoto, Y. Moriyama, 1995, Blood.

Characterization of pyruvate kinase from the liver of a patient with aberrant erythrocyte pyruvate kinase, PK Nagasaki.

K. Shinohara, H. Fujii, S. Miwa, 1977, The Journal of laboratory and clinical medicine.

Glycolytic inhibition by mutation of pyruvate kinase gene increases oxidative stress and causes apoptosis of a pyruvate kinase deficient cell line.

Jun Kanno, Ken-ichi Aisaki, J. Kanno, 2007, Experimental hematology.

Shared molecular targets in pediatric gliomas and ependymomas

M. Ōsawa, H. Fujii, Y. Okada, 2011, Pediatric blood & cancer.

Distribution of glucose-6-phosphate dehydrogenase mutations in Southeast Asia

H. Fujii, S. Miwa, F. Kawamoto, 2001, Human Genetics.

Fine structure of the spleen in autoimmune hemolytic anemia associated with systemic lupus erythematosus.

H. Fujii, S. Miwa, N. Matsumoto, 1978, The Tohoku journal of experimental medicine.

Carbamazepine-Induced Hemolytic and Aplastic Crises Associated with Reduced Glutathione Peroxidase Activity of Erythrocytes

H. Tsutsumi, N. Tachi, N. Hatakeyama, 2007, International journal of hematology.

Splenic Infarction after Epstein-Barr Virus Infection in a Patient with Hereditary Spherocytosis

K. Iwabuchi, M. Mukae, H. Fujii, 2007, International journal of hematology.

Ineffective erythropoiesis in mutant mice with deficient pyruvate kinase activity.

S. Aizawa, H. Fujii, H. Kanno, 2005, Experimental hematology.

Ineffective erythropoiesis in the spleen of a patient with pyruvate kinase deficiency

Yutaka Kawakami, Ken-ichi Aisaki, Masaki Hiramoto, 2003, American journal of hematology.

Glucose 6-Phosphate dehydrogenase variants: A unique variant (G6PD Kobe) showed an extremely increased affinity for galactose 6-phosphate and a new variant (G6PD Sapporo) resembling G6PD Pea Ridge

H. Fujii, S. Miwa, S. Nakayama, 1981, Human Genetics.

Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita

H. Fujii, S. Miwa, Kaneo Yamada, 1978, Human Genetics.

Four new electrophoretically slow‐moving glucose 6‐phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: Gd(‐) Kurume, Gd(‐) Fukushima, Gd(‐) Yamaguchi and Gd(‐) Wakayama

H. Fujii, S. Miwa, Y. Ishida, 1978, American journal of hematology.

Molecular Abnormality of Erythrocyte Pyruvate Kinase Deficiency in the Amish

H. Fujii, S. Miwa, S. Ballas, 1994 .

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

Y. Kitamura, M. Morimoto, T. Tsujimura, 2011 .

Genotypic analysis using a Y‐chromosome‐specific probe following bone marrow transplantation

S. Asano, T. Morisaki, H. Morisaki, 1988, American journal of hematology.

Homozygous intragenic deletion of type I hexokinase gene causes lethal hemolytic anemia of the affected fetus.

K. Ishikawa, H. Fujii, S. Miwa, 2002, Blood.

Delayed onset of hemolytic anemia in CBA-Pk-1slc/Pk-1slc mice with a point mutation of the gene encoding red blood cell type pyruvate kinase.

E. Morii, Y. Kitamura, K. Hashimoto, 1998, Blood.

Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a japanese family

Tomoaki Kato, H. Fujii, S. Miwa, 1981, American journal of hematology.

Alpha Hemoglobin Stabilizing Protein (AHSP) Is a Susceptibility Gene to Drug /Infection-Induced Hemolytic Anemia.

N. Kamatani, H. Fujii, S. Miwa, 2005 .

Double High-dose Chemotherapy Followed by Autologous Peripheral Blood Stem Cell Transplantation for Primary Disseminated Medulloblastoma: A Report of 3 Cases

T. Hori, T. Kawamata, M. Ōsawa, 2010, Journal of pediatric hematology/oncology.

Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.

H. Fujii, S. Miwa, 1996, American journal of hematology.

L. Luzzatto, E. Beutler, D. Paglia, 1989, Clinical and laboratory haematology.

Three cases of hereditary hemolytic anemia with pyrimidine 5′-nucleotidase deficiency in a Japanese family

H. Fujii, S. Miwa, K. Nomura, 1977, Human Genetics.

E. Beutler, D. Paglia, R. Rosa, 1989, Clinical and laboratory haematology.

Maturation of adult peripheral blood CD38(+)CD4(+) T cells demonstrated by cytokine production in response to a superantigen, TSST-1.

T. Uchiyama, K. Imanishi, H. Kato, 2003, Cellular immunology.

Erythrocyte enzyme activities in myelodysplastic syndromes: Elevated pyruvate kinase activity

S. Asano, H. Fujii, S. Miwa, 1989, American journal of hematology.

A combined system for the study of glutathione metabolism in erythrocytes.

H. Fujii, S. Miwa, Y. Ishida, 1979, Clinica chimica acta; international journal of clinical chemistry.

Ultrastructural study of immunoblastic lymphadenopathy.

H. Fujii, N. Matsumoto, T. Shiomura, 1977, The Tohoku journal of experimental medicine.

Imported malaria in Japan: hematological aspects.

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

Effect of Donor Blood Screening for Anti-HCV Antibody by the Second-generation Passive Hemagglutination Test on the Incidence of Post-Transfusion Hepatitis

Y. Sameshima, K. Nishioka, H. Fujii, 1994 .

[Photoradiation therapy of experimental glioma].

H. Abe, T. Asakura, H. Fujii, 1985, Neurologia medico-chirurgica.

Patient with pyruvate kinase deficiency developed acute myelogenous leukemia

F. Takaku, H. Fujii, S. Miwa, 1990, American journal of hematology/oncology.

Pyruvate kinase deficiency: Historical perspective and recent progress of molecular genetics

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

Haptoglobin therapy for acute favism: a Japanese boy with glucose‐6‐phosphate dehydrogenase Guadalajara

A. Matsuzaki, S. Ohga, A. Nomura, 1995, British journal of haematology.

Molecular abnormality of a unique japanese glucose‐6‐phosphate dehydrogenase variant (G6PD Kobe) with a greatly increased affinity for galactose‐6‐phosphate

H. Fujii, S. Miwa, S. Nakayama, 1994, American journal of hematology.

A Novel Homozygous Mutation of PKLR Gene in a Pyruvate-Kinase-Deficient Korean Family

H. Fujii, H. Kanno, W. Kim, 2005, Acta Haematologica.

A New Glucose-6-Phosphate Dehydrogenase Variant G6PD Sugao (826C→T) Exhibiting Chronic Hemolytic Anemia With Episodes of Hemolytic Crisis Immediately After Birth

M. Taki, H. Fujii, S. Miwa, 2001, International journal of hematology.

Two homozygous cases of erythrocyte pyruvate kinase (PK) deficiency in Japan: PK sendai and PK shinshu

T. Morisaki, T. Nakahata, K. Hayasaka, 1988, American journal of hematology/oncology.

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.

Cellulose‐treated blood is a good source of DNA for molecular analysis

H. Fujii, S. Miwa, A. Hirono, 1994, American journal of hematology.

Erythrocyte‐oxidized glutathione transport in pyrimidine 5′‐nucleotidase deficiency

Y. Ohtsuka, H. Fujii, S. Miwa, 1987, American journal of hematology.

Post-transfusion hepatitis in orthopedic surgery: Effects of Donor Screening with HCV Associated Antibodies (Anti C100 and Anti GOR) and GPT Levels and of Histories of Blood Transfusion to Recipients Anti-C100.

H. Fujii, Sumio Takahashi, M. Takanashi, 1991 .

[Circadian rhythm of estriol, dehydroepiandrosterone sulfate and cortisol levels in the maternal blood and their relationship with estriol production of the fetoplacental system].

H. Fujii, S. Sakamoto, K. Sato, 1974, Horumon to rinsho. Clinical endocrinology.

Molecular abnormality of a Japanese glucose-6-phosphate dehydrogenase variant (G6PD Tokyo) associated with hereditary non-spherocytic hemolytic anemia

H. Fujii, S. Miwa, H. Kanno, 2004, Human Genetics.

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

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

Two cases of phosphofructokinase deficiency associated with congenital hemolytic anemia found in Japan

A. Kuramoto, H. Fujii, S. Miwa, 1983, American journal of hematology.

Measurement of 5′‐methylthioadenosine in patients with neoplasms

T. Kumakawa, N. Kamatani, H. Fujii, 1990, International journal of cancer.

Autotransfusion supported by erythropoietin therapy in transurethral resection of the prostate.

T. Yagisawa, H. Fujii, M. Shimizu, 1998, Scandinavian journal of urology and nephrology.

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.

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.