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

Brain & development (Tokyo. 1979), 2013-04, Vol.35 (4), p.349-355

2013

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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

Internal Medicine, 2012, Vol.51(8), pp.917-920

2012

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Shared molecular targets in pediatric gliomas and ependymomas

Pediatric blood & cancer, 2011-12, Vol.57 (7), p.1117-1123

2011

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

Child's nervous system, 2011-06, Vol.27 (6), p.1019-1024

2011

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

Experimental hematology, 2007-08, Vol.35 (8), p.1190-1200

2007

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

Human genetics, 2001-06, Vol.108 (6), p.445-449

2001

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

Haematologica (Roma), 2007-06, Vol.92 (6), p.731-737

2007

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

International journal of hematology, 2007-11, Vol.86 (4), p.325-328

2007

Volltextzugriff (PDF)

Splenic infarction after epstein-barr virus infection in a patient with hereditary spherocytosis

International journal of hematology, 2007-06, Vol.85 (5), p.380-383

2007

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

Cancer chemotherapy and pharmacology, 2012-06, Vol.69 (6), p.1617-1624

2012

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

Proceedings of the Japan Academy, Series B, 2002, Vol.78(10), pp.287-292

2002

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

Biochemical and biophysical research communications, 1992-10, Vol.188 (2), p.516-523

1992

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A new glucose-6-phosphate dehydrogenase variant G6PD sugao (826C→T) exhibiting chronic hemolytic anemia with episodes of hemolytic crisis immediately after birth

International journal of hematology, 2001-08, Vol.74 (2), p.153-156

2001

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

American journal of hematology, 1993-01, Vol.42 (1), p.31-35

1993

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Measurement of glutathione

Nihon rinshō, 2004-12, Vol.62 Suppl 12, p.762

Fujii, Hisaichi

2004

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Other major red cell enzyme activities

Nihon rinshō, 2004-12, Vol.62 Suppl 12, p.840

Fujii, Hisaichi

2004

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

British journal of haematology, 2004-07, Vol.126 (2), p.265-271

2004

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Ineffective erythropoiesis in mutant mice with deficient pyruvate kinase activity

Experimental hematology, 2005-11, Vol.33 (11), p.1292-1298

2005

Volltextzugriff (PDF)

Double high-dose chemotherapy followed by autologous peripheral blood stem cell transplantation for primary disseminated medulloblastoma: a report of 3 cases

Journal of pediatric hematology/oncology, 2010-03, Vol.32 (2), p.e70-e74

2010

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

International journal of hematology, 1999-06, Vol.69 (4), p.234-236

1999

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Target Marker Gene Expressions and the Possibility of Molecular Therapy for Children's Brain Tumors

Blood, 2006-11, Vol.108 (11), p.5468-5468

2006

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

Blood, 2005-11, Vol.106 (11), p.1678-1678

2005

Volltextzugriff (PDF)

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

Blood, 2002-02, Vol.99 (4), p.1498-1498

2002

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

Genomics (San Diego, Calif.), 1988, Vol.2 (1), p.86-89

1988

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

Blood, 2002-09, Vol.100 (5), p.1930-1930

2002

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

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

Shared molecular targets in pediatric gliomas and ependymomas

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

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

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

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

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

Splenic infarction after epstein-barr virus infection in a patient with hereditary spherocytosis

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

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

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

A new glucose-6-phosphate dehydrogenase variant G6PD sugao (826C→T) exhibiting chronic hemolytic anemia with episodes of hemolytic crisis immediately after birth

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

Measurement of glutathione

Other major red cell enzyme activities

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

Ineffective erythropoiesis in mutant mice with deficient pyruvate kinase activity

Double high-dose chemotherapy followed by autologous peripheral blood stem cell transplantation for primary disseminated medulloblastoma: a report of 3 cases

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

Target Marker Gene Expressions and the Possibility of Molecular Therapy for Children's Brain Tumors

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

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

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

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

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