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In vitro excess ammonia production in human myeloma cell lines

Leukemia, 1998-07, Vol.12 (7), p.1149-1158

1998

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Progress in research on red cell membrane disorders: from the genome to the postgenome era

Rinshō ketsueki, 2001-05, Vol.42 (5), p.343

Yawata, Y

2001

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Expression of fibroblast growth factor and FGF-receptor family genes in human myeloma cells, including lines possessing t(4;14)(q16.3;q32. 3) and FGFR3 translocation

International journal of oncology, 1999-12, Vol.15 (6), p.1205

1999

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Red cell membrane disorders: historical perspectives from dawn to enlightenment (II)

Rinshō ketsueki, 1999-12, Vol.40 (12), p.1223

Yawata, Y

1999

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Red cell membrane disorders: historical perspectives from dawn to enlightenment (I)

Rinshō ketsueki, 1999-11, Vol.40 (11), p.1133

Yawata, Y

1999

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Expression of angiogenic factors including VEGFs and the effects of hypoxia and thalidomide on human myeloma cells

International journal of oncology, 2003-01, Vol.22 (1), p.165

2003

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Band 4.2 Abnormalities in Human Red Cells

The American journal of the medical sciences, 1994-03, Vol.307 (3), p.190-203

Yawata, Yoshihito

1994

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Characteristics of hereditary spherocytosis

Nihon Naika Gakkai zasshi, 1999-09, Vol.88 (9), p.1825-1833

Yawata, Y

1999

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Characteristics of red cell membrane disorders in the Japanese population

Rinsho byori. The Japanese journal of clinical pathology, 1997-04, Vol.45 (4), p.367

Yawata, Y

1997

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Integral proteins of red cell membranes: their genetic and phenotypic expressions

Nihon rinshō, 1996-09, Vol.54 (9), p.2348

Yawata, Y

1996

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Expression and In Vitro Modification of Parathyroid Hormone-Related Protein (PTHrP) and PTH/PTHrP-Receptor in Human Myeloma Cells

Leukemia & lymphoma, 2001, Vol.41 (3-4), p.397-409

2001

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Control of band 3 lateral and rotational mobility by band 4.2 in intact erythrocytes: release of band 3 oligomers from low-affinity binding sites

Biophysical journal, 1996-03, Vol.70 (3), p.1534-1542

1996

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Hemolytic anemia--recent findings--with special reference to erythrocyte membrane abnormalities

Nihon Naika Gakkai zasshi, 1997-03, Vol.86 (3), p.481-490

Yawata, Y

1997

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Congenital hemolytic anemia

Nihon rinshō, 2001-11, Vol.59 Suppl 7, p.416

2001

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Emergency therapy of disseminated intravascular coagulation

Nihon Naika Gakkai zasshi, 1995-11, Vol.84 (11), p.1858-1864

Yawata, Y

1995

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Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation

The Journal of clinical investigation, 1996-04, Vol.97 (8), p.1804-1817

1996

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Expression of Major Blood Group Antigens on Human Erythroid Cells in a Two Phase Liquid Culture System

Blood, 1990-01, Vol.75 (2), p.505-511

1990

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A surface replica method: a useful tool for studies of the cytoskeletal network in red cell membranes of normal subjects and patients with a β-spectrin mutant (spectrin Le Puy: β220/214)

Virchows Archiv : an international journal of pathology, 1994-10, Vol.425 (3), p.297-304

1994

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Establishment of CD7+ Human Myeloma Sister Cell Lines, KMS-21-PE and KMS-21-BM, Carrying t(11;14) and t(8;14)

Leukemia & lymphoma, 2001, Vol.42 (4), p.761-774

2001

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Hereditary stomatocytosis: phenotypical expression of sodium transport and band 7 peptides in 44 cases

British journal of haematology, 1992-09, Vol.82 (1), p.133-141

1992

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Red cell membrane disorders of congenital origin

Nihon rinshō, 1991-03, Vol.49 (3), p.647

Yawata, Y

1991

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Polycythaemia vera: response to treatment with angiotensin-converting enzyme inhibitor

European journal of haematology, 1996-07, Vol.57 (1), p.117-119

1996

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Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population

International journal of hematology, 2000-02, Vol.71 (2), p.118-135

2000

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Ankyrin gene mutations in Japanese patients with hereditary spherocytosis

International journal of hematology, 2001-01, Vol.73 (1), p.54-63

2001

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Abnormality of the glycolytic enzymes and erythrocyte membrane in congenital hemolytic anemia

Nihon Naika Gakkai zasshi, 1990-05, Vol.79 (5), p.625-631

Yawata, Y

1990

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In vitro excess ammonia production in human myeloma cell lines

Progress in research on red cell membrane disorders: from the genome to the postgenome era

Expression of fibroblast growth factor and FGF-receptor family genes in human myeloma cells, including lines possessing t(4;14)(q16.3;q32. 3) and FGFR3 translocation

Red cell membrane disorders: historical perspectives from dawn to enlightenment (II)

Red cell membrane disorders: historical perspectives from dawn to enlightenment (I)

Expression of angiogenic factors including VEGFs and the effects of hypoxia and thalidomide on human myeloma cells

Band 4.2 Abnormalities in Human Red Cells

Characteristics of hereditary spherocytosis

Characteristics of red cell membrane disorders in the Japanese population

Integral proteins of red cell membranes: their genetic and phenotypic expressions

Expression and In Vitro Modification of Parathyroid Hormone-Related Protein (PTHrP) and PTH/PTHrP-Receptor in Human Myeloma Cells

Control of band 3 lateral and rotational mobility by band 4.2 in intact erythrocytes: release of band 3 oligomers from low-affinity binding sites

Hemolytic anemia--recent findings--with special reference to erythrocyte membrane abnormalities

Congenital hemolytic anemia

Emergency therapy of disseminated intravascular coagulation

Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation

Expression of Major Blood Group Antigens on Human Erythroid Cells in a Two Phase Liquid Culture System

A surface replica method: a useful tool for studies of the cytoskeletal network in red cell membranes of normal subjects and patients with a β-spectrin mutant (spectrin Le Puy: β220/214)

Establishment of CD7+ Human Myeloma Sister Cell Lines, KMS-21-PE and KMS-21-BM, Carrying t(11;14) and t(8;14)

Hereditary stomatocytosis: phenotypical expression of sodium transport and band 7 peptides in 44 cases

Red cell membrane disorders of congenital origin

Polycythaemia vera: response to treatment with angiotensin-converting enzyme inhibitor

Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population

Ankyrin gene mutations in Japanese patients with hereditary spherocytosis

Abnormality of the glycolytic enzymes and erythrocyte membrane in congenital hemolytic anemia

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