Yawata Y - Search Results

1

DNA methylation in promoter regions of red cell membrane protein genes in healthy individuals and patients with hereditary membrane disorders.

Remus R, Kanzaki A, Yawata A, Nakanishi H, Wada H, Sugihara T, Zeschnigk M, Zuther I, Schmitz B, Naumann F, Doerfler W, Yawata Y. Remus R, et al. Among authors: yawata y, yawata a. Int J Hematol. 2005 Jun;81(5):385-95. doi: 10.1532/ijh97.04171. Int J Hematol. 2005. PMID: 16158818

2

Relationships between DNA methylation and expression in erythrocyte membrane protein (band 3, protein 4.2, and beta-spectrin) genes during human erythroid development and differentiation.

Remus R, Kanzaki A, Yawata A, Wada H, Nakanishi H, Sugihara T, Zeschnigk M, Zuther I, Schmitz B, Naumann F, Doerfler W, Yawata Y. Remus R, et al. Among authors: yawata y, yawata a. Int J Hematol. 2005 Dec;82(5):422-9. doi: 10.1532/IJH97.05058. Int J Hematol. 2005. PMID: 16533746

3

[Cytoskeleton anomalies in disorders of red cell membrane proteins].

Kanzaki A, Wada H, Yawata Y. Kanzaki A, et al. Among authors: yawata y. Rinsho Ketsueki. 1991 Jun;32(6):573-9. Rinsho Ketsueki. 1991. PMID: 1832469 Japanese.

4

Red cell membrane disorders in the Japanese population: clinical, biochemical, electron microscopic, and genetic studies.

Yawata Y, Kanzaki A, Inoue T, Ata K, Wada H, Okamoto N, Higo I, Yawata A, Sugihara T, Yamada O. Yawata Y, et al. Among authors: yawata a. Int J Hematol. 1994 Jul;60(1):23-38. Int J Hematol. 1994. PMID: 7919236 Review.

5

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

Yawata Y, Kanzaki A, Yawata A, Doerfler W, Ozcan R, Eber SW. Yawata Y, et al. Among authors: yawata a. Int J Hematol. 2000 Feb;71(2):118-35. Int J Hematol. 2000. PMID: 10745622

6

Ankyrin gene mutations in japanese patients with hereditary spherocytosis.

Nakanishi H, Kanzaki A, Yawata A, Yamada O, Yawata Y. Nakanishi H, et al. Among authors: yawata y, yawata a. Int J Hematol. 2001 Jan;73(1):54-63. doi: 10.1007/BF02981903. Int J Hematol. 2001. PMID: 11372755

7

Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.

Inoue T, Kanzaki A, Yawata A, Wada H, Okamoto N, Takahashi M, Sugihara T, Yamada O, Yawata Y. Inoue T, et al. Among authors: yawata y, yawata a. Int J Hematol. 1994 Dec;60(4):227-38. Int J Hematol. 1994. PMID: 7894027

8

Late expression of red cell membrane protein 4.2 in normal human erythroid maturation with seven isoforms of the protein 4.2 gene.

Wada H, Kanzaki A, Yawata A, Inoue T, Kaku M, Takezono M, Sugihara T, Yamada O, Yawata Y. Wada H, et al. Among authors: yawata y, yawata a. Exp Hematol. 1999 Jan;27(1):54-62. doi: 10.1016/s0301-472x(98)00014-9. Exp Hematol. 1999. PMID: 9923444 Free article.

9

Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied.

Yawata Y, Kanzaki A, Yawata A, Nakanishi H, Kaku M. Yawata Y, et al. Among authors: yawata a. Hematology. 2001;6(6):399-422. doi: 10.1080/10245332.2001.11746596. Hematology. 2001. PMID: 27405697 Free article.

10

[Cytoskeleton and membrane anomalies in disorders of red cell membrane proteins].

Kanzaki A, Yawata Y. Kanzaki A, et al. Among authors: yawata y. Rinsho Byori. 1991 Sep;Suppl 91:37-46. Rinsho Byori. 1991. PMID: 1836821 Japanese. No abstract available.

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