Nakanishi H - 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: nakanishi h. 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: nakanishi h. Int J Hematol. 2005 Dec;82(5):422-9. doi: 10.1532/IJH97.05058. Int J Hematol. 2005. PMID: 16533746

3

Ankyrin gene mutations in japanese patients with hereditary spherocytosis.

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

4

[Hereditary red cell membrane disorders in Japan: comparison with other countries].

Nakanishi H, Wada H, Suemori S, Sugihara T. Nakanishi H, et al. Rinsho Ketsueki. 2015 Jul;56(7):760-70. doi: 10.11406/rinketsu.56.760. Rinsho Ketsueki. 2015. PMID: 26251138 Japanese.

5

[Band 3 deficiency as a cause of hereditary spherocytosis].

Wada H, Suemori S, Nakanishi H, Sugihara T. Wada H, et al. Among authors: nakanishi h. Rinsho Ketsueki. 2015 Jul;56(7):837-45. doi: 10.11406/rinketsu.56.837. Rinsho Ketsueki. 2015. PMID: 26251147 Japanese.

6

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: nakanishi h. Hematology. 2001;6(6):399-422. doi: 10.1080/10245332.2001.11746596. Hematology. 2001. PMID: 27405697 Free article.

7

Analysis of Hereditary Elliptocytosis with Decreased Binding of Eosin-5-maleimide to Red Blood Cells.

Suemori S, Wada H, Nakanishi H, Tsujioka T, Sugihara T, Tohyama K. Suemori S, et al. Among authors: nakanishi h. Biomed Res Int. 2015;2015:451861. doi: 10.1155/2015/451861. Epub 2015 Oct 18. Biomed Res Int. 2015. PMID: 26557672 Free PMC article.

8

MLL/AF-1p fusion in therapy-related early pre-B acute lymphoblastic leukemia with t(1;11)(p32;q23) translocation developing in the relapse phase of acute promyelocytic leukemia.

Tsujioka T, Wada H, Yamamori S, Otsuki T, Suemori S, Kondo T, Nakanishi H, Suetsugu Y, Mikami M, Sugihara T. Tsujioka T, et al. Among authors: nakanishi h. Int J Hematol. 2003 Dec;78(5):439-42. doi: 10.1007/BF02983817. Int J Hematol. 2003. PMID: 14704037

9

[Acute myelogenous leukemia associated with severe esophageal stricture after chemotherapy].

Yata K, Yamada O, Iwato K, Kyo T, Otsuki T, Nakanishi H, Suetsugu Y, Mikami M, Wada H, Yawata Y, Sugihara T. Yata K, et al. Among authors: nakanishi h. Rinsho Ketsueki. 2002 Jan;43(1):41-3. Rinsho Ketsueki. 2002. PMID: 11868364 Review. Japanese.

10

[Seven patients with stage I and II primary testicular lymphoma].

Kondo T, Wada H, Yata K, Mikami M, Tsujioka T, Suemori S, Suetsugu Y, Nakanishi H, Otsuki T, Yamada O, Yawata Y, Morioka M, Tanaka H, Sadahira Y, Sugihara T. Kondo T, et al. Among authors: nakanishi h. Rinsho Ketsueki. 2002 Jun;43(6):473-6. Rinsho Ketsueki. 2002. PMID: 12134704 Japanese.

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