Saito H - Search Results

1

Possible absence of common polymorphisms in coagulation factor IX gene in Japanese subjects.

Kojima T, Tanimoto M, Kamiya T, Obata Y, Takahashi T, Ohno R, Kurachi K, Saito H. Kojima T, et al. Among authors: saito h. Blood. 1987 Jan;69(1):349-52. Blood. 1987. PMID: 2878695 Free article.

2

Extragenic factor IX gene RFLP is useful for detecting carriers of Japanese hemophilia B.

Tanimoto M, Kojima T, Ogata K, Hamaguchi M, Takamatsu J, Kamiya T, Saito H. Tanimoto M, et al. Among authors: saito h. Nihon Ketsueki Gakkai Zasshi. 1989 Jul;52(4):774-7. Nihon Ketsueki Gakkai Zasshi. 1989. PMID: 2575831

3

Carrier detection in Japanese hemophilia A by use of three intragenic and two extragenic factor VIII DNA probes: a study of 24 kindreds.

Suehiro K, Tanimoto M, Hamaguchi M, Kojima T, Takamatsu J, Ogata K, Kamiya T, Saito H. Suehiro K, et al. Among authors: saito h. J Lab Clin Med. 1988 Sep;112(3):314-8. J Lab Clin Med. 1988. PMID: 2900870

4

Three distinct point mutations in the factor IX gene of three Japanese CRM+ hemophilia B patients (factor IX BMNagoya 2, factor IX Nagoya 3 and 4).

Hamaguchi M, Matsushita T, Tanimoto M, Takahashi I, Yamamoto K, Sugiura I, Takamatsu J, Ogata K, Kamiya T, Saito H. Hamaguchi M, et al. Among authors: saito h. Thromb Haemost. 1991 May 6;65(5):514-20. Thromb Haemost. 1991. PMID: 1871712

5

DNA sequence analysis of three inhibitor-positive hemophilia B patients without gross gene deletion: identification of four novel mutations in factor IX gene.

Matsushita T, Tanimoto M, Yamamoto K, Sugiura I, Hamaguchi M, Takamatsu J, Kamiya T, Saito H. Matsushita T, et al. Among authors: saito h. J Lab Clin Med. 1990 Oct;116(4):492-7. J Lab Clin Med. 1990. PMID: 2212858

6

[Molecular diagnosis of inherited coagulation disorders--sequence analysis of hemophilia B patients with anti-factor IX antibodies].

Tanimoto M, Matsushita T, Takamatsu J, Saito H. Tanimoto M, et al. Among authors: saito h. Rinsho Byori. 1990 Sep;38(9):1041-6. Rinsho Byori. 1990. PMID: 2232265 Japanese.

7

[Molecular genetics and DNA diagnosis for inherited coagulation disorders].

Tanimoto M, Saito H. Tanimoto M, et al. Among authors: saito h. Nihon Rinsho. 1989 Apr;47(4):864-9. Nihon Rinsho. 1989. PMID: 2568509 Japanese. No abstract available.

8

Low incidence of acute graft-versus-host disease by the administration of methotrexate and cyclosporine in Japanese leukemia patients after bone marrow transplantation from human leukocyte antigen compatible siblings; possible role of genetic homogeneity. The Nagoya Bone Marrow Transplantation Group.

Morishima Y, Morishita Y, Tanimoto M, Ohno R, Saito H, Horibe K, Hamajima N, Naito K, Yamada K, Yokomaku S, et al. Morishima Y, et al. Among authors: saito h. Blood. 1989 Nov 1;74(6):2252-6. Blood. 1989. PMID: 2804362 Free article.

9

Phorbol ester induces interleukin-2 receptor on the cell surface of precursor thymocyte leukemia with no rearrangement of T cell receptor beta and gamma genes.

Morishima Y, Morishita Y, Adachi K, Tanimoto M, Ohno R, Saito H. Morishima Y, et al. Among authors: saito h. Blood. 1987 Nov;70(5):1291-6. Blood. 1987. PMID: 2822168 Free article.

10

[DNA analysis in the diagnosis of hemorrhagic diathesis].

Tanimoto M, Saito H. Tanimoto M, et al. Among authors: saito h. Rinsho Byori. 1987 Apr;Spec No 70:64-9. Rinsho Byori. 1987. PMID: 2886678 Review. Japanese. No abstract available.

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