Katsumi A - Search Results

1

High titer of ADAMTS13 inhibitor associated with thrombotic microangiopathy of the gut and skeletal muscle after allogeneic hematopoietic stem cell transplantation.

Adachi T, Matsushita T, Ichihashi R, Hirashima K, Ito M, Inukai A, Yokozawa T, Nishida T, Murata M, Hayashi M, Katsumi A, Kojima T, Saito H, Naoe T. Adachi T, et al. Among authors: katsumi a. Int J Hematol. 2006 Jun;83(5):415-9. doi: 10.1532/IJH97.05157. Int J Hematol. 2006. PMID: 16787872

2

Humoral and cellular immunity to an encoded protein induced by direct DNA injection.

Katsumi A, Emi N, Abe A, Hasegawa Y, Ito M, Saito H. Katsumi A, et al. Hum Gene Ther. 1994 Nov;5(11):1335-9. doi: 10.1089/hum.1994.5.11-1335. Hum Gene Ther. 1994. PMID: 7893804

3

A quantitative protein S deficiency associated with a novel nonsense mutation and markedly reduced levels of mutated mRNA.

Yamazaki T, Hamaguchi M, Katsumi A, Kagami K, Kojima T, Takamatsu J, Saito H. Yamazaki T, et al. Among authors: katsumi a. Thromb Haemost. 1995 Aug;74(2):590-5. Thromb Haemost. 1995. PMID: 8584989

4

Human ryudocan from endothelium-like cells binds basic fibroblast growth factor, midkine, and tissue factor pathway inhibitor.

Kojima T, Katsumi A, Yamazaki T, Muramatsu T, Nagasaka T, Ohsumi K, Saito H. Kojima T, et al. Among authors: katsumi a. J Biol Chem. 1996 Mar 8;271(10):5914-20. doi: 10.1074/jbc.271.10.5914. J Biol Chem. 1996. PMID: 8621465 Free article.

5

Protein C Nagoya, an elongated mutant of protein C, is retained within the endoplasmic reticulum and is associated with GRP78 and GRP94.

Katsumi A, Senda T, Yamashita Y, Yamazaki T, Hamaguchi M, Kojima T, Kobayashi S, Saito H. Katsumi A, et al. Blood. 1996 May 15;87(10):4164-75. Blood. 1996. PMID: 8639775 Free article.

6

Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474.

Yamazaki T, Katsumi A, Kagami K, Okamoto Y, Sugiura I, Hamaguchi M, Kojima T, Takamatsu J, Saito H. Yamazaki T, et al. Among authors: katsumi a. Blood. 1996 Jun 1;87(11):4643-50. Blood. 1996. PMID: 8639833 Free article.

7

[Carrier detection and prenatal diagnosis for hemophilia A using the inversion analysis of the factor VIII gene].

Okamoto Y, Kojima T, Katsumi A, Yamazaki T, Hamaguchi M, Nishida M, Suzumori K, Saito H. Okamoto Y, et al. Among authors: katsumi a. Rinsho Ketsueki. 1995 Nov;36(11):1252-6. Rinsho Ketsueki. 1995. PMID: 8691564 Japanese.

8

Analysis for antithrombin gene polymorphisms in Japanese subjects and cosegregation studies in families with hereditary antithrombin deficiency.

Yamazaki T, Katsumi A, Tsuzuki S, Sugiura I, Kojima T, Takamatsu J, Saito H. Yamazaki T, et al. Among authors: katsumi a. Thromb Res. 1996 May 1;82(3):275-80. doi: 10.1016/0049-3848(96)00074-6. Thromb Res. 1996. PMID: 8732631 No abstract available.

9

Structural organization and promoter activity of the human ryudocan gene.

Takagi A, Kojima T, Tsuzuki S, Katsumi A, Yamazaki T, Sugiura I, Hamaguchi M, Saito H. Takagi A, et al. Among authors: katsumi a. J Biochem. 1996 May;119(5):979-84. doi: 10.1093/oxfordjournals.jbchem.a021338. J Biochem. 1996. PMID: 8797100 Free article.

10

A novel nonsense mutation associated with an exon skipping in a patient with hereditary protein S deficiency type I.

Okamoto Y, Yamazaki T, Katsumi A, Kojima T, Takamatsu J, Nishida M, Saito H. Okamoto Y, et al. Among authors: katsumi a. Thromb Haemost. 1996 Jun;75(6):877-82. Thromb Haemost. 1996. PMID: 8822579

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