Katsumi A - Search Results

1

Impact of variation in reagent combinations for one-stage clotting assay on assay discrepancy in nonsevere haemophilia A.

Suzuki A, Suzuki N, Kanematsu T, Okamoto S, Tamura S, Kikuchi R, Katsumi A, Kiyoi H, Kojima T, Matsushita T. Suzuki A, et al. Among authors: katsumi a. Int J Lab Hematol. 2021 Feb;43(1):131-138. doi: 10.1111/ijlh.13335. Epub 2020 Sep 11. Int J Lab Hematol. 2021. PMID: 32915508 Clinical Trial.

2

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

3

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.

4

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.

5

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.

6

[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.

7

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.

8

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

9

Analysis for heterozygosity of protein S mRNA: application to genetic screening and family studies in hereditary protein S deficiency.

Yamazaki T, Hamaguchi M, Takamatsu J, Okamoto Y, Katsumi A, Kagami K, Sugiura I, Kojima T, Saito H. Yamazaki T, et al. Among authors: katsumi a. Int J Hematol. 1996 Aug;64(2):119-25. doi: 10.1016/0925-5710(96)00468-9. Int J Hematol. 1996. PMID: 8854569

10

Two distinct novel splice site mutations in a compound heterozygous patient with protein S deficiency.

Yamazaki T, Katsumi A, Okamoto Y, Takafuta T, Tsuzuki S, Kagami K, Sugiura I, Kojima T, Fujimura K, Saito H. Yamazaki T, et al. Among authors: katsumi a. Thromb Haemost. 1997 Jan;77(1):14-20. Thromb Haemost. 1997. PMID: 9031442

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

108 results

Search Page

Filters