Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

15,611 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Definite diagnosis in Japanese patients with protein C deficiency by identification of causative PROC mutations.
Takagi A, Tanaka R, Nakashima D, Fujimori Y, Yamada T, Okumura K, Murate T, Yamada M, Horikoshi Y, Yamamoto K, Katsumi A, Matsushita T, Naoe T, Kojima T. Takagi A, et al. Among authors: yamamoto k. Int J Hematol. 2009 May;89(4):555-557. doi: 10.1007/s12185-009-0312-7. Epub 2009 Apr 17. Int J Hematol. 2009. PMID: 19373522 No abstract available.
A novel splice site mutation in intron C of PROS1 leads to markedly reduced mutant mRNA level, absence of thrombin-sensitive region, and impaired secretion and cofactor activity of mutant protein S.
Okada H, Kunishima S, Hamaguchi M, Takagi A, Yamamoto K, Takamatsu J, Matsushita T, Saito H, Kojima T, Yamazaki T. Okada H, et al. Among authors: yamamoto k. Thromb Res. 2010 May;125(5):e246-50. doi: 10.1016/j.thromres.2009.11.029. Epub 2009 Dec 21. Thromb Res. 2010. PMID: 20022358
Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO mice.
Matsushita T, Hayashi H, Kunishima S, Hayashi M, Ikejiri M, Takeshita K, Yuzawa Y, Adachi T, Hirashima K, Sone M, Yamamoto K, Takagi A, Katsumi A, Kawai K, Nezu T, Takahashi M, Nakashima T, Naoe T, Kojima T, Saito H. Matsushita T, et al. Among authors: yamamoto k. Biochem Biophys Res Commun. 2004 Dec 24;325(4):1163-71. doi: 10.1016/j.bbrc.2004.10.147. Biochem Biophys Res Commun. 2004. PMID: 15555549
Recurrent mutations of factor XI gene in Japanese.
Okumura K, Kyotani M, Kawai R, Takagi A, Murate T, Yamamoto K, Takamatsu J, Matsushita T, Saito H, Kojima T. Okumura K, et al. Among authors: yamamoto k. Int J Hematol. 2006 Jun;83(5):462-3. doi: 10.1532/IJH97.06045. Int J Hematol. 2006. PMID: 16787881 No abstract available.
15,611 results
You have reached the last available page of results. Please see the User Guide for more information.