Urata M - Search Results

1

Successful therapy with argatroban for superior mesenteric vein thrombosis in a patient with congenital antithrombin deficiency.

Muta T, Okamura T, Kawamoto M, Ichimiya H, Yamanaka M, Wada Y, Urata M, Kayamori Y, Hamasaki N, Kato K, Eto T, Gondo H, Shibuya T. Muta T, et al. Among authors: urata m. Eur J Haematol. 2005 Aug;75(2):167-70. doi: 10.1111/j.1600-0609.2005.00480.x. Eur J Haematol. 2005. PMID: 16000134

2

Four missense mutations identified in the protein S gene of thrombosis patients with protein S deficiency: effects on secretion and anticoagulant activity of protein S.

Tsuda H, Urata M, Tsuda T, Wakiyama M, Iida H, Nakahara M, Kinoshita S, Hamasaki N. Tsuda H, et al. Among authors: urata m. Thromb Res. 2002 Feb 1;105(3):233-9. doi: 10.1016/s0049-3848(02)00015-4. Thromb Res. 2002. PMID: 11927129

3

A novel splice acceptor site mutation of protein S gene in affected individuals with type I protein S deficiency: allelic exclusion of the mutant gene.

Nakahara M, Iida H, Urata M, Fujise M, Wakiyama M, Kinoshita S, Tsuda H, Okamura T, Yao K, Yao T, Hamasaki N. Nakahara M, et al. Among authors: urata m. Thromb Res. 2001 Mar 1;101(5):387-93. doi: 10.1016/s0049-3848(01)00210-9. Thromb Res. 2001. PMID: 11297755

4

High-sensitivity detection of the A3243G mutation of mitochondrial DNA by a combination of allele-specific PCR and peptide nucleic acid-directed PCR clamping.

Urata M, Wada Y, Kim SH, Chumpia W, Kayamori Y, Hamasaki N, Kang D. Urata M, et al. Clin Chem. 2004 Nov;50(11):2045-51. doi: 10.1373/clinchem.2004.033761. Epub 2004 Sep 13. Clin Chem. 2004. PMID: 15364886

5

Failure in the detection of aberrant mRNA from the heterozygotic splice site mutant allele for protein S in a patient with protein S deficiency.

Iida H, Nakahara M, Komori K, Fujise M, Wakiyama M, Urata M, Kinoshita S, Tsuda H, Sugimachi K, Hamasaki N. Iida H, et al. Among authors: urata m. Thromb Res. 2001 May 1;102(3):187-96. doi: 10.1016/s0049-3848(01)00246-8. Thromb Res. 2001. PMID: 11369411

6

[A basic study of determination matrix metalloproteinase-3 and carbohydrate in rheumatoid factor in serum for diagnosis of rheumatoid arthritis].

Urata M, Nakamura N, Kinoshita S, Kayamori Y, Hamasaki N. Urata M, et al. Rinsho Byori. 2003 Aug;51(8):745-50. Rinsho Byori. 2003. PMID: 13677934 Japanese.

7

Paediatric presentation and outcome of congenital protein C deficiency in Japan.

Ohga S, Kang D, Kinjo T, Ochiai M, Doi T, Ishimura M, Kayamori Y, Urata M, Yamamoto J, Suenobu SI, Kanegane H, Ikenoue T, Shirahata A, Hara T. Ohga S, et al. Among authors: urata m. Haemophilia. 2013 May;19(3):378-84. doi: 10.1111/hae.12097. Epub 2013 Feb 4. Haemophilia. 2013. PMID: 23379934

8

Factor XII gene (F12) -4C/C polymorphism in combination with low protein S activity is associated with deep vein thrombosis.

Kanaji T, Watanabe K, Hattori S, Urata M, Iida H, Kinoshita S, Kayamori Y, Kang D, Hamasaki N. Kanaji T, et al. Among authors: urata m. Thromb Haemost. 2006 Dec;96(6):854-5. Thromb Haemost. 2006. PMID: 17139385 No abstract available.

9

A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene.

Iida H, Ishii E, Nakahara M, Urata M, Wakiyama M, Kurihara M, Watanabe K, Kai T, Ihara K, Kinoshita S, Hamasaki N. Iida H, et al. Among authors: urata m. Thromb Haemost. 2000 Jul;84(1):49-53. Thromb Haemost. 2000. PMID: 10928469

10

Platelet contamination causes large variation as well as overestimation of mitochondrial DNA content of peripheral blood mononuclear cells.

Urata M, Koga-Wada Y, Kayamori Y, Kang D. Urata M, et al. Ann Clin Biochem. 2008 Sep;45(Pt 5):513-4. doi: 10.1258/acb.2008.008008. Ann Clin Biochem. 2008. PMID: 18753426

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