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Items: 1 to 20 of 86

1.

Association of the smoothelin (SMTN) gene with cerebral infarction in men: a haplotype-based case-control study.

Jiang J, Nakayama T, Shimodaira M, Sato N, Aoi N, Sato M, Izumi Y, Kasamaki Y, Ohta M, Soma M, Matsumoto K, Kawamura H, Ozawa Y, Hinohara S, Doba N, Ma Y.

Vasc Med. 2012 Oct;17(5):317-25. doi: 10.1177/1358863X12453938.

PMID:
23033319
2.

Haplotype of smoothelin gene associated with essential hypertension.

Jiang J, Nakayama T, Shimodaira M, Sato N, Aoi N, Sato M, Izumi Y, Kasamaki Y, Ohta M, Soma M, Matsumoto K, Kawamura H, Ozawa Y, Ma Y.

Hereditas. 2012 Oct;149(5):178-85. doi: 10.1111/j.1601-5223.2012.02242.x. Epub 2012 Oct 18.

3.

A haplotype of the SMTN gene associated with myocardial infarction in Japanese women.

Jiang J, Nakayama T, Shimodaira M, Sato N, Aoi N, Sato M, Izumi Y, Kasamaki Y, Ohta M, Soma M, Matsumoto K, Kawamura H, Ozawa Y, Ma Y.

Genet Test Mol Biomarkers. 2012 Sep;16(9):1019-26. doi: 10.1089/gtmb.2012.0034.

PMID:
22963604
4.

The insulin-like growth factor-1 gene is associated with cerebral infarction in Japanese subjects.

Aoi N, Nakayama T, Soma M, Kosuge K, Haketa A, Sato M, Sato N, Hinohara S, Doba N, Asai S.

Hereditas. 2012 Oct;149(5):153-62. doi: 10.1111/j.1601-5223.2012.02257.x. Epub 2012 Sep 20.

5.

Purinergic receptor P2Y, G-protein coupled, 2 (P2RY2) gene is associated with cerebral infarction in Japanese subjects.

Wang Z, Nakayama T, Sato N, Yamaguchi M, Izumi Y, Kasamaki Y, Ohta M, Soma M, Aoi N, Ozawa Y, Ma Y, Doba N, Hinohara S.

Hypertens Res. 2009 Nov;32(11):989-96. doi: 10.1038/hr.2009.136. Epub 2009 Sep 18.

PMID:
19763137
6.

Relationship between haplotypes of KCNN4 gene and susceptibility to human vascular diseases in Japanese.

Yamaguchi M, Nakayama T, Fu Z, Naganuma T, Sato N, Soma M, Doba N, Hinohara S, Morita A, Mizutani T.

Med Sci Monit. 2009 Aug;15(8):CR389-97.

PMID:
19644414
7.

Association of the purinergic receptor P2Y, G-protein coupled, 2 (P2RY2) gene with myocardial infarction in Japanese men.

Wang ZX, Nakayama T, Sato N, Izumi Y, Kasamaki Y, Ohta M, Soma M, Aoi N, Matsumoto K, Ozawa Y, Ma YT, Doba N, Hinohara S.

Circ J. 2009 Dec;73(12):2322-9. Epub 2009 Oct 2.

8.

The haplotype of the CACNA1B gene associated with cerebral infarction in a Japanese population.

Yamaguchi M, Nakayama T, Fu Z, Sato N, Soma M, Morita A, Hinohara S, Doba N, Mizutani T.

Hereditas. 2010 Dec;147(6):313-9. doi: 10.1111/j.1601-5223.2009.02115.x.

9.

A haplotype of the CYP4F2 gene is associated with cerebral infarction in Japanese men.

Fu Z, Nakayama T, Sato N, Izumi Y, Kasamaki Y, Shindo A, Ohta M, Soma M, Aoi N, Sato M, Matsumoto K, Ozawa Y, Ma Y.

Am J Hypertens. 2008 Nov;21(11):1216-23. doi: 10.1038/ajh.2008.276. Epub 2008 Sep 11.

PMID:
18787519
10.

Haplotype-based case-control study of receptor (calcitonin) activity-modifying protein-1 gene in cerebral infarction.

Nakazato T, Nakayama T, Naganuma T, Sato N, Fu Z, Wang Z, Soma M, Sugama K, Hinohara S, Doba N.

J Hum Hypertens. 2010 May;24(5):351-8. doi: 10.1038/jhh.2009.68. Epub 2009 Aug 27.

PMID:
19710695
11.

Association of extracellular superoxide dismutase gene with cerebral infarction in women: a haplotype-based case-control study.

Naganuma T, Nakayama T, Sato N, Fu Z, Soma M, Aoi N, Hinohara S, Doba N, Usami R.

Hereditas. 2008 Dec;145(6):283-92. doi: 10.1111/j.1601-5223.2008.02086.x.

12.

The haplotype of the TGFβ1 gene associated with cerebral infarction in Chinese.

Tao HM, Chen GZ, Cheng GP, Shan XY.

Can J Neurol Sci. 2012 Sep;39(5):626-31.

PMID:
22931704
13.

Haplotype-based case-control study between human apurinic/apyrimidinic endonuclease 1/redox effector factor-1 gene and cerebral infarction.

Naganuma T, Nakayama T, Sato N, Fu Z, Yamaguchi M, Soma M, Aoi N, Usami R, Doba N, Hinohara S.

Clin Biochem. 2009 Oct;42(15):1493-9. doi: 10.1016/j.clinbiochem.2009.07.016. Epub 2009 Jul 23.

PMID:
19631633
14.

Analyses of single nucleotide polymorphisms and haplotype linkage of LOC387715 and the HTRA1 gene in exudative age-related macular degeneration in a Chinese cohort.

Jiang H, Qu Y, Dang G, Zhang X, Yin N, Zhang Y, Bi H, Pan X, Xu X, Zhou F, Dai H.

Retina. 2009 Jul-Aug;29(7):974-9. doi: 10.1097/IAE.0b013e3181a3b90e.

PMID:
19491722
15.

Relationship between the thromboxane A2 receptor gene and susceptibility to cerebral infarction.

Kaneko Y, Nakayama T, Saito K, Morita A, Sato I, Maruyama A, Soma M, Takahashi T, Sato N.

Hypertens Res. 2006 Sep;29(9):665-71.

PMID:
17249521
16.

[Variations within OLF1/EBF-associated zinc finger protein gene confer susceptibility to lupus nephritis in Chinese population].

Liang D, Huang XQ, Shen N, Mao HQ, Feng XB, Huang XF, Tang JP, Chen XX, Chen SL, Gu YY, Bao CD, Wang Y, Qian J.

Zhonghua Yi Xue Za Zhi. 2005 Apr 13;85(14):949-54. Chinese.

PMID:
16061000
17.

Association of genetic polymorphisms of ACADSB and COMT with human hypertension.

Kamide K, Kokubo Y, Yang J, Matayoshi T, Inamoto N, Takiuchi S, Horio T, Miwa Y, Yoshii M, Tomoike H, Tanaka C, Banno M, Okuda T, Kawano Y, Miyata T.

J Hypertens. 2007 Jan;25(1):103-10.

PMID:
17143180
18.

A haplotype of the GOSR2 gene is associated with myocardial infarction in Japanese men.

Pan S, Nakayama T, Sato N, Izumi Y, Soma M, Aoi N, Ma Y, Hinohara S, Doba N.

Genet Test Mol Biomarkers. 2013 Jun;17(6):481-8. doi: 10.1089/gtmb.2012.0379. Epub 2013 May 15.

19.

A haplotype of the GOSR2 gene is associated with essential hypertension in Japanese men.

Pan S, Nakayama T, Sato N, Izumi Y, Soma M, Aoi N, Ma Y.

Clin Biochem. 2013 Jun;46(9):760-5. doi: 10.1016/j.clinbiochem.2012.12.021. Epub 2013 Jan 11.

PMID:
23313660
20.

Haplotype-based case-control study of CYP4A11 gene and myocardial infarction.

Fu Z, Nakayama T, Sato N, Izumi Y, Kasamaki Y, Shindo A, Ohta M, Soma M, Aoi N, Sato M, Ozawa Y, Ma Y.

Hereditas. 2012 Jun;149(3):91-8. doi: 10.1111/j.1601-5223.2012.02247.x. Epub 2012 Jul 4.

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