Works matching IS 14345161 AND DT 2010 AND VI 55 AND IP 10

Results: 14

Polymorphisms and allele frequencies of the ABO blood group gene among the Jomon, Epi-Jomon and Okhotsk people in Hokkaido, northern Japan, revealed by ancient DNA analysis.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 691, doi. 10.1038/jhg.2010.90

By:

Sato, Takehiro;
Kazuta, Hisako;
Amano, Tetsuya;
Ono, Hiroko;
Ishida, Hajime;
Kodera, Haruto;
Matsumura, Hirofumi;
Yoneda, Minoru;
Dodo, Yukio;
Masuda, Ryuichi

Publication type:

Article

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 656, doi. 10.1038/jhg.2010.82

By:

Akiyama, Koichi;
Narita, Akira;
Nakaoka, Hirofumi;
Cui, Tailin;
Takahashi, Tomoko;
Yasuno, Katsuhito;
Tajima, Atsushi;
Krischek, Boris;
Yamamoto, Ken;
Kasuya, Hidetoshi;
Hata, Akira;
Inoue, Ituro

Publication type:

Article

Analysis of LDLR mRNA in patients with familial hypercholesterolemia revealed a novel mutation in intron 14, which activates a cryptic splice site.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 676, doi. 10.1038/jhg.2010.87

By:

Kulseth, Mari Ann;
Berge, Knut Erik;
Bogsrud, Martin Prøven;
Leren, Trond P.

Publication type:

Article

Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 649, doi. 10.1038/jhg.2010.79

By:

Sillén, Anna;
Brohede, Jesper;
Lilius, Lena;
Forsell, Charlotte;
Andrade, Jorge;
Odeberg, Jacob;
Ebise, Hayao;
Winblad, Bengt;
Graff, Caroline

Publication type:

Article

Association of polymorphisms in the RAGE gene with serum CRP levels and coronary artery disease in the Chinese Han population.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 668, doi. 10.1038/jhg.2010.85

By:

Jinxiong Gao;
Yahui Shao;
Wenyan Lai;
Hao Ren;
Dingli Xu

Publication type:

Article

GATA transcription factors in congenital heart defects: A Commentary on a novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.

Published in:

2010

By:

Kodo, Kazuki;
Yamagishi, Hiroyuki

Publication type:

Opinion

Genetic variants that affect length/height in infancy/early childhood in Vietnamese-Korean families.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 681, doi. 10.1038/jhg.2010.88

By:

Han-Na Kim;
Eun-Ju Lee;
Sung-Chul Jung;
Jong-Young Lee;
Hye Won Chung;
Hyung-Lae Kim

Publication type:

Article

A Commentary on genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms.

Published in:

2010

By:

Koizumi, Akio

Publication type:

Opinion

A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 662, doi. 10.1038/jhg.2010.84

By:

Xiaoping Lin;
Zhaoxia Huo;
Xingyuan Liu;
Yangyang Zhang;
Li Li;
Hong Zhao;
Biao Yan;
Ying Liu;
Yiqing Yang;
Yi-Han Chen

Publication type:

Article

Myocilin and optineurin coding variants in Hispanics of Mexican descent with POAG.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 697, doi. 10.1038/jhg.2010.91

By:

McDonald, Kristin K.;
Abramson, Karen;
Beltran, Marco A.;
Ramirez, Maria G.;
Alvarez, Miguel;
Ventura, Alice;
Santiago-Turla, Cecilia;
Schmidt, Silke;
Hauser, Michael A.;
Allingham, R. Rand

Publication type:

Article

Association of the leptin gene with knee osteoarthritis susceptibility in a Han Chinese population: a case-control study.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 704, doi. 10.1038/jhg.2010.86

By:

Jianghui Qin;
Dongquan Shi;
Jin Dai;
Lunqing Zhu;
Tsezou, Aspasia;
Qing Jiang

Publication type:

Article

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 639, doi. 10.1038/jhg.2010.96

By:

Mahdieh, Nejat;
Rabbani, Bahareh;
Wiley, Susan;
Akbari, Mohammad Taghi;
Zeinali, Sirous

Publication type:

Article

Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 701, doi. 10.1038/jhg.2010.83

By:

Nakanishi, Hiroshi;
Ohtsubo, Masafumi;
Iwasaki, Satoshi;
Hotta, Yoshihiro;
Mizuta, Kunihiro;
Mineta, Hiroyuki;
Minoshima, Shinsei

Publication type:

Article

Genome-wide pathway analysis implicates intracellular transmembrane protein transport in Alzheimer disease.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 707, doi. 10.1038/jhg.2010.92

By:

Mun-Gwan Hong;
Alexeyenko, Andrey;
Lambert, Jean-Charles;
Amouyel, Philippe;
Prince, Jonathan A.

Publication type:

Article