Works matching IS 14345161 AND DT 2010 AND VI 55 AND IP 11

Results: 14

Association between neuropeptide Y receptor 2 polymorphism and the smoking behavior of elderly Japanese.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 755, doi. 10.1038/jhg.2010.108

By:

Sato, Naomi;
Kageyama, Shinji;
Chen, Renyin;
Suzuki, Masaya;
Mori, Hiroki;
Tanioka, Fumihiko;
Yamada, Hidetaka;
Kamo, Takaharu;
Tao, Hong;
Shinmura, Kazuya;
Nozawa, Akiko;
Sugimura, Haruhiko

Publication type:

Article

Human endogenous retrovirus K14C drove genomic diversification of the Y chromosome during primate evolution.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 717, doi. 10.1038/jhg.2010.94

By:

Sin, Ho-Su;
Koh, Eitetsu;
Kim, Dae-Soo;
Murayama, Miho;
Sugimoto, Kazuhiro;
Maeda, Yuji;
Yoshida, Atsumi;
Namiki, Mikio

Publication type:

Article

Genetics of Moyamoya disease.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 711, doi. 10.1038/jhg.2010.103

By:

Roder, Constantin;
Nayak, Nikhil R;
Khan, Nadia;
Tatagiba, Marcos;
Inoue, Ituro;
Krischek, Boris

Publication type:

Article

Polymorphisms of the endothelial nitric oxide synthase gene in breast cancer: a genetic association study and meta-analysis.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 743, doi. 10.1038/jhg.2010.100

By:

Zintzaras, Elias;
Grammatikou, Maria;
Kitsios, Georgios D;
Doxani, Chrysa;
Zdoukopoulos, Nikos;
Papandreou, Christos

Publication type:

Article

Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 761, doi. 10.1038/jhg.2010.95

By:

Kaliakatsos, Marios;
Giannakopoulos, Aristeidis;
Fryssira, Helena;
Kanariou, Maria;
Skiathitou, Anna-Venetia;
Siahanidou, Tania;
Giannikou, Krinio;
Makrythanasis, Periklis;
Kanavakis, Emmanuel;
Tzetis, Maria

Publication type:

Article

Mutations in CLDN14 are associated with different hearing thresholds.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 767, doi. 10.1038/jhg.2010.104

By:

Bashir, Rasheeda;
Fatima, Amara;
Naz, Sadaf

Publication type:

Article

Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 749, doi. 10.1038/jhg.2010.101

By:

Dzhemileva, Lilya U;
Barashkov, Nikolay A;
Posukh, Olga L;
Khusainova, Rita I;
Akhmetova, Vita L;
Kutuev, Ildus A;
Gilyazova, Irina R;
Tadinova, Vera N;
Fedorova, Sardana A;
Khidiyatova, Irina M;
Lobov, Simeon L;
Khusnutdinova, Elza K

Publication type:

Article

Polymorphisms of the endothelial nitric oxide synthase gene in breast cancer: a genetic association study and meta-analysis.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 777, doi. 10.1038/jhg.2010.136

By:

Zintzaras, Elias;
Grammatikou, Maria;
Kitsios, Georgios D;
Doxani, Chrysa;
Zdoukopoulos, Nikos;
Papandreou, Christos

Publication type:

Article

Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 726, doi. 10.1038/jhg.2010.97

By:

Bae, Joon Seol;
Cheong, Hyun Sub;
Park, Byung Lae;
Kim, Lyoung Hyo;
Park, Tae Joon;
Kim, Jason Yongha;
Pasaje, Charisse Flerida A;
Lee, Jin Sol;
Cui, Tailin;
Inoue, Ituro;
Shin, Hyoung Doo

Publication type:

Article

Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese population.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 738, doi. 10.1038/jhg.2010.99

By:

Hotta, Kikuko;
Nakamura, Michihiro;
Nakamura, Takahiro;
Matsuo, Tomoaki;
Nakata, Yoshio;
Kamohara, Seika;
Miyatake, Nobuyuki;
Kotani, Kazuaki;
Komatsu, Ryoya;
Itoh, Naoto;
Mineo, Ikuo;
Wada, Jun;
Yoneda, Masato;
Nakajima, Atsushi;
Funahashi, Tohru;
Miyazaki, Shigeru;
Tokunaga, Katsuto;
Kawamoto, Manabu;
Masuzaki, Hiroaki;
Ueno, Takato

Publication type:

Article

A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 764, doi. 10.1038/jhg.2010.102

By:

Jeong, Seon-Yong;
Kim, Bo-Young;
Kim, Hyon J;
Yang, Jeong-A;
Kim, Ok-Hwa

Publication type:

Article

Influence of CYP3A5 and drug transporter polymorphisms on imatinib trough concentration and clinical response among patients with chronic phase chronic myeloid leukemia.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 731, doi. 10.1038/jhg.2010.98

By:

Takahashi, Naoto;
Miura, Masatomo;
Scott, Stuart A;
Kagaya, Hideaki;
Kameoka, Yoshihiro;
Tagawa, Hiroyuki;
Saitoh, Hirobumi;
Fujishima, Naohito;
Yoshioka, Tomoko;
Hirokawa, Makoto;
Sawada, Kenichi

Publication type:

Article

Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 771, doi. 10.1038/jhg.2010.106

By:

Abe, Akiko;
Nakamura, Kazuyuki;
Kato, Mitsuhiro;
Numakura, Chikahiko;
Honma, Tomomi;
Seiwa, Chizuru;
Shirahata, Emi;
Itoh, Aiko;
Kishikawa, Yumiko;
Hayasaka, Kiyoshi

Publication type:

Article

Gene flow between Zhuang and Han populations in the China-Vietnam borderland.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 11, p. 774, doi. 10.1038/jhg.2010.107

By:

Zhao, Qing;
Pan, Shangling;
Qin, Zhendong;
Cai, Xiaoyun;
Lu, Yan;
Farina, Sara E;
Liu, Chengwu;
Peng, Junhua;
Xu, Jieshun;
Yin, Ruixing;
Li, Shilin;
Li, Jin;
Li, Hui

Publication type:

Article