Works matching IS 1434-5161 AND VI 55 AND IP 11 AND DT 2010

Results: 14

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
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
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