Works matching IS 14345161 AND DT 2011 AND VI 56 AND IP 10

Results: 13

An association analysis of Per2 with panic disorder in the Japanese population.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 748, doi. 10.1038/jhg.2011.94

By:

Otowa, Takeshi;
Tochigi, Mamoru;
Kawamura, Yoshiya;
Sugaya, Nagisa;
Yoshida, Eiji;
Inoue, Ken;
Yasuda, Shin;
Umekage, Tadashi;
Ebisawa, Takashi;
Tanii, Hisashi;
Kaiya, Hisanobu;
Okazaki, Yuji;
Kato, Nobumasa;
Sasaki, Tsukasa

Publication type:

Article

Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 753, doi. 10.1038/jhg.2011.90

By:

Jeong, Seon-Yong;
Kim, Seo-Jin;
Yang, Jeong-A;
Hong, Ji-Hee;
Lee, Su-Jin;
Kim, Hyon J

Publication type:

Article

The generation of mitochondrial DNA large-scale deletions in human cells.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 689, doi. 10.1038/jhg.2011.97

By:

Chen, Tao;
He, Jing;
Huang, Yushan;
Zhao, Weiwei

Publication type:

Article

Common variants of FTO and the risk of obesity and type 2 diabetes in Indians.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 720, doi. 10.1038/jhg.2011.87

By:

Chauhan, Ganesh;
Tabassum, Rubina;
Mahajan, Anubha;
Dwivedi, Om Prakash;
Mahendran, Yuvaraj;
Kaur, Ismeet;
Nigam, Shubhanchi;
Dubey, Himanshu;
Varma, Binuja;
Madhu, Sri Venkata;
Mathur, Sandeep K;
Ghosh, Saurabh;
Tandon, Nikhil;
Bharadwaj, Dwaipayan

Publication type:

Article

HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 707, doi. 10.1038/jhg.2011.85

By:

Niihori, Tetsuya;
Aoki, Yoko;
Okamoto, Nobuhiko;
Kurosawa, Kenji;
Ohashi, Hirofumi;
Mizuno, Seiji;
Kawame, Hiroshi;
Inazawa, Johji;
Ohura, Toshihiro;
Arai, Hiroshi;
Nabatame, Shin;
Kikuchi, Kiyoshi;
Kuroki, Yoshikazu;
Miura, Masaru;
Tanaka, Toju;
Ohtake, Akira;
Omori, Isaku;
Ihara, Kenji;
Mabe, Hiroyo;
Watanabe, Kyoko

Publication type:

Article

Integration-free and stable expression of FVIII using a human artificial chromosome.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 727, doi. 10.1038/jhg.2011.88

By:

Kurosaki, Hajime;
Hiratsuka, Masaharu;
Imaoka, Natsuko;
Iida, Yuichi;
Uno, Narumi;
Kazuki, Yasuhiro;
Ishihara, Chie;
Yakura, Yuwna;
Mimuro, Jun;
Sakata, Youichi;
Takeya, Hiroyuki;
Oshimura, Mitsuo

Publication type:

Article

Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 742, doi. 10.1038/jhg.2011.93

By:

Mori, Satsuki;
Nakamura, Masayuki;
Yasuda, Takeshi;
Ueno, Shu-ichi;
Kaneko, Sunao;
Sano, Akira

Publication type:

Article

A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 701, doi. 10.1038/jhg.2011.84

By:

Kurban, Mazen;
Wajid, Muhammad;
Petukhova, Lynn;
Shimomura, Yutaka;
Christiano, Angela M

Publication type:

Article

Molecular and clinical studies of X-linked deafness among Pakistani families.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 752, doi. 10.1038/jhg.2011.89

By:

Waryah, Ali M;
Ahmed, Zubair M;
Binder, Munir A;
Choo, Daniel I;
Sisk, Robert A;
Shahzad, Mohsin;
Khan, Shaheen N;
Friedman, Thomas B;
Riazuddin, Sheikh;
Riazuddin, Saima

Publication type:

Article

Computed tomography analysis of the association between the SH2B1 rs7498665 single-nucleotide polymorphism and visceral fat area.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 716, doi. 10.1038/jhg.2011.86

By:

Hotta, Kikuko;
Kitamoto, Takuya;
Kitamoto, Aya;
Mizusawa, Seiho;
Matsuo, Tomoaki;
Nakata, Yoshio;
Hyogo, Hideyuki;
Ochi, Hidenori;
Kamohara, Seika;
Miyatake, Nobuyuki;
Kotani, Kazuaki;
Komatsu, Ryoya;
Itoh, Naoto;
Mineo, Ikuo;
Wada, Jun;
Yoneda, Masato;
Nakajima, Atsushi;
Funahashi, Tohru;
Miyazaki, Shigeru;
Tokunaga, Katsuto

Publication type:

Article

Mitochondrial DNA and Y-chromosome microstructure in Tunisia.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 734, doi. 10.1038/jhg.2011.92

By:

Ennafaa, Hajer;
Fregel, Rosa;
Khodjet-el-khil, Houssein;
González, Ana M;
Mahmoudi, Hejer Abdallah El;
Cabrera, Vicente M;
Larruga, José M;
Benammar-Elgaaïed, Amel

Publication type:

Article

Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 751, doi. 10.1038/jhg.2011.81

By:

Abe, Akiko;
Numakura, Chikahiko;
Kijima, Kazuki;
Hayashi, Makiko;
Hashimoto, Taeko;
Hayasaka, Kiyoshi

Publication type:

Article

Association of variants in genes involved in pancreatic β-cell development and function with type 2 diabetes in North Indians.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 10, p. 695, doi. 10.1038/jhg.2011.83

By:

Chavali, Sreenivas;
Mahajan, Anubha;
Tabassum, Rubina;
Dwivedi, Om Prakash;
Chauhan, Ganesh;
Ghosh, Saurabh;
Tandon, Nikhil;
Bharadwaj, Dwaipayan

Publication type:

Article