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
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
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
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