Works matching IS 14345161 AND DT 2009 AND VI 54 AND IP 2

Results: 10

Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 74, doi. 10.1038/jhg.2008.10

By:

Wu, Ye;
Pan, Yanxia;
Du, Li;
Wang, Jingmin;
Gu, Qiang;
Gao, Zhijie;
Li, Jie;
Leng, Xuerong;
Qin, Jiong;
Wu, Xiru;
Jiang, Yuwu

Publication type:

Article

Association between CYP19A1 polymorphisms and sex hormones in postmenopausal Japanese women.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 78, doi. 10.1038/jhg.2008.11

By:

Kidokoro, Kumiko;
Ino, Kazuhiko;
Hirose, Kaoru;
Kajiyama, Hiroaki;
Hosono, Satoyo;
Suzuki, Takeshi;
Kawase, Takakazu;
Hiraki, Akio;
Hamajima, Nobuyuki;
Tanaka, Hideo;
Tajima, Kazuo;
Kikkawa, Fumitaka;
Matsuo, Keitaro

Publication type:

Article

Origins of the Moken Sea Gypsies inferred from mitochondrial hypervariable region and whole genome sequences.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 86, doi. 10.1038/jhg.2008.12

By:

Dancause, Kelsey Needham;
Chan, Chim W;
Arunotai, Narumon Hinshiranan;
Lum, J. Koji

Publication type:

Article

Neurofilament light chain polypeptide gene mutations in Charcot–Marie–Tooth disease: nonsense mutation probably causes a recessive phenotype.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 94, doi. 10.1038/jhg.2008.13

By:

Abe, Akiko;
Numakura, Chikahiko;
Saito, Kayoko;
Koide, Hiroyoshi;
Oka, Nobuyuki;
Honma, Akira;
Kishikawa, Yumiko;
Hayasaka, Kiyoshi

Publication type:

Article

Case–control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 98, doi. 10.1038/jhg.2008.14

By:

Betcheva, Elitza T.;
Mushiroda, Taisei;
Takahashi, Atsushi;
Kubo, Michiaki;
Karachanak, Sena K.;
Zaharieva, Irina T.;
Vazharova, Radoslava V;
Dimova, Ivanka I;
Milanova, Vihra K;
Tolev, Todor;
Kirov, George;
Owen, Michael J.;
O'Donovan, Michael C.;
Kamatani, Naoyuki;
Nakamura, Yusuke;
Toncheva, Draga I

Publication type:

Article

HLA-DPB1 and NFKBIL1 may confer the susceptibility to chronic thromboembolic pulmonary hypertension in the absence of deep vein thrombosis.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 108, doi. 10.1038/jhg.2008.15

By:

Kominami, Satoshi;
Tanabe, Nobuhiro;
Ota, Masao;
Naruse, Taeko K;
Katsuyama, Yoshihiko;
Nakanishi, Norifumu;
Tomoike, Hitonobu;
Sakuma, Masahito;
Shirato, Kunio;
Takahashi, Megumi;
Shibata, Hiroki;
Yasunami, Michio;
Chen, Zhiyong;
Kasahara, Yasunori;
Tatsumi, Koichiro;
Kuriyama, Takayuki;
Kimura, Akinori

Publication type:

Article

Role of HCN4 channel in preventing ventricular arrhythmia.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 115, doi. 10.1038/jhg.2008.16

By:

Ueda, Kazuo;
Hirano, Yuji;
Higashiuesato, Yasushi;
Aizawa, Yoshiyasu;
Hayashi, Takeharu;
Inagaki, Natsuko;
Tana, Takeshi;
Ohya, Yusuke;
Takishita, Shuichi;
Muratani, Hiromi;
Hiraoka, Masayasu;
Kimura, Akinori

Publication type:

Article

Genome-wide association study of panic disorder in the Japanese population.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 122, doi. 10.1038/jhg.2008.17

By:

Otowa, Takeshi;
Yoshida, Eiji;
Sugaya, Nagisa;
Yasuda, Shin;
Nishimura, Yukika;
Inoue, Ken;
Tochigi, Mamoru;
Umekage, Tadashi;
Miyagawa, Taku;
Nishida, Nao;
Tokunaga, Katsushi;
Tanii, Hisashi;
Sasaki, Tsukasa;
Kaiya, Hisanobu;
Okazaki, Yuji

Publication type:

Article

Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45–55 of the Duchenne muscular dystrophy (DMD) gene.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 127, doi. 10.1038/jhg.2008.8

By:

Miyazaki, Daigo;
Yoshida, Kunihiro;
Fukushima, Kazuhiro;
Nakamura, Akinori;
Suzuki, Kayo;
Sato, Toshiyuki;
Takeda, Shin'ichi;
Ikeda, Shu-ichi

Publication type:

Article

Susceptibility genes for Kawasaki disease: toward implementation of personalized medicine.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 2, p. 67, doi. 10.1038/jhg.2008.9

By:

Hata, Akira;
Onouchi, Yoshihiro

Publication type:

Article