Works matching IS 14345161 AND DT 2011 AND VI 56 AND IP 8

Results: 14

Association studies getting broader: A commentary on A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 550, doi. 10.1038/jhg.2011.70

By:

Nakano, Masakazu;
Tashiro, Kei

Publication type:

Article

Association of interleukin-1β genetic polymorphisms with cognitive performance in elderly females without dementia.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 613, doi. 10.1038/jhg.2011.56

By:

Sasayama, Daimei;
Hori, Hiroaki;
Teraishi, Toshiya;
Hattori, Kotaro;
Ota, Miho;
Matsuo, Junko;
Kawamoto, Yumiko;
Kinoshita, Yukiko;
Higuchi, Teruhiko;
Amano, Naoji;
Kunugi, Hiroshi

Publication type:

Article

Genetic features of ancient West Siberian people of the Middle Ages, revealed by mitochondrial DNA haplogroup analysis.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 602, doi. 10.1038/jhg.2011.68

By:

Sato, Takehiro;
Razhev, Dmitry;
Amano, Tetsuya;
Masuda, Ryuichi

Publication type:

Article

Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 589, doi. 10.1038/jhg.2011.65

By:

Brown, Charlotte A;
Scharner, Juergen;
Felice, Kevin;
Meriggioli, Matthew N;
Tarnopolsky, Mark;
Bower, Matthew;
Zammit, Peter S;
Mendell, Jerry R;
Ellis, Juliet A

Publication type:

Article

A eulogy to the late Professor Eiji Inouye.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 549, doi. 10.1038/jhg.2011.67

By:

Asaka, Akio

Publication type:

Article

Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 617, doi. 10.1038/jhg.2011.63

By:

Mak, Chloe Miu;
Lam, Ching-wan;
Fong, Nai-chung;
Siu, Wai-kwan;
Lee, Han-chih Hencher;
Siu, Tak-shing;
Lai, Chi-kong;
Law, Chun-yiu;
Tong, Sui-fun;
Poon, Wing-tat;
Lam, David Shu-yan;
Ng, Ho-leung;
Yuen, Yuet-ping;
Tam, Sidney;
Que, Tak-lun;
Kwong, Ngai-shan;
Chan, Albert Yan-wo

Publication type:

Article

Loss-of-function mutation of collybistin is responsible for X-linked mental retardation associated with epilepsy.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 561, doi. 10.1038/jhg.2011.58

By:

Shimojima, Keiko;
Sugawara, Midori;
Shichiji, Minobu;
Mukaida, Souichi;
Takayama, Rumiko;
Imai, Katsumi;
Yamamoto, Toshiyuki

Publication type:

Article

Autosomal dominant nocturnal frontal lobe epilepsy: a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 609, doi. 10.1038/jhg.2011.69

By:

Hwang, Su-Kyeong;
Makita, Yoshio;
Kurahashi, Hirokazu;
Cho, Yong-Won;
Hirose, Shinichi

Publication type:

Article

A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 572, doi. 10.1038/jhg.2011.60

By:

Ratanajaraya, Chanavee;
Nishiyama, Hiroyuki;
Takahashi, Meiko;
Kawaguchi, Takahisa;
Saito, Ryoichi;
Mikami, Yoshiki;
Suyama, Mikita;
Lathrop, Mark;
Yamada, Ryo;
Ogawa, Osamu;
Matsuda, Fumihiko

Publication type:

Article

Ancient links between Siberians and Native Americans revealed by subtyping the Y chromosome haplogroup Q1a.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 583, doi. 10.1038/jhg.2011.64

By:

Malyarchuk, Boris;
Derenko, Miroslava;
Denisova, Galina;
Maksimov, Arkady;
Wozniak, Marcin;
Grzybowski, Tomasz;
Dambueva, Irina;
Zakharov, Ilya

Publication type:

Article

Copy number polymorphisms in new HapMap III and Singapore populations.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 552, doi. 10.1038/jhg.2011.54

By:

Ku, Chee-Seng;
Teo, Shu-Mei;
Naidoo, Nasheen;
Sim, Xueling;
Teo, Yik-Ying;
Pawitan, Yudi;
Seielstad, Mark;
Chia, Kee-Seng;
Salim, Agus

Publication type:

Article

Tumor suppressive microRNA-375 regulates oncogene AEG-1/MTDH in head and neck squamous cell carcinoma (HNSCC).

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 595, doi. 10.1038/jhg.2011.66

By:

Nohata, Nijiro;
Hanazawa, Toyoyuki;
Kikkawa, Naoko;
Mutallip, Muradil;
Sakurai, Daiju;
Fujimura, Lisa;
Kawakami, Kazumori;
Chiyomaru, Takeshi;
Yoshino, Hirofumi;
Enokida, Hideki;
Nakagawa, Masayuki;
Okamoto, Yoshitaka;
Seki, Naohiko

Publication type:

Article

Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 566, doi. 10.1038/jhg.2011.59

By:

Matsubara, Keiko;
Murakami, Nobuyuki;
Nagai, Toshiro;
Ogata, Tsutomu

Publication type:

Article

Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 8, p. 577, doi. 10.1038/jhg.2011.61

By:

Arai, Takashi;
Zhao, Meina;
Kanegane, Hirokazu;
van Zelm, Menno C;
Futatani, Takeshi;
Yamada, Masafumi;
Ariga, Tadashi;
Ochs, Hans D;
Miyawaki, Toshio;
Oh-ishi, Tsutomu

Publication type:

Article