Works matching IS 14345161 AND DT 2008 AND VI 53 AND IP 4

Results: 14

Dynamin 2 gene is a novel susceptibility gene for late-onset Alzheimer disease in non- APOE-ε4 carriers.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 296, doi. 10.1007/s10038-008-0251-9

By:

Aidaralieva, Nuripa Jenishbekovna;
Kamino, Kouzin;
Kimura, Ryo;
Yamamoto, Mitsuko;
Morihara, Takeshi;
Kazui, Hiroaki;
Hashimoto, Ryota;
Tanaka, Toshihisa;
Kudo, Takashi;
Kida, Tomoyuki;
Okuda, Jun-Ichiro;
Uema, Takeshi;
Yamagata, Hidehisa;
Miki, Tetsuro;
Akatsu, Hiroyasu;
Kosaka, Kenji;
Takeda, Masatoshi

Publication type:

Article

Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity.

Published in:

2008

By:

Mak, Chloe;
Lam, Ching-Wan;
Tam, Sidney;
Lai, Ching-Lung;
Chan, Lik-Yuen;
Fan, Sheung-Tat;
Lau, Yu-Lung;
Lai, Sik-To;
Yuen, Patrick;
Hui, Joannie;
Fu, Chun-Cheung;
Wong, Ka-Sing;
Mak, Wing-Lai;
Tze, Kong;
Tong, Sui-Fan;
Lau, Abby;
Leung, Nancy;
Hui, Aric;
Cheung, Ka-Ming;
Ko, Chun-Hung

Publication type:

Correction Notice

R1467H variant in the rho guanine nucleotide exchange factor 11 ( ARHGEF11) is associated with impaired glucose tolerance and type 2 diabetes in German Caucasians.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 365, doi. 10.1007/s10038-008-0252-8

By:

Böttcher, Yvonne;
Schleinitz, Dorit;
Tönjes, Anke;
Blüher, Matthias;
Stumvoll, Michael;
Kovacs, Peter

Publication type:

Article

A novel GDAP1 Q218E mutation in autosomal dominant Charcot-Marie-Tooth disease.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 360, doi. 10.1007/s10038-008-0249-3

By:

Ki Wha Chung;
Seung Min Kim;
Sunwoo, Il Nam;
Sun Young Cho;
Su Jin Hwang;
Joonki Kim;
Sung Hee Kang;
Kee-Duk Park;
Kyoung-Gyu Choi;
Il Saing Choi;
Byung-Ok Choi

Publication type:

Article

Association analyses confirming a susceptibility locus for intracranial aneurysm at chromosome 14q23.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 325, doi. 10.1007/s10038-008-0255-5

By:

Mineharu, Yohei;
Inoue, Kayoko;
Inoue, Sumiko;
Kikuchi, Kenji;
Ohishi, Hikaru;
Nozaki, Kazuhiko;
Hashimoto, Nobuo;
Koizumi, Akio

Publication type:

Article

Search for type 2 diabetes susceptibility genes on chromosomes 1q, 3q and 12q.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 314, doi. 10.1007/s10038-008-0254-6

By:

Takeuchi, F.;
Ochiai, Y.;
Serizawa, M.;
Yanai, K.;
Kuzuya, N.;
Kajio, H.;
Honjo, S.;
Takeda, N.;
Kaburagi, Y.;
Yasuda, K.;
Shirasawa, S.;
Sasazuki, T.;
Kato, N.

Publication type:

Article

Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 357, doi. 10.1007/s10038-008-0248-4

By:

Hinohara, Kunihiko;
Nakajima, Toshiaki;
Takahashi, Megumi;
Hohda, Shigeru;
Sasaoka, Taishi;
Nakahara, Ken-ichi;
Chida, Kouji;
Sawabe, Motoji;
Arimura, Takuro;
Sato, Akinori;
Lee, Bok-Soo;
Ban, Ji-min;
Yasunami, Michio;
Park, Jeong-Euy;
Izumi, Toru;
Kimura, Akinori

Publication type:

Article

Pinghua population as an exception of Han Chinese’s coherent genetic structure.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 303, doi. 10.1007/s10038-008-0250-x

By:

Rui-Jing Gan;
Shang-Ling Pan;
Mustavich, Laura F.;
Zhen-Dong Qin;
Xiao-Yun Cai;
Ji Qian;
Cheng-Wu Liu;
Jun-Hua Peng;
Shi-Lin Li;
Jie-Shun Xu;
Li Jin;
Hui Li

Publication type:

Article

Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangism.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 368, doi. 10.1007/s10038-008-0253-7

By:

Wei Yang;
Lihua Cao;
Wenli Liu;
Li Jiang;
Miao Sun;
Dai Zhang;
Shusen Wang;
Wilson H. Y. Lo;
Yang Luo;
Xue Zhang

Publication type:

Article

Mitochondrial DNA polymorphisms and haplogroups in Parkinson’s disease and control individuals with a similar genetic background.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 349, doi. 10.1007/s10038-008-0259-1

By:

Latsoudis, Helen;
Spanaki, Cleanthe;
Chlouverakis, Grigoris;
Plaitakis, Andreas

Publication type:

Article

Direct and accurate measurement of CAG repeat configuration in the ataxin-1 ( ATXN-1) gene by “dual-fluorescence labeled PCR-restriction fragment length analysis”.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 287, doi. 10.1007/s10038-007-0242-2

By:

Lin, Jiang X.;
Ishikawa, Kinya;
Sakamoto, Masaki;
Tsunemi, Taiji;
Ishiguro, Taro;
Amino, Takeshi;
Toru, Shuta;
Kondo, Ikuko;
Mizusawa, Hidehiro

Publication type:

Article

Methylenetetrahydrofolate reductase gene polymorphisms and lung cancer: a meta-analysis.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 340, doi. 10.1007/s10038-008-0262-6

By:

Renfang Mao;
Yihui Fan;
Yan Jin;
Jing Bai;
Songbin Fu

Publication type:

Article

Huntington disease mutation in Venezuela: age of onset, haplotype analyses and geographic aggregation.

Published in:

2008

By:

Paradisi, Irene;
Hernández, Alba;
Arias, Sergio

Publication type:

Correction Notice

Segregation distortion of wild-type alleles at the Machado-Joseph disease locus: a study in normal families from the Azores islands (Portugal).

Published in:

Journal of Human Genetics, 2008, v. 53, n. 4, p. 333, doi. 10.1007/s10038-008-0261-7

By:

Bettencourt, Conceição;
Fialho, Raquel Nunes;
Santos, Cristina;
Montiel, Rafael;
Bruges-Armas, Jácome;
Maciel, Patrícia;
Lima, Manuela

Publication type:

Article