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