Works matching IS 14345161 AND DT 2008 AND VI 53 AND IP 9

Results: 10

Linkage disequilibrium structure of the 5q31-33 region in a Thai population.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 850, doi. 10.1007/s10038-008-0309-8

By:

Nuchnoi, Pornlada;
Ohashi, Jun;
Naka, Izumi;
Nacapunchai, Duangporn;
Tokunaga, Katsushi;
Nishida, Nao;
Patarapotikul, Jintana

Publication type:

Article

Response to genetic manipulations of liver angiotensinogen in the physiological range.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 775, doi. 10.1007/s10038-008-0311-1

By:

Gociman, Barbu;
Rohrwasser, Andreas;
Hillas, Elaine;
Cheng, Tong;
Hunter, Grant;
Hunter, Jennifer;
Lott, Paul;
Monson, Smith;
Ying, Jian;
Lalouel, J.

Publication type:

Article

New correction algorithms for multiple comparisons in case–control multilocus association studies based on haplotypes and diplotype configurations.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 789, doi. 10.1007/s10038-008-0312-0

By:

Misawa, Kazuharu;
Fujii, Shoogo;
Yamazaki, Toshimasa;
Takahashi, Atsushi;
Takasaki, Junichi;
Yanagisawa, Masao;
Ohnishi, Yozo;
Nakamura, Yusuke;
Kamatani, Naoyuki

Publication type:

Article

Comparison of multivariate adaptive regression splines and logistic regression in detecting SNP–SNP interactions and their application in prostate cancer.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 802, doi. 10.1007/s10038-008-0313-z

By:

Lin, Hui-Yi;
Wang, Wenquan;
Liu, Yung-Hsin;
Soong, Seng-Jaw;
York, Timothy;
Myers, Leann;
Hu, Jennifer

Publication type:

Article

RET polymorphisms and the risk of Hirschsprung’s disease in a Chinese population.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 825, doi. 10.1007/s10038-008-0315-x

By:

Liu, Cuiping;
Jin, Lei;
Li, Hui;
Lou, Jintu;
Luo, Chunfen;
Zhou, Xuewu;
Li, Ji-Cheng

Publication type:

Article

Structural characterization of mutant α-galactosidases causing Fabry disease.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 812, doi. 10.1007/s10038-008-0316-9

By:

Sugawara, Kanako;
Ohno, Kazuki;
Saito, Seiji;
Sakuraba, Hitoshi

Publication type:

Article

INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 857, doi. 10.1007/s10038-008-0317-8

By:

Hotta, Kikuko;
Nakamura, Michihiro;
Nakata, Yoshio;
Matsuo, Tomoaki;
Kamohara, Seika;
Kotani, Kazuaki;
Komatsu, Ryoya;
Itoh, Naoto;
Mineo, Ikuo;
Wada, Jun;
Masuzaki, Hiroaki;
Yoneda, Masato;
Nakajima, Atsushi;
Miyazaki, Shigeru;
Tokunaga, Katsuto;
Kawamoto, Manabu;
Funahashi, Tohru;
Hamaguchi, Kazuyuki;
Yamada, Kentaro;
Hanafusa, Toshiaki

Publication type:

Article

No association between the oligodendrocyte-related gene PLP1 and schizophrenia in the Japanese population.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 863, doi. 10.1007/s10038-008-0318-7

By:

Aleksic, Branko;
Ikeda, Masashi;
Ishihara, Ryoko;
Saito, Shinichi;
Inada, Toshiya;
Iwata, Nakao;
Ozaki, Norio

Publication type:

Article

VSX1 gene variants are associated with keratoconus in unrelated Korean patients.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 842, doi. 10.1007/s10038-008-0319-6

By:

Mok, Jee-Won;
Baek, Sun-Jin;
Joo, Choun-Ki

Publication type:

Article

Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 9, p. 834, doi. 10.1007/s10038-008-0320-0

By:

Narumi, Yoko;
Aoki, Yoko;
Niihori, Tetsuya;
Sakurai, Masahiro;
Cavé, Hélène;
Verloes, Alain;
Nishio, Kimio;
Ohashi, Hirofumi;
Kurosawa, Kenji;
Okamoto, Nobuhiko;
Kawame, Hiroshi;
Mizuno, Seiji;
Kondoh, Tatsuro;
Addor, Marie-Claude;
Coeslier-Dieux, Anne;
Vincent-Delorme, Catherine;
Tabayashi, Koichi;
Aoki, Masashi;
Kobayashi, Tomoko;
Guliyeva, Afag

Publication type:

Article