Works matching IS 14345161 AND DT 2008 AND VI 53 AND IP 10

Results: 14

Genetic interactions model among Eotaxin gene polymorphisms in asthma.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 867, doi. 10.1007/s10038-008-0314-y

By:

June-Hyuk Lee;
Moore, Jason;
Sung-Woo Park;
An-Soo Jang;
Soo-Taek Uh;
Yong Kim;
Choon-Sik Park;
Byung Park;
Hyoung Shin

Publication type:

Article

Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan ( SGCE) gene.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 876, doi. 10.1007/s10038-008-0321-z

By:

Bonnet, C.;
Grégoire, M.-J.;
Vibert, M.;
Raffo, E.;
Leheup, B.;
Jonveaux, P.

Publication type:

Article

Appropriate data cleaning methods for genome-wide association study.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 886, doi. 10.1007/s10038-008-0322-y

By:

Miyagawa, Taku;
Nishida, Nao;
Ohashi, Jun;
Kimura, Ryosuke;
Fujimoto, Akihiro;
Kawashima, Minae;
Koike, Asako;
Sasaki, Tsukasa;
Tanii, Hisashi;
Otowa, Takeshi;
Momose, Yoshio;
Nakahara, Yasuo;
Gotoh, Jun;
Okazaki, Yuji;
Tsuji, Shoji;
Tokunaga, Katsushi

Publication type:

Article

A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 894, doi. 10.1007/s10038-008-0323-x

By:

Rasool, Mahmood;
Schuster, Jens;
Aslam, Muhammad;
Tariq, Muhammad;
Ahmad, Ilyas;
Ali, Amjad;
Entesarian, Miriam;
Dahl, Niklas;
Baig, Shahid

Publication type:

Article

Pharmacokinetic interaction between pravastatin and olmesartan in relation to SLCO1B1 polymorphism.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 899, doi. 10.1007/s10038-008-0324-9

By:

Suwannakul, Suttasinee;
Ieiri, Ichiro;
Kimura, Miyuki;
Kawabata, Kiyoshi;
Kusuhara, Hiroyuki;
Hirota, Takeshi;
Irie, Shin;
Sugiyama, Yuichi;
Higuchi, Shun

Publication type:

Article

Genetic imprint of the Mongol: signal from phylogeographic analysis of mitochondrial DNA.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 905, doi. 10.1007/s10038-008-0325-8

By:

Baoweng Cheng;
Wenru Tang;
Li He;
Yongli Dong;
Jing Lu;
Yunping Lei;
Haijing Yu;
Jiali Zhang;
Chunjie Xiao

Publication type:

Article

Case report of de novo dup(18p)/del(18q) and r(18) mosaicism.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 941, doi. 10.1007/s10038-008-0326-7

By:

Gereltzul, Enkhtuvshin;
Baba, Yoshiyuki;
Suda, Naoto;
Shiga, Momotoshi;
Inoue, Maristela;
Tsuji, Michiko;
Shin, Insik;
Hirata, Yukio;
Ohyama, Kimie;
Moriyama, Keiji

Publication type:

Article

Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 914, doi. 10.1007/s10038-008-0327-6

By:

Mizuguchi, Takeshi;
Hashimoto, Ryota;
Itokawa, Masanari;
Sano, Akira;
Shimokawa, Osamu;
Yoshimura, Yukiko;
Harada, Naoki;
Miyake, Noriko;
Nishimura, Akira;
Saitsu, Hirotomo;
Sosonkina, Nadiya;
Niikawa, Norio;
Kunugi, Hiroshi;
Matsumoto, Naomichi

Publication type:

Article

The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease).

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 947, doi. 10.1007/s10038-008-0328-5

By:

Tae-Joon Cho;
Hyuk Moon;
Dae-Yeon Cho;
Moon Park;
Dong Lee;
Won Yoo;
Chin Chung;
In Choi

Publication type:

Article

Monozygotic female twins discordant for Silver–Russell syndrome and hypomethylation of the H19-DMR.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 950, doi. 10.1007/s10038-008-0329-4

By:

Yamazawa, Kazuki;
Kagami, Masayo;
Fukami, Maki;
Matsubara, Keiko;
Ogata, Tsutomu

Publication type:

Article

Analysis of segregation patterns in Machado–Joseph disease pedigrees.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 920, doi. 10.1007/s10038-008-0330-y

By:

Bettencourt, Conceição;
Santos, Cristina;
Kay, Teresa;
Vasconcelos, João;
Lima, Manuela

Publication type:

Article

Mitochondrial DNA variant interactions modify breast cancer risk.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 924, doi. 10.1007/s10038-008-0331-x

By:

Covarrubias, Daniel;
Ren-Kui Bai;
Wong, Lee-Jun C.;
Leal, Suzanne M.

Publication type:

Article

Association and interaction analyses of NRG1 and ERBB4 genes with schizophrenia in a Japanese population.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 929, doi. 10.1007/s10038-008-0332-9

By:

Shiota, Sae;
Tochigi, Mamoru;
Shimada, Hiroko;
Ohashi, Jun;
Kasai, Kiyoto;
Kato, Nobumasa;
Tokunaga, Katsushi;
Sasaki, Tsukasa

Publication type:

Article

NEFL Pro22Arg mutation in Charcot-Marie-Tooth disease type 1.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 936, doi. 10.1007/s10038-008-0333-8

By:

Ji Shin;
Ki Chung;
Sun Cho;
Jiyoung Yun;
Su Hwang;
Sung Kang;
En Cho;
Seung-Min Kim;
Byung-Ok Choi

Publication type:

Article