Works matching IS 03406717 AND DT 2006 AND VI 120 AND IP 5

Results: 17

Identifying genes underlying skin pigmentation differences among human populations.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 613, doi. 10.1007/s00439-006-0256-4

By:

Myles, Sean;
Somel, Mehmet;
Kun Tang;
Kelso, Janet;
Stoneking, Mark

Publication type:

Article

Localization and replication of the systemic lupus erythematosus linkage signal at 4p16: interaction with 2p11, 12q24 and 19q13 in European Americans.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 623, doi. 10.1007/s00439-006-0248-4

By:

Chao Xing;
Sestak, Andrea L.;
Kelly, Jennifer A.;
Nguyen, Kim L.;
Bruner, Gail R.;
Harley, John B.;
Gray-McGuire, Courtney

Publication type:

Article

Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis–van Creveld syndrome patients.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 663, doi. 10.1007/s00439-006-0237-7

By:

Tompson, Stuart W. J.;
Ruiz-Perez, Victor L.;
Blair, Helen J.;
Barton, Stephanie;
Navarro, Victoria;
Robson, Joanne L.;
Wright, Michael J.;
Goodship, Judith A.

Publication type:

Article

A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 653, doi. 10.1007/s00439-006-0246-6

By:

Mendoza, Gustavo;
Pemberton, Trevor J.;
Kwanghyuk Lee;
Scarel-Caminaga, Raquel;
Mehrian-Shai, Ruty;
Gonzalez-Quevedo, Catalina;
Ninis, Vasiliki;
Hartiala, Jaana;
Allayee, Hooman;
Snead, Malcolm L.;
Leal, Suzanne M.;
Line, Sergio R. P.;
Patel, Pragna I.

Publication type:

Article

The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 633, doi. 10.1007/s00439-006-0249-3

By:

Clark, Rhonda;
De Biase, Irene;
Malykhina, Anna;
Al-Mahdawi, Sahar;
Pook, Mark;
Bidichandani, Sanjay

Publication type:

Article

Predictors of uptake of obesity genetic testing among affected adults.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 641, doi. 10.1007/s00439-006-0252-8

By:

Segal, Mary E.;
Polansky, Marcia;
Sankar, Pamela

Publication type:

Article

Lack of association between rs7566605 and obesity in a Chinese population.

Published in:

2006

By:

Yan Feng;
Hongxing Dong;
Qingyun Xiang;
Xiumei Hong;
Wilker, Elissa;
Yan Zhang;
Xiping Xu;
Xin Xu

Publication type:

Letter

Ian D. Young: Medical genetics.

Published in:

2006

By:

Leonard, Samantha

Publication type:

Book Review

Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 671, doi. 10.1007/s00439-006-0236-8

By:

Fornage, Myriam;
Mosley, Thomas H.;
Jack, Clifford R.;
de Andrade, Mariza;
Kardia, Sharon L. R.;
Boerwinkle, Eric;
Turner, Stephen T.

Publication type:

Article

Elevated male European and female African contributions to the genomes of African American individuals.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 713, doi. 10.1007/s00439-006-0261-7

By:

Lind, Joanne M.;
Hutcheson-Dilks, Holli B.;
Williams, Scott M.;
Moore, Jason H.;
Essex, Myron;
Ruiz-Pesini, Eduardo;
Wallace, Douglas C.;
Tishkoff, Sarah A.;
O'Brien, Stephen J.;
Smith, Michael W.

Publication type:

Article

A nonsense mutation-created intraexonic splice site is active in the lymphocytes, but not in the skeletal muscle of a DMD patient.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 737, doi. 10.1007/s00439-006-0241-y

By:

Van Khanh Tran;
Takeshima, Yasuhiro;
Zhujun Zhang;
Habara, Yasuaki;
Haginoya, Kazuhiro;
Nishiyama, Atsushi;
Yagi, Mariko;
Matsuo, Masafumi

Publication type:

Article

Association of Hck genetic polymorphisms with gene expression and COPD.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 681, doi. 10.1007/s00439-006-0253-7

By:

Xiaozhu Zhang;
Mahmudi-Azer, Salahaddin;
Connett, John;
Anthonisen, Nicholas;
Jian-Qing He;
Paré, Peter;
Sandford, Andrew

Publication type:

Article

High-resolution mapping of DNA methylation in human genome using oligonucleotide tiling array.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 701, doi. 10.1007/s00439-006-0254-6

By:

Hayashi, Hiroshi;
Nagae, Genta;
Tsutsumi, Shuichi;
Kaneshiro, Kiyofumi;
Kozaki, Takazumi;
Kaneda, Atsushi;
Sugisaki, Hajime;
Aburatani, Hiroyuki

Publication type:

Article

Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 691, doi. 10.1007/s00439-006-0255-5

By:

Celedón, Juan;
Soto-Quiros, Manuel;
Avila, Lydiana;
Lake, Stephen;
Liang, Catherine;
Fournier, Eduardo;
Spesny, Mitzi;
Hersh, Craig;
Sylvia, Jody;
Hudson, Thomas;
Verner, Andrei;
Klanderman, Barbara;
Freimer, Nelson;
Silverman, Edwin;
Weiss, Scott

Publication type:

Article

Genetics of preeclampsia: paradigm shifts.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 607, doi. 10.1007/s00439-006-0259-1

By:

Oudejans, Cees B. M.;
van Dijk, Marie;
Oosterkamp, Marjet;
Lachmeijer, Augusta;
Blankenstein, Marinus

Publication type:

Article

Fibrillin I gene polymorphism is associated with tall stature of normal individuals.

Published in:

Human Genetics, 2006, v. 120, n. 5, p. 733, doi. 10.1007/s00439-006-0263-5

By:

Mamada, Mitsukazu;
Yorifuji, Tohru;
Yorifuji, Junko;
Kurokawa, Keiji;
Kawai, Masahiko;
Momoi, Toru;
Nakahata, Tatsutoshi

Publication type:

Article

Paul Polani and the development of medical genetics.

Published in:

2006

By:

Harper, Peter

Publication type:

Editorial