Works matching IS 03406717 AND DT 2010 AND VI 128 AND IP 2

Results: 12

The CAG repeat in SCA12 functions as a cis element to up-regulate PPP2R2B expression.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 205, doi. 10.1007/s00439-010-0843-2

By:

Chih-Hsin Lin;
Chiung-Mei Chen;
Yi-Ting Hou;
Yih-Ru Wu;
Hsiu-Mei Hsieh-Li;
Ming-Tsan Su;
Guey-Jen Lee-Chen

Publication type:

Article

Association between genome-wide association studies reported SNPs and pediatric-onset Crohn’s disease in Canadian children.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 131, doi. 10.1007/s00439-010-0835-2

By:

Amre, Devendra K.;
Mack, David R.;
Morgan, Kenneth;
Israel, David;
Deslandres, Colette;
Seidman, Ernest G.;
Lambrette, Phlippe;
Costea, Irina;
Krupoves, Alfreda;
Fegury, Houda;
Jinsong Dong;
Zia Xhu;
Grimard, Guy;
Levy, Emile

Publication type:

Article

Identification of HAVCR1 gene haplotypes associated with mRNA expression levels and susceptibility to autoimmune diseases.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 221, doi. 10.1007/s00439-010-0844-1

By:

García-Lozano, José Raúl;
Abad, Cristina;
Escalera, Ana;
Torres, Belén;
Fernández, Olga;
García, Alicia;
Sánchez-Román, Julio;
Sabio, José-Mario;
Ortego-Centeno, Norberto;
Raya-Álvarez, Enrique;
Núñez-Roldán, Antonio;
Martín, Javier;
González-Escribano, María Francisca

Publication type:

Article

Polymorphisms in the GNB3 and ADD1 genes and blood pressure in a Chinese population.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 137, doi. 10.1007/s00439-010-0834-3

By:

Shufeng Chen;
Hongwei Wang;
Xiangfeng Lu;
De-Pei Liu;
Jing Chen;
Jaquish, Cashell E.;
Rao, Dabeeru C.;
Hixson, James E.;
Kelly, Tanika N.;
Liping Hou;
Laiyuan Wang;
Jianfeng Huang;
Chung-Shiuan Chen;
Rice, Treva K.;
Whelton, Paul K.;
Jiang He;
Dongfeng Gu

Publication type:

Article

Genome-wide analysis of the structure of the South African Coloured Population in the Western Cape.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 145, doi. 10.1007/s00439-010-0836-1

By:

de Wit, Erika;
Delport, Wayne;
Rugamika, Chimusa E.;
Meintjes, Ayton;
Möller, Marlo;
van Helden, Paul D.;
Seoighe, Cathal;
Hoal, Eileen G.

Publication type:

Article

Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs, David J. Weatherall: Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management.

Published in:

2010

By:

May, Alison

Publication type:

Book Review

A locus for juvenile myoclonic epilepsy maps to 2q33–q36.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 123, doi. 10.1007/s00439-010-0831-6

By:

Ratnapriya, Rinki;
Vijai, Joseph;
Kadandale, Jayaram S.;
Iyer, Rajesh S.;
Radhakrishnan, Kurupath;
Anand, Anuranjan

Publication type:

Article

Self-reported ethnicity, genetic structure and the impact of population stratification in a multiethnic study.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 165, doi. 10.1007/s00439-010-0841-4

By:

Hansong Wang;
Haiman, Christopher A.;
Kolonel, Laurence N.;
Henderson, Brian E.;
Wilkens, Lynne R.;
Le Marchand, Loïc;
Stram, Daniel O.

Publication type:

Article

Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 195, doi. 10.1007/s00439-010-0842-3

By:

Bostrom, Meredith A.;
Lingyi Lu;
Chou, Jeff;
Hicks, Pamela J.;
Jianzhao Xu;
Langefeld, Carl D.;
Bowden, Donald W.;
Freedman, Barry I.

Publication type:

Article

Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 179, doi. 10.1007/s00439-010-0837-0

By:

Qiao, Y.;
Harvard, C.;
Tyson, C.;
Liu, X.;
Fawcett, C.;
Pavlidis, P.;
Holden, J. J. A.;
Lewis, M. E. S.;
Rajcan-Separovic, E.

Publication type:

Article

Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 213, doi. 10.1007/s00439-010-0847-y

By:

Basit, Sulman;
Ali, Ghazanfar;
Wasif, Naveed;
Ansar, Muhammad;
Ahmad, Wasim

Publication type:

Article

Genetic determinants of autism in individuals with deletions of 18q.

Published in:

Human Genetics, 2010, v. 128, n. 2, p. 155, doi. 10.1007/s00439-010-0839-y

By:

O'Donnell, Louise;
Soileau, Bridgette;
Heard, Patricia;
Carter, Erika;
Sebold, Courtney;
Gelfond, Jon;
Hale, Daniel E.;
Cody, Jannine D.

Publication type:

Article