Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP suppl_2

Results: 22

The genetic architecture of normal variation in human pigmentation: an evolutionary perspective and model.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R176, doi. 10.1093/hmg/ddl217

By:

McEvoy, Brian;
Beleza, Sandra;
Shriver, Mark D.

Publication type:

Article

Mitochondrial DNA polymerase-γ and human disease.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R244, doi. 10.1093/hmg/ddl233

By:

Hudson, Gavin;
Chinnery, Patrick F.

Publication type:

Article

Planar cell polarity, ciliogenesis and neural tube defects.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R227, doi. 10.1093/hmg/ddl216

By:

Wallingford, John B.

Publication type:

Article

Genetics of obesity and the prediction of risk for health.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R124, doi. 10.1093/hmg/ddl215

By:

Walley, Andrew J.;
Blakemore, Alexandra I.F.;
Froguel, Philippe

Publication type:

Article

Molecular bases of progeroid syndromes.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R151, doi. 10.1093/hmg/ddl214

By:

Navarro, Claire L.;
Cau, Pierre;
Lévy, Nicolas

Publication type:

Article

Epigenetics of autism spectrum disorders.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R138, doi. 10.1093/hmg/ddl213

By:

Schanen, N. Carolyn

Publication type:

Article

Molecular components of the mammalian circadian clock.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R271, doi. 10.1093/hmg/ddl207

By:

Ko, Caroline H.;
Takahashi, Joseph S.

Publication type:

Article

Usher syndrome: molecular links of pathogenesis, proteins and pathways.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R262, doi. 10.1093/hmg/ddl205

By:

Kremer, Hannie;
van Wijk, Erwin;
Märker, Tina;
Wolfrum, Uwe;
Roepman, Ronald

Publication type:

Article

Recent advances in the genetics of amyotrophic lateral sclerosis and frontotemporal dementia: common pathways in neurodegenerative disease.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R182, doi. 10.1093/hmg/ddl202

By:

Talbot, Kevin;
Ansorge, Olaf

Publication type:

Article

How lifetimes shape epigenotype within and across generations.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R131, doi. 10.1093/hmg/ddl200

By:

Whitelaw, Nadia C.;
Whitelaw, Emma

Publication type:

Article

Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R220, doi. 10.1093/hmg/ddl197

By:

Gelb, Bruce D.;
Tartaglia, Marco

Publication type:

Article

The many facets of the Wilms' tumour gene, WT1.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R196, doi. 10.1093/hmg/ddl196

By:

Hohenstein, Peter;
Hastie, Nicholas D.

Publication type:

Article

Towards understanding CRUMBS function in retinal dystrophies.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R235, doi. 10.1093/hmg/ddl195

By:

Richard, Mélisande;
Roepman, Ronald;
Aartsen, Wendy M.;
van Rossum, Agnes G.S.H.;
den Hollander, Anneke I.;
Knust, Elisabeth;
Wijnholds, Jan;
Cremers, Frans P.M.

Publication type:

Article

Type-2 diabetes: a cocktail of genetic discovery.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R202, doi. 10.1093/hmg/ddl191

By:

Freeman, H.;
Cox, R.D.

Publication type:

Article

Untangling the tau gene association with neurodegenerative disorders.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R188, doi. 10.1093/hmg/ddl190

By:

Pittman, Alan M.;
Fung, Hon-Chung;
de Silva, Rohan

Publication type:

Article

The genetics of mental retardation.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R110, doi. 10.1093/hmg/ddl189

By:

Raymond, F. Lucy;
Tarpey, Patrick

Publication type:

Article

Genetic susceptibility to myocardial infarction and coronary artery disease.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R117, doi. 10.1093/hmg/ddl183

By:

Topol, Eric J.;
Smith, Jonathan;
Plow, Edward F.;
Wang, Qing K.

Publication type:

Article

Signatures of adaptive evolution within human non-coding sequence.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R170, doi. 10.1093/hmg/ddl182

By:

Ponting, Chris P.;
Lunter, Gerton

Publication type:

Article

RNA-dominant diseases.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R162, doi. 10.1093/hmg/ddl181

By:

Osborne, Robert J.;
Thornton, Charles A.

Publication type:

Article

Challenges and opportunities in dystrophin-deficient cardiomyopathy gene therapy.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R253, doi. 10.1093/hmg/ddl180

By:

Duan, Dongsheng

Publication type:

Article

New techniques to understand chromosome dosage: mouse models of aneuploidy.

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R103, doi. 10.1093/hmg/ddl179

By:

Tybulewicz, Victor L.J.;
Fisher, Elizabeth M.C.

Publication type:

Article

Signaling pathways in self-renewing hematopoietic and leukemic stem cells: do all stem cells need a niche?

Published in:

Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R210, doi. 10.1093/hmg/ddl175

By:

Rizo, Aleksandra;
Vellenga, Edo;
de Haan, Gerald;
Schuringa, Jan Jacob

Publication type:

Article