Works matching IS 09646906 AND DT 2002 AND VI 11 AND IP 20

Results: 20

Pharmacogenomics in schizophrenia: the quest for individualized therapy.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2517, doi. 10.1093/hmg/11.20.2517

By:

Basile, Vincenzo S.;
Masellis, Mario;
Potkin, Steven G.;
Kennedy, James L.

Publication type:

Article

Impaired dopamine storage resulting from α-synuclein mutations may contribute to the pathogenesis of Parkinson's disease.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2395, doi. 10.1093/hmg/11.20.2395

By:

Lotharius, Julie;
Brundin, Patrik

Publication type:

Article

Phenotypic diversity in hypertrophic cardiomyopathy.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2499, doi. 10.1093/hmg/11.20.2499

By:

Arad, Michael;
Seidman, J.G.;
Seidman, Christine E.

Publication type:

Article

Signals and their transduction pathways regulating alternative splicing: a new dimension of the human genome.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2409, doi. 10.1093/hmg/11.20.2409

By:

Stamm, Stefan

Publication type:

Article

Gene finding in genetically isolated populations.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2507, doi. 10.1093/hmg/11.20.2507

By:

Heutink, Peter;
Oostra, Ben A.

Publication type:

Article

Molecular genetics of calcium sensing in bone cells.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2377, doi. 10.1093/hmg/11.20.2377

By:

Purroy, Jesús;
Spurr, Nigel K.

Publication type:

Article

DiGeorge syndrome: the use of model organisms to dissect complex genetics.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2363, doi. 10.1093/hmg/11.20.2363

By:

Baldini, Antonio

Publication type:

Article

The NF-κB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2371, doi. 10.1093/hmg/11.20.2371

By:

Smahi, Asma;
Courtois, Gilles;
Rabia, Smail Hadj;
Döffinger, Rainer;
Bodemer, Christine;
Munnich, Arnold;
Casanova, Jean-Laurent;
Israël, Alain

Publication type:

Article

Gene therapy of muscular dystrophy.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2355, doi. 10.1093/hmg/11.20.2355

By:

Chamberlain, Jeffrey S.

Publication type:

Article

The pressure rises: update on the genetics of phaeochromocytoma.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2347, doi. 10.1093/hmg/11.20.2347

By:

Maher, Eamonn R.;
Eng, Charis

Publication type:

Article

The allelic architecture of human disease genes: common disease–common variant… or not?

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2417, doi. 10.1093/hmg/11.20.2417

By:

Pritchard, Jonathan K.;
Cox, Nancy J.

Publication type:

Article

Molecular genetics of too much bone.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2385, doi. 10.1093/hmg/11.20.2385

By:

Janssens, Katrien;
Van Hul, Wim

Publication type:

Article

Protecting genomic integrity during DNA replication: correlation between Werner's and Bloom's syndrome gene products and the MRE11 complex.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2447, doi. 10.1093/hmg/11.20.2447

By:

Franchitto, Annapaola;
Pichierri, Pietro

Publication type:

Article

Ion channels: structural bioinformatics and modelling.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2425, doi. 10.1093/hmg/11.20.2425

By:

Capener, Charlotte E.;
Kim, Hyun Ji;
Arinaminpathy, Yalini;
Sansom, Mark S.P.

Publication type:

Article

Susceptibility to malaria as a complex trait: big pressure from a tiny creature.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2469, doi. 10.1093/hmg/11.20.2469

By:

Fortin, A.;
Stevenson, M.M.;
Gros, P.

Publication type:

Article

Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2463, doi. 10.1093/hmg/11.20.2463

By:

Cordell, Heather J.

Publication type:

Article

The allelic structure of common disease.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2455, doi. 10.1093/hmg/11.20.2455

By:

Smith, Desmond J.;
Lusis, Aldons J.

Publication type:

Article

Understanding familial and non-familial renal cell cancer.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2489, doi. 10.1093/hmg/11.20.2489

By:

Bodmer, Daniëlle;
van den Hurk, Wilhelmina;
van Groningen, Jan J. M.;
Eleveld, Marc J.;
Martens, Gerard J. M.;
Weterman, Marian A. J.;
Geurts van Kessel, Ad

Publication type:

Article

Ion channel diseases.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2435, doi. 10.1093/hmg/11.20.2435

By:

Hübner, Christian A.;
Jentsch, Thomas J.

Publication type:

Article

Cancer epigenomics.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 20, p. 2479, doi. 10.1093/hmg/11.20.2479

By:

Plass, Christoph

Publication type:

Article