Works matching IS 09646906 AND DT 2004 AND VI 13 AND IP 13

Results: 10

Whole genome scanning identifies genotypes associated with recurrence and metastasis in prostate tumors.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1303, doi. 10.1093/hmg/ddh155

By:

Paris, Pamela L.;
Andaya, Armann;
Fridlyand, Jane;
Jain, Ajay N.;
Weinberg, Vivian;
Kowbel, David;
Brebner, John H.;
Simko, Jeff;
Watson, J.E. Vivienne;
Volik, Stas;
Albertson, Donna G.;
Pinkel, Daniel;
Alers, Janneke C.;
van der Kwast, Theodorus H.;
Vissers, Kees J.;
Schroder, Fritz H.;
Wildhagen, Mark F.;
Febbo, Phillip G.;
Chinnaiyan, Arul M.;
Pienta, Kenneth J.

Publication type:

Article

Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1333, doi. 10.1093/hmg/ddh154

By:

Amano, Kenji;
Sago, Haruhiko;
Uchikawa, Chiharu;
Suzuki, Taishi;
Kotliarova, Svetlana E.;
Nukina, Nobuyuki;
Epstein, Charles J.;
Yamakawa, Kazuhiro

Publication type:

Article

Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1373, doi. 10.1093/hmg/ddh153

By:

Kramerova, I.;
Kudryashova, E.;
Tidball, J.G.;
Spencer, Melissa J.

Publication type:

Article

Molecular pathogenesis of cystinosis: effect of CTNS mutations on the transport activity and subcellular localization of cystinosin.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1361, doi. 10.1093/hmg/ddh152

By:

Kalatzis, Vasiliki;
Nevo, Nathalie;
Cherqui, Stéphanie;
Gasnier, Bruno;
Antignac, Corinne

Publication type:

Article

Partial loss of presenilins causes seborrheic keratosis and autoimmune disease in mice.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1321, doi. 10.1093/hmg/ddh151

By:

Tournoy, Jos;
Bossuyt, Xavier;
Snellinx, An;
Regent, Marleen;
Garmyn, Marian;
Serneels, Lutgarde;
Saftig, Paul;
Craessaerts, Katleen;
De Strooper, Bart;
Hartmann, Dieter

Publication type:

Article

Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1291, doi. 10.1093/hmg/ddh150

By:

Mientjes, Edwin J.;
Willemsen, Rob;
Kirkpatrick, Laura L.;
Nieuwenhuizen, Ingeborg M.;
Hoogeveen-Westerveld, Marianne;
Verweij, Marcel;
Reis, Surya;
Bardoni, Barbara;
Hoogeveen, Andre T.;
Oostra, Ben A.;
Nelson, David L.

Publication type:

Article

Corticosteroid pharmacogenetics: association of sequence variants in CRHR1 with improved lung function in asthmatics treated with inhaled corticosteroids.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1353, doi. 10.1093/hmg/ddh149

By:

Tantisira, Kelan G.;
Lake, Stephen;
Silverman, Eric S.;
Palmer, Lyle J.;
Lazarus, Ross;
Silverman, Edwin K.;
Liggett, Stephen B.;
Gelfand, Erwin W.;
Rosenwasser, Lanny J.;
Richter, Brent;
Israel, Elliot;
Wechsler, Michael;
Gabriel, Stacey;
Altshuler, David;
Lander, Eric;
Drazen, Jeffrey;
Weiss, Scott T.

Publication type:

Article

Platelet-activating factor-acetylhydrolase and PAF-receptor gene haplotypes in relation to future cardiovascular event in patients with coronary artery disease.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1341, doi. 10.1093/hmg/ddh145

By:

Ninio, Ewa;
Tregouet, David;
Carrier, Jean-Luc;
Stengel, Dominique;
Bickel, Christoph;
Perret, Claire;
Rupprecht, Hans J.;
Cambien, François;
Blankenberg, Stefan;
Tiret, Laurence

Publication type:

Article

Progressive decrease in chaperone protein levels in a mouse model of Huntington's disease and induction of stress proteins as a therapeutic approach.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1389, doi. 10.1093/hmg/ddh144

By:

Hay, David G.;
Sathasivam, Kirupa;
Tobaben, Sönke;
Stahl, Bernd;
Marber, Michael;
Mestril, Ruben;
Mahal, Amarbirpal;
Smith, Donna L.;
Woodman, Ben;
Bates, Gillian P.

Publication type:

Article

GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 13, p. 1315, doi. 10.1093/hmg/ddh146

By:

Dibbens, Leanne M.;
Feng, Hua-Jun;
Richards, Michaella C.;
Harkin, Louise A.;
Hodgson, Bree L.;
Scott, Darren;
Jenkins, Misty;
Petrou, Steven;
Sutherland, Grant R.;
Scheffer, Ingrid E.;
Berkovic, Samuel F.;
Macdonald, Robert L.;
Mulley, John C.

Publication type:

Article