Works matching IS 09646906 AND DT 2007 AND VI 16 AND IP 16

Results: 11

SUT-1 enables tau-induced neurotoxicity in C. elegans.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 1959, doi. 10.1093/hmg/ddm143

By:

Kraemer, Brian C.;
Schellenberg, Gerard D.

Publication type:

Article

Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 1951, doi. 10.1093/hmg/ddm142

By:

Chao, Michael J.;
Barnardo, Martin C.N.M.;
Lui, Guang-zhi;
Lincoln, Matthew R.;
Ramagopalan, Sreeram V.;
Herrera, Blanca M.;
Dyment, David A.;
Sadovnick, A. Dessa;
Ebers, George C.

Publication type:

Article

Disease-associated mutations affect GPR56 protein trafficking and cell surface expression.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 1972, doi. 10.1093/hmg/ddm144

By:

Jin, Zhaohui;
Tietjen, Ian;
Bu, Lihong;
Liu-Yesucevitz, Liqun;
Gaur, Shantanu K.;
Walsh, Christopher A.;
Piao, Xianhua

Publication type:

Article

Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 1940, doi. 10.1093/hmg/ddm141

By:

Garcia-Gonzalez, Miguel A.;
Menezes, Luis F.;
Piontek, Klaus B.;
Kaimori, Junya;
Huso, David L.;
Watnick, Terry;
Onuchic, Luiz F.;
Guay-Woodford, Lisa M.;
Germino, Gregory G.

Publication type:

Article

GNAS transcripts in skeletal progenitors: evidence for random asymmetric allelic expression of Gsα.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 1921, doi. 10.1093/hmg/ddm139

By:

Michienzi, Stefano;
Cherman, Natasha;
Holmbeck, Kenn;
Funari, Alessia;
Collins, Michael T.;
Bianco, Paolo;
Robey, Pamela Gehron;
Riminucci, Mara

Publication type:

Article

Non-disjunction of chromosome 13.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 2004, doi. 10.1093/hmg/ddm148

By:

Bugge, Merete;
Collins, Andrew;
Hertz, Jens Michael;
Eiberg, Hans;
Lundsteen, Claes;
Brandt, Carsten A.;
Bak, Mads;
Hansen, Claus;
deLozier, Celia D.;
Lespinasse, James;
Tranebjaerg, Lisbeth;
Hahnemann, Johanne M.D.;
Rasmussen, Kirsten;
Bruun-Petersen, Gert;
Duprez, Laurence;
Tommerup, Niels;
Petersen, Michael B.

Publication type:

Article

Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 1986, doi. 10.1093/hmg/ddm146

By:

Spencer, Kylee L.;
Hauser, Michael A.;
Olson, Lana M.;
Schmidt, Silke;
Scott, William K.;
Gallins, Paul;
Agarwal, Anita;
Postel, Eric A.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.

Publication type:

Article

In vitro assays fail to predict in vivo effects of regulatory polymorphisms.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 1931, doi. 10.1093/hmg/ddm140

By:

Cirulli, Elizabeth T.;
Goldstein, David B.

Publication type:

Article

MPP1 links the Usher protein network and the Crumbs protein complex in the retina.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 1993, doi. 10.1093/hmg/ddm147

By:

Gosens, Ilse;
van Wijk, Erwin;
Kersten, Ferry F.J.;
Krieger, Elmar;
van der Zwaag, Bert;
Märker, Tina;
Letteboer, Stef J.F.;
Dusseljee, Simone;
Peters, Theo;
Spierenburg, Henk A.;
Punte, Ingrid M.;
Wolfrum, Uwe;
Cremers, Frans P.M.;
Kremer, Hannie;
Roepman, Ronald

Publication type:

Article

Huntingtin-deficient zebrafish exhibit defects in iron utilization and development.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 1905, doi. 10.1093/hmg/ddm138

By:

Lumsden, Amanda L.;
Henshall, Tanya L.;
Dayan, Sonia;
Lardelli, Michael T.;
Richards, Robert I.

Publication type:

Article

Mechanism of action of a sulphonylurea receptor SUR1 mutation (F132L) that causes DEND syndrome.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 16, p. 2011, doi. 10.1093/hmg/ddm149

By:

Proks, Peter;
Shimomura, Kenju;
Craig, Tim J.;
Girard, Christophe A.J.;
Ashcroft, Frances M.

Publication type:

Article