Works matching IS 09646906 AND DT 2003 AND VI 12 AND IP 6

Results: 11

Transgenic rat model of Huntington's disease.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 617, doi. 10.1093/hmg/ddg075

By:

von Hörsten, Stephan;
Schmitt, Ina;
Nguyen, Huu Phuc;
Holzmann, Carsten;
Schmidt, Thorsten;
Walther, Thomas;
Bader, Michael;
Pabst, Reinhard;
Kobbe, Philipp;
Krotova, Jana;
Stiller, Detlef;
Kask, Ants;
Vaarmann, Annika;
Rathke-Hartlieb, Silvia;
Schulz, Jörg B.;
Grasshoff, Ute;
Bauer, Ingrid;
Vieira-Saecker, Ana Maria Menezes;
Paul, Martin;
Jones, Lesley

Publication type:

Article

The dystrophin associated protein complex in zebrafish.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 601, doi. 10.1093/hmg/ddg071

By:

Guyon, J. R.;
Mosley, A. N.;
Zhou, Y.;
O'Brien, K. F.;
Sheng, X.;
Chiang, K.;
Davidson, A. J.;
Volinski, J. M.;
Zon, L. I.;
Kunkel, L. M.

Publication type:

Article

Atopy, respiratory function and HLA-DR in Aboriginal Australians.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 625, doi. 10.1093/hmg/ddg059

By:

Moffatt, Miriam F.;
Faux, Jennie A.;
Lester, Susan;
Paré, Peter;
McCluskey, James;
Spargo, Randy;
James, Alan;
Musk, A. William;
Cookson, William O. C. M.

Publication type:

Article

On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 657, doi. 10.1093/hmg/ddg060

By:

Schröder, Rolf;
Goudeau, Bertrand;
Simon, Monique Casteras;
Fischer, Dirk;
Eggermann, Thomas;
Clemen, Christoph S.;
Li, Zhenlin;
Reimann, Jens;
Xue, Zhigang;
Rudnik-Schöneborn, Sabine;
Zerres, Klaus;
van der Ven, Peter F. M.;
Fürst, Dieter O.;
Kunz, Wolfram S.;
Vicart, Patrick

Publication type:

Article

LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 631, doi. 10.1093/hmg/ddg062

By:

Gamp, Alexander-Christian;
Tanaka, Yoshitaka;
Lüllmann-Rauch, Renate;
Wittke, Dorothee;
D'Hooge, Rudi;
De Deyn, Peter P.;
Moser, Tobias;
Maier, Hannes;
Hartmann, Dieter;
Reiss, Karina;
Illert, Anna-Lena;
von Figura, Kurt;
Saftig, Paul

Publication type:

Article

A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 585, doi. 10.1093/hmg/ddg063

By:

Lyon, Mary F.;
Jamieson, Robyn V.;
Perveen, Rahat;
Glenister, Peter H.;
Griffiths, Robert;
Boyd, Yvonne;
Glimcher, Laurie H.;
Favor, Jack;
Munier, Francis L.;
Black, Graeme C. M.

Publication type:

Article

cDNA microarray analysis of individual Duchenne muscular dystrophy patients.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 595, doi. 10.1093/hmg/ddg065

By:

Noguchi, Satoru;
Tsukahara, Toshifumi;
Fujita, Masako;
Kurokawa, Rumi;
Tachikawa, Masaji;
Toda, Tatsushi;
Tsujimoto, Atsumi;
Arahata, Kiichi;
Nishino, Ichizo

Publication type:

Article

PKHDL1, a homolog of the autosomal recessive polycystic kidney disease gene, encodes a receptor with inducible T lymphocyte expression.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 685, doi. 10.1093/hmg/ddg068

By:

Hogan, Marie C.;
Griffin, Matthew D.;
Rossetti, Sandro;
Torres, Vicente E.;
Ward, Christopher J.;
Harris, Peter C.

Publication type:

Article

Haplotype-specific linkage disequilibrium patterns define the genetic topography of the human MHC.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 647, doi. 10.1093/hmg/ddg066

By:

Ahmad, Tariq;
Neville, Matt;
Marshall, Sara E.;
Armuzzi, Alessandro;
Mulcahy-Hawes, Kim;
Crawshaw, Jonathan;
Sato, Hiroe;
Ling, Khoon-Lin;
Barnardo, Martin;
Goldthorpe, Sue;
Walton, Robert;
Bunce, Mike;
Jewell, Derek P.;
Welsh, Ken I.

Publication type:

Article

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 671, doi. 10.1093/hmg/ddg070

By:

Hauser, Michael A.;
Li, Yi-Ju;
Takeuchi, Satoshi;
Walters, Robert;
Noureddine, Maher;
Maready, Melinda;
Darden, Tiffany;
Hulette, Christine;
Martin, Eden;
Hauser, Elizabeth;
Xu, Hong;
Schmechel, Don;
Stenger, Judith E.;
Dietrich, Fred;
Vance, Jeffery

Publication type:

Article

BMP2 exposure results in decreased PTEN protein degradation and increased PTEN levels.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 6, p. 679, doi. 10.1093/hmg/ddg069

By:

Waite, Kristin A.;
Eng, Charis

Publication type:

Article