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

Results: 11

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
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
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
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