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W Auerbach

Showing results (11-20 of 21) with videos related to

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The EMBO Journal|July 1, 1992
Regulation of CFTR expression and function during differentiation of intestinal epithelial cellsR Sood, C Bear, W Auerbach, et al.
Biotechniques|November 21, 2000
Establishment and chimera analysis of 129/SvEv- and C57BL/6-derived mouse embryonic stem cell linesW Auerbach, J H Dunmore, V Fairchild-Huntress, et al.
Mechanisms of Development|October 19, 2002
A novel gene, GliH1, with homology to the Gli zinc finger domain not required for mouse developmentM Nakashima, N Tanese, M Ito, et al.
Nature Genetics|December 17, 1997
Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansionJ K White, W Auerbach, M P Duyao, et al.
Journal of Cell Science|January 1, 1990
Transformed sweat gland and nasal epithelial cell lines from control and cystic fibrosis individualsJ A Buchanan, H Yeger, J A Tabcharani, et al.
Nature Genetics|March 1, 1996
Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factorR Rozmahel, M Wilschanski, A Matin, et al.
Human Molecular Genetics|November 16, 2001
The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtinW Auerbach, M S Hurlbert, P Hilditch-Maguire, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Targeted inactivation of the mouse Huntington's disease gene homolog HdhM E MacDonald, M Duyao, T Calzonetti, et al.
Human Molecular Genetics|January 15, 1999
Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouseV C Wheeler, W Auerbach, J K White, et al.
Human Molecular Genetics|March 4, 2000
Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in miceV C Wheeler, J K White, C A Gutekunst, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
The EMBO Journal|July 1, 1992
Regulation of CFTR expression and function during differentiation of intestinal epithelial cellsR Sood, C Bear, W Auerbach, et al.
Biotechniques|November 21, 2000
Establishment and chimera analysis of 129/SvEv- and C57BL/6-derived mouse embryonic stem cell linesW Auerbach, J H Dunmore, V Fairchild-Huntress, et al.
Mechanisms of Development|October 19, 2002
A novel gene, GliH1, with homology to the Gli zinc finger domain not required for mouse developmentM Nakashima, N Tanese, M Ito, et al.
Nature Genetics|December 17, 1997
Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansionJ K White, W Auerbach, M P Duyao, et al.
Journal of Cell Science|January 1, 1990
Transformed sweat gland and nasal epithelial cell lines from control and cystic fibrosis individualsJ A Buchanan, H Yeger, J A Tabcharani, et al.
Nature Genetics|March 1, 1996
Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factorR Rozmahel, M Wilschanski, A Matin, et al.
Human Molecular Genetics|November 16, 2001
The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtinW Auerbach, M S Hurlbert, P Hilditch-Maguire, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Targeted inactivation of the mouse Huntington's disease gene homolog HdhM E MacDonald, M Duyao, T Calzonetti, et al.
Human Molecular Genetics|January 15, 1999
Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouseV C Wheeler, W Auerbach, J K White, et al.
Human Molecular Genetics|March 4, 2000
Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in miceV C Wheeler, J K White, C A Gutekunst, et al.
Pageof 3