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Gilgenkrantz

Showing results (201-210 of 233) with videos related to

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Annales De Cardiologie Et D'Angeiologie|May 1, 1986
[Isotopic exercise tests and selection of cases of inferior infarction requiring coronarography]F Brunotte, M H Laurens, E Aliot, et al.
Gene Therapy|January 1, 1994
Adenovirus-mediated transfer of a human dystrophin gene to skeletal muscle of mdx mouseT Ragot, L D Stratford-Perricaudet, N Vincent, et al.
Cell|December 21, 1990
Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophiesJ Chelly, H Gilgenkrantz, M Lambert, et al.
Carcinogenesis|June 15, 2012
Combined hepatocellular-cholangiocarcinomas exhibit progenitor features and activation of Wnt and TGFβ signaling pathwaysCédric Coulouarn, Catherine Cavard, Laura Rubbia-Brandt, et al.
The American Journal of Pathology|June 12, 2002
The combination of ischemic preconditioning and liver Bcl-2 overexpression is a suitable strategy to prevent liver and lung damage after hepatic ischemia-reperfusionCarmen Peralta, José Carlos Perales, Ramón Bartrons, et al.
Human Molecular Genetics|May 1, 1994
Molecular cloning of the synovial sarcoma-specific translocation (X;18)(p11.2;q11.2) breakpointB de Leeuw, M Balemans, D O Weghuis, et al.
American Journal of Human Genetics|May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb regionN Dahl, L J Hu, M Chery, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Expression of the transcripts initiated in the 62nd intron of the dystrophin geneM Lambert, P Chafey, J P Hugnot, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 1992
Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissuesJ P Hugnot, H Gilgenkrantz, N Vincent, et al.
Human Genetics|December 1, 1988
Interstitial deletion of chromosome 15: two casesL D Formiga, L Poenaru, F Couronne, et al.
Pageof 24

Showing results (201-210 of 233) with videos related to

Sort By:
Pageof 24
Annales De Cardiologie Et D'Angeiologie|May 1, 1986
[Isotopic exercise tests and selection of cases of inferior infarction requiring coronarography]F Brunotte, M H Laurens, E Aliot, et al.
Gene Therapy|January 1, 1994
Adenovirus-mediated transfer of a human dystrophin gene to skeletal muscle of mdx mouseT Ragot, L D Stratford-Perricaudet, N Vincent, et al.
Cell|December 21, 1990
Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophiesJ Chelly, H Gilgenkrantz, M Lambert, et al.
Carcinogenesis|June 15, 2012
Combined hepatocellular-cholangiocarcinomas exhibit progenitor features and activation of Wnt and TGFβ signaling pathwaysCédric Coulouarn, Catherine Cavard, Laura Rubbia-Brandt, et al.
The American Journal of Pathology|June 12, 2002
The combination of ischemic preconditioning and liver Bcl-2 overexpression is a suitable strategy to prevent liver and lung damage after hepatic ischemia-reperfusionCarmen Peralta, José Carlos Perales, Ramón Bartrons, et al.
Human Molecular Genetics|May 1, 1994
Molecular cloning of the synovial sarcoma-specific translocation (X;18)(p11.2;q11.2) breakpointB de Leeuw, M Balemans, D O Weghuis, et al.
American Journal of Human Genetics|May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb regionN Dahl, L J Hu, M Chery, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Expression of the transcripts initiated in the 62nd intron of the dystrophin geneM Lambert, P Chafey, J P Hugnot, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 1992
Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissuesJ P Hugnot, H Gilgenkrantz, N Vincent, et al.
Human Genetics|December 1, 1988
Interstitial deletion of chromosome 15: two casesL D Formiga, L Poenaru, F Couronne, et al.
Pageof 24