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Gilgenkrantz

Showing results (191-200 of 233) with videos related to

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American Journal of Medical Genetics|July 1, 1993
No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome familiesW F Flintoff, M Bahuau, S Lyonnet, et al.
The Journal of Gene Medicine|October 25, 2000
Cardiac functional improvement by a human Bcl-2 transgene in a mouse model of ischemia/reperfusion injuryV Brocheriou, A A Hagège, A Oubenaïssa, et al.
European Heart Journal|April 1, 1988
Sustained improvement in myocardial perfusion four to six years after PTCA in patients with a satisfactory angiographic result, six months after the procedureN Danchin, A Haouzi, M Amor, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Myoblast transplantation between monozygotic twin girl carriers of Duchenne muscular dystrophyJ P Tremblay, J P Bouchard, F Malouin, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|December 16, 2006
Delayed liver regeneration in mice lacking liver serum response factorM Ujue Latasa, Dominique Couton, Claude Charvet, et al.
The Journal of Clinical Investigation|October 1, 1991
Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patientsJ Chelly, H Gilgenkrantz, J P Hugnot, et al.
Clinical Genetics|October 1, 1988
Coffin-Lowry syndrome: a multicenter studyS Gilgenkrantz, P Mujica, P Gruet, et al.
American Journal of Medical Genetics|February 1, 1991
New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA intervalI Oberlé, A Vincent, N Abbadi, et al.
Human Molecular Genetics|July 1, 1994
Cloning and characterization of the human choroideremia geneH van Bokhoven, J A van den Hurk, L Bogerd, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|March 1, 1987
[Outcome of 195 patients with Wolff-Parkinson-White syndrome]B Brembilla-Perrot, E Aliot, P Louis, et al.
Pageof 24

Showing results (191-200 of 233) with videos related to

Sort By:
Pageof 24
American Journal of Medical Genetics|July 1, 1993
No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome familiesW F Flintoff, M Bahuau, S Lyonnet, et al.
The Journal of Gene Medicine|October 25, 2000
Cardiac functional improvement by a human Bcl-2 transgene in a mouse model of ischemia/reperfusion injuryV Brocheriou, A A Hagège, A Oubenaïssa, et al.
European Heart Journal|April 1, 1988
Sustained improvement in myocardial perfusion four to six years after PTCA in patients with a satisfactory angiographic result, six months after the procedureN Danchin, A Haouzi, M Amor, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Myoblast transplantation between monozygotic twin girl carriers of Duchenne muscular dystrophyJ P Tremblay, J P Bouchard, F Malouin, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|December 16, 2006
Delayed liver regeneration in mice lacking liver serum response factorM Ujue Latasa, Dominique Couton, Claude Charvet, et al.
The Journal of Clinical Investigation|October 1, 1991
Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patientsJ Chelly, H Gilgenkrantz, J P Hugnot, et al.
Clinical Genetics|October 1, 1988
Coffin-Lowry syndrome: a multicenter studyS Gilgenkrantz, P Mujica, P Gruet, et al.
American Journal of Medical Genetics|February 1, 1991
New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA intervalI Oberlé, A Vincent, N Abbadi, et al.
Human Molecular Genetics|July 1, 1994
Cloning and characterization of the human choroideremia geneH van Bokhoven, J A van den Hurk, L Bogerd, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|March 1, 1987
[Outcome of 195 patients with Wolff-Parkinson-White syndrome]B Brembilla-Perrot, E Aliot, P Louis, et al.
Pageof 24