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J Capeau

Showing results (151-160 of 165) with videos related to

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Surgery|May 2, 2001
Survival and functions of encapsulated porcine hepatocytes after allotransplantation or xenotransplantation without immunosuppressionS Benoist, R Sarkis, V Barbu, et al.
The American Journal of Physiology|February 1, 1996
Deregulation of hexose transporter expression in Caco-2 cells by ras and polyoma middle T oncogenesS Baron-Delage, L Mahraoui, A Cadoret, et al.
Gene Therapy|February 4, 1999
Liposomes enhance delivery and expression of an RGD-oligolysine gene transfer vector in human tracheal cellsM Colin, R P Harbottle, A Knight, et al.
Gene Therapy|February 16, 2000
Cell delivery, intracellular trafficking and expression of an integrin-mediated gene transfer vector in tracheal epithelial cellsM Colin, M Maurice, G Trugnan, et al.
Pediatric Research|July 1, 1997
Major circadian variations of glucose homeostasis in a patient with Rabson-Mendenhall syndrome and primary insulin resistance due to a mutation (Cys284-->Tyr) in the insulin receptor alpha-subunitC Desbois-Mouthon, J Magré, J Duprey, et al.
Diabetes & Metabolism|December 4, 2010
Adiponectin and leptin in Afro-Caribbean men and women with HIV infection: association with insulin resistance and type 2 diabetesJ Deloumeaux, M Maachi, M-T Sow-Goerger, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2008
Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophyM C Vantyghem, D Vincent-Desplanques, F Defrance-Faivre, et al.
Diabetes|November 15, 2000
Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophyC Vigouroux, J Magré, M C Vantyghem, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2004
Serum leptin level is a regulator of bone massF Elefteriou, S Takeda, K Ebihara, et al.
Pageof 17

Showing results (151-160 of 165) with videos related to

Sort By:
Pageof 17
Surgery|May 2, 2001
Survival and functions of encapsulated porcine hepatocytes after allotransplantation or xenotransplantation without immunosuppressionS Benoist, R Sarkis, V Barbu, et al.
The American Journal of Physiology|February 1, 1996
Deregulation of hexose transporter expression in Caco-2 cells by ras and polyoma middle T oncogenesS Baron-Delage, L Mahraoui, A Cadoret, et al.
Gene Therapy|February 4, 1999
Liposomes enhance delivery and expression of an RGD-oligolysine gene transfer vector in human tracheal cellsM Colin, R P Harbottle, A Knight, et al.
Gene Therapy|February 16, 2000
Cell delivery, intracellular trafficking and expression of an integrin-mediated gene transfer vector in tracheal epithelial cellsM Colin, M Maurice, G Trugnan, et al.
Pediatric Research|July 1, 1997
Major circadian variations of glucose homeostasis in a patient with Rabson-Mendenhall syndrome and primary insulin resistance due to a mutation (Cys284-->Tyr) in the insulin receptor alpha-subunitC Desbois-Mouthon, J Magré, J Duprey, et al.
Diabetes & Metabolism|December 4, 2010
Adiponectin and leptin in Afro-Caribbean men and women with HIV infection: association with insulin resistance and type 2 diabetesJ Deloumeaux, M Maachi, M-T Sow-Goerger, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2008
Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophyM C Vantyghem, D Vincent-Desplanques, F Defrance-Faivre, et al.
Diabetes|November 15, 2000
Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophyC Vigouroux, J Magré, M C Vantyghem, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2004
Serum leptin level is a regulator of bone massF Elefteriou, S Takeda, K Ebihara, et al.
Pageof 17