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C Massart

Showing results (91-100 of 102) with videos related to

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Diabetes & Metabolism|November 21, 2016
Corrigendum to "Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism" [Diabetes Metab. 41 (2015) 331-337]M de Kerdanet, M Caron-Debarle, S Nivot, et al.
Pathologie-Biologie|June 1, 1986
New methods for detection of HLA genes polymorphism useful for associated diseases studiesI Le Gall, A M Chausse, A Marcadet, et al.
Annales De Biologie Clinique|March 30, 2004
[Recommendations for the standardization of growth hormone assays]M Bayle, D Chevenne, B Dousset, et al.
American Journal of Physiology. Cell Physiology|October 10, 2014
Anoctamin-1/TMEM16A is the major apical iodide channel of the thyrocyteL Twyffels, A Strickaert, M Virreira, et al.
Journal of Proteomics|July 6, 2010
Novel post-digest isotope coded protein labeling method for phospho- and glycoproteome analysisM Fleron, Y Greffe, D Musmeci, et al.
Kidney International|June 22, 2006
Inter-method variability in PTH measurement: implication for the care of CKD patientsJ-C Souberbielle, A Boutten, M-C Carlier, et al.
Diabetes & Metabolism|July 19, 2011
Vitamin D deficiency, vitamin D receptor gene polymorphisms and cardiovascular risk factors in Caribbean patients with type 2 diabetesF-L Vélayoudom-Céphise, L Larifla, J-P Donnet, et al.
Talanta|October 31, 2008
Validation of the CALUX bioassay for PCDD/F analyses in human blood plasma and comparison with GC-HRMSN Van Wouwe, I Windal, H Vanderperren, et al.
Muscle & Nerve|September 17, 2004
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutationsA Muchir, J Medioni, M Laluc, et al.
Neurology|May 31, 2007
Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?R Ben Yaou, A Toutain, T Arimura, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Diabetes & Metabolism|November 21, 2016
Corrigendum to "Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism" [Diabetes Metab. 41 (2015) 331-337]M de Kerdanet, M Caron-Debarle, S Nivot, et al.
Pathologie-Biologie|June 1, 1986
New methods for detection of HLA genes polymorphism useful for associated diseases studiesI Le Gall, A M Chausse, A Marcadet, et al.
Annales De Biologie Clinique|March 30, 2004
[Recommendations for the standardization of growth hormone assays]M Bayle, D Chevenne, B Dousset, et al.
American Journal of Physiology. Cell Physiology|October 10, 2014
Anoctamin-1/TMEM16A is the major apical iodide channel of the thyrocyteL Twyffels, A Strickaert, M Virreira, et al.
Journal of Proteomics|July 6, 2010
Novel post-digest isotope coded protein labeling method for phospho- and glycoproteome analysisM Fleron, Y Greffe, D Musmeci, et al.
Kidney International|June 22, 2006
Inter-method variability in PTH measurement: implication for the care of CKD patientsJ-C Souberbielle, A Boutten, M-C Carlier, et al.
Diabetes & Metabolism|July 19, 2011
Vitamin D deficiency, vitamin D receptor gene polymorphisms and cardiovascular risk factors in Caribbean patients with type 2 diabetesF-L Vélayoudom-Céphise, L Larifla, J-P Donnet, et al.
Talanta|October 31, 2008
Validation of the CALUX bioassay for PCDD/F analyses in human blood plasma and comparison with GC-HRMSN Van Wouwe, I Windal, H Vanderperren, et al.
Muscle & Nerve|September 17, 2004
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutationsA Muchir, J Medioni, M Laluc, et al.
Neurology|May 31, 2007
Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?R Ben Yaou, A Toutain, T Arimura, et al.
Pageof 11