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Caroline Silve

Showing results (21-30 of 53) with videos related to

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Stem Cell Reports|September 23, 2014
Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivativesVirginie Grybek, Laetitia Aubry, Stéphanie Maupetit-Méhouas, et al.
Annals of Surgical Oncology|April 27, 2019
GNAS but Not Extended RAS Mutations Spectrum are Associated with a Better Prognosis in Intraductal Pancreatic Mucinous NeoplasmsSébastien Gaujoux, Alina Parvanescu, Manuella Cesaretti, et al.
The Journal of Biological Chemistry|March 19, 2002
Parathyroid hormone and parathyroid hormone-related protein exert both pro- and anti-apoptotic effects in mesenchymal cellsHen-Li Chen, Burak Demiralp, Abraham Schneider, et al.
American Journal of Medical Genetics. Part A|December 8, 2015
Report of two novel mutations in PTHLH associated with brachydactyly type E and literature reviewCecile Thomas-Teinturier, Arrate Pereda, Intza Garin, et al.
The Journal of Biological Chemistry|September 26, 2015
Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney ComplexYara Rhayem, Catherine Le Stunff, Waed Abdel Khalek, et al.
Human Molecular Genetics|June 19, 2008
PTHR1 mutations associated with Ollier disease result in receptor loss of functionAlain Couvineau, Vinciane Wouters, Guylène Bertrand, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 19, 2017
Phenotypic Variability in a Family with Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of Protein Kinase-A PhosphorylationJulia Hoppmann, Julia Gesing, Caroline Silve, et al.
Medicine|December 20, 2019
McCune Albright syndrome is a genetic predisposition to intraductal papillary and mucinous neoplasms of the pancreas associated pancreatic cancer in relation with GNAS somatic mutation - a case reportSébastien Gaujoux, Eric Pasmant, Caroline Silve, et al.
The Journal of Clinical Endocrinology and Metabolism|June 28, 2008
Dominant-negative GCMB mutations cause an autosomal dominant form of hypoparathyroidismMichael Mannstadt, Guylène Bertrand, Mihaela Muresan, et al.
Human Molecular Genetics|October 11, 2017
Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3Claire Briet, Arrate Pereda, Catherine Le Stunff, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Stem Cell Reports|September 23, 2014
Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivativesVirginie Grybek, Laetitia Aubry, Stéphanie Maupetit-Méhouas, et al.
Annals of Surgical Oncology|April 27, 2019
GNAS but Not Extended RAS Mutations Spectrum are Associated with a Better Prognosis in Intraductal Pancreatic Mucinous NeoplasmsSébastien Gaujoux, Alina Parvanescu, Manuella Cesaretti, et al.
The Journal of Biological Chemistry|March 19, 2002
Parathyroid hormone and parathyroid hormone-related protein exert both pro- and anti-apoptotic effects in mesenchymal cellsHen-Li Chen, Burak Demiralp, Abraham Schneider, et al.
American Journal of Medical Genetics. Part A|December 8, 2015
Report of two novel mutations in PTHLH associated with brachydactyly type E and literature reviewCecile Thomas-Teinturier, Arrate Pereda, Intza Garin, et al.
The Journal of Biological Chemistry|September 26, 2015
Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney ComplexYara Rhayem, Catherine Le Stunff, Waed Abdel Khalek, et al.
Human Molecular Genetics|June 19, 2008
PTHR1 mutations associated with Ollier disease result in receptor loss of functionAlain Couvineau, Vinciane Wouters, Guylène Bertrand, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 19, 2017
Phenotypic Variability in a Family with Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of Protein Kinase-A PhosphorylationJulia Hoppmann, Julia Gesing, Caroline Silve, et al.
Medicine|December 20, 2019
McCune Albright syndrome is a genetic predisposition to intraductal papillary and mucinous neoplasms of the pancreas associated pancreatic cancer in relation with GNAS somatic mutation - a case reportSébastien Gaujoux, Eric Pasmant, Caroline Silve, et al.
The Journal of Clinical Endocrinology and Metabolism|June 28, 2008
Dominant-negative GCMB mutations cause an autosomal dominant form of hypoparathyroidismMichael Mannstadt, Guylène Bertrand, Mihaela Muresan, et al.
Human Molecular Genetics|October 11, 2017
Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3Claire Briet, Arrate Pereda, Catherine Le Stunff, et al.
Pageof 6