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Eric Clauser

Showing results (11-20 of 48) with videos related to

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Chronobiology International|March 9, 2010
Cardiovascular rhythms and cardiac baroreflex sensitivity in AT(1A) receptor gain-of-function mutant miceKesia Palma-Rigo, Véronique Baudrie, Dominique Laude, et al.
Annales De Biologie Clinique|September 8, 2011
[Assessment of AFP in amniotic fluid: comparison of three automated techniques]Marie-Clémence Leguy, Silvina Dos Reis Tavares, Vassili Tsatsaris, et al.
The Journal of Clinical Endocrinology and Metabolism|March 25, 2014
A feminizing adrenocortical carcinoma in the context of a late onset 21-hydroxylase deficiencyRossella Libé, Wiebke Arlt, Estelle Louiset, et al.
Journal of the American Society of Nephrology : JASN|April 11, 2019
Severe Arterial Hypertension from Cullin 3 Mutations Is Caused by Both Renal and Vascular EffectsWaed Abdel Khalek, Chloé Rafael, Irmine Loisel-Ferreira, et al.
International Journal of Molecular Sciences|May 14, 2022
Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and CyclingIlektra Kouranti, Waed Abdel Khalek, Stephani Mazurkiewicz, 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.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|November 10, 2016
Familial small-intestine carcinoids: Chromosomal alterations and germline inositol polyphosphate multikinase sequencingLouis de Mestier, Eric Pasmant, Clémence Fleury, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 3, 2016
Knock-In of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP-Dependent Protein Kinase A Activation: A Model of Type 1 AcrodysostosisCatherine Le Stunff, Francoise Tilotta, Jérémy Sadoine, et al.
Hormone Research in Paediatrics|May 7, 2011
Clinical features and treatment of pediatric somatotropinoma: case study of an aggressive tumor due to a new AIP mutation and extensive literature reviewClaire Personnier, Laure Cazabat, Jérôme Bertherat, et al.
Cancer Research|October 21, 2010
Transcriptome analysis reveals that p53 and {beta}-catenin alterations occur in a group of aggressive adrenocortical cancersBruno Ragazzon, Rossella Libé, Sébastien Gaujoux, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Chronobiology International|March 9, 2010
Cardiovascular rhythms and cardiac baroreflex sensitivity in AT(1A) receptor gain-of-function mutant miceKesia Palma-Rigo, Véronique Baudrie, Dominique Laude, et al.
Annales De Biologie Clinique|September 8, 2011
[Assessment of AFP in amniotic fluid: comparison of three automated techniques]Marie-Clémence Leguy, Silvina Dos Reis Tavares, Vassili Tsatsaris, et al.
The Journal of Clinical Endocrinology and Metabolism|March 25, 2014
A feminizing adrenocortical carcinoma in the context of a late onset 21-hydroxylase deficiencyRossella Libé, Wiebke Arlt, Estelle Louiset, et al.
Journal of the American Society of Nephrology : JASN|April 11, 2019
Severe Arterial Hypertension from Cullin 3 Mutations Is Caused by Both Renal and Vascular EffectsWaed Abdel Khalek, Chloé Rafael, Irmine Loisel-Ferreira, et al.
International Journal of Molecular Sciences|May 14, 2022
Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and CyclingIlektra Kouranti, Waed Abdel Khalek, Stephani Mazurkiewicz, 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.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|November 10, 2016
Familial small-intestine carcinoids: Chromosomal alterations and germline inositol polyphosphate multikinase sequencingLouis de Mestier, Eric Pasmant, Clémence Fleury, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 3, 2016
Knock-In of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP-Dependent Protein Kinase A Activation: A Model of Type 1 AcrodysostosisCatherine Le Stunff, Francoise Tilotta, Jérémy Sadoine, et al.
Hormone Research in Paediatrics|May 7, 2011
Clinical features and treatment of pediatric somatotropinoma: case study of an aggressive tumor due to a new AIP mutation and extensive literature reviewClaire Personnier, Laure Cazabat, Jérôme Bertherat, et al.
Cancer Research|October 21, 2010
Transcriptome analysis reveals that p53 and {beta}-catenin alterations occur in a group of aggressive adrenocortical cancersBruno Ragazzon, Rossella Libé, Sébastien Gaujoux, et al.
Pageof 5