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Eric Clauser

Showing results (41-50 of 48) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 5, 2010
Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotypeRossella Libé, Anelia Horvath, Delphine Vezzosi, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2012
PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistanceAgnès Linglart, Helena Fryssira, Olaf Hiort, et al.
The Journal of Clinical Investigation|December 1, 2020
TREM-1 orchestrates angiotensin II-induced monocyte trafficking and promotes experimental abdominal aortic aneurysmMarie Vandestienne, Yujiao Zhang, Icia Santos-Zas, et al.
The Journal of Clinical Investigation|August 14, 2020
Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosisHélène Louis-Dit-Picard, Ilektra Kouranti, Chloé Rafael, et al.
Nature Genetics|April 22, 2014
Integrated genomic characterization of adrenocortical carcinomaGuillaume Assié, Eric Letouzé, Martin Fassnacht, et al.
JCI Insight|September 22, 2017
Adrenal GIPR expression and chromosome 19q13 microduplications in GIP-dependent Cushing's syndromeAnne-Lise Lecoq, Constantine A Stratakis, Say Viengchareun, et al.
The Journal of Clinical Endocrinology and Metabolism|December 15, 2016
DNA Methylation Is an Independent Prognostic Marker of Survival in Adrenocortical CancerAnne Jouinot, Guillaume Assie, Rossella Libe, et al.
Human Molecular Genetics|February 5, 2013
Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort studyJulien Thevenon, Abderrahmane Bourredjem, Laurence Faivre, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
The Journal of Clinical Endocrinology and Metabolism|November 5, 2010
Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotypeRossella Libé, Anelia Horvath, Delphine Vezzosi, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2012
PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistanceAgnès Linglart, Helena Fryssira, Olaf Hiort, et al.
The Journal of Clinical Investigation|December 1, 2020
TREM-1 orchestrates angiotensin II-induced monocyte trafficking and promotes experimental abdominal aortic aneurysmMarie Vandestienne, Yujiao Zhang, Icia Santos-Zas, et al.
The Journal of Clinical Investigation|August 14, 2020
Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosisHélène Louis-Dit-Picard, Ilektra Kouranti, Chloé Rafael, et al.
Nature Genetics|April 22, 2014
Integrated genomic characterization of adrenocortical carcinomaGuillaume Assié, Eric Letouzé, Martin Fassnacht, et al.
JCI Insight|September 22, 2017
Adrenal GIPR expression and chromosome 19q13 microduplications in GIP-dependent Cushing's syndromeAnne-Lise Lecoq, Constantine A Stratakis, Say Viengchareun, et al.
The Journal of Clinical Endocrinology and Metabolism|December 15, 2016
DNA Methylation Is an Independent Prognostic Marker of Survival in Adrenocortical CancerAnne Jouinot, Guillaume Assie, Rossella Libe, et al.
Human Molecular Genetics|February 5, 2013
Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort studyJulien Thevenon, Abderrahmane Bourredjem, Laurence Faivre, et al.
Pageof 5