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Alain Calender

Showing results (41-50 of 71) with videos related to

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The American Journal of Surgical Pathology|February 28, 2008
Pituitary tumors and hyperplasia in multiple endocrine neoplasia type 1 syndrome (MEN1): a case-control study in a series of 77 patients versus 2509 non-MEN1 patientsJacqueline Trouillas, Françoise Labat-Moleur, Nathalie Sturm, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Hereditary hemorrhagic telangiectasia: evidence for regional founder effects of ACVRL1 mutations in French and Italian patientsGaetan Lesca, Emmanuelle Genin, Claire Blachier, et al.
Cells|August 27, 2021
Autophagy and Mitophagy-Related Pathways at the Crossroads of Genetic Pathways Involved in Familial Sarcoidosis and Host-Pathogen Interactions Induced by CoronavirusesYves Pacheco, Dominique Valeyre, Thomas El Jammal, et al.
Orphanet Journal of Rare Diseases|September 23, 2020
Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasiaSophie Giraud, Claire Bardel, Sophie Dupuis-Girod, et al.
Journal of Pharmaceutical and Biomedical Analysis|November 5, 2013
Metabolic expressivity of human genetic variants: NMR metabotyping of MEN1 pathogenic mutantsBenjamin J Blaise, Claire Lopez, Cécile Vercherat, et al.
Gastroenterology|September 9, 2008
MEN1 missense mutations impair sensitization to apoptosis induced by wild-type menin in endocrine pancreatic tumor cellsWissam Bazzi, Maud Renon, Cécile Vercherat, et al.
Human Mutation|March 15, 2019
Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variantsPauline Romanet, Marie-Françoise Odou, Marie-Odile North, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2018
UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French PopulationPauline Romanet, Amira Mohamed, Sophie Giraud, et al.
Human Mutation|March 17, 2004
Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in FranceGaëtan Lesca, Henri Plauchu, Florence Coulet, et al.
Human Mutation|May 18, 2006
Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patientsGaëtan Lesca, Nelly Burnichon, Grégory Raux, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
The American Journal of Surgical Pathology|February 28, 2008
Pituitary tumors and hyperplasia in multiple endocrine neoplasia type 1 syndrome (MEN1): a case-control study in a series of 77 patients versus 2509 non-MEN1 patientsJacqueline Trouillas, Françoise Labat-Moleur, Nathalie Sturm, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Hereditary hemorrhagic telangiectasia: evidence for regional founder effects of ACVRL1 mutations in French and Italian patientsGaetan Lesca, Emmanuelle Genin, Claire Blachier, et al.
Cells|August 27, 2021
Autophagy and Mitophagy-Related Pathways at the Crossroads of Genetic Pathways Involved in Familial Sarcoidosis and Host-Pathogen Interactions Induced by CoronavirusesYves Pacheco, Dominique Valeyre, Thomas El Jammal, et al.
Orphanet Journal of Rare Diseases|September 23, 2020
Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasiaSophie Giraud, Claire Bardel, Sophie Dupuis-Girod, et al.
Journal of Pharmaceutical and Biomedical Analysis|November 5, 2013
Metabolic expressivity of human genetic variants: NMR metabotyping of MEN1 pathogenic mutantsBenjamin J Blaise, Claire Lopez, Cécile Vercherat, et al.
Gastroenterology|September 9, 2008
MEN1 missense mutations impair sensitization to apoptosis induced by wild-type menin in endocrine pancreatic tumor cellsWissam Bazzi, Maud Renon, Cécile Vercherat, et al.
Human Mutation|March 15, 2019
Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variantsPauline Romanet, Marie-Françoise Odou, Marie-Odile North, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2018
UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French PopulationPauline Romanet, Amira Mohamed, Sophie Giraud, et al.
Human Mutation|March 17, 2004
Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in FranceGaëtan Lesca, Henri Plauchu, Florence Coulet, et al.
Human Mutation|May 18, 2006
Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patientsGaëtan Lesca, Nelly Burnichon, Grégory Raux, et al.
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