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Anne Barlier

Showing results (51-60 of 166) with videos related to

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The Journal of Endocrinology|November 5, 2004
Lentiviral vectors efficiently transduce human gonadotroph and somatotroph adenomas in vitro. Targeted expression of transgene by pituitary hormone promotersCatherine Roche, Alfredo J Zamora, David Taïeb, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2005
An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domainRachel Reynaud, Anne Barlier, Sophie Vallette-Kasic, et al.
Endocrine|May 11, 2020
MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectivesVincent Amodru, David Taieb, Carole Guerin, et al.
The Journal of Clinical Endocrinology and Metabolism|September 14, 2013
Sinonasal paraganglioma with long-delayed recurrence and metastases: genetic and imaging findingsJustin Michel, David Taïeb, Marianne Jolibert, et al.
Frontiers in Endocrinology|March 9, 2023
A novel <i>TBX19</i> gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical originThéo Charnay, Gregory Mougel, Cyril Amouroux, et al.
Annales D'Endocrinologie|March 21, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
Endocrine|June 4, 2020
Correction to: MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectivesVincent Amodru, David Taieb, Carole Guerin, et al.
Annales D'Endocrinologie|December 29, 2024
Tatton-Brown-Rahman syndrome: A new multiple endocrine neoplasia syndrome with intellectual disability?Lauriane Le Collen, Théo Charnay, Sang Ly, et al.
Endocrine|July 16, 2020
Correction to: MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectivesVincent Amodru, David Taieb, Carole Guerin, et al.
Oncogene|March 1, 2020
Hypoxia and the hypoxia inducible factor 1α activate protein kinase A by repressing RII beta subunit transcriptionKristin Lucia, Yonghe Wu, Jose Monteserin Garcia, et al.
Pageof 17

Showing results (51-60 of 166) with videos related to

Sort By:
Pageof 17
The Journal of Endocrinology|November 5, 2004
Lentiviral vectors efficiently transduce human gonadotroph and somatotroph adenomas in vitro. Targeted expression of transgene by pituitary hormone promotersCatherine Roche, Alfredo J Zamora, David Taïeb, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2005
An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domainRachel Reynaud, Anne Barlier, Sophie Vallette-Kasic, et al.
Endocrine|May 11, 2020
MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectivesVincent Amodru, David Taieb, Carole Guerin, et al.
The Journal of Clinical Endocrinology and Metabolism|September 14, 2013
Sinonasal paraganglioma with long-delayed recurrence and metastases: genetic and imaging findingsJustin Michel, David Taïeb, Marianne Jolibert, et al.
Frontiers in Endocrinology|March 9, 2023
A novel <i>TBX19</i> gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical originThéo Charnay, Gregory Mougel, Cyril Amouroux, et al.
Annales D'Endocrinologie|March 21, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
Endocrine|June 4, 2020
Correction to: MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectivesVincent Amodru, David Taieb, Carole Guerin, et al.
Annales D'Endocrinologie|December 29, 2024
Tatton-Brown-Rahman syndrome: A new multiple endocrine neoplasia syndrome with intellectual disability?Lauriane Le Collen, Théo Charnay, Sang Ly, et al.
Endocrine|July 16, 2020
Correction to: MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectivesVincent Amodru, David Taieb, Carole Guerin, et al.
Oncogene|March 1, 2020
Hypoxia and the hypoxia inducible factor 1α activate protein kinase A by repressing RII beta subunit transcriptionKristin Lucia, Yonghe Wu, Jose Monteserin Garcia, et al.
Pageof 17