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Laura Audi

Showing results (1-10 of 19) with videos related to

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Endocrine Development|August 26, 2011
Methods to study cartilage and bone developmentAnenisia C Andrade, Dionisios Chrysis, Laura Audi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 10, 2006
Genetically determined gonadal tumours in childrenLaura Audi, Nuria Torán, Carmen Piró, et al.
Journal of Pediatric Urology|November 20, 2012
Determinant factors of gender identity: a commentaryLih-Mei Liao, Laura Audi, Ellie Magritte, et al.
European Journal of Pediatrics|April 17, 2008
ACTH-dependent precocious pseudopuberty in an infant with DAX1 gene mutationDiego Yeste, Cristina González-Niño, Guiomar Pérez de Nanclares, et al.
The Journal of Clinical Endocrinology and Metabolism|October 22, 2010
Loss of the C terminus of melanocortin receptor 2 (MC2R) results in impaired cell surface expression and ACTH insensitivityAndrea Hirsch, Eirini Meimaridou, Monica Fernandez-Cancio, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 16, 2014
Promoter-dependent activity on androgen receptor N-terminal domain mutations in androgen insensitivity syndromeRieko Tadokoro-Cuccaro, John Davies, Nigel P Mongan, et al.
The Journal of Clinical Endocrinology and Metabolism|November 11, 2020
Response to Letter to the Editor: "A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness"Joel N Hirschhorn, Andrew Dauber, Laura Audi, et al.
Plos One|June 8, 2011
Characterization of novel StAR (steroidogenic acute regulatory protein) mutations causing non-classic lipoid adrenal hyperplasiaChrista E Flück, Amit V Pandey, Bernhard Dick, et al.
G3 (Bethesda, Md.)|February 28, 2016
Latitudinal Clines of the Human Vitamin D Receptor and Skin Color GenesDov Tiosano, Laura Audi, Sharlee Climer, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 2011
Absence of GH-releasing hormone (GHRH) mutations in selected patients with isolated GH deficiencyMarcela M França, Alexander A L Jorge, Kyriaki S Alatzoglou, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Endocrine Development|August 26, 2011
Methods to study cartilage and bone developmentAnenisia C Andrade, Dionisios Chrysis, Laura Audi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 10, 2006
Genetically determined gonadal tumours in childrenLaura Audi, Nuria Torán, Carmen Piró, et al.
Journal of Pediatric Urology|November 20, 2012
Determinant factors of gender identity: a commentaryLih-Mei Liao, Laura Audi, Ellie Magritte, et al.
European Journal of Pediatrics|April 17, 2008
ACTH-dependent precocious pseudopuberty in an infant with DAX1 gene mutationDiego Yeste, Cristina González-Niño, Guiomar Pérez de Nanclares, et al.
The Journal of Clinical Endocrinology and Metabolism|October 22, 2010
Loss of the C terminus of melanocortin receptor 2 (MC2R) results in impaired cell surface expression and ACTH insensitivityAndrea Hirsch, Eirini Meimaridou, Monica Fernandez-Cancio, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 16, 2014
Promoter-dependent activity on androgen receptor N-terminal domain mutations in androgen insensitivity syndromeRieko Tadokoro-Cuccaro, John Davies, Nigel P Mongan, et al.
The Journal of Clinical Endocrinology and Metabolism|November 11, 2020
Response to Letter to the Editor: "A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness"Joel N Hirschhorn, Andrew Dauber, Laura Audi, et al.
Plos One|June 8, 2011
Characterization of novel StAR (steroidogenic acute regulatory protein) mutations causing non-classic lipoid adrenal hyperplasiaChrista E Flück, Amit V Pandey, Bernhard Dick, et al.
G3 (Bethesda, Md.)|February 28, 2016
Latitudinal Clines of the Human Vitamin D Receptor and Skin Color GenesDov Tiosano, Laura Audi, Sharlee Climer, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 2011
Absence of GH-releasing hormone (GHRH) mutations in selected patients with isolated GH deficiencyMarcela M França, Alexander A L Jorge, Kyriaki S Alatzoglou, et al.
Pageof 2