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Louise C Gregory

Showing results (1-10 of 18) with videos related to

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Comprehensive Physiology|March 13, 2020
Development of the Pituitary GlandKyriaki S Alatzoglou, Louise C Gregory, Mehul T Dattani
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2023
Identification of genetic variants and phenotypic characterization of a large cohort of patients with congenital hypopituitarism and related disordersLouise C Gregory, Cecilia Cionna, Manuela Cerbone, et al.
Endocrine Development|November 28, 2012
Pituitary gland development: an updateRodrigo E Bancalari, Louise C Gregory, Mark J McCabe, et al.
The Journal of Clinical Endocrinology and Metabolism|March 26, 2013
Structural pituitary abnormalities associated with CHARGE syndromeLouise C Gregory, Evelien F Gevers, Joanne Baker, et al.
Molecular and Cellular Endocrinology|September 17, 2015
Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD)Mark J McCabe, Youli Hu, Louise C Gregory, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2019
Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and ArthrogryposisLouise C Gregory, Pratik Shah, Juliane R F Sanner, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2020
Loss-of-Function Variants in TBC1D32 Underlie Syndromic HypopituitarismJohanna Hietamäki, Louise C Gregory, Sandy Ayoub, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2013
Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasiaMark J McCabe, Carles Gaston-Massuet, Louise C Gregory, et al.
The Journal of Clinical Endocrinology and Metabolism|August 12, 2011
Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunctionMark J McCabe, Carles Gaston-Massuet, Vaitsa Tziaferi, et al.
Ebiomedicine|March 18, 2019
Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulationLouise C Gregory, Carolina B Ferreira, Sara K Young-Baird, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Comprehensive Physiology|March 13, 2020
Development of the Pituitary GlandKyriaki S Alatzoglou, Louise C Gregory, Mehul T Dattani
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2023
Identification of genetic variants and phenotypic characterization of a large cohort of patients with congenital hypopituitarism and related disordersLouise C Gregory, Cecilia Cionna, Manuela Cerbone, et al.
Endocrine Development|November 28, 2012
Pituitary gland development: an updateRodrigo E Bancalari, Louise C Gregory, Mark J McCabe, et al.
The Journal of Clinical Endocrinology and Metabolism|March 26, 2013
Structural pituitary abnormalities associated with CHARGE syndromeLouise C Gregory, Evelien F Gevers, Joanne Baker, et al.
Molecular and Cellular Endocrinology|September 17, 2015
Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD)Mark J McCabe, Youli Hu, Louise C Gregory, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2019
Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and ArthrogryposisLouise C Gregory, Pratik Shah, Juliane R F Sanner, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2020
Loss-of-Function Variants in TBC1D32 Underlie Syndromic HypopituitarismJohanna Hietamäki, Louise C Gregory, Sandy Ayoub, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2013
Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasiaMark J McCabe, Carles Gaston-Massuet, Louise C Gregory, et al.
The Journal of Clinical Endocrinology and Metabolism|August 12, 2011
Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunctionMark J McCabe, Carles Gaston-Massuet, Vaitsa Tziaferi, et al.
Ebiomedicine|March 18, 2019
Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulationLouise C Gregory, Carolina B Ferreira, Sara K Young-Baird, et al.
Pageof 2