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C A Stratakis

Showing results (111-120 of 166) with videos related to

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Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|October 1, 2014
Comparison of the effects of PRKAR1A and PRKAR2B depletion on signaling pathways, cell growth, and cell cycle control of adrenocortical cellsF Basso, F Rocchetti, S Rodriguez, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Synaptophysin immunoreactivity in primary pigmented nodular adrenocortical disease: neuroendocrine properties of tumors associated with Carney complexC A Stratakis, J A Carney, L S Kirschner, et al.
Molecular Genetics and Metabolism|October 6, 1998
Genetic heterogeneity of adrenocorticotropin (ACTH) resistance syndromes: identification of a novel mutation of the ACTH receptor gene in hereditary glucocorticoid deficiencyS M Wu, C A Stratakis, C H Chan, et al.
Genomics|December 10, 1999
Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomesL S Kirschner, S E Taymans, S Pack, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Comparative genomic hybridization analysis of adrenocortical tumors of childhoodB C Figueiredo, C A Stratakis, R Sandrini, et al.
Biochemical and Molecular Medicine|December 1, 1996
Dideoxyfingerprinting (ddF) analysis of the type X collagen gene (COL10A1) and identification of a novel mutation (S671P) in a kindred with Schmid metaphyseal chondrodysplasiaC A Stratakis, Z Orban, A L Burns, et al.
Journal of Psychosomatic Research|August 28, 1998
Chronic insomnia and activity of the stress system: a preliminary studyA N Vgontzas, C Tsigos, E O Bixler, et al.
The Journal of Clinical Investigation|February 1, 1996
Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2C A Stratakis, J A Carney, J P Lin, et al.
The Journal of Clinical Investigation|February 1, 1991
Point mutation causing a single amino acid substitution in the hormone binding domain of the glucocorticoid receptor in familial glucocorticoid resistanceD M Hurley, D Accili, C A Stratakis, et al.
Journal of Medical Genetics|November 10, 2000
A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)A R Lafferty, D J Torpy, M Stowasser, et al.
Pageof 17

Showing results (111-120 of 166) with videos related to

Sort By:
Pageof 17
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|October 1, 2014
Comparison of the effects of PRKAR1A and PRKAR2B depletion on signaling pathways, cell growth, and cell cycle control of adrenocortical cellsF Basso, F Rocchetti, S Rodriguez, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Synaptophysin immunoreactivity in primary pigmented nodular adrenocortical disease: neuroendocrine properties of tumors associated with Carney complexC A Stratakis, J A Carney, L S Kirschner, et al.
Molecular Genetics and Metabolism|October 6, 1998
Genetic heterogeneity of adrenocorticotropin (ACTH) resistance syndromes: identification of a novel mutation of the ACTH receptor gene in hereditary glucocorticoid deficiencyS M Wu, C A Stratakis, C H Chan, et al.
Genomics|December 10, 1999
Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomesL S Kirschner, S E Taymans, S Pack, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Comparative genomic hybridization analysis of adrenocortical tumors of childhoodB C Figueiredo, C A Stratakis, R Sandrini, et al.
Biochemical and Molecular Medicine|December 1, 1996
Dideoxyfingerprinting (ddF) analysis of the type X collagen gene (COL10A1) and identification of a novel mutation (S671P) in a kindred with Schmid metaphyseal chondrodysplasiaC A Stratakis, Z Orban, A L Burns, et al.
Journal of Psychosomatic Research|August 28, 1998
Chronic insomnia and activity of the stress system: a preliminary studyA N Vgontzas, C Tsigos, E O Bixler, et al.
The Journal of Clinical Investigation|February 1, 1996
Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2C A Stratakis, J A Carney, J P Lin, et al.
The Journal of Clinical Investigation|February 1, 1991
Point mutation causing a single amino acid substitution in the hormone binding domain of the glucocorticoid receptor in familial glucocorticoid resistanceD M Hurley, D Accili, C A Stratakis, et al.
Journal of Medical Genetics|November 10, 2000
A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)A R Lafferty, D J Torpy, M Stowasser, et al.
Pageof 17