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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 cells
F 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 complex
C 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 deficiency
S 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 chromosomes
L 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 childhood
B 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 chondrodysplasia
C 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 study
A 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 2
C 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 resistance
D 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.
Page
of 17
Search research articles
Search
Showing results (111-120 of 166) with videos related to
Sort By:
Page
of 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 cells
F 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 complex
C 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 deficiency
S 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 chromosomes
L 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 childhood
B 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 chondrodysplasia
C 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 study
A 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 2
C 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 resistance
D 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.
Page
of 17