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S E Taymans

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The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
Mutational analysis of the PRL receptor gene in human breast tumors with differential PRL receptor protein expressionA Glasow, L C Horn, S E Taymans, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 1998
Familial hyperaldosteronism type II: description of a large kindred and exclusion of the aldosterone synthase (CYP11B2) geneD J Torpy, R D Gordon, J P Lin, et al.
The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Ovarian lesions in Carney complex: clinical genetics and possible predisposition to malignancyC A Stratakis, T Papageorgiou, A Premkumar, et al.
Nature Genetics|September 6, 2000
Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complexL S Kirschner, J A Carney, S D Pack, et al.
Biochemical and Biophysical Research Communications|June 25, 1999
Cloning and characterization of a novel orphan G-protein-coupled receptor localized to human chromosome 2p16E E Tarttelin, L S Kirschner, J Bellingham, et al.
General and Comparative Endocrinology|April 1, 1997
The hypothalamic-pituitary-adrenal axis of prairie voles (Microtus ochrogaster): evidence for target tissue glucocorticoid resistanceS E Taymans, A C DeVries, M B DeVries, et al.
Biochemical and Biophysical Research Communications|January 28, 1999
Imbalanced expression of the glucocorticoid receptor isoforms in cultured lymphocytes from a patient with systemic glucocorticoid resistance and chronic lymphocytic leukemiaH Shahidi, A Vottero, C A Stratakis, et al.
Circulation|December 8, 1998
Identification of a novel genetic locus for familial cardiac myxomas and Carney complexM Casey, C Mah, A D Merliss, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic lociC A Stratakis, L S Kirschner, S E Taymans, et al.
Journal of Medical Genetics|May 4, 2004
Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriersC A Longui, S H V Lemos-Marini, B Figueiredo, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
Mutational analysis of the PRL receptor gene in human breast tumors with differential PRL receptor protein expressionA Glasow, L C Horn, S E Taymans, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 1998
Familial hyperaldosteronism type II: description of a large kindred and exclusion of the aldosterone synthase (CYP11B2) geneD J Torpy, R D Gordon, J P Lin, et al.
The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Ovarian lesions in Carney complex: clinical genetics and possible predisposition to malignancyC A Stratakis, T Papageorgiou, A Premkumar, et al.
Nature Genetics|September 6, 2000
Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complexL S Kirschner, J A Carney, S D Pack, et al.
Biochemical and Biophysical Research Communications|June 25, 1999
Cloning and characterization of a novel orphan G-protein-coupled receptor localized to human chromosome 2p16E E Tarttelin, L S Kirschner, J Bellingham, et al.
General and Comparative Endocrinology|April 1, 1997
The hypothalamic-pituitary-adrenal axis of prairie voles (Microtus ochrogaster): evidence for target tissue glucocorticoid resistanceS E Taymans, A C DeVries, M B DeVries, et al.
Biochemical and Biophysical Research Communications|January 28, 1999
Imbalanced expression of the glucocorticoid receptor isoforms in cultured lymphocytes from a patient with systemic glucocorticoid resistance and chronic lymphocytic leukemiaH Shahidi, A Vottero, C A Stratakis, et al.
Circulation|December 8, 1998
Identification of a novel genetic locus for familial cardiac myxomas and Carney complexM Casey, C Mah, A D Merliss, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic lociC A Stratakis, L S Kirschner, S E Taymans, et al.
Journal of Medical Genetics|May 4, 2004
Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriersC A Longui, S H V Lemos-Marini, B Figueiredo, et al.
Pageof 3