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C A Stratakis

Showing results (131-140 of 166) with videos related to

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Journal of Medical Genetics|April 5, 2003
Chromosome 2 (2p16) abnormalities in Carney complex tumoursL Matyakhina, S Pack, L S Kirschner, et al.
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.
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.
The Journal of Clinical Endocrinology and Metabolism|April 29, 1998
The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P450 aromatase gene transcriptionC A Stratakis, A Vottero, A Brodie, 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.
Journal of Medical Genetics|February 4, 2005
Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndromeJ S Lee, M Tartaglia, B D Gelb, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)C A Stratakis, R B Jenkins, E Pras, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 25, 2009
An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and proteinL Drori-Herishanu, A Horvath, M Nesterova, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2014
Vandetanib successfully controls medullary thyroid cancer-related Cushing syndrome in an adolescent patientA A Nella, M B Lodish, E Fox, 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.
Pageof 17

Showing results (131-140 of 166) with videos related to

Sort By:
Pageof 17
Journal of Medical Genetics|April 5, 2003
Chromosome 2 (2p16) abnormalities in Carney complex tumoursL Matyakhina, S Pack, L S Kirschner, et al.
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.
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.
The Journal of Clinical Endocrinology and Metabolism|April 29, 1998
The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P450 aromatase gene transcriptionC A Stratakis, A Vottero, A Brodie, 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.
Journal of Medical Genetics|February 4, 2005
Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndromeJ S Lee, M Tartaglia, B D Gelb, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)C A Stratakis, R B Jenkins, E Pras, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 25, 2009
An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and proteinL Drori-Herishanu, A Horvath, M Nesterova, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2014
Vandetanib successfully controls medullary thyroid cancer-related Cushing syndrome in an adolescent patientA A Nella, M B Lodish, E Fox, 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.
Pageof 17