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Aaron Chidakel

Showing results (1-10 of 4) with videos related to

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The Urologic Clinics of North America|May 3, 2016
Obesity and HypogonadismSteven Lamm, Aaron Chidakel, Rohan Bansal
Thyroid : Official Journal of the American Thyroid Association|August 8, 2006
Functional characterization of the 258 A/G (D2-ORFa-Gly3Asp) human type-2 deiodinase polymorphism: a naturally occurring variant increases the enzymatic activity by removing a putative repressor site in the 5' UTR of the geneGiuseppe Coppotelli, Aaron Summers, Aaron Chidakel, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 2008
The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3,5,3'-triiodothyronine toxicosis of McCune-Albright syndromeFrancesco S Celi, Giuseppe Coppotelli, Aaron Chidakel, et al.
The Journal of Clinical Endocrinology and Metabolism|March 3, 2005
Hereditary leiomyomatosis associated with bilateral, massive, macronodular adrenocortical disease and atypical cushing syndrome: a clinical and molecular genetic investigationLudmila Matyakhina, Reneé J Freedman, Isabelle Bourdeau, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
The Urologic Clinics of North America|May 3, 2016
Obesity and HypogonadismSteven Lamm, Aaron Chidakel, Rohan Bansal
Thyroid : Official Journal of the American Thyroid Association|August 8, 2006
Functional characterization of the 258 A/G (D2-ORFa-Gly3Asp) human type-2 deiodinase polymorphism: a naturally occurring variant increases the enzymatic activity by removing a putative repressor site in the 5' UTR of the geneGiuseppe Coppotelli, Aaron Summers, Aaron Chidakel, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 2008
The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3,5,3'-triiodothyronine toxicosis of McCune-Albright syndromeFrancesco S Celi, Giuseppe Coppotelli, Aaron Chidakel, et al.
The Journal of Clinical Endocrinology and Metabolism|March 3, 2005
Hereditary leiomyomatosis associated with bilateral, massive, macronodular adrenocortical disease and atypical cushing syndrome: a clinical and molecular genetic investigationLudmila Matyakhina, Reneé J Freedman, Isabelle Bourdeau, et al.
Pageof 1