Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Roy E Weiss

Showing results (51-60 of 111) with videos related to

Pageof 12
Sort By:
American Journal of Physiology. Endocrinology and Metabolism|August 10, 2002
Thyroid hormone and cardiac function in mice deficient in thyroid hormone receptor-alpha or -beta: an echocardiograph studyRoy E Weiss, Claudia Korcarz, Olivier Chassande, et al.
The Journal of Clinical Endocrinology and Metabolism|July 16, 2009
Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X)Caterina Di Cosmo, Neil McLellan, Xiao-Hui Liao, et al.
Endocrinology|April 23, 2005
Temperature homeostasis in transgenic mice lacking thyroid hormone receptor-alpha gene productsHusnia Marrif, Aria Schifman, Zaruhi Stepanyan, et al.
Science (New York, N.Y.)|April 5, 2014
Research funding. Science funding and short-term economic activityBruce A Weinberg, Jason Owen-Smith, Rebecca F Rosen, et al.
Thyroid : Official Journal of the American Thyroid Association|February 6, 2014
A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extractionSolomon Maximo Greenberg, Alfonso Massimiliano Ferrara, Everton S Nicholas, et al.
Endocrinology|September 14, 2013
Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levelsCaterina Di Cosmo, Xiao-Hui Liao, Honggang Ye, et al.
Molecular Endocrinology (Baltimore, Md.)|December 13, 2005
Repulsive separation of the cytoplasmic ends of transmembrane helices 3 and 6 is linked to receptor activation in a novel thyrotropin receptor mutant (M626I)Usanee Ringkananont, Joost Van Durme, Lucia Montanelli, et al.
Endocrinology|July 23, 2014
Placenta passage of the thyroid hormone analog DITPA to male wild-type and Mct8-deficient miceAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Pilar Gil-Ibáñez, et al.
Thyroid : Official Journal of the American Thyroid Association|October 31, 2018
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese FamiliesYui Watanabe, Ryan J Bruellman, Reham S Ebrhim, et al.
Thyroid : Official Journal of the American Thyroid Association|December 24, 2019
Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital HypothyroidismRyan Bruellman, Yui Watanabe, Reham Shareef, et al.
Pageof 12

Showing results (51-60 of 111) with videos related to

Sort By:
Pageof 12
American Journal of Physiology. Endocrinology and Metabolism|August 10, 2002
Thyroid hormone and cardiac function in mice deficient in thyroid hormone receptor-alpha or -beta: an echocardiograph studyRoy E Weiss, Claudia Korcarz, Olivier Chassande, et al.
The Journal of Clinical Endocrinology and Metabolism|July 16, 2009
Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X)Caterina Di Cosmo, Neil McLellan, Xiao-Hui Liao, et al.
Endocrinology|April 23, 2005
Temperature homeostasis in transgenic mice lacking thyroid hormone receptor-alpha gene productsHusnia Marrif, Aria Schifman, Zaruhi Stepanyan, et al.
Science (New York, N.Y.)|April 5, 2014
Research funding. Science funding and short-term economic activityBruce A Weinberg, Jason Owen-Smith, Rebecca F Rosen, et al.
Thyroid : Official Journal of the American Thyroid Association|February 6, 2014
A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extractionSolomon Maximo Greenberg, Alfonso Massimiliano Ferrara, Everton S Nicholas, et al.
Endocrinology|September 14, 2013
Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levelsCaterina Di Cosmo, Xiao-Hui Liao, Honggang Ye, et al.
Molecular Endocrinology (Baltimore, Md.)|December 13, 2005
Repulsive separation of the cytoplasmic ends of transmembrane helices 3 and 6 is linked to receptor activation in a novel thyrotropin receptor mutant (M626I)Usanee Ringkananont, Joost Van Durme, Lucia Montanelli, et al.
Endocrinology|July 23, 2014
Placenta passage of the thyroid hormone analog DITPA to male wild-type and Mct8-deficient miceAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Pilar Gil-Ibáñez, et al.
Thyroid : Official Journal of the American Thyroid Association|October 31, 2018
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese FamiliesYui Watanabe, Ryan J Bruellman, Reham S Ebrhim, et al.
Thyroid : Official Journal of the American Thyroid Association|December 24, 2019
Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital HypothyroidismRyan Bruellman, Yui Watanabe, Reham Shareef, et al.
Pageof 12