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Roy E Weiss

Showing results (61-70 of 111) with videos related to

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Endocrinology|March 19, 2002
Steroid receptor coactivator-1 deficiency causes variable alterations in the modulation of T(3)-regulated transcription of genes in vivoYoko Takeuchi, Yoshiharu Murata, Peter Sadow, et al.
Human Vaccines & Immunotherapeutics|October 15, 2025
SARS-CoV-2 breakthrough infections in a retrospective cohort of vaccinated university students and employeesJoana R N Lemos, Maritza Suarez, Shiby Thomas, et al.
Molecular and Cellular Endocrinology|June 5, 2003
Regulation of expression of thyroid hormone receptor isoforms and coactivators in liver and heart by thyroid hormonePeter M Sadow, Olivier Chassande, Eugene K Koo, et al.
Endocrinology|May 2, 2009
In vivo interaction of steroid receptor coactivator (SRC)-1 and the activation function-2 domain of the thyroid hormone receptor (TR) beta in TRbeta E457A knock-in and SRC-1 knockout miceManuela Alonso, Charles Goodwin, Xiaohui Liao, et al.
Journal of Investigative Medicine High Impact Case Reports|March 19, 2026
Real or Not Real? An Elevated TSHMarla E Sevilla-Alsina, Allison O Dumitriu Carcoana, Jane Y Yang, et al.
Thyroid : Official Journal of the American Thyroid Association|December 21, 2019
Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel <i>MCT8</i> VariantsJiao Fu, Manassawee Korwutthikulrangsri, Leigh Ramos-Platt, et al.
Molecular Endocrinology (Baltimore, Md.)|October 8, 2011
TSH compensates thyroid-specific IGF-I receptor knockout and causes papillary thyroid hyperplasiaKathrin Müller, Dagmar Führer, Jens Mittag, et al.
Endocrinology|May 23, 2013
Changes in thyroid status during perinatal development of MCT8-deficient male miceAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Pilar Gil-Ibáñez, et al.
The Journal of Clinical Endocrinology and Metabolism|December 24, 2019
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital HypothyroidismRyan J Bruellman, Yui Watanabe, Reham S Ebrhim, et al.
Hormone Research in Paediatrics|January 9, 2020
Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβReham S Ebrhim, Ryan J Bruellman, Yui Watanabe, et al.
Pageof 12

Showing results (61-70 of 111) with videos related to

Sort By:
Pageof 12
Endocrinology|March 19, 2002
Steroid receptor coactivator-1 deficiency causes variable alterations in the modulation of T(3)-regulated transcription of genes in vivoYoko Takeuchi, Yoshiharu Murata, Peter Sadow, et al.
Human Vaccines & Immunotherapeutics|October 15, 2025
SARS-CoV-2 breakthrough infections in a retrospective cohort of vaccinated university students and employeesJoana R N Lemos, Maritza Suarez, Shiby Thomas, et al.
Molecular and Cellular Endocrinology|June 5, 2003
Regulation of expression of thyroid hormone receptor isoforms and coactivators in liver and heart by thyroid hormonePeter M Sadow, Olivier Chassande, Eugene K Koo, et al.
Endocrinology|May 2, 2009
In vivo interaction of steroid receptor coactivator (SRC)-1 and the activation function-2 domain of the thyroid hormone receptor (TR) beta in TRbeta E457A knock-in and SRC-1 knockout miceManuela Alonso, Charles Goodwin, Xiaohui Liao, et al.
Journal of Investigative Medicine High Impact Case Reports|March 19, 2026
Real or Not Real? An Elevated TSHMarla E Sevilla-Alsina, Allison O Dumitriu Carcoana, Jane Y Yang, et al.
Thyroid : Official Journal of the American Thyroid Association|December 21, 2019
Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel <i>MCT8</i> VariantsJiao Fu, Manassawee Korwutthikulrangsri, Leigh Ramos-Platt, et al.
Molecular Endocrinology (Baltimore, Md.)|October 8, 2011
TSH compensates thyroid-specific IGF-I receptor knockout and causes papillary thyroid hyperplasiaKathrin Müller, Dagmar Führer, Jens Mittag, et al.
Endocrinology|May 23, 2013
Changes in thyroid status during perinatal development of MCT8-deficient male miceAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Pilar Gil-Ibáñez, et al.
The Journal of Clinical Endocrinology and Metabolism|December 24, 2019
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital HypothyroidismRyan J Bruellman, Yui Watanabe, Reham S Ebrhim, et al.
Hormone Research in Paediatrics|January 9, 2020
Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβReham S Ebrhim, Ryan J Bruellman, Yui Watanabe, et al.
Pageof 12