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Plos One|May 14, 2014
Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 inactivationBárbara Núñez, Raquel Martínez de Mena, Maria Jesus Obregon, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2017
Fetal Exposure to High Maternal Thyroid Hormone Levels Causes Central Resistance to Thyroid Hormone in Adult Humans and MicePanudda Srichomkwun, João Anselmo, Xiao-Hui Liao, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2004
A de novo mutation in an already mutant nucleotide of the thyroid hormone receptor beta gene perpetuates resistance to thyroid hormoneJoaquin Lado-Abeal, Alexandra M Dumitrescu, Xiao-Hui Liao, et al.
The Journal of Clinical Endocrinology and Metabolism|September 21, 2012
Diiodothyropropionic acid (DITPA) in the treatment of MCT8 deficiencyCharles F Verge, Daniel Konrad, Michal Cohen, et al.
Endocrinology|February 3, 2011
Distinct roles of deiodinases on the phenotype of Mct8 defect: a comparison of eight different mouse genotypesXiao-Hui Liao, Caterina Di Cosmo, Alexandra M Dumitrescu, et al.
The Journal of Clinical Endocrinology and Metabolism|February 22, 2020
Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) MutationsJiao Fu, Manassawee Korwutthikulrangsri, E Nazli Gönç, et al.
Nature Genetics|October 18, 2005
Mutations in SECISBP2 result in abnormal thyroid hormone metabolismAlexandra M Dumitrescu, Xiao-Hui Liao, Mohamed S Y Abdullah, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 2014
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancerAlfonso Massimiliano Ferrara, Theodora Pappa, Jiao Fu, et al.
Thyroid : Official Journal of the American Thyroid Association|March 30, 2022
AAV9-MCT8 Delivery at Juvenile Stage Ameliorates Neurological and Behavioral Deficits in a Mouse Model of MCT8-DeficiencyXiao-Hui Liao, Pablo Avalos, Oksana Shelest, et al.
Thyroid : Official Journal of the American Thyroid Association|August 5, 2020
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene MutationSamuel Refetoff, Theodora Pappa, Meredith K Williams, et al.
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