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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.
Endocrinology|September 8, 2007
Type 3 deiodinase deficiency results in functional abnormalities at multiple levels of the thyroid axisArturo Hernandez, M Elena Martinez, Xiao-Hui Liao, et al.
European Thyroid Journal|January 4, 2022
TSHB R75G is a founder variant and prevalent cause of low or undetectable TSH in Indian JewsDavid Shaki, Marina Eskin-Schwartz, Noam Hadar, 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.
JCI Insight|September 9, 2025
Thyroidal expression of ER molecular chaperone GRP170 is required for efficient TSH-mediated thyroid hormone synthesisXiaohan Zhang, Crystal Young, Xiao-Hui Liao, et al.
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.
The Journal of Clinical Endocrinology and Metabolism|February 26, 2009
Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous communityYardena Tenenbaum-Rakover, Helmut Grasberger, Sunee Mamanasiri, et al.
Human Genetics|September 29, 2005
Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1Helmut Grasberger, Martine Vaxillaire, Silvana Pannain, et al.
Endocrinology|January 17, 2009
Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3,5,3'-triiodo-L-thyronineAinhoa Ceballos, Monica M Belinchon, Eduardo Sanchez-Mendoza, et al.
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