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International Journal of Pediatric Endocrinology|April 16, 2015
A new family with an activating mutation (G431S) in the TSH receptor gene: a phenotype discussion and review of the literatureCæcilie C Larsen, Lefkothea P Karaviti, Victor Seghers, et al.
Endocrinology|September 1, 2015
The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 DeficiencyAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Honggang Ye, et al.
Endocrine-Related Cancer|July 12, 2014
Obatoclax overcomes resistance to cell death in aggressive thyroid carcinomas by countering Bcl2a1 and Mcl1 overexpressionDevora Champa, Marika A Russo, Xiao-Hui Liao, et al.
Thyroid : Official Journal of the American Thyroid Association|February 26, 2016
Aberrant Cerebellar Development in Mice Lacking Dual Oxidase Maturation FactorsIzuki Amano, Yusuke Takatsuru, Syutaro Toya, et al.
The Journal of Clinical Endocrinology and Metabolism|May 6, 2004
Partial deficiency of thyroxine-binding globulin-Allentown is due to a mutation in the signal peptideAnja Fingerhut, Sirimon Reutrakul, Sebastian D Knuedeler, et al.
The Journal of Clinical Endocrinology and Metabolism|June 29, 2006
Mosaicism of a thyroid hormone receptor-beta gene mutation in resistance to thyroid hormoneSunee Mamanasiri, Sena Yesil, Alexandra M Dumitrescu, et al.
Thyroid : Official Journal of the American Thyroid Association|December 31, 2021
Severe Resistance to Thyroid Hormone Beta in a Patient with AthyreosisFederico Salas-Lucia, Monica M França, James A Amrhein, et al.
Molecular Endocrinology (Baltimore, Md.)|February 4, 2012
Mice deficient in dual oxidase maturation factors are severely hypothyroidHelmut Grasberger, Xavier De Deken, Olga Barca Mayo, et al.
Endocrinology|March 19, 2002
Thyroid function in mice with compound heterozygous and homozygous disruptions of SRC-1 and TIF-2 coactivators: evidence for haploinsufficiencyRoy E Weiss, Martine Gehin, Jianming Xu, et al.
Thyroid : Official Journal of the American Thyroid Association|September 16, 2024
Combined Levothyroxine and Propylthiouracil Treatment in Children with Monocarboxylate Transporter 8 Deficiency: A Multicenter Case Series of 12 PatientsRoy E Weiss, Joana R N Lemos, Alexandra M Dumitrescu, et al.
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