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Mice deficient in the steroid receptor co-activator 1 (SRC-1) are resistant to thyroid hormone.
- Published in:
- EMBO Journal, 1999, v. 18, n. 7, p. 1900, doi. 10.1093/emboj/18.7.1900
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- Publication type:
- Article
Genomic organization of mouse ZAKI-4 gene that encodes ZAKI-4 α and β isoforms, endogenous calcineurin inhibitors, and changes in the expression of these isoforms by thyroid hormone in adult mouse brain and heart.
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- European Journal of Endocrinology, 2004, v. 150, n. 3, p. 0371
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- Publication type:
- Article
Autoantibodies from patients with autoimmune thyroid disease do not interfere with the activity of the human iodide symporter gene stably transfected in CHO cells.
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- European Journal of Endocrinology, 2001, v. 144, n. 6, p. 611, doi. 10.1530/eje.0.1440611
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- Article
Effect of the Fetal THRB Genotype on the Placenta.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 10, p. e944, doi. 10.1210/clinem/dgad243
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- Publication type:
- Article
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
- Published in:
- 2019
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- Publication type:
- journal article
Small-molecule MAPK inhibitors restore radioiodine incorporation in mouse thyroid cancers with conditional BRAF activation.
- Published in:
- 2011
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- Publication type:
- journal article
Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion.
- Published in:
- 2010
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- Publication type:
- journal article
Negative regulation by thyroid hormone receptor requires an intact coactivator-binding surface.
- Published in:
- 2005
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- Publication type:
- journal article
Effects of ligand and thyroid hormone receptor isoforms on hepatic gene expression profiles of thyroid hormone receptor knockout mice.
- Published in:
- EMBO Reports, 2003, v. 4, n. 6, p. 581, doi. 10.1038/sj.embor.embor862
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- Publication type:
- Article
Resistance to thyroid hormone and its molecular basis.
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- Pediatrics International, 1994, v. 36, n. 1, p. 1, doi. 10.1111/j.1442-200X.1994.tb03121.x
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- Publication type:
- Article
Pseudomalabsorption of Levothyroxine.
- Published in:
- JAMA: Journal of the American Medical Association, 1991, v. 266, n. 15, p. 2118, doi. 10.1001/jama.1991.03470150090036
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- Article
Neonatal Detection of Generalized Resistance to Thyroid Hormone.
- Published in:
- 1990
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- Case Study
Transient Elevation of Serum Thyroid Hormone Concentration After Initiation of Replacement Therapy in Myxedema.
- Published in:
- Annals of Internal Medicine, 1980, v. 92, n. 4, p. 491, doi. 10.7326/0003-4819-92-4-491
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- Publication type:
- Article
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism.
- Published in:
- Nature Genetics, 2005, v. 37, n. 11, p. 1247, doi. 10.1038/ng1654
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- Publication type:
- Article
Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical Implications.
- Published in:
- 2017
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- Publication type:
- journal article
Fetal Exposure to High Maternal Thyroid Hormone Levels Causes Central Resistance to Thyroid Hormone in Adult Humans and Mice.
- Published in:
- 2017
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- Publication type:
- journal article
Mutations of the thyroid hormone transporter MCT8 cause prenatal brain damage and persistent hypomyelination.
- Published in:
- 2014
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- Publication type:
- journal article
Coexistence of THRB and TBG gene mutations in a Turkish family.
- Published in:
- 2013
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- Publication type:
- journal article
Management of differentiated thyroid cancer in the presence of resistance to thyroid hormone and TSH-secreting adenomas: a report of four cases and review of the literature.
- Published in:
- 2013
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- Publication type:
- journal article
Diiodothyropropionic acid (DITPA) in the treatment of MCT8 deficiency.
- Published in:
- 2012
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- Publication type:
- journal article
Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.
- Published in:
- 2012
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- Publication type:
- journal article
The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation.
- Published in:
- 2011
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- Publication type:
- journal article
Mutations in the NKX2.5 gene and the PAX8 promoter in a girl with thyroid dysgenesis.
- Published in:
- 2011
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- Publication type:
- journal article
A single copy of the recently identified dual oxidase maturation factor (DUOXA) 1 gene produces only mild transient hypothyroidism in a patient with a novel biallelic DUOXA2 mutation and monoallelic DUOXA1 deletion.
- Published in:
- 2011
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- Publication type:
- journal article
Resistance to Thyroid Hormone.
- Published in:
- Reviews in Endocrine & Metabolic Disorders, 2000, v. 1, n. 1/2, p. 97, doi. 10.1023/A:1010072605757
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- Publication type:
- Article
FALSE ELEVATION OF FREE THYROXINE AND TRIIODOTHYRONINE DUE TO THE PRESENCE OF ANTIBODIES TO IODOTHYRONINES.
- Published in:
- Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi, 2016, v. 79, n. 1, p. 51, doi. 10.18017/iuitfd.01011
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- Publication type:
- Article
Iatrogenic Hydrothorax.
- Published in:
- Annals of Internal Medicine, 1965, v. 63, n. 5, p. 869, doi. 10.7326/0003-4819-63-5-869
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- Publication type:
- Article
Increased Oxidative Metabolism and Neurotransmitter Cycling in the Brain of Mice Lacking the Thyroid Hormone Transporter Slc16a2 (Mct8).
- Published in:
- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0074621
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- Publication type:
- Article
Distinct and Histone-Specific Modifications Mediate Positive versus Negative Transcriptional Regulation of TSHα Promoter.
- Published in:
- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009853
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- Publication type:
- Article
White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene.
- Published in:
- Developmental Medicine & Child Neurology, 2010, v. 52, n. 5, p. 475, doi. 10.1111/j.1469-8749.2009.03471.x
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- Publication type:
- Article
Approach to the patient with resistance to thyroid hormone and pregnancy.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Autoimmunity in patients with resistance to thyroid hormone.
- Published in:
- 2010
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- Publication type:
- journal article
Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X).
- Published in:
- 2009
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- Publication type:
- journal article
Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous community.
- Published in:
- 2009
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- Publication type:
- journal article
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.
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- 2008
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- Publication type:
- journal article
Pendred syndrome in two Galician families: insights into clinical phenotypes through cellular, genetic, and molecular studies.
- Published in:
- 2008
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- Publication type:
- journal article
A Familial Thyrotropin (TSH) Receptor Mutation Provides in Vivo Evidence that the Inositol Phosphates/Ca<sup>2+</sup> Cascade Mediates TSH Action on Thyroid Hormone Synthesis.
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- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 7, p. 2816, doi. 10.1210/jc.2007-0366
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- Publication type:
- Article
Mosaicism of a Thyroid Hormone Receptor-β Gene Mutation in Resistance to Thyroid Hormone.
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- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 9, p. 3471, doi. 10.1210/jc.2006-0727
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- Publication type:
- Article
A Novel Thyroid Hormone Receptor-β Mutation That Fails to Bind Nuclear Receptor Corepressor in a Patient as an Apparent Cause of Severe, Predominantly Pituitary Resistance to Thyroid Hormone.
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- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 5, p. 1887, doi. 10.1210/jc.2005-2428
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- Publication type:
- Article
Identification of a functional polymorphism of the human type 5 17beta-hydroxysteroid dehydrogenase gene associated with polycystic ovary syndrome.
- Published in:
- 2006
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- Publication type:
- journal article
A De Novo Mutation in an Already Mutant Nucleotide of the Thyroid Hormone Receptor β Gene Perpetuates Resistance to Thyroid Hormone.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 3, p. 1760, doi. 10.1210/jc.2004-1488
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- Publication type:
- Article
Thyroid Hormone Responsive Genes in Cultured Human Fibroblasts.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 2, p. 936, doi. 10.1210/jc.2004-1768
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- Publication type:
- Article
Partial deficiency of thyroxine-binding globulin-Allentown is due to a mutation in the signal peptide.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 5, p. 2477, doi. 10.1210/jc.2003-031613
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- Publication type:
- Article
Congenital Secondary Hypothyroidism Caused by Exon Skipping due to a Homozygous Donor Splice Site Mutation in the TSHβ-Subunit Gene.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 1, p. 336, doi. 10.1210/jcem.87.1.8154
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- Publication type:
- Article
Three Novel Mutations Causing Complete T<sub>4</sub>-Binding Globulin Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 10, p. 5039, doi. 10.1210/jcem.86.10.7916
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- Publication type:
- Article
Resistance to Thyroid Hormone Does Not Abrogate the Transient Thyrotoxicosis Associated with Gestation: Report of a Case.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 9, p. 4273, doi. 10.1210/jcem.86.9.7858
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- Publication type:
- Article
Search for Abnormalities of Nuclear Corepressors, Coactivators, and a Coregulator in Families with Resistance to Thyroid Hormone without Mutations in Thyroid Hormone Receptor β or α Genes.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 10, p. 3609, doi. 10.1210/jcem.85.10.6873
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- Publication type:
- Article
Failure of Membrane Targeting Causes the Functional Defect of Two Mutant Sodium Iodide Symporters.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 7, p. 2366, doi. 10.1210/jcem.85.7.6700
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- Publication type:
- Article
Identification of Thyroxine-Binding Globulin-San Diego in a Family from Houston and Its Characterization by in Vitro Expression Using Xenopus Oocytes.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 1, p. 368, doi. 10.1210/jcem.85.1.6317
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- Publication type:
- Article
Five New Families with Resistance to Thyroid Hormone not Caused by Mutations in the Thyroid Hormone Receptor β Gene.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 11, p. 3919, doi. 10.1210/jcem.84.11.6080
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- Publication type:
- Article