| Item Type | Name |
|
Concept
|
Acid Phosphatase
|
|
Concept
|
Amino Acid Sequence
|
|
Concept
|
Central Nervous System Diseases
|
|
Concept
|
Biological Transport
|
|
Concept
|
Endocrine System Diseases
|
|
Concept
|
Hypothalamo-Hypophyseal System
|
|
Concept
|
Fatty Acids, Unsaturated
|
|
Concept
|
Nucleic Acid Hybridization
|
|
Concept
|
Nucleic Acid Conformation
|
|
Concept
|
Regulatory Sequences, Nucleic Acid
|
|
Concept
|
Receptors, Retinoic Acid
|
|
Concept
|
Amino Acid Substitution
|
|
Concept
|
Monocarboxylic Acid Transporters
|
|
Concept
|
Organic Cation Transport Proteins
|
|
Concept
|
Organic Anion Transporters, Sodium-Independent
|
|
Concept
|
Organic Anion Transporters
|
|
Concept
|
Pituitary-Adrenal System
|
|
Concept
|
Membrane Transport Proteins
|
|
Concept
|
Amino Acid Transport System y+
|
|
Concept
|
Amino Acid Transport System y+L
|
|
Concept
|
Glucose Transporter Type 4
|
|
Concept
|
Young Adult
|
|
Academic Article
|
The relative expression of mutant and normal thyroid hormone receptor genes in patients with generalized resistance to thyroid hormone determined by estimation of their specific messenger ribonucleic acid products.
|
|
Academic Article
|
Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine.
|
|
Academic Article
|
Complete thyroxine-binding globulin (TBG) deficiency produced by a mutation in acceptor splice site causing frameshift and early termination of translation (TBG-Kankakee).
|
|
Academic Article
|
RXR receptor agonist suppression of thyroid function: central effects in the absence of thyroid hormone receptor.
|
|
Academic Article
|
Effects of ligand and thyroid hormone receptor isoforms on hepatic gene expression profiles of thyroid hormone receptor knockout mice.
|
|
Academic Article
|
Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice.
|
|
Academic Article
|
A de novo mutation in an already mutant nucleotide of the thyroid hormone receptor beta gene perpetuates resistance to thyroid hormone.
|
|
Academic Article
|
Effects of maternal levels of thyroid hormone (TH) on the hypothalamus-pituitary-thyroid set point: studies in TH receptor beta knockout mice.
|
|
Academic Article
|
Transformation of a pituitary macroadenoma into to a corticotropin-secreting carcinoma over 16 years.
|
|
Academic Article
|
Effect of pioglitazone on adrenocorticotropic hormone and cortisol secretion in Cushing's disease.
|
|
Academic Article
|
Doctor . . . could it be my thyroid?
|
|
Academic Article
|
A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport.
|
|
Academic Article
|
Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion.
|
|
Academic Article
|
Homozygous thyroid hormone receptor ß-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.
|
|
Academic Article
|
Human thyroxine-binding globulin gene: complete sequence and transcriptional regulation.
|
|
Academic Article
|
The syndromes of resistance to thyroid hormone.
|
|
Academic Article
|
A novel thyroid hormone receptor-beta mutation that fails to bind nuclear receptor corepressor in a patient as an apparent cause of severe, predominantly pituitary resistance to thyroid hormone.
|
|
Academic Article
|
The nuclear receptor corepressor (NCoR) controls thyroid hormone sensitivity and the set point of the hypothalamic-pituitary-thyroid axis.
|
|
Academic Article
|
Low intelligence but not attention deficit hyperactivity disorder is associated with resistance to thyroid hormone caused by mutation R316H in the thyroid hormone receptor beta gene.
|
|
Academic Article
|
Pituitary-thyroid setpoint and thyrotropin receptor expression in consomic rats.
|
|
Academic Article
|
Distinct roles of deiodinases on the phenotype of Mct8 defect: a comparison of eight different mouse genotypes.
|
|
Academic Article
|
Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site.
|
|
Academic Article
|
A novel point mutation in cluster 3 of the thyroid hormone receptor beta gene (P247L) causing mild resistance to thyroid hormone.
|
|
Academic Article
|
Repulsive separation of the cytoplasmic ends of transmembrane helices 3 and 6 is linked to receptor activation in a novel thyrotropin receptor mutant (M626I).
|
|
Academic Article
|
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice.
|
|
Academic Article
|
Calcitonin stimulates bone formation when administered prior to initiation of osteogenesis.
|
|
Academic Article
|
Effect of 13-cis-retinoic acid and alpha-interferon on transforming growth factor beta1 in patients with rising prostate-specific antigen.
|
|
Academic Article
|
In vitro trial of the pilot prototype of the prostate mechanical imaging system.
|
|
Academic Article
|
Diiodothyropropionic acid (DITPA) in the treatment of MCT8 deficiency.
|
|
Academic Article
|
Thyroid hormone receptor-ß agonists prevent hepatic steatosis in fat-fed rats but impair insulin sensitivity via discrete pathways.
|
|
Academic Article
|
Changes in thyroid status during perinatal development of MCT8-deficient male mice.
|
|
Academic Article
|
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.
|
|
Academic Article
|
Placenta passage of the thyroid hormone analog DITPA to male wild-type and Mct8-deficient mice.
|
|
Academic Article
|
A study of recurrence and death from papillary thyroid cancer with 27 years of median follow-up.
|
|
Academic Article
|
Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levels.
|
|
Academic Article
|
A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction.
|
|
Academic Article
|
Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism.
|
|
Academic Article
|
Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism.
|
|
Academic Article
|
Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism.
|
|
Academic Article
|
The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 Deficiency.
|
|
Academic Article
|
Adeno Associated Virus 9-Based Gene Therapy Delivers a Functional Monocarboxylate Transporter 8, Improving Thyroid Hormone Availability to the Brain of Mct8-Deficient Mice.
|
|
Academic Article
|
Understanding Transgender Men's Experiences with and Preferences for Cervical Cancer Screening: A Rapid Assessment Survey.
|
|
Academic Article
|
An Essential Physiological Role for MCT8 in Bone in Male Mice.
|
|
Academic Article
|
A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism.
|
|
Academic Article
|
Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical Implications.
|
|
Academic Article
|
Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel MCT8 Variants.
|
|
Academic Article
|
Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHß.
|
|
Academic Article
|
Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations.
|
|
Academic Article
|
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation.
|
|
Academic Article
|
Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Monocarboxylate Transporter 8 Deficiency.
|