| Item Type | Name |
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Concept
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Dependovirus
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Concept
|
Acid Phosphatase
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Concept
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Aged, 80 and over
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|
Concept
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Adolescent
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Concept
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Aged
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Concept
|
Algorithms
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Concept
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Amino Acid Sequence
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Concept
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Adult
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Concept
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Central Nervous System Diseases
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Concept
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Animals
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Concept
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Animals, Newborn
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Concept
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Base Sequence
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Concept
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Biological Transport
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Concept
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Cattle
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Concept
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Child
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Concept
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Diagnosis, Computer-Assisted
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Concept
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Homozygote
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Concept
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Interviews as Topic
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Concept
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Endocrine System Diseases
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Concept
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Child, Preschool
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Concept
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HIV
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Concept
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Litter Size
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Concept
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Hypothalamo-Hypophyseal System
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Concept
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Family
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Concept
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Fishes
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Concept
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Fatty Liver
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Concept
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Infant, Newborn
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Concept
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Mice, Inbred C3H
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Concept
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Fatty Acids, Unsaturated
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Concept
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Terminology as Topic
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|
Concept
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Goldfish
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Concept
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Nucleic Acid Hybridization
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Concept
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Liver Neoplasms
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Concept
|
Enzyme-Linked Immunosorbent Assay
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Concept
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Feedback
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Concept
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Infant
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Concept
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Leucine
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Concept
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Lung Diseases
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Concept
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Leukocytes
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Concept
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Mice, Inbred Strains
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Concept
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Mice, Transgenic
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Concept
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Molecular Sequence Data
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|
Concept
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Monte Carlo Method
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Concept
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Mycobacterium tuberculosis
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|
Concept
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Mice, Inbred BALB C
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Concept
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Mice, Inbred C57BL
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Concept
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Mice, Nude
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Concept
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Middle Aged
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Concept
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Cricetinae
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Concept
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Laminin
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Concept
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Laparoscopy
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Concept
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Nucleic Acid Conformation
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|
Concept
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Ligands
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Concept
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Liver
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Concept
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Primates
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Concept
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Infant, Low Birth Weight
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Concept
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Research Personnel
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Concept
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Rats, Zucker
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|
Concept
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Quality of Life
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|
Concept
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Xenopus
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Concept
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Regulatory Sequences, Nucleic Acid
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|
Concept
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Polymorphism, Restriction Fragment Length
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Concept
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Humans
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|
Concept
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Leeches
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Concept
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Lung
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Concept
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Lymph Node Excision
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|
Concept
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Models, Animal
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|
Concept
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Likelihood Functions
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|
Concept
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Mice, Inbred DBA
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|
Concept
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Lymph Nodes
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|
Concept
|
Lymphatic Metastasis
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|
Concept
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Rats, Sprague-Dawley
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Concept
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Rats, Wistar
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Concept
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Neoplasm Recurrence, Local
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|
Concept
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Receptors, Retinoic Acid
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|
Concept
|
Mice, Knockout
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|
Concept
|
Basic-Leucine Zipper Transcription Factors
|
|
Concept
|
Rats, Inbred Dahl
|
|
Concept
|
Fusion Regulatory Protein 1, Light Chains
|
|
Concept
|
Mental Retardation, X-Linked
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|
Concept
|
Diagnostic and Statistical Manual of Mental Disorders
|
|
Concept
|
Amino Acid Substitution
|
|
Concept
|
Leptin
|
|
Concept
|
Papillomaviridae
|
|
Concept
|
Monocarboxylic Acid Transporters
|
|
Concept
|
Organic Cation Transport Proteins
|
|
Concept
|
Organic Anion Transporters, Sodium-Independent
|
|
Concept
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Animals, Genetically Modified
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|
Concept
|
Mice
|
|
Concept
|
Rats, Inbred BN
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|
Concept
|
Research Design
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|
Concept
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Acute Lung Injury
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|
Concept
|
Rats
|
|
Concept
|
Logistic Models
|
|
Concept
|
Mice, 129 Strain
|
|
Concept
|
Organic Anion Transporters
|
|
Concept
|
Ventilator-Induced Lung Injury
|
|
Concept
|
Siblings
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|
Concept
|
Cell Line, Tumor
|
|
Concept
|
Lipid Metabolism
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|
Concept
|
Cell Line
|
|
Concept
|
Heterozygote
|
|
Concept
|
Luteinizing Hormone
|
|
Concept
|
Genetic Linkage
|
|
Concept
|
Longitudinal Studies
|
|
Concept
|
Lymphocytes
|
|
Concept
|
Mice, Mutant Strains
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|
Concept
|
Mothers
|
|
Concept
|
Numerical Analysis, Computer-Assisted
|
|
Concept
|
Phylogeny
|
|
Concept
|
Pituitary-Adrenal System
|
|
Concept
|
User-Computer Interface
|
|
Concept
|
Membrane Transport Proteins
|
|
Concept
|
Amino Acid Transport System y+
|
|
Concept
|
Amino Acid Transport System y+L
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|
Concept
|
Glucose Transporter Type 4
|
|
Concept
|
Young Adult
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|
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.
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Academic Article
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Resistance to thyrotropin (TSH) in three families is not associated with mutations in the TSH receptor or TSH.
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|
Academic Article
|
Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping.
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|
Academic Article
|
Selective pituitary resistance to thyroid hormone produced by expression of a mutant thyroid hormone receptor beta gene in the pituitary gland of transgenic mice.
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Academic Article
|
Effect of thyroid hormone on growth. Lessons from the syndrome of resistance to thyroid hormone.
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Academic Article
|
Dominant inheritance of resistance to thyroid hormone not linked to defects in the thyroid hormone receptor alpha or beta genes may be due to a defective cofactor.
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|
Academic Article
|
Thyroid hormone action on liver, heart, and energy expenditure in thyroid hormone receptor beta-deficient mice.
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|
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.
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|
Academic Article
|
Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene.
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|
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).
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|
Academic Article
|
Rapid localization of mutations in the thyroid hormone receptor-beta gene by denaturing gradient gel electrophoresis in 18 families with thyroid hormone resistance.
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|
Academic Article
|
Improved radioimmunoassay for measurement of mouse thyrotropin in serum: strain differences in thyrotropin concentration and thyrotroph sensitivity to thyroid hormone.
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|
Academic Article
|
Steroid receptor coactivator-1 deficiency causes variable alterations in the modulation of T(3)-regulated transcription of genes in vivo.
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|
Academic Article
|
Search for abnormalities of nuclear corepressors, coactivators, and a coregulator in families with resistance to thyroid hormone without mutations in thyroid hormone receptor beta or alpha genes.
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|
Academic Article
|
Specificity of thyroid hormone receptor subtype and steroid receptor coactivator-1 on thyroid hormone action.
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|
Academic Article
|
RXR receptor agonist suppression of thyroid function: central effects in the absence of thyroid hormone receptor.
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|
Academic Article
|
Familial dysalbuminemic hyperthyroxinemia: a rare example of albumin polymorphism and its rapid molecular diagnosis.
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|
Academic Article
|
Effects of ligand and thyroid hormone receptor isoforms on hepatic gene expression profiles of thyroid hormone receptor knockout mice.
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|
Academic Article
|
Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice.
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|
Academic Article
|
Fetal loss associated with excess thyroid hormone exposure.
|
|
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
|
Regulation of expression of thyroid hormone receptor isoforms and coactivators in liver and heart by thyroid hormone.
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|
Academic Article
|
Autosomal dominant resistance to thyrotropin as a distinct entity in five multigenerational kindreds: clinical characterization and exclusion of candidate loci.
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|
Academic Article
|
Open versus laparoscopic simultaneous bilateral adrenalectomy.
|
|
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.
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|
Academic Article
|
Effect of pioglitazone on adrenocorticotropic hormone and cortisol secretion in Cushing's disease.
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|
Academic Article
|
Doctor . . . could it be my thyroid?
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|
Academic Article
|
Tissue responses to thyroid hormone in a kindred with resistance to thyroid hormone harboring a commonly occurring mutation in the thyroid hormone receptor beta gene (P453T).
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|
Academic Article
|
The syndrome of inherited partial SBP2 deficiency in humans.
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|
Academic Article
|
A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport.
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|
Academic Article
|
Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion.
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|
Academic Article
|
A lack of thyroid hormones rather than excess thyrotropin causes abnormal skeletal development in hypothyroidism.
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|
Academic Article
|
Homozygous thyroid hormone receptor ß-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.
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Academic Article
|
Transsphenoidal surgery for Cushing disease: experience with 136 patients.
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|
Academic Article
|
Role of type 2 deiodinase in response to acute lung injury (ALI) in mice.
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|
Academic Article
|
The interaction between nuclear receptor corepressor and histone deacetylase 3 regulates both positive and negative thyroid hormone action in vivo.
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|
Academic Article
|
Human thyroxine-binding globulin gene: complete sequence and transcriptional regulation.
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|
Academic Article
|
The syndromes of resistance to thyroid hormone.
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|
Academic Article
|
Sleep disturbances, daytime sleepiness, and quality of life in adults with growth hormone deficiency.
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|
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.
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|
Academic Article
|
The nuclear receptor corepressor (NCoR) controls thyroid hormone sensitivity and the set point of the hypothalamic-pituitary-thyroid axis.
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|
Academic Article
|
Mosaicism of a thyroid hormone receptor-beta gene mutation in resistance to thyroid hormone.
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|
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.
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|
Academic Article
|
Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred.
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|
Academic Article
|
Distinct roles of deiodinases on the phenotype of Mct8 defect: a comparison of eight different mouse genotypes.
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|
Academic Article
|
Behavioral effects of liothyronine (L-T3) in children with attention deficit hyperactivity disorder in the presence and absence of resistance to thyroid hormone.
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|
Academic Article
|
Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site.
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|
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
|
Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alpha.
|
|
Academic Article
|
Genetic analysis reveals different functions for the products of the thyroid hormone receptor alpha locus.
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|
Academic Article
|
Reciprocal interactions between the GH axis and sleep.
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|
Academic Article
|
Temperature homeostasis in transgenic mice lacking thyroid hormone receptor-alpha gene products.
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Academic Article
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Repulsive separation of the cytoplasmic ends of transmembrane helices 3 and 6 is linked to receptor activation in a novel thyrotropin receptor mutant (M626I).
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|
Academic Article
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Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice.
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|
Academic Article
|
"They have ears but do not hear" (Psalms 135:17): non-thyroid hormone receptor beta (non-TRbeta) resistance to thyroid hormone.
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Academic Article
|
Abrogation of the invasion of human bladder tumor cells by using protease inhibitor(s).
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Academic Article
|
Calcitonin stimulates bone formation when administered prior to initiation of osteogenesis.
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Academic Article
|
Somatostatin can locally inhibit proliferation and differentiation of cartilage and bone precursor cells.
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Academic Article
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Synthesis and localization of fibronectin during collagenous matrix-mesenchymal cell interaction and differentiation of cartilage and bone in vivo.
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Academic Article
|
Penile replantation using the leech Hirudo medicinalis.
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Academic Article
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Lymphatic mapping and intraoperative lymphoscintigraphy for identifying the sentinel node in penile tumors.
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|
Academic Article
|
Ureteroenteric anastomosis in continent urinary diversion: long-term results and complications of direct versus nonrefluxing techniques.
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Academic Article
|
State-of-the-art prostate cancer treatment and research. A report from the Cancer Institute of New Jersey.
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Academic Article
|
Effect of 13-cis-retinoic acid and alpha-interferon on transforming growth factor beta1 in patients with rising prostate-specific antigen.
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Academic Article
|
In vitro trial of the pilot prototype of the prostate mechanical imaging system.
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Academic Article
|
Behçet's syndrome with left ventricular aneurysm and ruptured renal artery pseudoaneurysm.
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|
Academic Article
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Diiodothyropropionic acid (DITPA) in the treatment of MCT8 deficiency.
|
|
Academic Article
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Thyroid hormone receptor-ß agonists prevent hepatic steatosis in fat-fed rats but impair insulin sensitivity via discrete pathways.
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|
Academic Article
|
Review of staging modalities in clinically localized prostate cancer.
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|
Academic Article
|
Changes in thyroid status during perinatal development of MCT8-deficient male mice.
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Academic Article
|
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.
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Academic Article
|
Sodium currents during differentiation in a human neuroblastoma cell line.
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Academic Article
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Placenta passage of the thyroid hormone analog DITPA to male wild-type and Mct8-deficient mice.
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Academic Article
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On Bayesian calculations for mixture likelihoods and priors.
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Academic Article
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A study of recurrence and death from papillary thyroid cancer with 27 years of median follow-up.
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Academic Article
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Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levels.
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Academic Article
|
Steroid-induced diabetes: a clinical and molecular approach to understanding and treatment.
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|
Academic Article
|
A new family with an activating mutation (G431S) in the TSH receptor gene: a phenotype discussion and review of the literature.
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|
Academic Article
|
A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction.
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Academic Article
|
Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism.
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Academic Article
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Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism.
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Academic Article
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Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism.
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Academic Article
|
Evaluation of the validity of the Quality of Well-being Scale in Trinidad and Tobago.
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Academic Article
|
The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 Deficiency.
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|
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.
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Academic Article
|
Laparoscopic renal cryoablation of small renal tumors: An alternative treatment option in elderly patients at high risk.
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Academic Article
|
Thyroid Hormone Action on Liver, Heart, and Energy Expenditure in Thyroid Hormone Receptor ß-Deficient Mice* * Presented in part at the 69th Annual Meeting of the American Thyroid Association Meeting, November 14-17, 1996, San Diego, California. This study was supported in part by the National Institutes of Health Grant DK-17050 and the Seymour J. Abrams Thyroid Research Center; a grant from the Ministry of Health and Welfare, Japan (to H.S.); and Grant-in-Aid for Scientific Research (0967104...
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Academic Article
|
Understanding Transgender Men's Experiences with and Preferences for Cervical Cancer Screening: A Rapid Assessment Survey.
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Academic Article
|
Fetal Exposure to High Maternal Thyroid Hormone Levels Causes Central Resistance to Thyroid Hormone in Adult Humans and Mice.
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Academic Article
|
An Essential Physiological Role for MCT8 in Bone in Male Mice.
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|
Academic Article
|
A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism.
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Academic Article
|
Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical Implications.
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Academic Article
|
Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel MCT8 Variants.
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|
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.
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|
Academic Article
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Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation.
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|
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.
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|
Concept
|
Transgender Persons
|
|
Concept
|
Non-alcoholic Fatty Liver Disease
|
|
Academic Article
|
Combined Use of RT-qPCR and NGS for Identification and Surveillance of SARS-CoV-2 Variants of Concern in Residual Clinical Laboratory Samples in Miami-Dade County, Florida.
|