Item Type | Name |
Concept
|
Acne Vulgaris
|
Concept
|
Age Factors
|
Concept
|
Adenoma, Chromophobe
|
Concept
|
Antibodies, Neoplasm
|
Concept
|
Adrenal Gland Neoplasms
|
Concept
|
Ethanol
|
Concept
|
Alkaline Phosphatase
|
Concept
|
Australia
|
Concept
|
Haplorhini
|
Concept
|
Autophagy
|
Concept
|
Adenoids
|
Concept
|
Adenylyl Cyclases
|
Concept
|
Adenoma
|
Concept
|
Cyclic AMP
|
Concept
|
Acromegaly
|
Concept
|
alpha 1-Antitrypsin
|
Concept
|
Amniotic Fluid
|
Concept
|
Aging
|
Concept
|
Alleles
|
Concept
|
Administration, Intranasal
|
Concept
|
Adrenocorticotropic Hormone
|
Concept
|
Agranulocytosis
|
Concept
|
Albuminuria
|
Concept
|
Blood Protein Disorders
|
Concept
|
Carcinoma, Papillary
|
Concept
|
Chiari-Frommel Syndrome
|
Concept
|
Amitrole
|
Concept
|
Aneuploidy
|
Concept
|
Antineoplastic Combined Chemotherapy Protocols
|
Concept
|
Androgens
|
Concept
|
Chloromercuribenzoates
|
Concept
|
Analysis of Variance
|
Concept
|
Anthropometry
|
Concept
|
Antibodies, Monoclonal
|
Concept
|
B-Lymphocytes
|
Concept
|
Base Sequence
|
Concept
|
Benzamides
|
Concept
|
Diabetes Mellitus, Experimental
|
Concept
|
Blood Urea Nitrogen
|
Concept
|
Body Height
|
Concept
|
Autoradiography
|
Concept
|
Athetosis
|
Concept
|
Autoantibodies
|
Concept
|
Birth Weight
|
Concept
|
Blood Glucose
|
Concept
|
Body Temperature
|
Concept
|
Dihydroxyphenylalanine
|
Concept
|
beta-Endorphin
|
Concept
|
Biopsy, Needle
|
Concept
|
Biopsy
|
Concept
|
Blood Protein Electrophoresis
|
Concept
|
Body Weight
|
Concept
|
Adipose Tissue, Brown
|
Concept
|
Calcification, Physiologic
|
Concept
|
Cattle
|
Concept
|
Bromocriptine
|
Concept
|
Evaluation Studies as Topic
|
Concept
|
Chromosomes, Human, Pair 15
|
Concept
|
Chromosomes, Human, Pair 3
|
Concept
|
Catalase
|
Concept
|
Fetal Diseases
|
Concept
|
Foot Diseases
|
Concept
|
Chromosomes, Human, 6-12 and X
|
Concept
|
Colonic Neoplasms
|
Concept
|
Chicago
|
Concept
|
Child Development
|
Concept
|
Chromosome Deletion
|
Concept
|
Chromosome Mapping
|
Concept
|
Codon
|
Concept
|
Blood-Brain Barrier
|
Concept
|
Genes, Synthetic
|
Concept
|
Genetic Vectors
|
Concept
|
Glucose-6-Phosphatase
|
Concept
|
Ovarian Follicle
|
Concept
|
Guinea Pigs
|
Concept
|
Corticotropin-Releasing Hormone
|
Concept
|
Cricetulus
|
Concept
|
Chorea
|
Concept
|
Chromatography, Ion Exchange
|
Concept
|
Hearing Loss, Sensorineural
|
Concept
|
Hematocrit
|
Concept
|
Cytosine Nucleotides
|
Concept
|
Homozygote
|
Concept
|
Hormones
|
Concept
|
Culture Media
|
Concept
|
Immunogenetics
|
Concept
|
Diagnostic Errors
|
Concept
|
DNA Transposable Elements
|
Concept
|
DNA, Mitochondrial
|
Concept
|
Cushing Syndrome
|
Concept
|
Cycloheximide
|
Concept
|
Cysteine Endopeptidases
|
Concept
|
Cystine
|
Concept
|
Dexamethasone
|
Concept
|
Immunoglobulin Fab Fragments
|
Concept
|
Injections, Intraperitoneal
|
Concept
|
Inositol Phosphates
|
Concept
|
Congenital Hypothyroidism
|
Concept
|
Cystinosis
|
Concept
|
Dithiothreitol
|
Concept
|
DNA, Bacterial
|
Concept
|
Catecholamines
|
Concept
|
DNA Mutational Analysis
|
Concept
|
DNA, Neoplasm
|
Concept
|
DNA, Recombinant
|
Concept
|
Dogs
|
Concept
|
Dosage Compensation, Genetic
|
Concept
|
Electrophoresis, Starch Gel
|
Concept
|
Electrophoresis, Polyacrylamide Gel
|
Concept
|
Fetal Resorption
|
Concept
|
Gene Frequency
|
Concept
|
Ghana
|
Concept
|
Glucocorticoids
|
Concept
|
Chorionic Gonadotropin
|
Concept
|
Heparitin Sulfate
|
Concept
|
Hybridomas
|
Concept
|
Enzyme Inhibitors
|
Concept
|
Estradiol
|
Concept
|
Litter Size
|
Concept
|
Hypothalamo-Hypophyseal System
|
Concept
|
Chromones
|
Concept
|
Exons
|
Concept
|
Mass Screening
|
Concept
|
Dextrans
|
Concept
|
Deafness
|
Concept
|
Dimethylformamide
|
Concept
|
Diphenylamine
|
Concept
|
Double-Blind Method
|
Concept
|
Follicle Stimulating Hormone
|
Concept
|
Fibroblasts
|
Concept
|
Introns
|
Concept
|
Electrophoresis
|
Concept
|
Enzyme Activation
|
Concept
|
Mice, Inbred C3H
|
Concept
|
Fluorescence
|
Concept
|
gamma-Globulins
|
Concept
|
Gene Expression Regulation
|
Concept
|
Genes, Dominant
|
Concept
|
Glucosamine
|
Concept
|
Genes
|
Concept
|
False Positive Reactions
|
Concept
|
Fasting
|
Concept
|
Fibronectins
|
Concept
|
Israel
|
Concept
|
Karyotyping
|
Concept
|
Genes, Recessive
|
Concept
|
Diagnostic Techniques, Endocrine
|
Concept
|
Nucleic Acid Hybridization
|
Concept
|
Obesity
|
Concept
|
Oncogenes
|
Concept
|
Osteoblasts
|
Concept
|
Histocytochemistry
|
Concept
|
Hematopoietic Stem Cells
|
Concept
|
Electroencephalography
|
Concept
|
Electromyography
|
Concept
|
DNA, Viral
|
Concept
|
Dwarfism, Pituitary
|
Concept
|
Hydrogen Peroxide
|
Concept
|
Hydrogen-Ion Concentration
|
Concept
|
Immune Sera
|
Concept
|
beta-Lipotropin
|
Concept
|
Liver Neoplasms
|
Concept
|
Long-Acting Thyroid Stimulator
|
Concept
|
Indium
|
Concept
|
Endocrinology
|
Concept
|
Enzyme-Linked Immunosorbent Assay
|
Concept
|
Eosinophilia
|
Concept
|
Herpesvirus 4, Human
|
Concept
|
Escherichia coli
|
Concept
|
Hydrocortisone
|
Concept
|
Feedback
|
Concept
|
Flow Cytometry
|
Concept
|
Fluorescent Antibody Technique
|
Concept
|
Immunosorbent Techniques
|
Concept
|
Immunodiffusion
|
Concept
|
Gene Amplification
|
Concept
|
Isoelectric Focusing
|
Concept
|
Isoenzymes
|
Concept
|
Multigene Family
|
Concept
|
Gigantism
|
Concept
|
Goats
|
Concept
|
Goiter, Endemic
|
Concept
|
Light
|
Concept
|
Heme
|
Concept
|
Lung Diseases
|
Concept
|
Macrophages
|
Concept
|
Mast Cells
|
Concept
|
Isoelectric Point
|
Concept
|
Metanephrine
|
Concept
|
Carcinoma, Hepatocellular
|
Concept
|
Maternal Age
|
Concept
|
Labor, Obstetric
|
Concept
|
Leukocytes
|
Concept
|
Leydig Cells
|
Concept
|
Gonadotropin-Releasing Hormone
|
Concept
|
Hydrolysis
|
Concept
|
Hypoproteinemia
|
Concept
|
Mice, Inbred Strains
|
Concept
|
Mosaicism
|
Concept
|
Phenolsulfonphthalein
|
Concept
|
Mice, Transgenic
|
Concept
|
Models, Genetic
|
Concept
|
Mannose
|
Concept
|
Estrogens
|
Concept
|
Ethchlorvynol
|
Concept
|
Prenatal Diagnosis
|
Concept
|
Immunohistochemistry
|
Concept
|
Organ Size
|
Concept
|
Nelson Syndrome
|
Concept
|
Glycogen
|
Concept
|
Graves Disease
|
Concept
|
Growth
|
Concept
|
Mice, Inbred BALB C
|
Concept
|
Mice, Inbred C57BL
|
Concept
|
Random Allocation
|
Concept
|
Receptors, Estrogen
|
Concept
|
Molecular Biology
|
Concept
|
Muscular Atrophy
|
Concept
|
Mutation
|
Concept
|
Cricetinae
|
Concept
|
Hot Temperature
|
Concept
|
Iodine Isotopes
|
Concept
|
Laminin
|
Concept
|
Phosphatidylinositols
|
Concept
|
Nucleic Acid Conformation
|
Concept
|
Osteoclasts
|
Concept
|
Ovarian Diseases
|
Concept
|
Lung Neoplasms
|
Concept
|
Serum Albumin, Radio-Iodinated
|
Concept
|
Oocytes
|
Concept
|
Pedigree
|
Concept
|
Pituitary Function Tests
|
Concept
|
Pituitary Gland, Anterior
|
Concept
|
Morpholines
|
Concept
|
Polymorphism, Genetic
|
Concept
|
Operon
|
Concept
|
Osteogenesis
|
Concept
|
Oxygen
|
Concept
|
Feeding Behavior
|
Concept
|
Embryonic and Fetal Development
|
Concept
|
Fetus
|
Concept
|
Prealbumin
|
Concept
|
Pituitary Gland
|
Concept
|
Plasmids
|
Concept
|
Protein Processing, Post-Translational
|
Concept
|
Globins
|
Concept
|
Glycogen Storage Disease Type I
|
Concept
|
Hypopituitarism
|
Concept
|
Immunoglobulin G
|
Concept
|
Immunoelectrophoresis
|
Concept
|
Immunoenzyme Techniques
|
Concept
|
Regression Analysis
|
Concept
|
Guanethidine
|
Concept
|
Guanine
|
Concept
|
Haplotypes
|
Concept
|
Rabbits
|
Concept
|
Rats, Zucker
|
Concept
|
Receptors, LH
|
Concept
|
Pronase
|
Concept
|
RNA-Directed DNA Polymerase
|
Concept
|
Puberty, Precocious
|
Concept
|
Insulin Resistance
|
Concept
|
Intestinal Absorption
|
Concept
|
Intestinal Mucosa
|
Concept
|
Iodine
|
Concept
|
Iopanoic Acid
|
Concept
|
Cohort Studies
|
Concept
|
Rats, Inbred Lew
|
Concept
|
Regulatory Sequences, Nucleic Acid
|
Concept
|
Polymorphism, Restriction Fragment Length
|
Concept
|
Retina
|
Concept
|
RNA Splicing
|
Concept
|
Seasons
|
Concept
|
Sex Chromosomes
|
Concept
|
Sensitivity and Specificity
|
Concept
|
Swine
|
Concept
|
Thyroid Function Tests
|
Concept
|
Thyroxine-Binding Proteins
|
Concept
|
Sheep
|
Concept
|
Humans
|
Concept
|
Hypogonadism
|
Concept
|
Immunization
|
Concept
|
Incidence
|
Concept
|
Cluster Analysis
|
Concept
|
Tomography, X-Ray Computed
|
Concept
|
Tretinoin
|
Concept
|
Thyrotoxicosis
|
Concept
|
Statistics as Topic
|
Concept
|
Triiodothyronine
|
Concept
|
Tritium
|
Concept
|
Thyroid Crisis
|
Concept
|
Genome
|
Concept
|
Ultrasonography
|
Concept
|
Triglycerides
|
Concept
|
Tamoxifen
|
Concept
|
Genetic Variation
|
Concept
|
Iodine Radioisotopes
|
Concept
|
Kidney Failure, Chronic
|
Concept
|
Germ-Line Mutation
|
Concept
|
Deoxyribonuclease EcoRI
|
Concept
|
Multicenter Studies as Topic
|
Concept
|
Liver Glycogen
|
Concept
|
Antithyroid Agents
|
Concept
|
Codon, Terminator
|
Concept
|
Weight Loss
|
Concept
|
Neonatal Screening
|
Concept
|
Risk Assessment
|
Concept
|
Drug Resistance, Neoplasm
|
Concept
|
Reverse Transcriptase Polymerase Chain Reaction
|
Concept
|
Turner Syndrome
|
Concept
|
RNA Splice Sites
|
Concept
|
Vitamins
|
Concept
|
Wakefulness
|
Concept
|
Up-Regulation
|
Concept
|
Deoxyribonucleases, Type II Site-Specific
|
Concept
|
17-Hydroxysteroid Dehydrogenases
|
Concept
|
Prevalence
|
Concept
|
DNA, Antisense
|
Concept
|
Metabolic Clearance Rate
|
Concept
|
Methimazole
|
Concept
|
Mice, Inbred DBA
|
Concept
|
Mice, Inbred ICR
|
Concept
|
Exercise
|
Concept
|
Weight Gain
|
Concept
|
Interleukin-4
|
Concept
|
Culture Media, Conditioned
|
Concept
|
Genomic Library
|
Concept
|
Rats, Sprague-Dawley
|
Concept
|
Rats, Wistar
|
Concept
|
Mutagenesis, Site-Directed
|
Concept
|
Sequence Alignment
|
Concept
|
Myxedema
|
Concept
|
Case-Control Studies
|
Concept
|
Alternative Splicing
|
Concept
|
In Situ Hybridization
|
Concept
|
Sequence Analysis, DNA
|
Concept
|
Methionine
|
Concept
|
Methylation
|
Concept
|
Genes, Reporter
|
Concept
|
Mice, Obese
|
Concept
|
Treatment Outcome
|
Concept
|
Point Mutation
|
Concept
|
Gene Transfer Techniques
|
Concept
|
Nafarelin
|
Concept
|
Gene Deletion
|
Concept
|
Sequence Deletion
|
Concept
|
Fetal Development
|
Concept
|
MAP Kinase Kinase 1
|
Concept
|
Hepatoblastoma
|
Concept
|
Mice, Knockout
|
Concept
|
Gene Expression Regulation, Developmental
|
Concept
|
DNA, Complementary
|
Concept
|
Cell Proliferation
|
Concept
|
Hyperthyroxinemia, Familial Dysalbuminemic
|
Concept
|
Chemokines
|
Concept
|
GTP-Binding Protein alpha Subunits, Gs
|
Concept
|
Epitope Mapping
|
Concept
|
Th2 Cells
|
Concept
|
Hepatocyte Nuclear Factor 1-alpha
|
Concept
|
3-Iodobenzylguanidine
|
Concept
|
Multiple Endocrine Neoplasia Type 2a
|
Concept
|
Transgenes
|
Concept
|
Rats, Inbred Dahl
|
Concept
|
Smad1 Protein
|
Concept
|
Chondrocytes
|
Concept
|
Mutation, Missense
|
Concept
|
Fusion Regulatory Protein 1, Light Chains
|
Concept
|
Cross-Over Studies
|
Concept
|
Gene Knockout Techniques
|
Concept
|
Nucleic Acid Denaturation
|
Concept
|
Reactive Oxygen Species
|
Concept
|
In Situ Hybridization, Fluorescence
|
Concept
|
Genetic Association Studies
|
Concept
|
Molecular Diagnostic Techniques
|
Concept
|
Exome
|
Concept
|
Genetic Diseases, X-Linked
|
Concept
|
Early Diagnosis
|
Concept
|
Primary Cell Culture
|
Concept
|
Mental Retardation, X-Linked
|
Concept
|
Positron-Emission Tomography
|
Concept
|
Genetic Structures
|
Concept
|
Hepatocyte Nuclear Factor 1
|
Concept
|
Chromatin Immunoprecipitation
|
Concept
|
Proto-Oncogene Proteins c-bcl-2
|
Concept
|
Clinical Laboratory Techniques
|
Concept
|
COS Cells
|
Concept
|
Microscopy, Confocal
|
Concept
|
Amino Acid Substitution
|
Concept
|
Proto-Oncogene Proteins B-raf
|
Concept
|
Alu Elements
|
Concept
|
5' Untranslated Regions
|
Concept
|
Response Elements
|
Concept
|
Congenital Disorders of Glycosylation
|
Concept
|
Oligonucleotide Array Sequence Analysis
|
Concept
|
Active Transport, Cell Nucleus
|
Concept
|
Genetic Diseases, Inborn
|
Concept
|
Databases, Genetic
|
Concept
|
Gene Expression Profiling
|
Concept
|
Physical Examination
|
Concept
|
Polycystic Ovary Syndrome
|
Concept
|
Monocarboxylic Acid Transporters
|
Concept
|
Precipitin Tests
|
Concept
|
Prolactin
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Pseudohypoparathyroidism
|
Concept
|
Mice
|
Concept
|
Nuclear Receptor Coactivator 2
|
Concept
|
Rats, Inbred BN
|
Concept
|
Pyrroles
|
Concept
|
Radioimmunoassay
|
Concept
|
Radionuclide Imaging
|
Concept
|
Rats, Inbred Strains
|
Concept
|
Ribonucleases
|
Concept
|
Saccharomyces cerevisiae
|
Concept
|
Serum Albumin
|
Concept
|
Severity of Illness Index
|
Concept
|
Reflex, Stretch
|
Concept
|
Respiratory Distress Syndrome, Newborn
|
Concept
|
Sampling Studies
|
Concept
|
Serum Globulins
|
Concept
|
Congenital Hyperinsulinism
|
Concept
|
Testosterone
|
Concept
|
Thyroglobulin
|
Concept
|
Heredity
|
Concept
|
Acute Lung Injury
|
Concept
|
Unfolded Protein Response
|
Concept
|
Compassionate Use Trials
|
Concept
|
MAP Kinase Kinase Kinase 2
|
Concept
|
Rats
|
Concept
|
Dried Blood Spot Testing
|
Concept
|
Palatine Tonsil
|
Concept
|
Cathepsin G
|
Concept
|
Kruppel-Like Transcription Factors
|
Concept
|
Epithelial-Mesenchymal Transition
|
Concept
|
Pituitary ACTH Hypersecretion
|
Concept
|
Trypsin
|
Concept
|
Uremia
|
Concept
|
Sex Factors
|
Concept
|
MAP Kinase Kinase Kinase 1
|
Concept
|
Adaptor Proteins, Signal Transducing
|
Concept
|
Temperature
|
Concept
|
Blotting, Western
|
Concept
|
Glycoprotein Hormones, alpha Subunit
|
Concept
|
Down-Regulation
|
Concept
|
PTEN Phosphohydrolase
|
Concept
|
Survival Analysis
|
Concept
|
Evoked Potentials, Auditory, Brain Stem
|
Concept
|
Thyroxine-Binding Globulin
|
Concept
|
Thyroid Neoplasms
|
Concept
|
Thyrotropin-Releasing Hormone
|
Concept
|
Frameshift Mutation
|
Concept
|
Mice, 129 Strain
|
Concept
|
Transfection
|
Concept
|
Phosphatidylinositol 3-Kinase
|
Concept
|
Blotting, Southern
|
Concept
|
Blotting, Northern
|
Concept
|
Electrophoresis, Gel, Two-Dimensional
|
Concept
|
Reproducibility of Results
|
Concept
|
Genetic Therapy
|
Concept
|
Minor Histocompatibility Antigens
|
Concept
|
Gene Expression Regulation, Enzymologic
|
Concept
|
Codon, Nonsense
|
Concept
|
Odds Ratio
|
Concept
|
Polymerase Chain Reaction
|
Concept
|
Proto-Oncogene Proteins p21(ras)
|
Concept
|
Genes, erbA
|
Concept
|
Phlebotomy
|
Concept
|
GTP-Binding Proteins
|
Concept
|
NADPH Oxidases
|
Concept
|
Dietary Supplements
|
Concept
|
Nystagmus, Congenital
|
Concept
|
Sequence Analysis, Protein
|
Concept
|
Gene Silencing
|
Concept
|
Gene Targeting
|
Concept
|
Gene Dosage
|
Concept
|
Immunoglobulins, Thyroid-Stimulating
|
Concept
|
Leukocyte Elastase
|
Concept
|
Phosphatidylinositol 3-Kinases
|
Concept
|
Two-Hybrid System Techniques
|
Concept
|
Dystonic Disorders
|
Concept
|
Placental Circulation
|
Concept
|
Extracellular Signal-Regulated MAP Kinases
|
Concept
|
Infusions, Intraventricular
|
Concept
|
Hepatocyte Nuclear Factor 1-beta
|
Concept
|
Smad5 Protein
|
Concept
|
Transcriptome
|
Concept
|
Ventilator-Induced Lung Injury
|
Concept
|
Nuclear Receptor Coactivator 1
|
Concept
|
Organogenesis
|
Concept
|
Ribosomal Protein S6 Kinases, 70-kDa
|
Concept
|
Cyclin-Dependent Kinase Inhibitor p27
|
Concept
|
Gene Knock-In Techniques
|
Concept
|
Nuclear Receptor Co-Repressor 1
|
Concept
|
Th17 Cells
|
Concept
|
Alpha-Globulins
|
Concept
|
Antibodies
|
Concept
|
Binding, Competitive
|
Concept
|
Bone Development
|
Concept
|
Carcinoembryonic Antigen
|
Concept
|
Chromatin
|
Concept
|
Chromosomes
|
Concept
|
Clinical Trials as Topic
|
Concept
|
Cloning, Molecular
|
Concept
|
Crosses, Genetic
|
Concept
|
Deoxycytidine
|
Concept
|
Drug Eruptions
|
Concept
|
Diabetes Mellitus
|
Concept
|
Disease Models, Animal
|
Concept
|
DNA Restriction Enzymes
|
Concept
|
Drinking
|
Concept
|
Drug Administration Schedule
|
Concept
|
Drug Screening Assays, Antitumor
|
Concept
|
Ecuador
|
Concept
|
Electrophoresis, Agar Gel
|
Concept
|
Enhancer Elements, Genetic
|
Concept
|
Epinephrine
|
Concept
|
Erythrocytes
|
Concept
|
Estriol
|
Concept
|
Estrone
|
Concept
|
Follow-Up Studies
|
Concept
|
Genetic Counseling
|
Concept
|
Genetic Testing
|
Concept
|
Genotype
|
Concept
|
Gestational Age
|
Concept
|
Heart Rate
|
Concept
|
Hemagglutination Tests
|
Concept
|
Heterozygote
|
Concept
|
Histidine
|
Concept
|
Horses
|
Concept
|
Hyperkinesis
|
Concept
|
Hypothalamus
|
Concept
|
Immunoglobulins
|
Concept
|
Monoiodotyrosine
|
Concept
|
Iran
|
Concept
|
Kinetics
|
Concept
|
Luteinizing Hormone
|
Concept
|
Genetic Linkage
|
Concept
|
Longitudinal Studies
|
Concept
|
Lymphocyte Activation
|
Concept
|
Lymphocytes
|
Concept
|
Magnetic Resonance Imaging
|
Concept
|
Metabolism, Inborn Errors
|
Concept
|
Mice, Mutant Strains
|
Concept
|
Microscopy, Fluorescence
|
Concept
|
Mothers
|
Concept
|
Niacin
|
Concept
|
Norepinephrine
|
Concept
|
Patient Compliance
|
Concept
|
Pituitary Neoplasms
|
Concept
|
Plasma Volume
|
Concept
|
Predictive Value of Tests
|
Concept
|
Propylthiouracil
|
Concept
|
Prospective Studies
|
Concept
|
Radiation Effects
|
Concept
|
Recombinant Fusion Proteins
|
Concept
|
Reticulocytes
|
Concept
|
Retrospective Studies
|
Concept
|
Sex Hormone-Binding Globulin
|
Concept
|
Thymus Gland
|
Concept
|
Umbilical Cord
|
Concept
|
X Chromosome
|
Concept
|
Restriction Mapping
|
Concept
|
Transcriptional Activation
|
Concept
|
Gene Expression Regulation, Neoplastic
|
Concept
|
Cytokines
|
Concept
|
Mutagenesis, Insertional
|
Concept
|
Age of Onset
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Polymorphism, Single Nucleotide
|
Concept
|
Collagen Type IV
|
Concept
|
Amino Acid Transport System y+
|
Concept
|
Amino Acid Transport System y+L
|
Concept
|
Chromosomes, Human, X
|
Concept
|
Epigenesis, Genetic
|
Concept
|
Protein Kinase Inhibitors
|
Concept
|
Neurogenesis
|
Concept
|
Class III Phosphatidylinositol 3-Kinases
|
Concept
|
Early Medical Intervention
|
Academic Article
|
Phenotype differences of resistance to thyroid hormone in two unrelated families with an identical mutation in the thyroid hormone receptor beta gene (R320C).
|
Academic Article
|
Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type I.
|
Academic Article
|
Resistance to thyroid hormone caused by two mutant thyroid hormone receptors beta, R243Q and R243W, with marked impairment of function that cannot be explained by altered in vitro 3,5,3'-triiodothyroinine binding affinity.
|
Academic Article
|
A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center study.
|
Academic Article
|
New insights on the mechanism(s) of the dominant negative effect of mutant thyroid hormone receptor in generalized resistance to thyroid hormone.
|
Academic Article
|
Resistance to thyrotropin (TSH) in three families is not associated with mutations in the TSH receptor or TSH.
|
Academic Article
|
Thyroxine-binding globulin: organization of the gene and variants.
|
Academic Article
|
A new mutation in the thyroid hormone receptor (TR) beta gene (V458A) in a family with resistance to thyroid hormone (RTH).
|
Academic Article
|
Thyrotropin regulation by thyroid hormone in thyroid hormone receptor beta-deficient mice.
|
Academic Article
|
Iodination-deiodination. A radiochemical method for detection of structure and changes in structure in RNA.
|
Academic Article
|
Effect of thyroid hormone on growth. Lessons from the syndrome of resistance to thyroid hormone.
|
Academic Article
|
Congenital central isolated hypothyroidism caused by a homozygous mutation in the TSH-beta subunit gene.
|
Academic Article
|
Sequencing of the variant thyroxine-binding globulin (TBG)-San Diego reveals two nucleotide substitutions.
|
Academic Article
|
Identification of thyroxine-binding globulin-San Diego in a family from Houston and its characterization by in vitro expression using Xenopus oocytes.
|
Academic Article
|
Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene.
|
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
|
Aberrant alternative splicing of thyroid hormone receptor in a TSH-secreting pituitary tumor is a mechanism for hormone resistance.
|
Academic Article
|
Thyroid hormone resistance.
|
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.
|
Academic Article
|
Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene.
|
Academic Article
|
RXR receptor agonist suppression of thyroid function: central effects in the absence of thyroid hormone receptor.
|
Academic Article
|
Hypothyroidism in thyroid transcription factor 1 haploinsufficiency is caused by reduced expression of the thyroid-stimulating hormone receptor.
|
Academic Article
|
Genomic organization of mouse ZAKI-4 gene that encodes ZAKI-4 alpha and beta isoforms, endogenous calcineurin inhibitors, and changes in the expression of these isoforms by thyroid hormone in adult mouse brain and heart.
|
Academic Article
|
Characterization and primary structures of bovine and porcine thyroxine-binding globulin.
|
Academic Article
|
The syndrome of resistance to thyroid hormone, misdiagnosed and treated as thyrotoxicosis.
|
Academic Article
|
Autosomal dominant resistance to thyrotropin as a distinct entity in five multigenerational kindreds: clinical characterization and exclusion of candidate loci.
|
Academic Article
|
Identification of a serum protein polymorphism via two-dimensional electrophoresis. Family and population studies in two genetically isolated groups: North American Hutterites and Australian aborigines.
|
Academic Article
|
Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1.
|
Academic Article
|
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism.
|
Academic Article
|
Thyroid hormone mediated changes in gene expression can be initiated by cytosolic action of the thyroid hormone receptor beta through the phosphatidylinositol 3-kinase pathway.
|
Academic Article
|
Delineation of the discontinuous-conformational epitope of a monoclonal antibody displaying full in vitro and in vivo thyrotropin activity.
|
Academic Article
|
Molecular basis for the properties of the thyroxine-binding globulin-slow variant in American blacks.
|
Academic Article
|
Syndromes of reduced sensitivity to thyroid hormone: genetic defects in hormone receptors, cell transporters and deiodination.
|
Academic Article
|
Familial juvenile autoimmune hypothyroidism, pituitary enlargement, obesity, and insulin resistance.
|
Academic Article
|
Sleep deprivation in the rat: XI. The effect of guanethidine-induced sympathetic blockade on the sleep deprivation syndrome.
|
Academic Article
|
A novel splice variant involving the 5' untranslated region of thyroid hormone receptor beta1 (TRbeta1).
|
Academic Article
|
Multiple endocrine neoplasia 2A syndrome presenting as peripartum cardiomyopathy due to catecholamine excess.
|
Academic Article
|
Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3,5,3'-triiodo-L-thyronine.
|
Academic Article
|
Sleep deprivation in the rat: V. Energy use and mediation.
|
Academic Article
|
Autoimmunity in patients with resistance to thyroid hormone.
|
Academic Article
|
Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion.
|
Academic Article
|
Oncogenic Kras requires simultaneous PI3K signaling to induce ERK activation and transform thyroid epithelial cells in vivo.
|
Academic Article
|
Thyrocyte-specific inactivation of p53 and Pten results in anaplastic thyroid carcinomas faithfully recapitulating human tumors.
|
Academic Article
|
Homozygous thyroid hormone receptor ß-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.
|
Academic Article
|
Two new inherited defects of the thyroxine-binding globulin (TBG) molecule presenting as partial TBG deficiency.
|
Academic Article
|
Effect of estrogen on the synthesis and secretion of thyroxine-binding globulin by a human hepatoma cell line, Hep G2.
|
Academic Article
|
Normal cellular uptake of thyroxine from serum of patients with familial dysalbuminemic hyperthyroxinemia or elevated thyroxine-binding globulin.
|
Academic Article
|
Thyroid hormone inhibits fibronectin synthesis by cultured human skin fibroblasts.
|
Academic Article
|
Isoelectric focusing variant thyroxine-binding globulin in American blacks: increased heat lability and reduced serum concentration.
|
Academic Article
|
X-chromosome-linked inheritance of the variant thyroxine-binding globulin in Australian aborigines.
|
Academic Article
|
The effects of low doses of depot estradiol and testosterone in teenagers with ovarian failure and Turner's syndrome.
|
Academic Article
|
Resistance to thyroid hormone: an historical overview.
|
Academic Article
|
The syndromes of resistance to thyroid hormone.
|
Academic Article
|
Variant thyroxine-binding globulin in serum of Australian aborigines: a comparison with familial TBG deficiency in Caucasians and American blacks.
|
Academic Article
|
Suppression of serum thyrotropin (TSH) by L-dopa in chronic hypothyroidism: interrelationships in the regulation of TSH and prolactin secretion.
|
Academic Article
|
Effects of 7, 12-dimethylbenz(a)anthracene and estrogen on the transplantation and growth of a rat pituitary tumor.
|
Academic Article
|
Inherited X chromosome linked thyroxine-binding globulin (TBG) deficiency in a homozygous female.
|
Academic Article
|
Mosaicism of a thyroid hormone receptor-beta gene mutation in resistance to thyroid hormone.
|
Academic Article
|
The role of glycosylation in the molecular conformation and secretion of thyroxine-binding globulin.
|
Academic Article
|
Translation of thyroglobulin 33S messenger RNA as a means of determining thyroglobulin quaternary structure.
|
Academic Article
|
Cross-talk between PI3K and estrogen in the mouse thyroid predisposes to the development of follicular carcinomas with a higher incidence in females.
|
Academic Article
|
Stanniocalcin 1 induction by thyroid hormone depends on thyroid hormone receptor ß and phosphatidylinositol 3-kinase activation.
|
Academic Article
|
The preparation of carrier-free iodine isotope-substituted cytosine nucleotides.
|
Academic Article
|
Gene screening in Japanese families with complete deficiency of thyroxine-binding globulin demonstrates that a nucleotide deletion at codon 352 may be a race specific mutation.
|
Academic Article
|
Relationship of oligosaccharide modification to the cause of serum thyroxine-binding globulin excess.
|
Academic Article
|
Disappearance rate of endogenous and exogenous human growth hormone in man.
|
Academic Article
|
Direct application of radioiodinated aminoacyl tRNA for radiolabeling nascent proteins.
|
Academic Article
|
Measurement of thyroxine uptake from serum by cultured human hepatocytes as an index of thyroid status: reduced thyroxine uptake from serum of patients with nonthyroidal illness.
|
Academic Article
|
Resistance to thyroid hormone diagnosed by the reduced response of fibroblasts to the triiodothyronine-induced suppression of fibronectin synthesis.
|
Academic Article
|
Circadian and ultradian variations of ACTH and cortisol secretion.
|
Academic Article
|
Peroxidase defect in congenital goiter with complete organification block.
|
Academic Article
|
Hyperthyroidism and adult celiac disease.
|
Academic Article
|
High prevalence of thyroxine-binding globulin deficiency among Bedouin infants in southern Israel.
|
Academic Article
|
Thyroid dysfunction in chronic renal failure. A study of the pituitary-thyroid axis and peripheral turnover kinetics of thyroxine and triiodothyronine.
|
Academic Article
|
Expression of a thyroid hormone-responsive recombinant gene introduced into adult mice livers by replication-defective adenovirus can be regulated by endogenous thyroid hormone receptor.
|
Academic Article
|
How clinical observations of a congenital disease can be translated in terms of molecular biology.
|
Academic Article
|
Transient iodide trapping defect in Hashimoto's thyroiditis detected by the combination of radionuclide and fluorescent scanning.
|
Academic Article
|
Use of 131-I-CEA antibody as a tumor scanning agent.
|
Academic Article
|
Pituitary-thyroid setpoint and thyrotropin receptor expression in consomic rats.
|
Academic Article
|
Brief report: resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene.
|
Academic Article
|
Carcinoembryonic antigen and humoral antibody response in patients with thyroid carcinoma.
|
Academic Article
|
Radioiodine labeling of ribopolymers for special applications in biology.
|
Academic Article
|
Sleep deprivation in the rat: XIX. Effects of thyroxine administration.
|
Academic Article
|
Interrelationships in the regulation of TSH and prolactin secretion in man: effects of L-dopa, TRH and thyroid hormone in various combinations.
|
Academic Article
|
Familial goitre with partial iodine organification defect, lack of thyroglobulin, and high levels of thyroid peroxidase.
|
Academic Article
|
Resistance to thyroid hormone and its molecular basis.
|
Academic Article
|
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 mice.
|
Academic Article
|
Approach to the patient with resistance to thyroid hormone and pregnancy.
|
Academic Article
|
Translation of prolactin and growth hormone messenger RNA from rat pituitary tumour cells. Stimulation of GH mRNA activity by triiodothyronine [proceedings].
|
Academic Article
|
The effect of dexamethasone on the 24-hour profiles of adrenocorticotropin and cortisol in Cushing's syndrome.
|
Academic Article
|
Multifactorial control of the 24-hour secretory profiles of pituitary hormones.
|
Academic Article
|
Nuclear thyroid hormone receptors in cultured human fibroblasts: improved method of isolation, partial characterization, and interaction with chromatin.
|
Academic Article
|
Inherited abnormality of thyroxine-binding globulin with no demonstrable thyroxine-binding activity and high serum levels of denatured thyroxine-binding globulin.
|
Academic Article
|
Homogeneous apoenzyme reactivation immunoassay for thyroxin-binding globulin in serum.
|
Academic Article
|
Evidence for two subtypes of Cushing's disease based on the analysis of episodic cortisol secretion.
|
Academic Article
|
Variant thyroxine-binding globulin in serum of Australian aborigines: its physical, chemical and biological properties.
|
Academic Article
|
The consequences of inappropriate treatment because of failure to recognize the syndrome of pituitary and peripheral tissue resistance to thyroid hormone.
|
Academic Article
|
Response to challenge with gonadotropin-releasing hormone agonist in a mother and her two sons with a constitutively activating mutation of the luteinizing hormone receptor--a clinical research center study.
|
Academic Article
|
Dopaminergic control of prolactin mRNA accumulation in the pituitary of the male rat.
|
Academic Article
|
Molecular cloning of an orphan G-protein-coupled receptor that constitutively activates adenylate cyclase.
|
Academic Article
|
Probing the cause of thyroid dysgenesis.
|
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.
|
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
|
Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alpha.
|
Academic Article
|
Molecular cloning and primary structure of rat thyroxine-binding globulin.
|
Academic Article
|
Thyroid hormone induces rapid activation of Akt/protein kinase B-mammalian target of rapamycin-p70S6K cascade through phosphatidylinositol 3-kinase in human fibroblasts.
|
Academic Article
|
Resistance to thyroid hormone associated with autoimmune thyroid disease in a Turkish family.
|
Academic Article
|
Thyroid hormone receptor beta gene mutation (P453A) in a family producing resistance to thyroid hormone.
|
Academic Article
|
The action of thyroid hormone.
|
Academic Article
|
Leukocyte alkaline phosphatase in hypothyroidism and hyperthyroidism. Response to initiation of thyroxine replacement therapy.
|
Academic Article
|
Detection of the thyroxine-binding globulin (TBG) gene in six unrelated families with complete TBG deficiency.
|
Academic Article
|
Inherited heat-stable variant thyroxine-binding globulin (TBG-Chicago).
|
Academic Article
|
Reduced affinity for thyroxine in two of three structural thyroxine-binding prealbumin variants associated with familial amyloidotic polyneuropathy.
|
Academic Article
|
Reduced clearance rate of thyroxine-binding globulin (TBG) with increased sialylation: a mechanism for estrogen-induced elevation of serum TBG concentration.
|
Academic Article
|
A study on the inheritance of thyroxine-binding globulin (TBG) deficiency from data obtained in 13 families detected by a neonatal screening program.
|
Academic Article
|
Sex hormone-binding globulin in the diagnosis of peripheral tissue resistance to thyroid hormone: the value of changes after short term triiodothyronine administration.
|
Academic Article
|
Radioimmunoassay of anterior pituitary hormones.
|
Academic Article
|
Do clinical manifestations of resistance to thyroid hormone correlate with the functional alteration of the corresponding mutant thyroid hormone-beta receptors?
|
Academic Article
|
The syndromes of reduced sensitivity to thyroid hormone.
|
Academic Article
|
The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 Deficiency.
|
Academic Article
|
Diiodothyropropionic acid (DITPA) cross-reacts with thyroid function assays on different immunoassay platforms.
|
Academic Article
|
Fetal Exposure to High Maternal Thyroid Hormone Levels Causes Central Resistance to Thyroid Hormone in Adult Humans and Mice.
|
Academic Article
|
An Essential Physiological Role for MCT8 in Bone in Male Mice.
|
Academic Article
|
Oncogene-induced senescence and its evasion in a mouse model of thyroid neoplasia.
|
Academic Article
|
Resistance to thyrotropin.
|
Academic Article
|
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families.
|
Academic Article
|
Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical Implications.
|
Academic Article
|
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.
|
Academic Article
|
Reduced Sensitivity to Thyroid Hormone as a Transgenerational Epigenetic Marker Transmitted Along the Human Male Line.
|
Academic Article
|
A Liver-Specific Thyromimetic, VK2809, Decreases Hepatosteatosis in Glycogen Storage Disease Type Ia.
|
Academic Article
|
Clinical recognition and evaluation of patients with inherited serum thyroid hormone-binding protein mutations.
|
Academic Article
|
Interconnection between circadian clocks and thyroid function.
|
Academic Article
|
Very Severe Resistance to Thyroid Hormone ß in One of Three Affected Members of a Family with a Novel Mutation in the THRB Gene.
|
Academic Article
|
Increased Anaplastic Lymphoma Kinase Activity Induces a Poorly Differentiated Thyroid Carcinoma in Mice.
|
Academic Article
|
Class III PI3K Vps34 Controls Thyroid Hormone Production by Regulating Thyroglobulin Iodination, Lysosomal Proteolysis, and Tissue Homeostasis.
|
Academic Article
|
Intracerebroventricular administration of the thyroid hormone analog TRIAC increases its brain content in the absence of MCT8.
|
Academic Article
|
Free Thyroxine Concentrations in Sera of Individuals with Familial Dysalbuminemic Hyperthyroxinemia: A Comparison of Three Methods of Measurement.
|
Academic Article
|
Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel MCT8 Variants.
|
Academic Article
|
Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism.
|
Academic Article
|
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
|
Academic Article
|
Nonautoimmune Hyperthyroidism Caused by a Somatic Mosaic GNAS Mutation Involving Part of the Thyroid Gland.
|
Academic Article
|
Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHß.
|
Academic Article
|
A Novel G385E Variant in the Cold Region of the T3-Binding Domain of Thyroid Hormone Receptor Beta Gene and Investigations to Assess Its Clinical Significance.
|
Academic Article
|
Re: "Goiter in Residents of Salta, Argentina: An Artistic Rendition" by Jonklaas et al. (Thyroid 2020:30;34-36. DOI: 10.1089/thy.2019.0639).
|
Academic Article
|
Intranasal delivery of Thyroid hormones in MCT8 deficiency.
|
Academic Article
|
Mice Hypomorphic for Keap1, a Negative Regulator of the Nrf2 Antioxidant Response, Show Age-Dependent Diffuse Goiter with Elevated Thyrotropin Levels.
|
Academic Article
|
Human Type 1 Iodothyronine Deiodinase (DIO1) Mutations Cause Abnormal Thyroid Hormone Metabolism.
|
Academic Article
|
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation.
|
Academic Article
|
Early Diagnosis and Treatment of an Infant with a Novel Thyroid Hormone Receptor a Gene (pC380SfsX9) Mutation.
|
Academic Article
|
SWI/SNF Complex Mutations Promote Thyroid Tumor Progression and Insensitivity to Redifferentiation Therapies.
|
Academic Article
|
Increased Hepatic Fat Content in Patients with Resistance to Thyroid Hormone Beta.
|
Academic Article
|
Resistance to Thyroid Hormone Beta: A Focused Review.
|
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.
|
Academic Article
|
Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism.
|
Academic Article
|
XB130 Deficiency Causes Congenital Hypothyroidism in Mice due to Disorganized Apical Membrane Structure and Function of Thyrocytes.
|
Academic Article
|
Triiodothyroacetic Acid Cross-Reacts With Measurement of Triiodothyronine (T3) on Various Immunoassay Platforms.
|
Academic Article
|
XB130 Plays an Essential Role in Folliculogenesis Through Mediating Interactions Between Microfilament and Microtubule Systems in Thyrocytes.
|
Academic Article
|
Pathogenesis of Multinodular Goiter in Elderly XB130-Deficient Mice: Alteration of Thyroperoxidase Affinity with Iodide and Hydrogen Peroxide.
|
Academic Article
|
TSHB R75G is a founder variant and prevalent cause of low or undetectable TSH in Indian Jews.
|
Academic Article
|
Severe Resistance to Thyroid Hormone Beta in a Patient with Athyreosis.
|
Academic Article
|
Thyroidal Transcriptomic Profiles of Pathoadaptive Responses to Congenital Hypothyroidism in XB130 Knockout Mice.
|
Academic Article
|
AAV9-MCT8 Delivery at Juvenile Stage Ameliorates Neurological and Behavioral Deficits in a Mouse Model of MCT8-Deficiency.
|
Academic Article
|
A Novel Pathogenic Variant in PAX8 Leads to Familial Congenital Hypothyroidism.
|
Academic Article
|
Maintaining the thyroid gland in mutant thyroglobulin-induced hypothyroidism requires thyroid cell proliferation that must continue in adulthood.
|
Academic Article
|
Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).
|
Academic Article
|
Transplantable human thyroid organoids generated from embryonic stem cells to rescue hypothyroidism.
|
Academic Article
|
Foxe1 Deletion in the Adult Mouse Is Associated With Increased Thyroidal Mast Cells and Hypothyroidism.
|
Academic Article
|
Iodotyrosines Are Biomarkers for Preclinical Stages of Iodine-Deficient Hypothyroidism in Dehal1-Knockout Mice.
|
Concept
|
Cellular Reprogramming Techniques
|
Concept
|
Kelch-Like ECH-Associated Protein 1
|
Concept
|
Homeobox Protein Nkx-2.5
|
Concept
|
Serum Albumin, Human
|
Concept
|
Dual Oxidases
|
Concept
|
Symptom Assessment
|
Concept
|
Myeloid Cell Leukemia Sequence 1 Protein
|
Concept
|
Calcineurin Inhibitors
|
Grant
|
3RD INTERNATL WORKSHOP ON RESISTANCE TO THYROID HORMONE
|
Academic Article
|
Endoplasmic reticulum stress in the intestinal epithelium initiates purine metabolite synthesis and promotes Th17 cell differentiation in the gut.
|
Academic Article
|
Effect of the Fetal THRB Genotype on the Placenta.
|
Academic Article
|
Perturbation of endoplasmic reticulum proteostasis triggers tissue injury in the thyroid gland.
|
Academic Article
|
Increased cardiovascular morbidity and mortality in patients with resistance to thyroid hormone.
|
Academic Article
|
ASIC1a affects hypothalamic signaling and regulates the daily rhythm of body temperature in mice.
|
Academic Article
|
The Relationship Between Fetal THRB Genotype and Maternal Thyroid Function.
|
Academic Article
|
Impaired T3 uptake and action in MCT8-deficient cerebral organoids underlie Allan-Herndon-Dudley syndrome.
|