Item Type | Name |
Concept
|
Acne Vulgaris
|
Concept
|
Abortion, Spontaneous
|
Concept
|
Adenocarcinoma
|
Concept
|
Addison Disease
|
Concept
|
Adenoma, Chromophobe
|
Concept
|
Amyloidosis
|
Concept
|
Adrenal Gland Neoplasms
|
Concept
|
Arrhythmias, Cardiac
|
Concept
|
Adenocarcinoma, Papillary
|
Concept
|
Adenoma
|
Concept
|
Acromegaly
|
Concept
|
Amenorrhea
|
Concept
|
Brain Damage, Chronic
|
Concept
|
Agranulocytosis
|
Concept
|
Albuminuria
|
Concept
|
Blood Protein Disorders
|
Concept
|
Carcinoma, Papillary
|
Concept
|
Central Nervous System Diseases
|
Concept
|
Chiari-Frommel Syndrome
|
Concept
|
Aneuploidy
|
Concept
|
Carcinoma
|
Concept
|
Autoimmune Diseases
|
Concept
|
Constipation
|
Concept
|
Celiac Disease
|
Concept
|
Diabetes Mellitus, Experimental
|
Concept
|
Attention Deficit Disorder with Hyperactivity
|
Concept
|
DNA Damage
|
Concept
|
Bone Neoplasms
|
Concept
|
Athetosis
|
Concept
|
Developmental Disabilities
|
Concept
|
Child Behavior Disorders
|
Concept
|
Fetal Diseases
|
Concept
|
Foot Diseases
|
Concept
|
Colonic Neoplasms
|
Concept
|
Cell Transformation, Neoplastic
|
Concept
|
Chromosome Deletion
|
Concept
|
Cardiovascular Diseases
|
Concept
|
Goiter
|
Concept
|
Growth Disorders
|
Concept
|
Chorea
|
Concept
|
Hearing Loss, Sensorineural
|
Concept
|
Hypothermia
|
Concept
|
Cushing Syndrome
|
Concept
|
Endocrine System Diseases
|
Concept
|
Congenital Hypothyroidism
|
Concept
|
Cystinosis
|
Concept
|
Dose-Response Relationship, Radiation
|
Concept
|
Fetal Resorption
|
Concept
|
Chondrodysplasia Punctata
|
Concept
|
Chronic Disease
|
Concept
|
Deafness
|
Concept
|
Diseases in Twins
|
Concept
|
Fatty Liver
|
Concept
|
Factitious Disorders
|
Concept
|
Muscle Hypotonia
|
Concept
|
Neoplasms, Radiation-Induced
|
Concept
|
Obesity
|
Concept
|
Dose-Response Relationship, Drug
|
Concept
|
Dwarfism, Pituitary
|
Concept
|
Edema
|
Concept
|
Liver Neoplasms
|
Concept
|
Eosinophilia
|
Concept
|
Hyperparathyroidism
|
Concept
|
Gigantism
|
Concept
|
Goiter, Endemic
|
Concept
|
Lactation Disorders
|
Concept
|
Lung Diseases
|
Concept
|
Carcinoma, Hepatocellular
|
Concept
|
Hyperplasia
|
Concept
|
Hypoproteinemia
|
Concept
|
Movement Disorders
|
Concept
|
Nerve Compression Syndromes
|
Concept
|
Protein Denaturation
|
Concept
|
Nelson Syndrome
|
Concept
|
Goiter, Nodular
|
Concept
|
Graves Disease
|
Concept
|
Intellectual Disability
|
Concept
|
Muscular Atrophy
|
Concept
|
Hepatitis
|
Concept
|
Paralysis
|
Concept
|
Parathyroid Diseases
|
Concept
|
Nervous System Diseases
|
Concept
|
Leg Dermatoses
|
Concept
|
Ovarian Diseases
|
Concept
|
Lung Neoplasms
|
Concept
|
Sleep Stages
|
Concept
|
Pheochromocytoma
|
Concept
|
Pituitary Diseases
|
Concept
|
Pregnancy in Diabetics
|
Concept
|
Genetic Markers
|
Concept
|
Glycogen Storage Disease Type I
|
Concept
|
Glutens
|
Concept
|
Hyperthyroidism
|
Concept
|
Hypopituitarism
|
Concept
|
Hypothyroidism
|
Concept
|
Psychomotor Disorders
|
Concept
|
Puerperal Disorders
|
Concept
|
Quadriplegia
|
Concept
|
Puberty, Precocious
|
Concept
|
Insulin Resistance
|
Concept
|
Sleep Deprivation
|
Concept
|
Thyroid Diseases
|
Concept
|
Thyroiditis, Autoimmune
|
Concept
|
Hypogonadism
|
Concept
|
Thyrotoxicosis
|
Concept
|
Trophoblastic Neoplasms
|
Concept
|
Thyroid Crisis
|
Concept
|
Thyroiditis
|
Concept
|
Syndrome
|
Concept
|
Kidney Failure, Chronic
|
Concept
|
Weight Loss
|
Concept
|
Turner Syndrome
|
Concept
|
LDL-Receptor Related Protein-Associated Protein
|
Concept
|
Weight Gain
|
Concept
|
Myxedema
|
Concept
|
Cardiomyopathies
|
Concept
|
Neoplasm Metastasis
|
Concept
|
Neoplasms, Experimental
|
Concept
|
Sequence Deletion
|
Concept
|
Hepatoblastoma
|
Concept
|
Thyroid Hormone Resistance Syndrome
|
Concept
|
Hyperthyroxinemia, Familial Dysalbuminemic
|
Concept
|
Oxidative Stress
|
Concept
|
Adenocarcinoma, Follicular
|
Concept
|
Multiple Endocrine Neoplasia Type 2a
|
Concept
|
Jet Lag Syndrome
|
Concept
|
Genetic Association Studies
|
Concept
|
Megalencephaly
|
Concept
|
Endoplasmic Reticulum Stress
|
Concept
|
Genetic Diseases, X-Linked
|
Concept
|
Mental Retardation, X-Linked
|
Concept
|
Congenital Disorders of Glycosylation
|
Concept
|
Genetic Diseases, Inborn
|
Concept
|
Myopathies, Structural, Congenital
|
Concept
|
Polycystic Ovary Syndrome
|
Concept
|
Prenatal Exposure Delayed Effects
|
Concept
|
Postoperative Complications
|
Concept
|
Pregnancy Complications
|
Concept
|
Pseudohypoparathyroidism
|
Concept
|
Respiratory Distress Syndrome, Newborn
|
Concept
|
Structure-Activity Relationship
|
Concept
|
Congenital Hyperinsulinism
|
Concept
|
Acute Lung Injury
|
Concept
|
Lingual Goiter
|
Concept
|
Tooth Abnormalities
|
Concept
|
Pituitary ACTH Hypersecretion
|
Concept
|
Uremia
|
Concept
|
Autoimmunity
|
Concept
|
NF-E2-Related Factor 2
|
Concept
|
Thyroid Neoplasms
|
Concept
|
Nystagmus, Congenital
|
Concept
|
Low Density Lipoprotein Receptor-Related Protein-2
|
Concept
|
Chemical and Drug Induced Liver Injury
|
Concept
|
Dystonic Disorders
|
Concept
|
Thyroid Dysgenesis
|
Concept
|
Ventilator-Induced Lung Injury
|
Concept
|
Bone Diseases, Developmental
|
Concept
|
Depression, Chemical
|
Concept
|
Drug Eruptions
|
Concept
|
Diabetes Mellitus
|
Concept
|
Disease Models, Animal
|
Concept
|
Fetal Death
|
Concept
|
Heart Rate
|
Concept
|
Hyperkinesis
|
Concept
|
Hyperthyroxinemia
|
Concept
|
Infant, Newborn, Diseases
|
Concept
|
Infant, Premature, Diseases
|
Concept
|
Metabolism, Inborn Errors
|
Concept
|
Neoplasm Invasiveness
|
Concept
|
Pituitary Neoplasms
|
Concept
|
Mutagenesis, Insertional
|
Concept
|
Age of Onset
|
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
|
Neurocognitive characteristics of individuals with resistance to thyroid hormone: comparisons with individuals with attention-deficit hyperactivity disorder.
|
Academic Article
|
Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type I.
|
Academic Article
|
Structure-function relationships of two loss-of-function mutations of the thyrotropin receptor gene.
|
Academic Article
|
Mice with a targeted mutation in the thyroid hormone beta receptor gene exhibit impaired growth and resistance to thyroid hormone.
|
Academic Article
|
Pseudomalabsorption of levothyroxine.
|
Academic Article
|
Preferential megalin-mediated transcytosis of low-hormonogenic thyroglobulin: a control mechanism for thyroid hormone release.
|
Academic Article
|
Defective thyroglobulin storage in LDL receptor-associated protein-deficient mice.
|
Academic Article
|
Elevated serum thyroglobulin level in congenital thyroxine-binding globulin deficiency.
|
Academic Article
|
Mice deficient in dual oxidase maturation factors are severely hypothyroid.
|
Academic Article
|
The relationship between episodic variations of plasma prolactin and REM-non-REM cyclicity is an artifact.
|
Academic Article
|
Continuing occurrence of thyroid carcinoma after irradiation to the neck in infancy and childhood.
|
Academic Article
|
Stanniocalcin 1 induction by thyroid hormone depends on thyroid hormone receptor ß and phosphatidylinositol 3-kinase activation.
|
Academic Article
|
Relationship of oligosaccharide modification to the cause of serum thyroxine-binding globulin excess.
|
Academic Article
|
Chiari-Frommel syndrome in a patient with primary adrenocortical insufficiency.
|
Academic Article
|
Familial thyroxine-binding globulin deficiency in a patient with Turner's syndrome (XO). Genetic study of a kindred.
|
Academic Article
|
Hyperthyroidism and adult celiac disease.
|
Academic Article
|
Thyroid hormone relationships between maternal and fetal circulations in human pregnancy at term: a study in patients with normal and abnormal thyroid function.
|
Academic Article
|
White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene.
|
Academic Article
|
The effect of dexamethasone on the 24-hour profiles of adrenocorticotropin and cortisol in Cushing's syndrome.
|
Academic Article
|
Serum thyrotropin and prolactin in the syndrome of generalized resistance to thyroid hormone: responses to thyrotropin-releasing hormone stimulation and short term triiodothyronine suppression.
|
Academic Article
|
Metabolism of thyroxine-binding globulin in man. Abnormal rate of synthesis in inherited thyroxine-binding globulin deficiency and excess.
|
Academic Article
|
The action of thyroid hormone.
|
Academic Article
|
Study of four new kindreds with inherited thyroxine-binding globulin abnormalities. Possible mutations of a single gene locus.
|
Academic Article
|
Coexisting thyroid and parathyroid disease--are they related?
|
Academic Article
|
Obatoclax overcomes resistance to cell death in aggressive thyroid carcinomas by countering Bcl2a1 and Mcl1 overexpression.
|
Academic Article
|
Modeling Psychomotor Retardation using iPSCs from MCT8-Deficient Patients Indicates a Prominent Role for the Blood-Brain Barrier.
|
Academic Article
|
NFE2-Related Transcription Factor 2 Coordinates Antioxidant Defense with Thyroglobulin Production and Iodination in the Thyroid Gland.
|
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
|
Thyroidal Transcriptomic Profiles of Pathoadaptive Responses to Congenital Hypothyroidism in XB130 Knockout Mice.
|
Concept
|
Thyroid Carcinoma, Anaplastic
|
Grant
|
THYROID PHYSIOLOGY STUDIES OF INHERITED DISORDERS
|
Grant
|
Thyroid Physiology Studies of Inherited Disorders
|
Academic Article
|
The Relationship Between Fetal THRB Genotype and Maternal Thyroid Function.
|