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Weiss, Roy Emanuel

One or more keywords matched the following items that are connected to Weiss, Roy Emanuel

Item Type	Name
Concept	Thyroxine-Binding Proteins
Concept	Thyroxine
Concept	Thyroxine-Binding Globulin
Academic Article	Multiple genetic factors in the heterogeneity of thyroid hormone resistance.
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	Thyrotropin regulation by thyroid hormone in thyroid hormone receptor beta-deficient mice.
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.
Academic Article	Mice deficient in the steroid receptor co-activator 1 (SRC-1) are resistant to thyroid hormone.
Academic Article	Thyroid hormone action on liver, heart, and energy expenditure in thyroid hormone receptor beta-deficient mice.
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	Clear fluid from a thyroid cyst.
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	Congenital hypothyroidism in a child with unsuspected familial dysalbuminemic hyperthyroxinemia caused by a mutation (R218H) in the human albumin gene.
Academic Article	Specificity of thyroid hormone receptor subtype and steroid receptor coactivator-1 on thyroid hormone action.
Academic Article	Thyroid function in mice with compound heterozygous and homozygous disruptions of SRC-1 and TIF-2 coactivators: evidence for haploinsufficiency.
Academic Article	RXR receptor agonist suppression of thyroid function: central effects in the absence of thyroid hormone receptor.
Academic Article	Familial dysalbuminemic hyperthyroxinemia: a rare example of albumin polymorphism and its rapid molecular diagnosis.
Academic Article	Thyroid function and effect of aging in combined hetero/homozygous mice deficient in thyroid hormone receptors alpha and beta genes.
Academic Article	Thyroid function tests and neurocognitive functioning in children referred for attention deficit/hyperactivity disorder.
Academic Article	Neonatal detection of generalized resistance to thyroid hormone.
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	Thyroid hormone receptor a and regulation of type 3 deiodinase.
Academic Article	Role of type 2 deiodinase in response to acute lung injury (ALI) in mice.
Academic Article	The interaction between nuclear receptor corepressor and histone deacetylase 3 regulates both positive and negative thyroid hormone action in vivo.
Academic Article	Human thyroxine-binding globulin gene: complete sequence and transcriptional regulation.
Academic Article	The nuclear receptor corepressor (NCoR) controls thyroid hormone sensitivity and the set point of the hypothalamic-pituitary-thyroid axis.
Academic Article	Mosaicism of a thyroid hormone receptor-beta gene mutation in resistance to thyroid hormone.
Academic Article	Pituitary-thyroid setpoint and thyrotropin receptor expression in consomic rats.
Academic Article	Molecular basis of inherited thyroxine-binding globulin defects.
Academic Article	Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred.
Academic Article	An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families.
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	Complete deficiency of thyroxine-binding globulin (TBG-CD Buffalo) caused by a new nonsense mutation in the thyroxine-binding globulin gene.
Academic Article	Genetic analysis reveals different functions for the products of the thyroid hormone receptor alpha locus.
Academic Article	Temperature homeostasis in transgenic mice lacking thyroid hormone receptor-alpha gene products.
Academic Article	Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice.
Academic Article	"They have ears but do not hear" (Psalms 135:17): non-thyroid hormone receptor beta (non-TRbeta) resistance to thyroid hormone.
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	Delayed development of specific thyroid hormone-regulated events in transthyretin null mice.
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 novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction.
Academic Article	Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism.
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	Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism.

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Thyroxine