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Asymmetric spermatic cord vessel enhancement on CT: a sign of epididymitis or testicular neoplasm.
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Dumitrescu, Alexandra M.
One or more keywords matched the following items that are connected to
Dumitrescu, Alexandra M.
Item Type
Name
Concept
DNA-Binding Proteins
Concept
Thyroxine-Binding Proteins
Concept
RNA-Binding Proteins
Concept
GTP-Binding Protein alpha Subunits, Gs
Concept
Iron-Binding Proteins
Concept
Organic Cation Transport Proteins
Concept
Membrane Transport Proteins
Academic Article
Complete thyroxine-binding globulin (TBG) deficiency in two families without mutations in coding or promoter regions of the TBG genes: in vitro demonstration of exon skipping.
Academic Article
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism.
Academic Article
Novel biological and clinical aspects of thyroid hormone metabolism.
Academic Article
Syndromes of reduced sensitivity to thyroid hormone: genetic defects in hormone receptors, cell transporters and deiodination.
Academic Article
Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3,5,3'-triiodo-L-thyronine.
Academic Article
The syndrome of inherited partial SBP2 deficiency in humans.
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
Selenium supplementation fails to correct the selenoprotein synthesis defect in subjects with SBP2 gene mutations.
Academic Article
Inherited defects of thyroid hormone metabolism.
Academic Article
Distinct roles of deiodinases on the phenotype of Mct8 defect: a comparison of eight different mouse genotypes.
Academic Article
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice.
Academic Article
Thyroid hormone-regulated mouse cerebral cortex genes are differentially dependent on the source of the hormone: a study in monocarboxylate transporter-8- and deiodinase-2-deficient mice.
Academic Article
The syndromes of reduced sensitivity to thyroid hormone.
Academic Article
Changes in thyroid status during perinatal development of MCT8-deficient male mice.
Academic Article
Placenta passage of the thyroid hormone analog DITPA to male wild-type and Mct8-deficient mice.
Academic Article
Inherited defects of thyroid hormone-cell-membrane transport: review of recent findings.
Academic Article
Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levels.
Academic Article
Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 inactivation.
Academic Article
Inherited defects in thyroid hormone cell-membrane 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
An Essential Physiological Role for MCT8 in Bone in Male Mice.
Academic Article
A Novel Homozygous Selenocysteine Insertion Sequence Binding Protein 2 (SECISBP2, SBP2) Gene Mutation in a Turkish Boy.
Academic Article
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families.
Academic Article
Thyroid Hormone Metabolism Defects in a Mouse Model of SBP2 Deficiency.
Academic Article
Role of the Thyroid Gland in Expression of the Thyroid Phenotype of Sbp2-Deficient Mice.
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
Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations.
Academic Article
Selenocysteine insertion sequence binding protein 2 (Sbp2) in the sex-specific regulation of selenoprotein gene expression in mouse pancreatic islets.
Academic Article
Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism.
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Carrier Proteins