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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
Iodide Peroxidase
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
A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport.
Academic Article
Role of type 2 deiodinase in response to acute lung injury (ALI) in mice.
Academic Article
The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation.
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
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
Changes in thyroid status during perinatal development of MCT8-deficient male mice.
Academic Article
An Essential Physiological Role for MCT8 in Bone in Male Mice.
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
Paradigms of Dynamic Control of Thyroid Hormone Signaling.
Academic Article
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
Academic Article
Human Type 1 Iodothyronine Deiodinase (DIO1) Mutations Cause Abnormal Thyroid Hormone Metabolism.
Academic Article
Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism.
Academic Article
Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).
Search Criteria
Peroxidase