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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
Heterozygote
Academic Article
Thyroid function in mice with compound heterozygous and homozygous disruptions of SRC-1 and TIF-2 coactivators: evidence for haploinsufficiency.
Academic Article
Thyroid function and effect of aging in combined hetero/homozygous mice deficient in thyroid hormone receptors alpha and beta genes.
Academic Article
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism.
Academic Article
Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion.
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
Repulsive separation of the cytoplasmic ends of transmembrane helices 3 and 6 is linked to receptor activation in a novel thyrotropin receptor mutant (M626I).
Academic Article
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families.
Academic Article
A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism.
Academic Article
Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations.
Academic Article
Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism.
Search Criteria
Heterozygote