Alanine

iodothyronine deiodinase 2 ; Homo sapiens







6 Article(s)
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1 32436183 Thr92Ala polymorphism in the type 2 deiodinase gene: an evolutionary perspective. 2020 Dec 1
2 23193417 Thr92Ala polymorphism of human type 2 deiodinase gene (hD2) affects the development of Graves' disease, treatment efficiency, and rate of remission. 2012 3
3 15542398 Screening of SNPs at 18 positional candidate genes, located within the GD-1 locus on chromosome 14q23-q32, for susceptibility to Graves' disease: a TDT study. 2004 Nov 2
4 11897672 Substitution of cysteine for a conserved alanine residue in the catalytic center of type II iodothyronine deiodinase alters interaction with reducing cofactor. 2002 Apr 1
5 10698189 Substrate-induced down-regulation of human type 2 deiodinase (hD2) is mediated through proteasomal degradation and requires interaction with the enzyme's active center. 2000 Mar 1
6 11108274 The role of selenocysteine 133 in catalysis by the human type 2 iodothyronine deiodinase. 2000 Dec 2