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Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts during infancy and presenile cataracts in the adult population. 再加上，我们可以发Galactokinase 1 蛋白 (66) 和 Galactokinase 1 试剂盒 (8)和数多这个蛋白质的别的产品。
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The GALK1 gene was included in this interval and direct sequencing.
Data indicate taht the interactions between galactokinase (GALK) and its potential inhibitors by molecular dynamics simulations.
The study highlighted the importance of GALK gene analysis in diagnosis of galactosemia in Indian population.
A possible mechanism for the unfolding caused by the Pro(28)Thr (显示 TRH 抗体) point mutation of human galactokinase.
Pathogenic mutations in GALK1 that are responsible for autosomal recessive congenital cataracts in consanguineous Pakistani families, are reported.
2 new GALK1 mutations near the ATP-binding site were found in a homozygotic Turkish immigrant: S142I and G148C.
In this northern Italian population age-related cataract does not appear to be associated with GALK1 alleles.
structure and function of galactokinase, and role in type II galactosemia [review]
Mutations in GALK1 resulted in reduction of GALK activity and caused GALK deficiency.
These results suggest that the elevated GALK1 activity resulted from enhanced gene expression, due to nucleotide variation within GALK1 promoter
Egr-1 (显示 EGR1 抗体) and galactokinase have roles in a developmentally regulated chain to prepare the neonate for suckling
Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts during infancy and presenile cataracts in the adult population.
, galactose kinase