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Integrating transcriptome and metabolome reveals sex-dependent meat quality regulation in Qiandongnan Xiaoxiang chickens. [PDF]
BMC GenomicsHao M, Xie Y, Li C.
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A New Variant of Galactokinase
Human Heredity, 1982A new variant of human galactokinase activity is described. This enzyme shows reduced catalytic activity both in red and white blood cells, lower Km for ATPMg2-, and increased in vivo instability when compared to the normal enzyme. Thermostability and pH optimum are not modified.
MAGNANI, MAURO +3 more
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Galactokinase activity in Streptococcus thermophilus
Applied and Environmental Microbiology, 1985ATP-dependent phosphorylation of [14C]galactose by 11 strains of Streptococcus thermophilus indicated that these organisms possessed the Leloir enzyme, galactokinase (galK). Activities were 10 times higher in fully induced, galactose-fermenting (Gal+) strains than in galactose-nonfermenting (Gal-) strains.
Hutkins, Robert W. +2 more
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Galactokinase deficiency and mental retardation
The Journal of Pediatrics, 1979Abstract: Mental retardation has been previously associated with galactosemia resulting from a deficiency in a different enzyme, galactose-1-phosphate uridyl transferase. Cataracts are normally symptomatic of galactosemia, and are caused by galactose toxicity. Both severely retarded patients with galactosemia had cataracts.
S, Segal, J Y, Rutman, G W, Frimpter
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Functional studies of rat galactokinase
Journal of Biotechnology, 2009Galactokinase is an ATP-dependent enzyme that catalyzes the phosphorylation of galactose to form galactose-1-phosphate. The defect in human galactokinase can result in the disease of galactosemia. On the other hand, the control of galactose-1-phosphate production by inhibiting galactokinase is a potential therapy for another disease referred to as ...
Xiusheng, Chu +3 more
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Human Erythrocyte Galactokinase: A Population Survey
Human Heredity, 1982Erythrocyte galactokinase activity was measured in a random sample of 620 Italian individuals to estimate the frequency of the gene responsible for the form of galactosemia due to galactokinase deficiency. 3 individuals had an activity about one-half the normal value.
MAGNANI, MAURO +6 more
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Some inferences from galactokinase deficiency
Pediatrics, 1974The observations made by Olambiwonnu et al. in this issue on twins with galactokinase deficiency raise several issues of practical importance. The first point, which is not new but cannot be too often reemphasized, is the necessity to use a chemical reducing method, such as the Clinitest® tablet, for routine screening of urines for sugars.
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Galactokinase Deficiency in Twins
Pediatrics, 1974The recent article by Olabiwonnu et al., reporting two new cases of galactokinase deficiency, deserves comment. The authors reported the results of serum and urine studies for galactose and galactose derivatives on their patients while on a "galactose-free diet." The urine galactose and galactitol levels were rather high.
James A. Monteleone +3 more
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Galactokinase deficiency presenting as pseudotumor cerebri
The Journal of Pediatrics, 1975DISTURBANCES in galactose metabolism from deficiency of the enzyme galactose uridyl transferase may cause cataracts and liver and brain damage. The more recently discovered deficiency of galactokinase has been thought to be a benign condition other than causing cataracts.
N, Litman, A I, Kanter, L, Finberg
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