lactase

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  • noun

Synonyms for lactase

any of a group of enzymes (trade name Lactaid) that hydrolyze lactose to glucose and galactose

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References in periodicals archive ?
The top three genes with a high absolute value of coefficient factor, namely, 2583 (B4GALNT1), 2720 (GLB1), and 3074 (HEXB), are selected to represent genes for this canonical variable (Figure 4(b), Table 1).
The responsible gene of GMl-gangliosidosis, GLB1, contains 16 exons and encodes by alternative splicing to the lysosomal enzyme [beta]-galactosidase and the elastin binding protein [9].
One candidate is GLB1, since this enzyme cleaves terminal [beta]-linked galactosyl residues from gangliosides.
cDNA clone of a wheat storage globulin, Glb1, linked to islet damage," The Journal of Biological Chemistry, vol.
Almost all the proteins that were upregulated at all time points are classified into the fourth cluster including GLB1, AKT1, COQ7, INSR, and PIK3R1.
Yang et al., "Overexpression of the novel senescence marker [beta]-galactosidase (GLB1) in prostate cancer predicts reduced PSA recurrence," PLoS ONE, vol.
El gen que codifica la enzima [beta]-galactosidasa (GLB1) esta ubicado en el brazo corto del cromosoma 3 (3p21.33) [7].
As shown in Table 2, there were 2 nominally replicable pathways (based on 50kb flanking) enriched in alcohol dependence-related genes in both EAs (0.015 [less than or equal to] p [less than or equal to] 0.035) and AAs (0.025 [less than or equal to] p [less than or equal to] 0.050): the 'Na+/Cl- dependent neurotransmitter transporters' pathway (#15) (specified above), and the 'other glycan degradation' pathway (#20) (AGA, HEXA, HEXB, ENGASE, FUCA2, FUCA1, MANBA, GLB1, MAN2C1, MAN2B2, NEU1, NEU3, MAN2B1, NEU2, GBA, and NEU4).
The disorder is "caused by mutations in the GLB1 gene, which encodes an enzyme called beta-galactosidase necessary for recycling of a molecule (GM1-ganglioside) in neurons.
Kelly et al., "A type 1 diabetes-related protein from wheat (Triticum aestivum): cDNA clone of a wheat storage globulin, Glb1, linked to islet damage," The Journal of Biological Chemistry, vol.
A genetic defect has been identified in the N-acetyl-galactosamine-6-sulphate sulphatase (GALNS gene) in Morquio's syndrome type IVA or beta-galactosidase (GLB1 gene) in Morquio's syndrome type IVB.