3.2.1.62 Brain Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=4287968&form=6&db=m [On cerebrosidase of the glial tissue of brain tumors] diagnostic usage,ongoing research,unassigned 1,4,0 3.2.1.62 Brain Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=4935035&form=6&db=m [The cerebrosidase activity of the human brain and brain tumors] diagnostic usage,ongoing research,unassigned 3,4,0 3.2.1.62 Colonic Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8574790&form=6&db=m Activity of the rat lactase gene promoter in transfected human colon cancer cells. ongoing research,unassigned 4,0 3.2.1.62 Colonic Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17350584&form=6&db=m Novel fucogangliosides found in human colon adenocarcinoma tissues by means of glycomic analysis. diagnostic usage,ongoing research,unassigned 1,1,0 3.2.1.62 Colorectal Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17478481&form=6&db=m Genotyping of the lactase-phlorizin hydrolase c/t-13910 polymorphism by means of a new rapid denaturing high-performance liquid chromatography-based assay in healthy subjects and colorectal cancer patients. causal interaction,diagnostic usage,ongoing research,therapeutic application 3,3,2,1 3.2.1.62 Cryptococcosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22072709&form=6&db=m Quality control of fungus-specific glucosylceramide in Cryptococcus neoformans by endoglycoceramidase-related protein 1 (EGCrP1). unassigned - 3.2.1.62 Gangliosidosis, GM1 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=819652&form=6&db=m Krabbe's globoid cell leucodystrophy. Studies on galactosylceramide beta-galactosidase and non-specific beta-galactosidase of leucocytes, cultured skin fibroblasts, and amniotic fluid cells. diagnostic usage,therapeutic application,unassigned 3,1,0 3.2.1.62 Gastrointestinal Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=108036&form=6&db=m Immunoelectrophoretic studies on human small intestinal brush border proteins. A quantitative study of brush border enzymes from single small intestinal biopsies. ongoing research,unassigned 1,0 3.2.1.62 Gaucher Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33446243&form=6&db=m Cross-talks among GBA mutations, glucocerebrosidase, and ?-synuclein in GBA-associated Parkinson's disease and their targeted therapeutic approaches: a comprehensive review. causal interaction,therapeutic application,unassigned 3,1,0 3.2.1.62 Genetic Diseases, Inborn http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30813293&form=6&db=m Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives. causal interaction,unassigned 4,0 3.2.1.62 Glioma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=5822027&form=6&db=m [On the cerebrosidase activity of brain gliomas] diagnostic usage,ongoing research,unassigned 3,1,0 3.2.1.62 Immunoglobulin Light-chain Amyloidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10620102&form=6&db=m Systemic AL amyloidosis in Gaucher disease. A case report and review of the literature. diagnostic usage,ongoing research,unassigned 1,1,0 3.2.1.62 Influenza, Human http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10075706&form=6&db=m Hierarchy of sorting signals in chimeras of intestinal lactase-phlorizin hydrolase and the influenza virus hemagglutinin. therapeutic application,unassigned 1,0 3.2.1.62 lactase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8514062&form=6&db=m Immunocytochemical heterogeneity of lactase-phlorizin hydrolase in adult lactase deficiency. causal interaction,diagnostic usage,ongoing research,unassigned 4,2,4,0 3.2.1.62 lactase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9758622&form=6&db=m Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene. causal interaction,unassigned 3,0 3.2.1.62 lactase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30813293&form=6&db=m Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives. causal interaction,unassigned 4,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1902057&form=6&db=m Structure of the chromosomal gene and cDNAs coding for lactase-phlorizin hydrolase in humans with adult-type hypolactasia or persistence of lactase. therapeutic application,unassigned 1,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1916106&form=6&db=m Lactose intolerance and the genetic regulation of intestinal lactase-phlorizin hydrolase. causal interaction,diagnostic usage,ongoing research,unassigned 4,2,1,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1976654&form=6&db=m Biogenesis of intestinal lactase-phlorizin hydrolase in adults with lactose intolerance. Evidence for reduced biosynthesis and slowed-down maturation in enterocytes. causal interaction,unassigned 2,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8514062&form=6&db=m Immunocytochemical heterogeneity of lactase-phlorizin hydrolase in adult lactase deficiency. causal interaction,diagnostic usage,ongoing research,unassigned 4,2,4,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11332711&form=6&db=m Molecular and cellular aspects and regulation of intestinal lactase-phlorizin hydrolase. causal interaction,unassigned 4,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11788828&form=6&db=m Identification of a variant associated with adult-type hypolactasia. causal interaction,unassigned 1,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12692047&form=6&db=m Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia. causal interaction,diagnostic usage,unassigned 2,2,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16301215&form=6&db=m T-13910 DNA variant associated with lactase persistence interacts with Oct-1 and stimulates lactase promoter activity in vitro. causal interaction,unassigned 1,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16373956&form=6&db=m The myth of increased lactose intolerance in African-Americans. causal interaction,diagnostic usage,unassigned 3,3,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16391332&form=6&db=m Genotyping of the lactase-phlorizin hydrolase -13910 polymorphism by LightCycler PCR and implications for the diagnosis of lactose intolerance. causal interaction,diagnostic usage,unassigned 3,4,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17015546&form=6&db=m The effects of adult-type hypolactasia on body height growth and dietary calcium intake from childhood into young adulthood: a 21-year follow-up study--the Cardiovascular Risk in Young Finns Study. unassigned - 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17133732&form=6&db=m Hypolactasia as a molecular basis of lactose intolerance. causal interaction,ongoing research,unassigned 2,1,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17478481&form=6&db=m Genotyping of the lactase-phlorizin hydrolase c/t-13910 polymorphism by means of a new rapid denaturing high-performance liquid chromatography-based assay in healthy subjects and colorectal cancer patients. causal interaction,diagnostic usage,ongoing research,therapeutic application 3,3,2,1 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17934640&form=6&db=m Correlation between lactose absorption and the C/T-13910 and G/A-22018 mutations of the lactase-phlorizin hydrolase (LCT) gene in adult-type hypolactasia. unassigned - 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24361938&form=6&db=m Detecting and measuring selection from gene frequency data. causal interaction,diagnostic usage,unassigned 3,1,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25281930&form=6&db=m Lactose intolerance genetic testing: is it useful as routine screening? Results on 1426 south-central Italy patients. causal interaction,diagnostic usage,therapeutic application,unassigned 3,2,1,0 3.2.1.62 Lactose Intolerance http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28443769&form=6&db=m The C/C_????? and G/G_????? Genotypes for Adult-type Hypolactasia are not Associated with Inflammatory Bowel Disease. causal interaction,diagnostic usage,ongoing research,unassigned 1,2,3,0 3.2.1.62 Proteinuria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10620102&form=6&db=m Systemic AL amyloidosis in Gaucher disease. A case report and review of the literature. diagnostic usage,ongoing research,unassigned 1,1,0 3.2.1.62 Vesicular Stomatitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16230359&form=6&db=m A novel type of detergent-resistant membranes may contribute to an early protein sorting event in epithelial cells. ongoing research,unassigned 2,0