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707 Possible Causes for Glycolipids

  • Urinary Tract Infection

    P fimbriae , which attach to globoseries-type glycolipids found in the colon and urinary epithelium, are associated with pyelonephritis and cystitis and are found in many[emedicine.medscape.com] […] of the ABH blood antigens appear to be at higher risk for recurrent UTIs; this may occur because of a lack of specific glycosyltransferases that modify epithelial surface glycolipids[emedicine.medscape.com]

  • Dementia

    […] antigens, and although these pathways have been revised as new information was obtained, the basic premise was correct. 2 The primary structure of these antigens is either a glycolipid[ncbi.nlm.nih.gov] […] the mouth, gastrointestinal tract, lung, bladder, breast, uterine cervix, and prostate have ABH antigens, but these antigens are often missing from the glycoproteins and glycolipids[ncbi.nlm.nih.gov] Selectins, integrins, the IgSF, the cartilage link protein family, and sialomucins play a role in hematopoiesis. 16 , 60 RBCs, especially sickled red cells, contain sialylated glycolipids[ncbi.nlm.nih.gov]

  • Tuberculosis

    This glycolipid had previously been observed only in a smooth isolate of M. tuberculosis obtained in 1969 by Canetti in France.[doi.org] Recent studies clarified the unusual structures of arabinogalactan as well as of extractable cell wall lipids, such as trehalose-based lipooligosaccharides, phenolic glycolipids[ncbi.nlm.nih.gov] […] strains described thus far by having only a single copy of insertion sequence IS 1081 , an unusual composition of the direct repeat cluster, and a characteristic phenolic glycolipid[doi.org]

  • GM2 Gangliosidosis Variant AB

    Abstract GM2-gangliosidoses are neurological disorders caused by a genetic deficiency of either the beta-hexosaminidase A or the GM2 activator, a glycolipid binding protein[ncbi.nlm.nih.gov] Evidence is presented that this factor is defective in the AB-variant of infantile GM2 gangliosidosis which is characterized by an accumulation of glycolipids GM2 and GA2[wwww.unboundmedicine.com] Links PMC Free PDF PMC Free Full Text patent databases Authors , Source MeSH Enzyme Activation G(M2) Ganglioside Gangliosides Gangliosidoses Glycolipids Hexosaminidases Hot[wwww.unboundmedicine.com]

  • Fucosidosis

    Abstract Neutral glycolipids from the brain of a patient with Fucosidosis were analyzed and two complex glycolipids containing five and eight sugars were isolated from the[ncbi.nlm.nih.gov] A lack of enzyme activity results in an incomplete breakdown of glycolipids and glycoproteins.[ghr.nlm.nih.gov] With the lack of this enzyme activity, the result is incomplete breakdown of glycolipids and glycoproteins.[en.wikipedia.org]

  • Alpha-Galactosidase

    There is no urinary excretion of glycolipids or mucopolysaccharides. Yet this patient has an accumulation of material in his fibroblasts and renal cells.[ncbi.nlm.nih.gov] This enzyme is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins.[cloud-clone.com] […] differ from that in the pathway view due to the constraints in pathway layout Alpha-galactosidase A (GLA) (Bishop et al. 1986) removes the terminal galactose residue from glycolipids[reactome.org]

  • Schindler Disease, Type 1

    Mutations of this gene interfere with the ability of the enzyme to do its job in breaking down glycoproteins and glycolipids.[wiki.ggc.usg.edu] Category Inherited metabolic disease; Lysosomal storage disease Brite Human diseases [BR: br08402 ] Congenital disorders of metabolism Congenital disorders of lipid/glycolipid[kegg.jp] […] alpha-N-acetylgalactosaminidase.This enzyme works in the lysosomes (compartments within cells that digest and recycle materials) to help break down complexes called glycoproteins and glycolipids[rarediseases.info.nih.gov]

  • Fabry Disease

    Evidence indicates that these glycolipids can activate toll-like receptors, thus triggering inflammation and fibrosis cascades.[ncbi.nlm.nih.gov] These glycolipids accumulate in the lysosomes as a consequence of defects in the lysosomal hydrolase, α-galactosidase A.[themedicalbiochemistrypage.org] Klionsky: Fabry disease: Classification as a sphingolipidosis and partial characterization of a novel glycolipid.[whonamedit.com]

  • Schindler Disease

    Mutations of this gene interfere with the ability of the enzyme to do its job in breaking down glycoproteins and glycolipids.[wiki.ggc.usg.edu] Category Inherited metabolic disease; Lysosomal storage disease Brite Human diseases [BR: br08402 ] Congenital disorders of metabolism Congenital disorders of lipid/glycolipid[kegg.jp] […] metabolism of alpha-N-acetylgalactosaminidase-deficient fibroblasts using native and artificial glycolipids. ( 1418679 ) Klima B....Egge H. 1992 22 Lysosomal alpha-N-acetylgalactosaminidase[malacards.org]

  • Mycobacterium Leprae

    By enzyme-linked immunosorbent assay, C3 binds selectively to phenolic glycolipid-1 (PGL-1), a major surface molecule of the leprosy bacillus.[jem.rupress.org] […] leprae DNA was detected through quantitative polymerase chain reaction in nasal vestibule, nasal turbinate mucosa, and peripheral blood samples, along with anti-phenolic glycolipid[ncbi.nlm.nih.gov] […] to clarify the involvement of Rab5, Rab7, and trytophan aspartate-containing coat protein (TACO) from host macrophage and leprae lipoarabinomannan (Lep-LAM) and phenolic glycolipid[ncbi.nlm.nih.gov]

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