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369 Possible Causes for PGL3b, glycosphingolipid

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  • Urinary Tract Infection

    Since the glycosphingolipids (GSLs) globotriaosylceramide (Gb3Cer) and globotetraosylceramide (Gb4Cer) are well-known receptors for Stx but also for P fimbriae, a major virulence[ncbi.nlm.nih.gov] Glycosphingolipids of human urinary tract epithelial cells as possible receptors for adhering Escherichia coli bacteria.[guiasalud.es]

    Missing: PGL3b
  • Vascular Dementia

    Abstract Fabry's disease, a rare X-linked disorder of glycosphingolipid metabolism, can present as an insidious dementia in middle or later life.[ncbi.nlm.nih.gov] This genetic disorder produces a deficiency of alpha-galactosidase A which results in the deposition of glycosphingolipids in blood vessel walls in the brain as well as in[ncbi.nlm.nih.gov]

    Missing: PGL3b
  • Barth Syndrome

    Chapter 35, Disorders of Phospholipid and Glycosphingolipid Synthesis; p. 485–495.[invitae.com] Chapter 35, Disorders of Phospholipid and Glycosphingolipid Synthesis; p. 485–495. Mangat, J, et al.[invitae.com]

    Missing: PGL3b
  • Arterial Thrombosis

    […] concentrations of circulating von Willebrand Factor and other endothelial cell adhesion molecules, ABO antigens are also present on several platelet surface glycoproteins and glycosphingolipids[ncbi.nlm.nih.gov]

    Missing: PGL3b
  • Staphylococcal Toxemia

    Accession Number : ADA332016 Title : Glycosphingolipids as Putative Receptor for Staphylococcal Enterotoxin-B in Cultured Human Kidney Cells.[dtic.mil]

    Missing: PGL3b
  • Gaucher Disease Type 1

    […] of biosynthesis of glycosphingolipids to counteract the catabolic defect (i.e. substrate reduction therapy).[ncbi.nlm.nih.gov] Abstract Gaucher disease type 1 (GD1) is an autosomal recessive lysosomal storage disorder, characterised by accumulation of glycosphingolipids in visceral organs.[ncbi.nlm.nih.gov] Abstract Gaucher disease is a rare autosomal recessive disorder of glycosphingolipid metabolism resulting from deficient activity of the lysosomal enzyme beta-glucocerebrosidase[ncbi.nlm.nih.gov]

    Missing: PGL3b
  • Proteinuria

    Abstract Fabry disease is a rare X-linked lysosomal storage disorder of glycosphingolipids, caused by the partial or complete deficiency of the lysosomal enzyme alpha-galactosidase[ncbi.nlm.nih.gov]

    Missing: PGL3b
  • Intoxication

    Finally, CT gavage produces an intact diarrheal response in knockout mice lacking GM1 even after additional reduction of glycosphingolipids.[ncbi.nlm.nih.gov] Inhibition of glycosphingolipid synthesis or sialylation in GM1-deficient C6 rat glioma cells results in sensitization to CT-mediated intoxication.[ncbi.nlm.nih.gov]

    Missing: PGL3b
  • Cholera

    Finally, CT gavage produces an intact diarrheal response in knockout mice lacking GM1 even after additional reduction of glycosphingolipids.[ncbi.nlm.nih.gov] Cholera toxin subunit B (CTB) is investigated to facilitate multifunctional glioma-targeted drug delivery by targeting the glycosphingolipid GM1 expressed in the blood-brain[ncbi.nlm.nih.gov] Inhibition of glycosphingolipid synthesis or sialylation in GM1-deficient C6 rat glioma cells results in sensitization to CT-mediated intoxication.[ncbi.nlm.nih.gov]

    Missing: PGL3b
  • Left Ventricular Hypertrophy

    A deficiency of this enzyme leads to the lysosomal accumulation of glycosphingolipids, which may cause left ventricular hypertrophy that is typically concentric and symmetric[ncbi.nlm.nih.gov] AFD is a rare X linked recessive disorder, resulting in a deficiency of the enzyme, α-galactosidase A, with subsequent glycosphingolipid accumulation.[heart.bmj.com]

    Missing: PGL3b

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