Results 111 to 120 of about 35,445 (258)

Convenient and rapid removal of detergent from glycolipids in detergent-resistant membrane microdomains

open access: yesJournal of Lipid Research, 2012
Although detergents are often essential in protocols, they are usually incompatible with further biochemical analysis. There are several methods for detergent removal, but the procedures are complicated or suffer from sample loss.
Yusuke Suzuki, Kazuya Kabayama
doaj   +1 more source

Identification of plasma glycosphingolipids as potential biomarkers for prostate cancer (PCA) status

open access: green, 2023
Ashley J. Snider   +16 more
openalex   +1 more source

Miglustat Reverts the Impairment of Synaptic Plasticity in a Mouse Model of NPC Disease [PDF]

open access: yes, 2016
Niemann-Pick type C disease is an autosomal recessive storage disorder, characterized by abnormal sequestration of unesterified cholesterol within the late endolysosomal compartment of cells and accumulation of gangliosides and other sphingolipids ...
Cardinale, A   +9 more
core   +4 more sources

Reduced sphingolipid hydrolase activities, substrate accumulation and ganglioside decline in Parkinson’s disease

open access: yesMolecular Neurodegeneration, 2019
Background Haploinsufficiency in the Gaucher disease GBA gene, which encodes the lysosomal glucocerebrosidase GBA, and ageing represent major risk factors for developing Parkinson’s disease (PD). Recently, more than fifty other lysosomal storage disorder
Mylene Huebecker   +6 more
doaj   +1 more source

The Glycosphingolipid, Lactosylceramide, Regulates β1-Integrin Clustering and Endocytosis [PDF]

open access: bronze, 2005
Deepak Sharma   +5 more
openalex   +1 more source

Supplementary table S1 from Efficacy and Safety of Glycosphingolipid SSEA-4 Targeting CAR-T Cells in an Ovarian Carcinoma Model

open access: gold, 2023
Héctor J. Monzó   +17 more
openalex   +1 more source

Histo-blood group antigens of glycosphingolipids predict susceptibility of human intestinal enteroids to norovirus infection [PDF]

open access: hybrid, 2020
Inga Rimkutė   +12 more
openalex   +1 more source

Emerging targeted strategies for the treatment of autosomal dominant polycystic kidney disease. [PDF]

open access: yes, 2018
Autosomal dominant polycystic kidney disease (ADPKD) is a widespread genetic disease that leads to renal failure in the majority of patients. The very first pharmacological treatment, tolvaptan, received Food and Drug Administration approval in 2018 ...
Bourgeois, Bryan C   +4 more
core   +1 more source

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