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Published in 2019 at "Journal of hepatology"
DOI: 10.1016/j.jhep.2018.09.028
Abstract: BACKGROUND & AIMS Lysosomal acid lipase deficiency (LAL-D) is an autosomal recessive condition that may present in a mild form (cholesteryl ester storage disease [CESD]), which mimics non-alcoholic fatty liver disease (NAFLD). It has been…
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Keywords:
lal;
condition;
lysosomal acid;
disease ... See more keywords
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Published in 2019 at "Nature chemical biology"
DOI: 10.1038/s41589-019-0341-3
Abstract: The flagellar hook protein FlgE from spirochaete bacteria self-catalyzes the formation of an unusual inter-subunit lysinoalanine (Lal) crosslink that is critical for cell motility. Unlike other known examples of Lal biosynthesis, conserved cysteine and lysine…
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Keywords:
lysinoalanine crosslinking;
lal;
chemistry;
chemistry lysinoalanine ... See more keywords
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Published in 2017 at "Oncotarget"
DOI: 10.18632/oncotarget.16673
Abstract: Degradation of lysosomal lipids requires lysosomal acid lipase (LAL), the only intracellular lipase known to be active at acidic pH. We found LAL to be expressed in murine immune cells with highest mRNA expression in…
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Keywords:
lal;
lipid mediator;
mediator synthesis;
lipid hydrolysis ... See more keywords
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Published in 2022 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2022.1013266
Abstract: Lysosomal acid lipase (LAL), encoded by the gene LIPA, is the sole neutral lipid hydrolase in lysosomes, responsible for cleavage of cholesteryl esters and triglycerides into their component parts. Inherited forms of complete (Wolman Disease,…
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Keywords:
lal;
fatty liver;
disease;
lysosomal acid ... See more keywords