2014
DOI: 10.1038/nm.3449
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RIPK3 as a potential therapeutic target for Gaucher's disease

Abstract: Gaucher's disease (GD), an inherited metabolic disorder caused by mutations in the glucocerebrosidase gene (GBA), is the most common lysosomal storage disease. Heterozygous mutations in GBA are a major risk factor for Parkinson's disease. GD is divided into three clinical subtypes based on the absence (type 1) or presence (types 2 and 3) of neurological signs. Type 1 GD was the first lysosomal storage disease (LSD) for which enzyme therapy became available, and although infusions of recombinant glucocerebrosid… Show more

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Cited by 145 publications
(140 citation statements)
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“…38 Altogether, these findings suggest opportunities for RIPK3 inhibitors in the treatment of diseases where high RIPK3 kinase activity promotes human pathologies, also including steatohepatitis 36 and Gaucher's disease. 39 Materials and Methods Cell lines. Primary MEFs were generated by mating animals of the required genotypes and harvesting embryos at E12-E14 based on palpation.…”
Section: Discussionmentioning
confidence: 99%
“…38 Altogether, these findings suggest opportunities for RIPK3 inhibitors in the treatment of diseases where high RIPK3 kinase activity promotes human pathologies, also including steatohepatitis 36 and Gaucher's disease. 39 Materials and Methods Cell lines. Primary MEFs were generated by mating animals of the required genotypes and harvesting embryos at E12-E14 based on palpation.…”
Section: Discussionmentioning
confidence: 99%
“…Studies in recent years have demonstrated the involvement of necroptosis in a number of pathophysiological processes, such as atherosclerosis (6), skin inflammation (7)(8)(9), chronic intestinal inflammation (10, 11), Gaucher's disease (12), acute liver injury (13,14), and heightened intestinal inflammation (15).…”
mentioning
confidence: 99%
“…RIP3 knockout can significantly ameliorate the development of disease and prolong the survival of animals. [38] Amyotrophic lateral sclerosis (ALS) is the most adult onset motor neuron degenerative disease, in which inflammation is the most striking hallmark of pathological changes. Recently, it has been demonstrated that in the spinal cord of the ALS model, motor neurons also undergo necroptosis.…”
Section: Necroptosis and Neurological Diseasesmentioning
confidence: 99%