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Lysosomal lipid alterations caused by glucocerebrosidase deficiency promote lysosomal dysfunction, chaperone-mediated-autophagy deficiency, and alpha-synuclein pathology.

Navarro-Romero A, Fernandez-Gonzalez I, Riera J, Montpeyo M, Albert-Bayo M, Lopez-Royo T, Castillo-Sanchez P, Carnicer-Caceres C, Arranz-Amo JA, Castillo-Ribelles L, Pradas E, Casas J, Vila M, Martinez-Vicente M.

NPJ Parkinsons Dis · 2022-10-06

DOI: 10.1038/s41531-022-00397-6PMID: 36202848

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Urinary bis(monacylglycerol) phosphate (BMP) levels are higher in LRRK2 and GBA1 variant carriers but do not predict disease progression in PPMI cohorts

Merchant K, Simuni T, Fedler J, Caspell-Garcia C, Brumm M, Nudelman K, Tengstrand E, Hsieh F, Alcalay R, Coffey C, Chahine L, Foroud T, Singleton A, weintraub d, Hutten S, Sherer T, Siderowf A, Mollenhauer B, Tanner C, Marek K.

· 2022-10-05

DOI: 10.21203/rs.3.rs-2065993/v1

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

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