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2. The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. Straniero L; Rimoldi V; Samarani M; Goldwurm S; Di Fonzo A; Krüger R; Deleidi M; Aureli M; Soldà G; Duga S; Asselta R Sci Rep; 2017 Oct; 7(1):12702. PubMed ID: 28983119 [TBL] [Abstract][Full Text] [Related]
3. Sex distribution and classification of GBA1 variants in an Italian cohort of Parkinson's disease patients analyzed over the last seventeen years. Panteghini C; Reale C; Colangelo I; Suerz M; Catania A; Garavaglia B; Invernizzi F Parkinsonism Relat Disord; 2023 Dec; 117():105919. PubMed ID: 37948831 [TBL] [Abstract][Full Text] [Related]
4. A genetic variation in the CpG island of pseudogene GBAP1 promoter is associated with gastric cancer susceptibility. Ma G; Liu H; Du M; Zhang G; Lin Y; Ge Y; Wang M; Jin G; Zhao Q; Chu H; Gong W; Zhang Z Cancer; 2019 Jul; 125(14):2465-2473. PubMed ID: 30951202 [TBL] [Abstract][Full Text] [Related]
5. Glucocerebrosidase deficiency in dopaminergic neurons induces microglial activation without neurodegeneration. Soria FN; Engeln M; Martinez-Vicente M; Glangetas C; López-González MJ; Dovero S; Dehay B; Normand E; Vila M; Favereaux A; Georges F; Lo Bianco C; Bezard E; Fernagut PO Hum Mol Genet; 2017 Jul; 26(14):2603-2615. PubMed ID: 28520872 [TBL] [Abstract][Full Text] [Related]
6. The relationship between glucocerebrosidase mutations and Parkinson disease. Migdalska-Richards A; Schapira AH J Neurochem; 2016 Oct; 139 Suppl 1(Suppl Suppl 1):77-90. PubMed ID: 26860875 [TBL] [Abstract][Full Text] [Related]
7. Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation. Sheth J; Bhavsar R; Mistri M; Pancholi D; Bavdekar A; Dalal A; Ranganath P; Girisha KM; Shukla A; Phadke S; Puri R; Panigrahi I; Kaur A; Muranjan M; Goyal M; Ramadevi R; Shah R; Nampoothiri S; Danda S; Datar C; Kapoor S; Bhatwadekar S; Sheth F BMC Med Genet; 2019 Feb; 20(1):31. PubMed ID: 30764785 [TBL] [Abstract][Full Text] [Related]
8. PGRN deficiency exacerbates, whereas a brain penetrant PGRN derivative protects, Zhao X; Lin Y; Liou B; Fu W; Jian J; Fannie V; Zhang W; Setchell KDR; Grabowski GA; Sun Y; Liu CJ Proc Natl Acad Sci U S A; 2023 Jan; 120(1):e2210442120. PubMed ID: 36574647 [TBL] [Abstract][Full Text] [Related]
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11. Glucocerebrosidase and its relevance to Parkinson disease. Do J; McKinney C; Sharma P; Sidransky E Mol Neurodegener; 2019 Aug; 14(1):36. PubMed ID: 31464647 [TBL] [Abstract][Full Text] [Related]
12. Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease. Yildiz Y; Hoffmann P; Vom Dahl S; Breiden B; Sandhoff R; Niederau C; Horwitz M; Karlsson S; Filocamo M; Elstein D; Beck M; Sandhoff K; Mengel E; Gonzalez MC; Nöthen MM; Sidransky E; Zimran A; Mattheisen M Orphanet J Rare Dis; 2013 Sep; 8():151. PubMed ID: 24070122 [TBL] [Abstract][Full Text] [Related]
13. Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytes. Burke DG; Rahim AA; Waddington SN; Karlsson S; Enquist I; Bhatia K; Mehta A; Vellodi A; Heales S J Inherit Metab Dis; 2013 Sep; 36(5):869-72. PubMed ID: 23151684 [TBL] [Abstract][Full Text] [Related]
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18. The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease. Duran R; Mencacci NE; Angeli AV; Shoai M; Deas E; Houlden H; Mehta A; Hughes D; Cox TM; Deegan P; Schapira AH; Lees AJ; Limousin P; Jarman PR; Bhatia KP; Wood NW; Hardy J; Foltynie T Mov Disord; 2013 Feb; 28(2):232-236. PubMed ID: 23225227 [TBL] [Abstract][Full Text] [Related]
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