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Page 1
Animal Models for the Study of Gaucher Disease.
Int J Mol Sci. 2023 Nov 7;24(22):16035. doi: 10.3390/ijms242216035.
Int J Mol Sci. 2023.
PMID: 38003227
Free PMC article.
Review.
The Uncovered Function of the Drosophila GBA1a-Encoded Protein.
Cabasso O, Paul S, Maor G, Pasmanik-Chor M, Kallemeijn W, Aerts J, Horowitz M.
Cabasso O, et al.
Cells. 2021 Mar 12;10(3):630. doi: 10.3390/cells10030630.
Cells. 2021.
PMID: 33809074
Free PMC article.
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Drosophila melanogaster Mutated in its GBA1b Ortholog Recapitulates Neuronopathic Gaucher Disease.
Cabasso O, Paul S, Dorot O, Maor G, Krivoruk O, Pasmanik-Chor M, Mirzaian M, Ferraz M, Aerts J, Horowitz M.
Cabasso O, et al.
J Clin Med. 2019 Sep 9;8(9):1420. doi: 10.3390/jcm8091420.
J Clin Med. 2019.
PMID: 31505865
Free PMC article.
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SUMOylation of EHD3 Modulates Tubulation of the Endocytic Recycling Compartment.
Cabasso O, Pekar O, Horowitz M.
Cabasso O, et al.
PLoS One. 2015 Jul 30;10(7):e0134053. doi: 10.1371/journal.pone.0134053. eCollection 2015.
PLoS One. 2015.
PMID: 26226295
Free PMC article.
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The contribution of mutant GBA to the development of Parkinson disease in Drosophila.
Maor G, Cabasso O, Krivoruk O, Rodriguez J, Steller H, Segal D, Horowitz M.
Maor G, et al. Among authors: cabasso o.
Hum Mol Genet. 2016 Jul 1;25(13):2712-2727. doi: 10.1093/hmg/ddw129. Epub 2016 May 9.
Hum Mol Genet. 2016.
PMID: 27162249
Free PMC article.
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