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marrocchella r[au]
(4 results)?
C9ORF72-derived poly-GA DPRs undergo endocytic uptake in iAstrocytes and spread to motor neurons.
Life Sci Alliance. 2022 May 13;5(9):e202101276. doi: 10.26508/lsa.202101276. Print 2022 Sep.
Life Sci Alliance. 2022.
PMID: 35568435
Free PMC article.
SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction.
Marrone L, Marchi PM, Webster CP, Marroccella R, Coldicott I, Reynolds S, Alves-Cruzeiro J, Yang ZL, Higginbottom A, Khundadze M, Shaw PJ, Hübner CA, Livesey MR, Azzouz M.
Marrone L, et al. Among authors: marroccella r.
Hum Mol Genet. 2022 Aug 23;31(16):2693-2710. doi: 10.1093/hmg/ddac063.
Hum Mol Genet. 2022.
PMID: 35313342
Free PMC article.
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Ap4b1-knockout mouse model of hereditary spastic paraplegia type 47 displays motor dysfunction, aberrant brain morphology and ATG9A mislocalization.
Scarrott JM, Alves-Cruzeiro J, Marchi PM, Webster CP, Yang ZL, Karyka E, Marroccella R, Coldicott I, Thomas H, Azzouz M.
Scarrott JM, et al. Among authors: marroccella r.
Brain Commun. 2023 Jan 6;5(1):fcac335. doi: 10.1093/braincomms/fcac335. eCollection 2023.
Brain Commun. 2023.
PMID: 36632189
Free PMC article.
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