Galper J - Search Results

1

Lipid pathway dysfunction is prevalent in patients with Parkinson's disease.

Galper J, Dean NJ, Pickford R, Lewis SJG, Halliday GM, Kim WS, Dzamko N. Galper J, et al. Brain. 2022 Oct 21;145(10):3472-3487. doi: 10.1093/brain/awac176. Brain. 2022. PMID: 35551349 Free PMC article.

2

Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice.

McCann EP, Fifita JA, Grima N, Galper J, Mehta P, Freckleton SE, Zhang KY, Henden L, Hogan AL, Chan Moi Fat S, Wu SS, Jagaraj CJ, Berning BA, Williams KL, Twine NA, Bauer D, Piguet O, Hodges J, Kwok JBJ, Halliday GM, Kiernan MC, Atkin J, Rowe DB, Nicholson GA, Walker AK, Blair IP, Yang S. McCann EP, et al. Among authors: galper j. J Neurol Neurosurg Psychiatry. 2020 Feb;91(2):162-171. doi: 10.1136/jnnp-2019-321790. Epub 2019 Nov 5. J Neurol Neurosurg Psychiatry. 2020. PMID: 31690696

3

Cytokines and Gaucher Biomarkers in Glucocerebrosidase Carriers with and Without Parkinson Disease.

Galper J, Balwani M, Fahn S, Waters C, Krohn L, Gan-Or Z, Dzamko N, Alcalay RN. Galper J, et al. Mov Disord. 2021 Jun;36(6):1451-1455. doi: 10.1002/mds.28525. Epub 2021 Feb 11. Mov Disord. 2021. PMID: 33570220 Free PMC article.

4

LRRK2 and Lipid Pathways: Implications for Parkinson's Disease.

Galper J, Kim WS, Dzamko N. Galper J, et al. Biomolecules. 2022 Oct 30;12(11):1597. doi: 10.3390/biom12111597. Biomolecules. 2022. PMID: 36358947 Free PMC article. Review.

5

A protective role of ABCA5 in response to elevated sphingomyelin levels in Parkinson's disease.

Fu Y, Pickford R, Galper J, Phan K, Wu P, Li H, Kim YB, Dzamko N, Halliday GM, Kim WS. Fu Y, et al. Among authors: galper j. NPJ Parkinsons Dis. 2024 Jan 11;10(1):20. doi: 10.1038/s41531-024-00632-2. NPJ Parkinsons Dis. 2024. PMID: 38212656 Free PMC article.

6

Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis.

Fifita JA, Zhang KY, Galper J, Williams KL, McCann EP, Hogan AL, Saunders N, Bauer D, Tarr IS, Pamphlett R, Nicholson GA, Rowe D, Yang S, Blair IP. Fifita JA, et al. Among authors: galper j. Neurodegener Dis. 2017;17(6):304-312. doi: 10.1159/000481258. Epub 2017 Nov 11. Neurodegener Dis. 2017. PMID: 29131108

7

Cyclin F: A component of an E3 ubiquitin ligase complex with roles in neurodegeneration and cancer.

Galper J, Rayner SL, Hogan AL, Fifita JA, Lee A, Chung RS, Blair IP, Yang S. Galper J, et al. Int J Biochem Cell Biol. 2017 Aug;89:216-220. doi: 10.1016/j.biocel.2017.06.011. Epub 2017 Jun 24. Int J Biochem Cell Biol. 2017. PMID: 28652210 Review.

8

Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagy.

Lee A, Rayner SL, Gwee SSL, De Luca A, Shahheydari H, Sundaramoorthy V, Ragagnin A, Morsch M, Radford R, Galper J, Freckleton S, Shi B, Walker AK, Don EK, Cole NJ, Yang S, Williams KL, Yerbury JJ, Blair IP, Atkin JD, Molloy MP, Chung RS. Lee A, et al. Among authors: galper j. Cell Mol Life Sci. 2018 Jan;75(2):335-354. doi: 10.1007/s00018-017-2632-8. Epub 2017 Aug 29. Cell Mol Life Sci. 2018. PMID: 28852778

9

ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis.

Parakh S, Jagaraj CJ, Vidal M, Ragagnin AMG, Perri ER, Konopka A, Toth RP, Galper J, Blair IP, Thomas CJ, Walker AK, Yang S, Spencer DM, Atkin JD. Parakh S, et al. Among authors: galper j. Hum Mol Genet. 2018 Apr 15;27(8):1311-1331. doi: 10.1093/hmg/ddy041. Hum Mol Genet. 2018. PMID: 29409023

10

Theme 3 In vitro experimental models.

Yang S, Wu S, Fifita J, McCann E, Fat SCM, Galper J, Freckleton S, Zhang KY, Blair IP. Yang S, et al. Among authors: galper j. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Nov;20(sup1):135-159. doi: 10.1080/21678421.2019.1646991. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 31702460

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