Grierson AJ - Search Results

1

Spastin recovery in hereditary spastic paraplegia by preventing neddylation-dependent degradation.

Sardina F, Pisciottani A, Ferrara M, Valente D, Casella M, Crescenzi M, Peschiaroli A, Casali C, Soddu S, Grierson AJ, Rinaldo C. Sardina F, et al. Among authors: grierson aj. Life Sci Alliance. 2020 Oct 26;3(12):e202000799. doi: 10.26508/lsa.202000799. Print 2020 Dec. Life Sci Alliance. 2020. PMID: 33106322 Free PMC article.

2

Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation.

McDermott CJ, Grierson AJ, Wood JD, Bingley M, Wharton SB, Bushby KM, Shaw PJ. McDermott CJ, et al. Among authors: grierson aj. Ann Neurol. 2003 Dec;54(6):748-59. doi: 10.1002/ana.10757. Ann Neurol. 2003. PMID: 14681884

3

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients.

Kasher PR, De Vos KJ, Wharton SB, Manser C, Bennett EJ, Bingley M, Wood JD, Milner R, McDermott CJ, Miller CC, Shaw PJ, Grierson AJ. Kasher PR, et al. Among authors: grierson aj. J Neurochem. 2009 Jul;110(1):34-44. doi: 10.1111/j.1471-4159.2009.06104.x. Epub 2009 Apr 22. J Neurochem. 2009. PMID: 19453301 Free article.

4

The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene.

Wharton SB, McDermott CJ, Grierson AJ, Wood JD, Gelsthorpe C, Ince PG, Shaw PJ. Wharton SB, et al. Among authors: grierson aj. J Neuropathol Exp Neurol. 2003 Nov;62(11):1166-77. doi: 10.1093/jnen/62.11.1166. J Neuropathol Exp Neurol. 2003. PMID: 14656074

5

New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP).

Hewamadduma C, McDermott C, Kirby J, Grierson A, Panayi M, Dalton A, Rajabally Y, Shaw P. Hewamadduma C, et al. Neurogenetics. 2009 Apr;10(2):105-10. doi: 10.1007/s10048-008-0163-z. Epub 2008 Nov 26. Neurogenetics. 2009. PMID: 19034539

6

C9ORF72-derived poly-GA DPRs undergo endocytic uptake in iAstrocytes and spread to motor neurons.

Marchi PM, Marrone L, Brasseur L, Coens A, Webster CP, Bousset L, Destro M, Smith EF, Walther CG, Alfred V, Marroccella R, Graves EJ, Robinson D, Shaw AC, Wan LM, Grierson AJ, Ebbens SJ, De Vos KJ, Hautbergue GM, Ferraiuolo L, Melki R, Azzouz M. Marchi PM, et al. Among authors: grierson aj. 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.

7

Systemic delivery of scAAV9 expressing SMN prolongs survival in a model of spinal muscular atrophy.

Valori CF, Ning K, Wyles M, Mead RJ, Grierson AJ, Shaw PJ, Azzouz M. Valori CF, et al. Among authors: grierson aj. Sci Transl Med. 2010 Jun 9;2(35):35ra42. doi: 10.1126/scitranslmed.3000830. Sci Transl Med. 2010. PMID: 20538619

8

C9orf72 plays a central role in Rab GTPase-dependent regulation of autophagy.

Webster CP, Smith EF, Grierson AJ, De Vos KJ. Webster CP, et al. Among authors: grierson aj. Small GTPases. 2018 Sep 3;9(5):399-408. doi: 10.1080/21541248.2016.1240495. Epub 2016 Oct 21. Small GTPases. 2018. PMID: 27768524 Free PMC article. Review.

9

Use of zebrafish models to investigate rare human disease.

Adamson KI, Sheridan E, Grierson AJ. Adamson KI, et al. Among authors: grierson aj. J Med Genet. 2018 Oct;55(10):641-649. doi: 10.1136/jmedgenet-2018-105358. Epub 2018 Jul 31. J Med Genet. 2018. PMID: 30065072 Review.

10

Cyclin D2 interacts with cdk-5 and modulates cellular cdk-5/p35 activity.

Guidato S, McLoughlin DM, Grierson AJ, Miller CC. Guidato S, et al. Among authors: grierson aj. J Neurochem. 1998 Jan;70(1):335-40. doi: 10.1046/j.1471-4159.1998.70010335.x. J Neurochem. 1998. PMID: 9422379 Free article.

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