Cleeter MW - Search Results

1

Complex I function in familial and sporadic dystonia.

Schapira AH, Warner T, Gash MT, Cleeter MW, Marinho CF, Cooper JM. Schapira AH, et al. Among authors: cleeter mw. Ann Neurol. 1997 Apr;41(4):556-9. doi: 10.1002/ana.410410421. Ann Neurol. 1997. PMID: 9124815

2

Mitochondria in the etiology and pathogenesis of Parkinson's disease.

Schapira AH, Gu M, Taanman JW, Tabrizi SJ, Seaton T, Cleeter M, Cooper JM. Schapira AH, et al. Ann Neurol. 1998 Sep;44(3 Suppl 1):S89-98. doi: 10.1002/ana.410440714. Ann Neurol. 1998. PMID: 9749579 Review.

3

Biochemical abnormalities and excitotoxicity in Huntington's disease brain.

Tabrizi SJ, Cleeter MW, Xuereb J, Taanman JW, Cooper JM, Schapira AH. Tabrizi SJ, et al. Among authors: cleeter mw. Ann Neurol. 1999 Jan;45(1):25-32. doi: 10.1002/1531-8249(199901)45:1<25::aid-art6>3.0.co;2-e. Ann Neurol. 1999. PMID: 9894873

4

Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons.

Schapira AH, Cleeter MW, Muddle JR, Workman JM, Cooper JM, King RH. Schapira AH, et al. Among authors: cleeter mw. Ann Neurol. 2006 Aug;60(2):253-5. doi: 10.1002/ana.20934. Ann Neurol. 2006. PMID: 16862591

5

Irreversible inhibition of mitochondrial complex I by 1-methyl-4-phenylpyridinium: evidence for free radical involvement.

Cleeter MW, Cooper JM, Schapira AH. Cleeter MW, et al. J Neurochem. 1992 Feb;58(2):786-9. doi: 10.1111/j.1471-4159.1992.tb09789.x. J Neurochem. 1992. PMID: 1729421

6

Free radicals and mitochondrial dysfunction in Parkinson's disease.

Schapira AH, Hartley A, Cleeter MW, Cooper JM. Schapira AH, et al. Among authors: cleeter mw. Biochem Soc Trans. 1993 May;21(2):367-70. doi: 10.1042/bst0210367. Biochem Soc Trans. 1993. PMID: 8359498 Review.

7

Nitric oxide enhances MPP(+) inhibition of complex I.

Cleeter MW, Cooper JM, Schapira AH. Cleeter MW, et al. FEBS Lett. 2001 Aug 24;504(1-2):50-2. doi: 10.1016/s0014-5793(01)02763-6. FEBS Lett. 2001. PMID: 11522295 Free article.

8

Reversible inhibition of cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, by nitric oxide. Implications for neurodegenerative diseases.

Cleeter MW, Cooper JM, Darley-Usmar VM, Moncada S, Schapira AH. Cleeter MW, et al. FEBS Lett. 1994 May 23;345(1):50-4. doi: 10.1016/0014-5793(94)00424-2. FEBS Lett. 1994. PMID: 8194600 Free article.

9

Screening for mutations in the phosphatidylinositol 4-kinase 2-alpha gene in autosomal recessive hereditary spastic paraplegia.

Cleeter M, Houlden H, Simons P, Al-Shawi R, Stevanin G, Durr A, Hsuan J, Warner TT. Cleeter M, et al. Amyotroph Lateral Scler. 2011 Mar;12(2):148-9. doi: 10.3109/17482968.2010.543689. Epub 2010 Dec 30. Amyotroph Lateral Scler. 2011. PMID: 21190509

10

Glucocerebrosidase inhibition causes mitochondrial dysfunction and free radical damage.

Cleeter MW, Chau KY, Gluck C, Mehta A, Hughes DA, Duchen M, Wood NW, Hardy J, Mark Cooper J, Schapira AH. Cleeter MW, et al. Neurochem Int. 2013 Jan;62(1):1-7. doi: 10.1016/j.neuint.2012.10.010. Epub 2012 Oct 23. Neurochem Int. 2013. PMID: 23099359 Free PMC article.

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