Lockhart PJ - Search Results

1

Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism.

Lee MJ, Mata IF, Lin CH, Tzen KY, Lincoln SJ, Bounds R, Lockhart PJ, Hulihan MM, Farrer MJ, Wu RM. Lee MJ, et al. Among authors: lockhart pj. Mov Disord. 2009 Jan 15;24(1):104-8. doi: 10.1002/mds.22093. Mov Disord. 2009. PMID: 19006224

2

Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism.

Lockhart PJ, Bounds R, Hulihan M, Kachergus J, Lincoln S, Lin CH, Wu RM, Farrer MJ. Lockhart PJ, et al. Mov Disord. 2004 Sep;19(9):1065-9. doi: 10.1002/mds.20082. Mov Disord. 2004. PMID: 15372597

3

It's a double knock-out! The quaking mouse is a spontaneous deletion of parkin and parkin co-regulated gene (PACRG).

Lockhart PJ, O'Farrell CA, Farrer MJ. Lockhart PJ, et al. Mov Disord. 2004 Jan;19(1):101-4. doi: 10.1002/mds.20000. Mov Disord. 2004. PMID: 14743368

4

Lack of evidence for association of a parkin promoter polymorphism with early-onset Parkinson's disease in a Chinese population.

Taylor JM, Wu RM, Lin CH, Delatycki MB, Lockhart PJ. Taylor JM, et al. Among authors: lockhart pj. Parkinsonism Relat Disord. 2009 Feb;15(2):149-52. doi: 10.1016/j.parkreldis.2008.02.010. Epub 2008 Apr 2. Parkinsonism Relat Disord. 2009. PMID: 18387843

5

Analysis of PArkin Co-Regulated Gene in a Taiwanese-ethnic Chinese cohort with early-onset Parkinson's disease.

Taylor JM, Wu RM, Farrer MJ, Delatycki MB, Lockhart PJ. Taylor JM, et al. Among authors: lockhart pj. Parkinsonism Relat Disord. 2009 Jul;15(6):417-21. doi: 10.1016/j.parkreldis.2008.11.009. Epub 2009 Feb 3. Parkinsonism Relat Disord. 2009. PMID: 19196541

6

DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function.

Lockhart PJ, Lincoln S, Hulihan M, Kachergus J, Wilkes K, Bisceglio G, Mash DC, Farrer MJ. Lockhart PJ, et al. J Med Genet. 2004 Mar;41(3):e22. doi: 10.1136/jmg.2003.011106. J Med Genet. 2004. PMID: 14985393 Free PMC article. No abstract available.

7

Parkin genetics: one model for Parkinson's disease.

Mata IF, Lockhart PJ, Farrer MJ. Mata IF, et al. Among authors: lockhart pj. Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R127-33. doi: 10.1093/hmg/ddh089. Epub 2004 Feb 19. Hum Mol Genet. 2004. PMID: 14976155 Review.

8

The emerging role of Rab GTPases in the pathogenesis of Parkinson's disease.

Gao Y, Wilson GR, Stephenson SEM, Bozaoglu K, Farrer MJ, Lockhart PJ. Gao Y, et al. Among authors: lockhart pj. Mov Disord. 2018 Feb;33(2):196-207. doi: 10.1002/mds.27270. Epub 2018 Jan 9. Mov Disord. 2018. PMID: 29315801 Review.

9

SCA2 may present as levodopa-responsive parkinsonism.

Payami H, Nutt J, Gancher S, Bird T, McNeal MG, Seltzer WK, Hussey J, Lockhart P, Gwinn-Hardy K, Singleton AA, Singleton AB, Hardy J, Farrer M. Payami H, et al. Mov Disord. 2003 Apr;18(4):425-9. doi: 10.1002/mds.10375. Mov Disord. 2003. PMID: 12671950

10

Identification of a novel gene linked to parkin via a bi-directional promoter.

West AB, Lockhart PJ, O'Farell C, Farrer MJ. West AB, et al. Among authors: lockhart pj. J Mol Biol. 2003 Feb 7;326(1):11-9. doi: 10.1016/s0022-2836(02)01376-1. J Mol Biol. 2003. PMID: 12547187

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