Lockhart PJ - Search Results

1

Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse.

Wilson GR, Wang HX, Egan GF, Robinson PJ, Delatycki MB, O'Bryan MK, Lockhart PJ. Wilson GR, et al. Among authors: lockhart pj. Hum Mol Genet. 2010 Apr 15;19(8):1593-602. doi: 10.1093/hmg/ddq031. Epub 2010 Jan 27. Hum Mol Genet. 2010. PMID: 20106870

2

Gene amplification of the Menkes (MNK; ATP7A) P-type ATPase gene of CHO cells is associated with copper resistance and enhanced copper efflux.

Camakaris J, Petris MJ, Bailey L, Shen P, Lockhart P, Glover TW, Barcroft C, Patton J, Mercer JF. Camakaris J, et al. Hum Mol Genet. 1995 Nov;4(11):2117-23. doi: 10.1093/hmg/4.11.2117. Hum Mol Genet. 1995. PMID: 8589689

3

Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease.

Grimes A, Hearn CJ, Lockhart P, Newgreen DF, Mercer JF. Grimes A, et al. Hum Mol Genet. 1997 Jul;6(7):1037-42. doi: 10.1093/hmg/6.7.1037. Hum Mol Genet. 1997. PMID: 9215672

4

Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutants.

La Fontaine S, Firth SD, Lockhart PJ, Brooks H, Camakaris J, Mercer JF. La Fontaine S, et al. Among authors: lockhart pj. Hum Mol Genet. 1999 Jun;8(6):1069-75. doi: 10.1093/hmg/8.6.1069. Hum Mol Genet. 1999. PMID: 10332039

5

Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene.

Fahey MC, Knight MA, Shaw JH, Gardner RJ, du Sart D, Lockhart PJ, Delatycki MB, Gates PC, Storey E. Fahey MC, et al. Among authors: lockhart pj. J Neurol Neurosurg Psychiatry. 2005 Dec;76(12):1720-2. doi: 10.1136/jnnp.2004.044115. J Neurol Neurosurg Psychiatry. 2005. PMID: 16291902 Free PMC article.

6

Parkin Co-Regulated Gene (PACRG) is regulated by the ubiquitin-proteasomal system and is present in the pathological features of Parkinsonian diseases.

Taylor JM, Song YJ, Huang Y, Farrer MJ, Delatycki MB, Halliday GM, Lockhart PJ. Taylor JM, et al. Among authors: lockhart pj. Neurobiol Dis. 2007 Aug;27(2):238-47. doi: 10.1016/j.nbd.2007.04.014. Epub 2007 May 18. Neurobiol Dis. 2007. PMID: 17590346

7

Regional and cellular localisation of Parkin co-regulated gene in developing and adult mouse brain.

Brody KM, Taylor JM, Wilson GR, Delatycki MB, Lockhart PJ. Brody KM, et al. Among authors: lockhart pj. Brain Res. 2008 Mar 27;1201:177-86. doi: 10.1016/j.brainres.2008.01.050. Epub 2008 Jan 30. Brain Res. 2008. PMID: 18295750

8

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

9

Identification and validation of control cell lines for accurate parkin dosage analysis.

Taylor JM, Delatycki MB, Lockhart PJ. Taylor JM, et al. Among authors: lockhart pj. J Neurosci Methods. 2009 Jan 30;176(2):68-71. doi: 10.1016/j.jneumeth.2008.08.029. Epub 2008 Sep 5. J Neurosci Methods. 2009. PMID: 18817813

10

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

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