Zheng K - Search Results

1

Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination.

Venkateswaran S, Zheng K, Sacchetti M, Gagne D, Arnold DL, Sadovnick AD, Scherer SW, Banwell B, Bar-Or A, Simon DK; Canadian Pediatric Demyelinating Disease Network. Venkateswaran S, et al. Among authors: zheng k. Neurology. 2011 Mar 1;76(9):774-80. doi: 10.1212/WNL.0b013e31820ee1bb. Epub 2011 Feb 2. Neurology. 2011. PMID: 21288980 Free PMC article.

2

A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease.

Zheng K, Heydari B, Simon DK. Zheng K, et al. Arch Neurol. 2003 May;60(5):722-5. doi: 10.1001/archneur.60.5.722. Arch Neurol. 2003. PMID: 12756136

3

Mitochondrial complex I gene variant associated with early age at onset in spinocerebellar ataxia type 2.

Simon DK, Zheng K, Velázquez L, Santos N, Almaguer L, Figueroa KP, Pulst SM. Simon DK, et al. Among authors: zheng k. Arch Neurol. 2007 Jul;64(7):1042-4. doi: 10.1001/archneur.64.7.1042. Arch Neurol. 2007. PMID: 17620498

4

Somatic mitochondrial DNA mutations in single neurons and glia.

Cantuti-Castelvetri I, Lin MT, Zheng K, Keller-McGandy CE, Betensky RA, Johns DR, Beal MF, Standaert DG, Simon DK. Cantuti-Castelvetri I, et al. Among authors: zheng k. Neurobiol Aging. 2005 Nov-Dec;26(10):1343-55. doi: 10.1016/j.neurobiolaging.2004.11.008. Epub 2004 Dec 29. Neurobiol Aging. 2005. PMID: 16243605

5

Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease.

Clark J, Reddy S, Zheng K, Betensky RA, Simon DK. Clark J, et al. Among authors: zheng k. BMC Med Genet. 2011 May 19;12:69. doi: 10.1186/1471-2350-12-69. BMC Med Genet. 2011. PMID: 21595954 Free PMC article.

6

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

Lin MT, Cantuti-Castelvetri I, Zheng K, Jackson KE, Tan YB, Arzberger T, Lees AJ, Betensky RA, Beal MF, Simon DK. Lin MT, et al. Among authors: zheng k. Ann Neurol. 2012 Jun;71(6):850-4. doi: 10.1002/ana.23568. Ann Neurol. 2012. PMID: 22718549 Free PMC article.

7

Somatic mitochondrial DNA mutations do not increase neuronal vulnerability to MPTP in young POLG mutator mice.

Dai Y, Clark J, Zheng K, Kujoth GC, Prolla TA, Simon DK. Dai Y, et al. Among authors: zheng k. Neurotoxicol Teratol. 2014 Nov-Dec;46:62-7. doi: 10.1016/j.ntt.2014.10.004. Neurotoxicol Teratol. 2014. PMID: 25450660 Free PMC article.

8

Rapamycin drives selection against a pathogenic heteroplasmic mitochondrial DNA mutation.

Dai Y, Zheng K, Clark J, Swerdlow RH, Pulst SM, Sutton JP, Shinobu LA, Simon DK. Dai Y, et al. Among authors: zheng k. Hum Mol Genet. 2014 Feb 1;23(3):637-47. doi: 10.1093/hmg/ddt450. Epub 2013 Sep 18. Hum Mol Genet. 2014. PMID: 24101601 Free PMC article.

9

Oral N-acetyl-cysteine attenuates loss of dopaminergic terminals in alpha-synuclein overexpressing mice.

Clark J, Clore EL, Zheng K, Adame A, Masliah E, Simon DK. Clark J, et al. Among authors: zheng k. PLoS One. 2010 Aug 23;5(8):e12333. doi: 10.1371/journal.pone.0012333. PLoS One. 2010. PMID: 20808797 Free PMC article.

10

Behavioral and metabolic characterization of heterozygous and homozygous POLG mutator mice.

Dai Y, Kiselak T, Clark J, Clore E, Zheng K, Cheng A, Kujoth GC, Prolla TA, Maratos-Flier E, Simon DK. Dai Y, et al. Among authors: zheng k. Mitochondrion. 2013 Jul;13(4):282-91. doi: 10.1016/j.mito.2013.03.006. Epub 2013 Mar 27. Mitochondrion. 2013. PMID: 23542163 Free PMC article.

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