Zhang L - Search Results

1

Mitochondrial localization of the Parkinson's disease related protein DJ-1: implications for pathogenesis.

Zhang L, Shimoji M, Thomas B, Moore DJ, Yu SW, Marupudi NI, Torp R, Torgner IA, Ottersen OP, Dawson TM, Dawson VL. Zhang L, et al. Hum Mol Genet. 2005 Jul 15;14(14):2063-73. doi: 10.1093/hmg/ddi211. Epub 2005 Jun 8. Hum Mol Genet. 2005. PMID: 15944198

2

A missense mutation (L166P) in DJ-1, linked to familial Parkinson's disease, confers reduced protein stability and impairs homo-oligomerization.

Moore DJ, Zhang L, Dawson TM, Dawson VL. Moore DJ, et al. Among authors: zhang l. J Neurochem. 2003 Dec;87(6):1558-67. doi: 10.1111/j.1471-4159.2003.02265.x. J Neurochem. 2003. PMID: 14713311 Free article.

3

Association of DJ-1 and parkin mediated by pathogenic DJ-1 mutations and oxidative stress.

Moore DJ, Zhang L, Troncoso J, Lee MK, Hattori N, Mizuno Y, Dawson TM, Dawson VL. Moore DJ, et al. Among authors: zhang l. Hum Mol Genet. 2005 Jan 1;14(1):71-84. doi: 10.1093/hmg/ddi007. Epub 2004 Nov 3. Hum Mol Genet. 2005. PMID: 15525661

4

Absence of inclusion body formation in the MPTP mouse model of Parkinson's disease.

Shimoji M, Zhang L, Mandir AS, Dawson VL, Dawson TM. Shimoji M, et al. Among authors: zhang l. Brain Res Mol Brain Res. 2005 Mar 24;134(1):103-8. doi: 10.1016/j.molbrainres.2005.01.012. Brain Res Mol Brain Res. 2005. PMID: 15790534

5

Role of nitric oxide in Parkinson's disease.

Zhang L, Dawson VL, Dawson TM. Zhang L, et al. Pharmacol Ther. 2006 Jan;109(1-2):33-41. doi: 10.1016/j.pharmthera.2005.05.007. Epub 2005 Jul 7. Pharmacol Ther. 2006. PMID: 16005074 Review.

6

DJ-1 gene deletion reveals that DJ-1 is an atypical peroxiredoxin-like peroxidase.

Andres-Mateos E, Perier C, Zhang L, Blanchard-Fillion B, Greco TM, Thomas B, Ko HS, Sasaki M, Ischiropoulos H, Przedborski S, Dawson TM, Dawson VL. Andres-Mateos E, et al. Among authors: zhang l. Proc Natl Acad Sci U S A. 2007 Sep 11;104(37):14807-12. doi: 10.1073/pnas.0703219104. Epub 2007 Aug 31. Proc Natl Acad Sci U S A. 2007. PMID: 17766438 Free PMC article.

7

Unexpected lack of hypersensitivity in LRRK2 knock-out mice to MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine).

Andres-Mateos E, Mejias R, Sasaki M, Li X, Lin BM, Biskup S, Zhang L, Banerjee R, Thomas B, Yang L, Liu G, Beal MF, Huso DL, Dawson TM, Dawson VL. Andres-Mateos E, et al. Among authors: zhang l. J Neurosci. 2009 Dec 16;29(50):15846-50. doi: 10.1523/JNEUROSCI.4357-09.2009. J Neurosci. 2009. PMID: 20016100 Free PMC article.

8

Kabuki syndrome stem cell models reveal locus specificity of histone methyltransferase 2D (KMT2D/MLL4).

Jefri M, Zhang X, Stumpf PS, Zhang L, Peng H, Hettige N, Theroux JF, Aouabed Z, Wilson K, Deshmukh S, Antonyan L, Ni A, Alsuwaidi S, Zhang Y, Jabado N, Garcia BA, Schuppert A, Bjornsson HT, Ernst C. Jefri M, et al. Among authors: zhang l, zhang x, zhang y. Hum Mol Genet. 2022 Oct 28;31(21):3715-3728. doi: 10.1093/hmg/ddac121. Hum Mol Genet. 2022. PMID: 35640156 Free PMC article.

9

Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities.

Sobreira N, Brucato M, Zhang L, Ladd-Acosta C, Ongaco C, Romm J, Doheny KF, Mingroni-Netto RC, Bertola D, Kim CA, Perez AB, Melaragno MI, Valle D, Meloni VA, Bjornsson HT. Sobreira N, et al. Among authors: zhang l. Eur J Hum Genet. 2017 Dec;25(12):1335-1344. doi: 10.1038/s41431-017-0023-0. Epub 2017 Nov 7. Eur J Hum Genet. 2017. PMID: 29255178 Free PMC article.

10

Precocious neuronal differentiation and disrupted oxygen responses in Kabuki syndrome.

Carosso GA, Boukas L, Augustin JJ, Nguyen HN, Winer BL, Cannon GH, Robertson JD, Zhang L, Hansen KD, Goff LA, Bjornsson HT. Carosso GA, et al. Among authors: zhang l. JCI Insight. 2019 Oct 17;4(20):e129375. doi: 10.1172/jci.insight.129375. JCI Insight. 2019. PMID: 31465303 Free PMC article.

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