Ding J - Search Results

1

Targeted Mutation (R100W) of the Gene Encoding NGF Leads to Deficits in the Peripheral Sensory Nervous System.

Yang W, Sung K, Zhou F, Xu W, Rissman RA, Ding J, Wu C. Yang W, et al. Among authors: ding j. Front Aging Neurosci. 2018 Nov 13;10:373. doi: 10.3389/fnagi.2018.00373. eCollection 2018. Front Aging Neurosci. 2018. PMID: 30524266 Free PMC article.

2

BPAG1n4 is essential for retrograde axonal transport in sensory neurons.

Liu JJ, Ding J, Kowal AS, Nardine T, Allen E, Delcroix JD, Wu C, Mobley W, Fuchs E, Yang Y. Liu JJ, et al. Among authors: ding j. J Cell Biol. 2003 Oct 27;163(2):223-9. doi: 10.1083/jcb.200306075. J Cell Biol. 2003. PMID: 14581450 Free PMC article.

3

Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport.

Liu JJ, Ding J, Wu C, Bhagavatula P, Cui B, Chu S, Mobley WC, Yang Y. Liu JJ, et al. Among authors: ding j. Proc Natl Acad Sci U S A. 2007 Feb 13;104(7):2223-8. doi: 10.1073/pnas.0602222104. Epub 2007 Feb 7. Proc Natl Acad Sci U S A. 2007. PMID: 17287360 Free PMC article.

4

A functional dynein-microtubule network is required for NGF signaling through the Rap1/MAPK pathway.

Wu C, Ramirez A, Cui B, Ding J, Delcroix JD, Valletta JS, Liu JJ, Yang Y, Chu S, Mobley WC. Wu C, et al. Among authors: ding j. Traffic. 2007 Nov;8(11):1503-20. doi: 10.1111/j.1600-0854.2007.00636.x. Epub 2007 Sep 6. Traffic. 2007. PMID: 17822405 Free article.

5

CALHM1 P86L polymorphism is a risk factor for Alzheimer's disease in the Chinese population.

Cui PJ, Zheng L, Cao L, Wang Y, Deng YL, Wang G, Xu W, Tang HD, Ma JF, Zhang T, Ding JQ, Cheng Q, Chen SD. Cui PJ, et al. J Alzheimers Dis. 2010;19(1):31-5. doi: 10.3233/JAD-2010-1207. J Alzheimers Dis. 2010. PMID: 20061624

6

Association study of clusterin polymorphism rs11136000 with late onset Alzheimer's disease in Chinese Han population.

Ma JF, Liu LH, Zhang Y, Wang Y, Deng YL, Huang Y, Wang G, Xu W, Cui PJ, Fei QZ, Ding JQ, Tang HD, Chen SD. Ma JF, et al. Am J Alzheimers Dis Other Demen. 2011 Dec;26(8):627-30. doi: 10.1177/1533317511432735. Epub 2012 Jan 31. Am J Alzheimers Dis Other Demen. 2011. PMID: 22296908 Free PMC article.

7

Genetic variation in LINGO-1 (rs9652490) and risk of Parkinson's disease: twelve studies and a meta-analysis.

Wu Y, Wang X, Xu W, Liu W, Fang F, Ding J, Song Y, Chen S. Wu Y, et al. Among authors: ding j. Neurosci Lett. 2012 Jul 26;522(1):67-72. doi: 10.1016/j.neulet.2012.06.018. Epub 2012 Jun 15. Neurosci Lett. 2012. PMID: 22710005

8

The genetic variation of SORCS1 is associated with late-onset Alzheimer's disease in Chinese Han population.

Xu W, Xu J, Wang Y, Tang H, Deng Y, Ren R, Wang G, Niu W, Ma J, Wu Y, Zheng J, Chen S, Ding J. Xu W, et al. Among authors: ding j. PLoS One. 2013 May 20;8(5):e63621. doi: 10.1371/journal.pone.0063621. Print 2013. PLoS One. 2013. PMID: 23700427 Free PMC article.

9

Lack of association between TOR1A and THAP1 mutations and sporadic adult-onset primary focal dystonia in a Chinese population.

Wang L, Duan C, Gao Y, Xu W, Ding J, Liu VT, Wu Y. Wang L, et al. Among authors: ding j. Clin Neurol Neurosurg. 2016 Mar;142:26-30. doi: 10.1016/j.clineuro.2016.01.018. Epub 2016 Jan 12. Clin Neurol Neurosurg. 2016. PMID: 26803725

10

Amyloid precursor protein-mediated endocytic pathway disruption induces axonal dysfunction and neurodegeneration.

Xu W, Weissmiller AM, White JA 2nd, Fang F, Wang X, Wu Y, Pearn ML, Zhao X, Sawa M, Chen S, Gunawardena S, Ding J, Mobley WC, Wu C. Xu W, et al. Among authors: ding j. J Clin Invest. 2016 May 2;126(5):1815-33. doi: 10.1172/JCI82409. Epub 2016 Apr 11. J Clin Invest. 2016. PMID: 27064279 Free PMC article.

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