Wexler NS - Search Results

1

Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington's disease patients.

Lee CYD, Wang N, Shen K, Stricos M, Langfelder P, Cheon KH, Cortés EP, Vinters HV, Vonsattel JP, Wexler NS, Damoiseaux R, Frydman J, Yang XW. Lee CYD, et al. Among authors: wexler ns. Sci Rep. 2020 Nov 20;10(1):20295. doi: 10.1038/s41598-020-77164-1. Sci Rep. 2020. PMID: 33219289 Free PMC article.

2

Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain.

Shelbourne PF, Keller-McGandy C, Bi WL, Yoon SR, Dubeau L, Veitch NJ, Vonsattel JP, Wexler NS; US-Venezuela Collaborative Research Group; Arnheim N, Augood SJ. Shelbourne PF, et al. Among authors: wexler ns. Hum Mol Genet. 2007 May 15;16(10):1133-42. doi: 10.1093/hmg/ddm054. Epub 2007 Apr 4. Hum Mol Genet. 2007. PMID: 17409200

3

Oligonucleotide Treatment for Huntington's Disease.

Fischbeck KH, Wexler NS. Fischbeck KH, et al. Among authors: wexler ns. N Engl J Med. 2019 Jun 13;380(24):2373-2374. doi: 10.1056/NEJMe1904861. Epub 2019 May 6. N Engl J Med. 2019. PMID: 31059640 No abstract available.

4

Aberrantly spliced HTT, a new player in Huntington's disease pathogenesis.

Gipson TA, Neueder A, Wexler NS, Bates GP, Housman D. Gipson TA, et al. Among authors: wexler ns. RNA Biol. 2013 Nov;10(11):1647-52. doi: 10.4161/rna.26706. Epub 2013 Oct 11. RNA Biol. 2013. PMID: 24256709 Free PMC article.

5

Pope Francis champions Huntington's disease.

Wexler NS. Wexler NS. Brain. 2018 Feb 1;141(2):e8. doi: 10.1093/brain/awx322. Brain. 2018. PMID: 29240886 No abstract available.

6

Molecular approaches to hereditary diseases of the nervous system: Huntington's disease as a paradigm.

Wexler NS, Rose EA, Housman DE. Wexler NS, et al. Annu Rev Neurosci. 1991;14:503-29. doi: 10.1146/annurev.ne.14.030191.002443. Annu Rev Neurosci. 1991. PMID: 1827708 Review. No abstract available.

7

The Prevalence of Huntington's Disease.

Rawlins MD, Wexler NS, Wexler AR, Tabrizi SJ, Douglas I, Evans SJ, Smeeth L. Rawlins MD, et al. Among authors: wexler ns. Neuroepidemiology. 2016;46(2):144-53. doi: 10.1159/000443738. Epub 2016 Jan 30. Neuroepidemiology. 2016. PMID: 26824438 Free article. Review.

8

Huntington disease expansion mutations in humans can occur before meiosis is completed.

Yoon SR, Dubeau L, de Young M, Wexler NS, Arnheim N. Yoon SR, et al. Among authors: wexler ns. Proc Natl Acad Sci U S A. 2003 Jul 22;100(15):8834-8. doi: 10.1073/pnas.1331390100. Epub 2003 Jul 11. Proc Natl Acad Sci U S A. 2003. PMID: 12857955 Free PMC article.

9

Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism.

Leeflang EP, Tavaré S, Marjoram P, Neal CO, Srinidhi J, MacFarlane H, MacDonald ME, Gusella JF, de Young M, Wexler NS, Arnheim N. Leeflang EP, et al. Among authors: wexler ns. Hum Mol Genet. 1999 Feb;8(2):173-83. doi: 10.1093/hmg/8.2.173. Hum Mol Genet. 1999. PMID: 9931325

10

Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum.

Leeflang EP, Zhang L, Tavaré S, Hubert R, Srinidhi J, MacDonald ME, Myers RH, de Young M, Wexler NS, Gusella JF, et al. Leeflang EP, et al. Among authors: wexler ns. Hum Mol Genet. 1995 Sep;4(9):1519-26. doi: 10.1093/hmg/4.9.1519. Hum Mol Genet. 1995. PMID: 8541834

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