Cheng TH - Search Results

1

Reply to: "Low Frequency of p.S510G in PIAS1 Challenges Its Relevance for Modifying Repeat Expansion Disorders".

Lee YH, Lee YC, Tsai YS, Yang UC, Cheng TH, Chern Y, Soong BW. Lee YH, et al. Among authors: cheng th. Mov Disord. 2022 Oct;37(10):2169. doi: 10.1002/mds.29192. Mov Disord. 2022. PMID: 36250496 No abstract available.

2

Human mesenchymal stem cells prolong survival and ameliorate motor deficit through trophic support in Huntington's disease mouse models.

Lin YT, Chern Y, Shen CK, Wen HL, Chang YC, Li H, Cheng TH, Hsieh-Li HM. Lin YT, et al. Among authors: cheng th. PLoS One. 2011;6(8):e22924. doi: 10.1371/journal.pone.0022924. Epub 2011 Aug 5. PLoS One. 2011. PMID: 21850243 Free PMC article.

3

Spt4 is selectively required for transcription of extended trinucleotide repeats.

Liu CR, Chang CR, Chern Y, Wang TH, Hsieh WC, Shen WC, Chang CY, Chu IC, Deng N, Cohen SN, Cheng TH. Liu CR, et al. Among authors: cheng th. Cell. 2012 Feb 17;148(4):690-701. doi: 10.1016/j.cell.2011.12.032. Cell. 2012. PMID: 22341442 Free article.

4

Enhancement of brain-type creatine kinase activity ameliorates neuronal deficits in Huntington's disease.

Lin YS, Cheng TH, Chang CP, Chen HM, Chern Y. Lin YS, et al. Among authors: cheng th. Biochim Biophys Acta. 2013 Jun;1832(6):742-53. doi: 10.1016/j.bbadis.2013.02.006. Epub 2013 Feb 15. Biochim Biophys Acta. 2013. PMID: 23416527 Free article.

5

Effects on murine behavior and lifespan of selectively decreasing expression of mutant huntingtin allele by supt4h knockdown.

Cheng HM, Chern Y, Chen IH, Liu CR, Li SH, Chun SJ, Rigo F, Bennett CF, Deng N, Feng Y, Lin CS, Yan YT, Cohen SN, Cheng TH. Cheng HM, et al. Among authors: cheng th. PLoS Genet. 2015 Mar 11;11(3):e1005043. doi: 10.1371/journal.pgen.1005043. eCollection 2015 Mar. PLoS Genet. 2015. PMID: 25760041 Free PMC article.

6

A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy.

Tsai PC, Soong BW, Mademan I, Huang YH, Liu CR, Hsiao CT, Wu HT, Liu TT, Liu YT, Tseng YT, Lin KP, Yang UC, Chung KW, Choi BO, Nicholson GA, Kennerson ML, Chan CC, De Jonghe P, Cheng TH, Liao YC, Züchner S, Baets J, Lee YC. Tsai PC, et al. Among authors: cheng th. Brain. 2017 May 1;140(5):1252-1266. doi: 10.1093/brain/awx058. Brain. 2017. PMID: 28369220 Free PMC article.

7

A PIAS1 Protective Variant S510G Delays polyQ Disease Onset by Modifying Protein Homeostasis.

Lee YH, Tsai YS, Chang CC, Ho CC, Shih HM, Chen HM, Lai HL, Lee CW, Lee YC, Liao YC, Yang UC, Cheng TH, Chern Y, Soong BW. Lee YH, et al. Among authors: cheng th. Mov Disord. 2022 Apr;37(4):767-777. doi: 10.1002/mds.28896. Epub 2021 Dec 23. Mov Disord. 2022. PMID: 34951052

8

Chemical interference with DSIF complex formation lowers synthesis of mutant huntingtin gene products and curtails mutant phenotypes.

Deng N, Wu YY, Feng Y, Hsieh WC, Song JS, Lin YS, Tseng YH, Liao WJ, Chu YF, Liu YC, Chang EC, Liu CR, Sheu SY, Su MT, Kuo HC, Cohen SN, Cheng TH. Deng N, et al. Among authors: cheng th. Proc Natl Acad Sci U S A. 2022 Aug 9;119(32):e2204779119. doi: 10.1073/pnas.2204779119. Epub 2022 Aug 1. Proc Natl Acad Sci U S A. 2022. PMID: 35914128 Free PMC article.

9

Flap endonuclease Rad27 cleaves the RNA of R-loop structures to suppress telomere recombination.

Liu CC, Chan HR, Su GC, Hsieh YZ, Lei KH, Kato T, Yu TY, Kao YW, Cheng TH, Chi P, Lin JJ. Liu CC, et al. Among authors: cheng th. Nucleic Acids Res. 2023 May 22;51(9):4398-4414. doi: 10.1093/nar/gkad236. Nucleic Acids Res. 2023. PMID: 36999631 Free PMC article.

10

DSIF modulates RNA polymerase II occupancy according to template G + C content.

Deng N, Zhang Y, Ma Z, Lin R, Cheng TH, Tang H, Snyder MP, Cohen SN. Deng N, et al. Among authors: cheng th. NAR Genom Bioinform. 2022 Jul 27;4(3):lqac054. doi: 10.1093/nargab/lqac054. eCollection 2022 Sep. NAR Genom Bioinform. 2022. PMID: 35910045 Free PMC article.

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