TMEM230-WT-pEGFP(isoform 1) Citations (2)
Originally described in: Identification of TMEM230 mutations in familial Parkinson's disease.Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, Xu Y, Chan P, Huang B, Gao XP, Song Z, Liu Z, Fecto F, Siddique N, Foroud T, Jankovic J, Ghetti B, Nicholson DA, Krainc D, Melen O, Vance JM, Pericak-Vance MA, Ma YC, Rajput AH, Siddique T Nat Genet. 2016 Jul;48(7):733-9. doi: 10.1038/ng.3589. Epub 2016 Jun 6. PubMed Journal
Articles Citing TMEM230-WT-pEGFP(isoform 1)
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| Quantitative chemoproteomics reveals O-GlcNAcylation of cystathionine gamma-lyase (CSE) represses trophoblast syncytialization. Liu J, Shao X, Qin W, Zhang Y, Dang F, Yang Q, Yu X, Li YX, Chen X, Wang C, Wang YL. Cell Chem Biol. 2021 Jun 17;28(6):788-801.e5. doi: 10.1016/j.chembiol.2021.01.024. Epub 2021 Feb 23. PubMed |
| TREX2 deficiency suppresses spontaneous and genotoxin-associated mutagenesis. Marple T, Son MY, Cheng X, Ko JH, Sung P, Hasty P. Cell Rep. 2024 Jan 23;43(1):113637. doi: 10.1016/j.celrep.2023.113637. Epub 2024 Jan 3. PubMed |
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