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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1974 1
1992 1
1994 1
2003 2
2004 2
2005 1
2008 3
2009 2
2010 5
2011 2
2012 1
2013 5
2015 4
2016 4
2017 2
2018 3
2019 1
2020 1
2023 0

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PubMed (Bookshelf cited) for id: 40363

37 results

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Page 1
Renal disease in Cockayne syndrome.
Stern-Delfils A, Spitz MA, Durand M, Obringer C, Calmels N, Olagne J, Pillay K, Fieggen K, Laugel V, Zaloszyc A. Stern-Delfils A, et al. Eur J Med Genet. 2020 Jan;63(1):103612. doi: 10.1016/j.ejmg.2019.01.002. Epub 2019 Jan 7. Eur J Med Genet. 2020. PMID: 30630117
Cockayne syndrome group A and B proteins converge on transcription-linked resolution of non-B DNA.
Scheibye-Knudsen M, Tseng A, Borch Jensen M, Scheibye-Alsing K, Fang EF, Iyama T, Bharti SK, Marosi K, Froetscher L, Kassahun H, Eckley DM, Maul RW, Bastian P, De S, Ghosh S, Nilsen H, Goldberg IG, Mattson MP, Wilson DM 3rd, Brosh RM Jr, Gorospe M, Bohr VA. Scheibye-Knudsen M, et al. Proc Natl Acad Sci U S A. 2016 Nov 1;113(44):12502-12507. doi: 10.1073/pnas.1610198113. Epub 2016 Oct 18. Proc Natl Acad Sci U S A. 2016. PMID: 27791127 Free PMC article.
A ubiquitylation site in Cockayne syndrome B required for repair of oxidative DNA damage, but not for transcription-coupled nucleotide excision repair.
Ranes M, Boeing S, Wang Y, Wienholz F, Menoni H, Walker J, Encheva V, Chakravarty P, Mari PO, Stewart A, Giglia-Mari G, Snijders AP, Vermeulen W, Svejstrup JQ. Ranes M, et al. Nucleic Acids Res. 2016 Jun 20;44(11):5246-55. doi: 10.1093/nar/gkw216. Epub 2016 Apr 7. Nucleic Acids Res. 2016. PMID: 27060134 Free PMC article.
CSB-PGBD3 Mutations Cause Premature Ovarian Failure.
Qin Y, Guo T, Li G, Tang TS, Zhao S, Jiao X, Gong J, Gao F, Guo C, Simpson JL, Chen ZJ. Qin Y, et al. PLoS Genet. 2015 Jul 28;11(7):e1005419. doi: 10.1371/journal.pgen.1005419. eCollection 2015 Jul. PLoS Genet. 2015. PMID: 26218421 Free PMC article.
37 results