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

Year Number of Results
1991 1
1995 3
1996 3
1997 1
1998 2
2001 1
2002 3
2003 1
2004 3
2005 8
2006 5
2007 4
2009 1
2010 2
2011 10
2012 6
2013 6
2014 9
2015 9
2016 8
2017 6
2018 6
2019 5
2020 12
2021 4
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Similar articles for PMID: 21474761

104 results
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Page 1
Association of TALS developmental disorder with defect in minor splicing component U4atac snRNA.
Edery P, Marcaillou C, Sahbatou M, Labalme A, Chastang J, Touraine R, Tubacher E, Senni F, Bober MB, Nampoothiri S, Jouk PS, Steichen E, Berland S, Toutain A, Wise CA, Sanlaville D, Rousseau F, Clerget-Darpoux F, Leutenegger AL. Edery P, et al. Science. 2011 Apr 8;332(6026):240-3. doi: 10.1126/science.1202205. Science. 2011. PMID: 21474761 Free article.
Mutations in U4atac snRNA, a component of the minor spliceosome, in the developmental disorder MOPD I.
He H, Liyanarachchi S, Akagi K, Nagy R, Li J, Dietrich RC, Li W, Sebastian N, Wen B, Xin B, Singh J, Yan P, Alder H, Haan E, Wieczorek D, Albrecht B, Puffenberger E, Wang H, Westman JA, Padgett RA, Symer DE, de la Chapelle A. He H, et al. Science. 2011 Apr 8;332(6026):238-40. doi: 10.1126/science.1200587. Science. 2011. PMID: 21474760 Free PMC article.
Genetics. Minor splicing, disrupted.
Pessa HK, Frilander MJ. Pessa HK, et al. Science. 2011 Apr 8;332(6026):184-5. doi: 10.1126/science.1205503. Science. 2011. PMID: 21474744 No abstract available.
Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome.
Putoux A, Alqahtani A, Pinson L, Paulussen AD, Michel J, Besson A, Mazoyer S, Borg I, Nampoothiri S, Vasiljevic A, Uwineza A, Boggio D, Champion F, de Die-Smulders CE, Gardeitchik T, van Putten WK, Perez MJ, Musizzano Y, Razavi F, Drunat S, Verloes A, Hennekam R, Guibaud L, Alix E, Sanlaville D, Lesca G, Edery P. Putoux A, et al. Clin Genet. 2016 Dec;90(6):550-555. doi: 10.1111/cge.12781. Epub 2016 Jun 2. Clin Genet. 2016. PMID: 27040866
Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing.
Merico D, Roifman M, Braunschweig U, Yuen RK, Alexandrova R, Bates A, Reid B, Nalpathamkalam T, Wang Z, Thiruvahindrapuram B, Gray P, Kakakios A, Peake J, Hogarth S, Manson D, Buncic R, Pereira SL, Herbrick JA, Blencowe BJ, Roifman CM, Scherer SW. Merico D, et al. Nat Commun. 2015 Nov 2;6:8718. doi: 10.1038/ncomms9718. Nat Commun. 2015. PMID: 26522830 Free PMC article.
104 results
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