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

Year Number of Results
1985 1
1986 11
1987 35
1988 56
1989 78
1990 94
1991 135
1992 152
1993 206
1994 183
1995 181
1996 217
1997 217
1998 239
1999 212
2000 243
2001 265
2002 181
2003 196
2004 228
2005 241
2006 247
2007 290
2008 258
2009 277
2010 306
2011 368
2012 343
2013 324
2014 304
2015 303
2016 344
2017 279
2018 272
2019 201
2020 18
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6,978 results
Results by year
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Page 1
Universal Alternative Splicing of Noncoding Exons.
Deveson IW, Brunck ME, Blackburn J, Tseng E, Hon T, Clark TA, Clark MB, Crawford J, Dinger ME, Nielsen LK, Mattick JS, Mercer TR. Deveson IW, et al. Cell Syst. 2018 Feb 28;6(2):245-255.e5. doi: 10.1016/j.cels.2017.12.005. Epub 2018 Jan 24. Cell Syst. 2018. PMID: 29396323 Free article.
The importance of DNA methylation of exons on alternative splicing.
Shayevitch R, Askayo D, Keydar I, Ast G. Shayevitch R, et al. RNA. 2018 Oct;24(10):1351-1362. doi: 10.1261/rna.064865.117. Epub 2018 Jul 12. RNA. 2018. PMID: 30002084 Free PMC article.
Reduced mutation rate in exons due to differential mismatch repair.
Frigola J, Sabarinathan R, Mularoni L, Muiños F, Gonzalez-Perez A, López-Bigas N. Frigola J, et al. Nat Genet. 2017 Dec;49(12):1684-1692. doi: 10.1038/ng.3991. Epub 2017 Nov 6. Nat Genet. 2017. PMID: 29106418 Free PMC article.
Exons of Leukemia Suppressor Genes: Creative Assembly Required.
Asnani M, Thomas-Tikhonenko A. Asnani M, et al. Trends Cancer. 2018 Dec;4(12):796-798. doi: 10.1016/j.trecan.2018.10.005. Epub 2018 Oct 28. Trends Cancer. 2018. PMID: 30470300 Free PMC article. Review.
Exon Junction Complex Shapes the Transcriptome by Repressing Recursive Splicing.
Blazquez L, Emmett W, Faraway R, Pineda JMB, Bajew S, Gohr A, Haberman N, Sibley CR, Bradley RK, Irimia M, Ule J. Blazquez L, et al. Mol Cell. 2018 Nov 1;72(3):496-509.e9. doi: 10.1016/j.molcel.2018.09.033. Mol Cell. 2018. PMID: 30388411 Free PMC article.
Origins and impacts of new mammalian exons.
Merkin JJ, Chen P, Alexis MS, Hautaniemi SK, Burge CB. Merkin JJ, et al. Cell Rep. 2015 Mar 31;10(12):1992-2005. doi: 10.1016/j.celrep.2015.02.058. Epub 2015 Mar 19. Cell Rep. 2015. PMID: 25801031 Free PMC article.
Identification of novel candidate disease genes from de novo exonic copy number variants.
Gambin T, Yuan B, Bi W, Liu P, Rosenfeld JA, Coban-Akdemir Z, Pursley AN, Nagamani SCS, Marom R, Golla S, Dengle L, Petrie HG, Matalon R, Emrick L, Proud MB, Treadwell-Deering D, Chao HT, Koillinen H, Brown C, Urraca N, Mostafavi R, Bernes S, Roeder ER, Nugent KM, Bader PI, Bellus G, Cummings M, Northrup H, Ashfaq M, Westman R, Wildin R, Beck AE, Immken L, Elton L, Varghese S, Buchanan E, Faivre L, Lefebvre M, Schaaf CP, Walkiewicz M, Yang Y, Kang SL, Lalani SR, Bacino CA, Beaudet AL, Breman AM, Smith JL, Cheung SW, Lupski JR, Patel A, Shaw CA, Stankiewicz P. Gambin T, et al. Genome Med. 2017 Sep 21;9(1):83. doi: 10.1186/s13073-017-0472-7. Genome Med. 2017. PMID: 28934986 Free PMC article.
Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder.
Krupp DR, Barnard RA, Duffourd Y, Evans SA, Mulqueen RM, Bernier R, Rivière JB, Fombonne E, O'Roak BJ. Krupp DR, et al. Am J Hum Genet. 2017 Sep 7;101(3):369-390. doi: 10.1016/j.ajhg.2017.07.016. Epub 2017 Aug 31. Am J Hum Genet. 2017. PMID: 28867142 Free PMC article.
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