Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1991 16
1992 30
1993 48
1994 56
1995 61
1996 59
1997 59
1998 93
1999 82
2000 153
2001 156
2002 105
2003 98
2004 157
2005 141
2006 145
2007 165
2008 158
2009 168
2010 198
2011 222
2012 164
2013 145
2014 114
2015 110
2016 87
2017 87
2018 118
2019 83
2020 10
Text availability
Article attribute
Article type
Publication date

Search Results

3,012 results
Results by year
Filters applied: . Clear all
Page 1
Alternative splicing regulates stochastic NLRP3 activity.
Hoss F, Mueller JL, Rojas Ringeling F, Rodriguez-Alcazar JF, Brinkschulte R, Seifert G, Stahl R, Broderick L, Putnam CD, Kolodner RD, Canzar S, Geyer M, Hoffman HM, Latz E. Hoss F, et al. Nat Commun. 2019 Jul 19;10(1):3238. doi: 10.1038/s41467-019-11076-1. Nat Commun. 2019. PMID: 31324763 Free PMC article.
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.
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.
Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia.
Latham SL, Ehmke N, Reinke PYA, Taft MH, Eicke D, Reindl T, Stenzel W, Lyons MJ, Friez MJ, Lee JA, Hecker R, Frühwald MC, Becker K, Neuhann TM, Horn D, Schrock E, Niehaus I, Sarnow K, Grützmann K, Gawehn L, Klink B, Rump A, Chaponnier C, Figueiredo C, Knöfler R, Manstein DJ, Di Donato N. Latham SL, et al. Nat Commun. 2018 Oct 12;9(1):4250. doi: 10.1038/s41467-018-06713-0. Nat Commun. 2018. PMID: 30315159 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.
The exon junction complex: a lifelong guardian of mRNA fate.
Woodward LA, Mabin JW, Gangras P, Singh G. Woodward LA, et al. Wiley Interdiscip Rev RNA. 2017 May;8(3). doi: 10.1002/wrna.1411. Epub 2016 Dec 23. Wiley Interdiscip Rev RNA. 2017. PMID: 28008720 Review.
Exonic mutations and exon skipping: Lessons learned from DFNA5.
Booth KT, Azaiez H, Kahrizi K, Wang D, Zhang Y, Frees K, Nishimura C, Najmabadi H, Smith RJ. Booth KT, et al. Hum Mutat. 2018 Mar;39(3):433-440. doi: 10.1002/humu.23384. Epub 2018 Jan 11. Hum Mutat. 2018. PMID: 29266521 Free PMC article.
Novel PLVAP Mutation in Protein Losing Enteropathy.
Gorukmez O, Gorukmez O, Demiroren K. Gorukmez O, et al. Fetal Pediatr Pathol. 2019 Dec;38(6):534-537. doi: 10.1080/15513815.2019.1627624. Epub 2019 Jun 19. Fetal Pediatr Pathol. 2019. PMID: 31215290
Exome sequencing identifies the cause of a mendelian disorder.
Ng SB, Buckingham KJ, Lee C, Bigham AW, Tabor HK, Dent KM, Huff CD, Shannon PT, Jabs EW, Nickerson DA, Shendure J, Bamshad MJ. Ng SB, et al. Nat Genet. 2010 Jan;42(1):30-5. doi: 10.1038/ng.499. Epub 2009 Nov 13. Nat Genet. 2010. PMID: 19915526 Free PMC article.
3,012 results
Jump to page
Feedback