共 155 条
[1]
Wang Z(2008)Splicing regulation: from a parts list of regulatory elements to an integrated splicing code RNA 14 802-813
[2]
Burge CB(2007)Splicing in disease: disruption of the splicing code and the decoding machinery Nat Rev Genet. 8 749-761
[3]
Wang GS(2011)Loss of exon identity is a common mechanism of human inherited disease Genome Res 21 1563-1571
[4]
Cooper TA(2014)Exon identity crisis: disease-causing mutations that disrupt the splicing code Genome Biol 15 201-238
[5]
Sterne-Weiler T(2004)Allele-specific transcript isoforms in human FEBS Lett 577 233-231
[6]
Howard J(2007)Identification of common genetic variation that modulates alternative splicing PLoS Genet 3 e99-554
[7]
Mort M(2008)Genome-wide analysis of transcript isoform variation in humans Nat Genet 40 225-592
[8]
Cooper DN(2009)Fine-scale variation and genetic determinants of alternative splicing across individuals PLoS Genet 5 e1000766-772
[9]
Sanford JR(2011)RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression Genome Res 21 545-777
[10]
Sterne-Weiler T(2012)Genetic variation of pre-mRNA alternative splicing in human populations Wiley Interdiscip Rev RNA 3 581-511