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Genes & Development|May 17, 2012
Widespread recognition of 5' splice sites by noncanonical base-pairing to U1 snRNA involving bulged nucleotidesXavier Roca, Martin Akerman, Hans Gaus, et al.Molecular and Cellular Biology|March 24, 2010
Arginine methylation controls the subcellular localization and functions of the oncoprotein splicing factor SF2/ASFRahul Sinha, Eric Allemand, Zuo Zhang, et al.Molecular and Cellular Biology|September 7, 2002
Nuclear export and retention signals in the RS domain of SR proteinsDemian Cazalla, Jun Zhu, Lisa Manche, et al.Human Mutation|January 12, 2005
Functional significance of a deep intronic mutation in the ATM gene and evidence for an alternative exon 28aGabriela Coutinho, Jiuyong Xie, Liutao Du, et al.Proceedings of the National Academy of Sciences of the United States of America|March 2, 2005
Regulation of heterogenous nuclear ribonucleoprotein A1 transport by phosphorylation in cells stressed by osmotic shockEric Allemand, Sònia Guil, Michael Myers, et al.Plos One|June 21, 2007
Control of pre-mRNA splicing by the general splicing factors PUF60 and U2AF(65)Michelle L Hastings, Eric Allemand, Dominik M Duelli, et al.Nature Structural & Molecular Biology|December 21, 2004
An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sitesMichelle L Hastings, Nicoletta Resta, Daniel Traum, et al.Nature Communications|May 27, 2022
Gene-specific nonsense-mediated mRNA decay targeting for cystic fibrosis therapyYoung Jin Kim, Tomoki Nomakuchi, Foteini Papaleonidopoulou, et al.Nucleic Acids Research|August 18, 2006
Comprehensive splice-site analysis using comparative genomicsNihar Sheth, Xavier Roca, Michelle L Hastings, et al.American Journal of Human Genetics|December 31, 2005
Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2Luca Cartegni, Michelle L Hastings, John A Calarco, et al.Pageof 21