| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/J.TIG.2004.12.004 |
| P698 | PubMed publication ID | 15661351 |
| P50 | author | Brendan J. Frey | Q18684996 |
| Benjamin J. Blencowe | Q63212972 | ||
| Quaid D Morris | Q63646478 | ||
| P2093 | author name string | Timothy R Hughes | |
| Wen Zhang | |||
| Qun Pan | |||
| Malina A Bakowski | |||
| P433 | issue | 2 | |
| P921 | main subject | alternative mRNA splicing, via spliceosome | Q21114084 |
| P304 | page(s) | 73-77 | |
| P577 | publication date | 2005-02-01 | |
| P1433 | published in | Trends in Genetics | Q2451468 |
| P1476 | title | Alternative splicing of conserved exons is frequently species-specific in human and mouse | |
| P478 | volume | 21 |
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| Q34921189 | Ab initio prediction of mutation-induced cryptic splice-site activation and exon skipping. |
| Q36504877 | Alternative splicing and RNA selection pressure--evolutionary consequences for eukaryotic genomes |
| Q34618555 | Alternative splicing and evolution: diversification, exon definition and function |
| Q39372815 | Alternative splicing networks regulated by signaling in human T cells. |
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| Q36090387 | Alternative splicing: a potential source of functional innovation in the eukaryotic genome |
| Q36503778 | Assessing the fraction of short-distance tandem splice sites under purifying selection |
| Q33261411 | Assessing the number of ancestral alternatively spliced exons in the human genome |
| Q33710087 | Assessment of orthologous splicing isoforms in human and mouse orthologous genes |
| Q43104534 | Characterization of intron loss events in mammals |
| Q38610057 | Characterization of lincRNA expression in the human retinal pigment epithelium and differentiated induced pluripotent stem cells. |
| Q37430071 | Complex tissue-specific patterns and distribution of multiple RAGE splice variants in different mammals |
| Q38157823 | Complexity of the alternative splicing landscape in plants. |
| Q28750125 | Computational prediction of splicing regulatory elements shared by Tetrapoda organisms |
| Q36311097 | Correspondence of D. melanogaster and C. elegans developmental stages revealed by alternative splicing characteristics of conserved exons |
| Q24684177 | Distinct class of putative "non-conserved" promoters in humans: comparative studies of alternative promoters of human and mouse genes |
| Q34964532 | Divergence of exonic splicing elements after gene duplication and the impact on gene structures. |
| Q38586911 | Diverse regulation of 3' splice site usage |
| Q36742729 | Dual function of C/D box small nucleolar RNAs in rRNA modification and alternative pre-mRNA splicing |
| Q36002580 | Dual-specificity splice sites function alternatively as 5' and 3' splice sites |
| Q35757637 | Epigenetic mechanisms for breakdown of self-incompatibility in interspecific hybrids. |
| Q39239706 | Estimating the prevalence of functional exonic splice regulatory information |
| Q33302676 | Evolution of Nova-dependent splicing regulation in the brain |
| Q33980314 | Evolution of alternative splicing in primate brain transcriptomes |
| Q24810664 | Evolutionarily conserved and diverged alternative splicing events show different expression and functional profiles |
| Q37053510 | Evolutionary conservation of alternative splicing in chicken. |
| Q38258263 | Evolutionary dynamics of coding and non-coding transcriptomes |
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| Q38938771 | Global 3' UTR shortening has a limited effect on protein abundance in proliferating T cells |
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| Q28744540 | Identification and functional characterization in vivo of a novel splice variant of LDLR in rhesus macaques |
| Q37052723 | Improved identification of conserved cassette exons using Bayesian networks. |
| Q41488512 | Limitations of animal models of Parkinson's disease |
| Q36580173 | Microarray analysis of RNA processing and modification |
| Q21245331 | Noisy splicing, more than expression regulation, explains why some exons are subject to nonsense-mediated mRNA decay |
| Q33258810 | Phylogenetic reconstruction of orthology, paralogy, and conserved synteny for dog and human |
| Q24646896 | Positive selection acting on splicing motifs reflects compensatory evolution |
| Q35493751 | Post-transcriptional exon shuffling events in humans can be evolutionarily conserved and abundant. |
| Q24812842 | Protein modularity of alternatively spliced exons is associated with tissue-specific regulation of alternative splicing |
| Q34324095 | Quantitative microarray profiling provides evidence against widespread coupling of alternative splicing with nonsense-mediated mRNA decay to control gene expression |
| Q42734570 | RNA Splicing Modulation Selectively Impairs Leukemia Stem Cell Maintenance in Secondary Human AML |
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| Q35568660 | RNA-Seq: Improving Our Understanding of Retinal Biology and Disease |
| Q34588437 | Regulation of alternative splicing by the core spliceosomal machinery |
| Q36748147 | Regulation of multiple core spliceosomal proteins by alternative splicing-coupled nonsense-mediated mRNA decay |
| Q35556982 | Regulation of toll-like receptor signaling by the SF3a mRNA splicing complex. |
| Q36877029 | Review: Alternative Splicing (AS) of Genes As An Approach for Generating Protein Complexity. |
| Q33305142 | SERpredict: detection of tissue- or tumor-specific isoforms generated through exonization of transposable elements |
| Q33618915 | Sex-specific and lineage-specific alternative splicing in primates |
| Q99724533 | Sex-specific selection drives the evolution of alternative splicing in birds |
| Q33982260 | Smg1 is required for embryogenesis and regulates diverse genes via alternative splicing coupled to nonsense-mediated mRNA decay |
| Q37397927 | Splice site strength-dependent activity and genetic buffering by poly-G runs |
| Q33478140 | Splicing in the eukaryotic ancestor: form, function and dysfunction |
| Q33471943 | Stochastic noise in splicing machinery |
| Q37298563 | Structural implication of splicing stochastics |
| Q33306111 | The "alternative" choice of constitutive exons throughout evolution |
| Q36139994 | The Mouse-Specific Splice Variant mRAGE_v4 Encodes a Membrane-Bound RAGE That Is Resistant to Shedding and Does Not Contribute to the Production of Soluble RAGE. |
| Q33269611 | The dystrotelin, dystrophin and dystrobrevin superfamily: new paralogues and old isoforms. |
| Q35826230 | The evolutionary fate of alternatively spliced homologous exons after gene duplication |
| Q34983597 | The relationship between gene isoform multiplicity, number of exons and protein divergence |
| Q41884066 | Tissue-specific splicing of disordered segments that embed binding motifs rewires protein interaction networks |
| Q34832437 | Transcriptome analyses of the human retina identify unprecedented transcript diversity and 3.5 Mb of novel transcribed sequence via significant alternative splicing and novel genes |
| Q29615085 | Understanding alternative splicing: towards a cellular code |
| Q35664036 | Using several pair-wise informant sequences for de novo prediction of alternatively spliced transcripts |
| Q34609175 | Verification of alternative splicing variants based on domain integrity, truncation length and intrinsic protein disorder |
| Q37890153 | When orthologs diverge between human and mouse |
| Q33381615 | Width of gene expression profile drives alternative splicing |
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