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Jing Zhang et al.
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Alternative isoform regulation in human tissue transcriptomes
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Expression of 24,426 human alternative splicing events and predicted cis regulation in 48 tissues and cell lines
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Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing
Qun Pan et al.
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Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe stargardt-like disease
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Mutations in splicing factor PRPF3, causing retinal degeneration, form detrimental aggregates in photoreceptor cells
Antonella Comitato et al.
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Discovery of tissue-specific exons using comprehensive human exon microarrays
Tyson A. Clark et al.
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Computational analysis of tissue-specific combinatorial gene regulation: predicting interaction between transcription factors in human tissues
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Alternative splicing: New insights from global analyses
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Ames waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts
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Alternative promoter usage of the membrane glycoprotein CD36
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Unusual intron conservation near tissue-regulated exons found by splicing microarrays
Charles W. Sugnet et al.
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Mutations in PRPF31 inhibit pre-mRNA splicing of rhodopsin gene and cause apoptosis of retinal cells
LY Yuan et al.
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Alternative splicing in disease and therapy
MA Garcia-Blanco et al.
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Developmental analyses of 5A11/Basigin, 5A11/Basigin-2 and their putative binding partner MCTI in the mouse eye
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Genomic analysis of mouse retinal development
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5A11/Basigin gene products are necessary for proper maturation and function of the retina
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Variation in alternative splicing across human tissues
G Yeo et al.
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Retina-specific expression of 5A11/Basigin-2, a member of the immunoglobulin gene superfamily
JD Ochrietor et al.
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Predictive identification of exonic splicing enhancers in human genes
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SCIENCE (2002)
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa
CF Chakarova et al.
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A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11)
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Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)
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Genome-wide detection of alternative splicing in expressed sequences of human genes
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Protein diversity from alternative splicing: A challenge for bioinformatics and post-genome biology
DL Black
CELL (2000)