ExonSkipDB

Functional annotation of exon skipping event in human. Exon skipping (ES), the most common alternative splicing event, has been reported to contribute to diverse human diseases due to the loss of functional domains sites or frame shifting of open reading frame (ORF) and noticed as therapeutic targets

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ExonSkipDB: functional annotation of exon skipping event in human
PMID: 31642488

metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:22.886049

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• ExonSkipDB: functional annotation of exon skipping event in human PubMed citations: 16.

  16 articles citing: ExonSkipDB: functional annotation of exon skipping event in human

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  lncRNAfunc: a knowledgebase of lncRNA function in human cancer. PMID:34791419

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  A Review on the Carcinogenic Roles of DSCAM-AS1. PMID:34708048

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  OncoSplicing: an updated database for clinically relevant alternative splicing in 33 human cancers. PMID:34554251

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  Antisense Oligonucleotide-Mediated Exon-skipping Therapies: Precision Medicine Spreading from Duchenne Muscular Dystrophy. PMID:34414317

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  Measuring and interpreting pervasive heterogeneity, poikilosis. PMID:34377957

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  Systemic characterization of alternative splicing related to prognosis and immune infiltration in malignant mesothelioma. PMID:34294080

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  Alternative Splicing Dynamics of the Hypothalamus-Pituitary-Ovary Axis During Pubertal Transition in Gilts. PMID:33995469

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  MET Exon 14 Skipping: A Case Study for the Detection of Genetic Variants in Cancer Driver Genes by Deep Learning. PMID:33921709

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  The Functional Impact of Alternative Splicing on the Survival Prognosis of Triple-Negative Breast Cancer. PMID:33519909

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  ExonSkipAD provides the functional genomic landscape of exon skipping events in Alzheimer's disease. PMID:33497435

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  Prpf31 is essential for the survival and differentiation of retinal progenitor cells by modulating alternative splicing. PMID:33476374

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  Androgen receptor and its splice variant, AR-V7, differentially induce mRNA splicing in prostate cancer cells. PMID:33446905

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  Dual Fluorescence Splicing Reporter Minigene Identifies an Antisense Oligonucleotide to Skip Exon v8 of the CD44 Gene. PMID:33266296

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  Comprehensive Analysis of Alternative Splicing Signature in Gastric Cancer Prognosis Based on The Cancer Genome Atlas (TCGA) and SpliceSeq Databases. PMID:33219199

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  MeDAS: a Metazoan Developmental Alternative Splicing database. PMID:33084905

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  Systematics for types and effects of RNA variations. PMID:32951567

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gene transcripts

metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:22.886049

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rna splicing

metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:22.886049

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oncology

metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:22.886049

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genetic variation

metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:22.886049

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small molecules

metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:22.886049

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gene transcripts rna splicing oncology genetic variation small molecule