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Conserved role for spliceosomal component PRPF40A in microexon splicing
Mouse hippocampi transcriptomics of Daam1 microexon KO (RNA-seq)
Limited Evidence of Microexon Skipping in Parkinson’s Disease and Spinocerebellar Ataxia Type 3
Alternative splicing of microexons tend to be tissue-specific. Greatly investigated in brain development and autism spectrum disorders, little is known about microexons in other tissues. Humans have two highly homologous clathrin heavy chains (CLTC and CLTCL1). Ubiquitously expressed, CLTC drives cl...
ORGANISM(S): Mus musculus (Mouse) 
2026-09-10 | PXD082922 | Pride
X-linked dystonia-parkinsonism is a neurodegenerative disease, which is caused by a SVA retrotransposon insertion within TAF1, gene encoding an integral component of the basal transcription factor TFIID. The SVA insertion has been shown to induce defects both in biosynthesis and in alternative splic...
ORGANISM(S): Homo sapiens (Human) 
2020-05-26 | PXD009905 | Pride
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