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Article

A Novel Function for SMN, the Spinal Muscular Atrophy Disease Gene Product, in Pre-mRNA Splicing

1 Nov 1998

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Share to Neurogenetic and Muscular Disorders Research
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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9845364
DOI: 10.1016/s0092-8674(00)81632-3

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Related research

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A Novel Function for SMN, the Spinal Muscular Atrophy Disease Gene Product, in Pre-mRNA SplicingPMID 9845364Read ↗

The Spinal Muscular Atrophy Disease Gene Product, SMN, and Its Associated Protein SIP1 Are in a Complex with Spliceosomal snRNP ProteinsSemantic proximity Read ↗

Spliceosomal small nuclear ribonucleoprotein biogenesis defects and motor neuron selectivity in spinal muscular atrophy.Semantic proximity Read ↗

SMN in spinal muscular atrophy and snRNP biogenesisSemantic proximity Read ↗

Alternative Splicing Role in New Therapies of Spinal Muscular AtrophySemantic proximity Read ↗

The Impact of Splicing Dysregulation on Neuromuscular Disorders and Current Neuromuscular Genetic TherapiesSemantic proximity Read ↗

Alternative splicing in spinal muscular atrophy underscores the role of an intron definition modelSemantic proximity Read ↗

Spinal muscular atrophy.Semantic proximity Read ↗

Genome-wide identification of mRNAs associated with the protein SMN whose depletion decreases their axonal localizationSemantic proximity Read ↗

RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent intronsSemantic proximity Read ↗

Mitochondrial Dysfunction in Spinal Muscular AtrophySemantic proximity Read ↗

The SMN-ribosome interplay: a new opportunity for Spinal Muscular Atrophy therapies.Semantic proximity Read ↗

Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2.Semantic proximity Read ↗

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