Related references
Note: Only part of the references are listed.Minimal functional domains of paralogues hnRNP L and hnRNP LL exhibit mechanistic differences in exonic splicing repression
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hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome
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Polypyrimidine tract binding protein controls the transition from exon definition to an intron defined spliceosome
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A cell-based screen for splicing regulators identifies hnRNP LL as a distinct signal-induced repressor of CD45 variable exon 4
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SCIENCE (2008)
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hnRNP A1 functions with specificity in repression of SMN2 exon 7 splicing
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Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs)
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GENOME RESEARCH (2007)
Splicing regulation in neurologic disease
Donny D. Licatalosi et al.
NEURON (2006)
An exonic splicing silencer represses spliceosome assembly after ATP-dependent exon recognition
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A peptide motif in Raver1 mediates splicing repression by interaction with the PTB RRM2 domain
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Novel modes of splicing repression by PTB
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Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2
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AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Differential expression of CD45 isoforms is controlled by the combined activity of basal and inducible splicing-regulatory elements in each of the variable exons
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HnRNP L represses exon splicing via a regulated exonic splicing silencer
CR Rothrock et al.
EMBO JOURNAL (2005)
Binding of hnRNP L to the Pre-mRNA processing enhancer of the herpes simplex virus thymidine kinase gene enhances both polyadenylation and nucleocytoplasmic export of intronless mRNAs
SH Guang et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
Intronic CA-repeat and CA-rich elements:: a new class of regulators of mammalian alternative splicing
JY Hui et al.
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A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy
T Kashima et al.
NATURE GENETICS (2003)
Novel functional role of CA repeats and hnRNP L in RNA stability
JY Hui et al.
RNA (2003)
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NATURE REVIEWS NEUROSCIENCE (2003)
Missense mutations in hMLH1 and hMSH2 are associated with exonic splicing enhancers
IP Gorlov et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Alu-containing exons are alternatively spliced
R Sorek et al.
GENOME RESEARCH (2002)
Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1
L Cartegni et al.
NATURE GENETICS (2002)
Polypyrimidine tract binding protein antagonizes exon definition
EJ Wagner et al.
MOLECULAR AND CELLULAR BIOLOGY (2001)
Functional association of U2 snRNP with the ATP-independent spliceosomal complex E
R Das et al.
MOLECULAR CELL (2000)
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