Related references
Note: Only part of the references are listed.hnRNP M facilitates exon 7 inclusion of SMN2 pre-mRNA in spinal muscular atrophy by targeting an enhancer on exon 7
Sunghee Cho et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS (2014)
Mechanisms for U2AF to define 3′ splice sites and regulate alternative splicing in the human genome
Changwei Shao et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2014)
Regulation of gene expression programmes by serine-arginine rich splicing factors
Minna-Liisa Aenkoe
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2014)
hnRNP A1 contacts exon 5 to promote exon 6 inclusion of apoptotic Fas gene
Hyun Kyung Oh et al.
APOPTOSIS (2013)
Position-dependent splicing activation and repression by SR and hnRNP proteins rely on common mechanisms
Steffen Erkelenz et al.
RNA (2013)
Validation of trans-acting elements that promote exon 7 skipping of SMN2 in SMN2-GFP stable cell line
Sunghee Cho et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2012)
Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of > 72 400 specimens
Elaine A. Sugarman et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2012)
hnRNP A1 Proofreads 3′ Splice Site Recognition by U2AF
Joao Paulo Tavanez et al.
MOLECULAR CELL (2012)
Control of alternative splicing by forskolin through hnRNP K during neuronal differentiation
Wenguang Cao et al.
NUCLEIC ACIDS RESEARCH (2012)
YB-1 binds to CAUC motifs and stimulates exon inclusion by enhancing the recruitment of U2AF to weak polypyrimidine tracts
Wen-Juan Wei et al.
NUCLEIC ACIDS RESEARCH (2012)
Evolution of SR protein and hnRNP splicing regulatory factors
Anke Busch et al.
WILEY INTERDISCIPLINARY REVIEWS-RNA (2012)
RNA-Seq analysis in mutant zebrafish reveals role of U1C protein in alternative splicing regulation
Tanja Dorothe Roesel et al.
EMBO JOURNAL (2011)
G Run-mediated Recognition of Proteolipid Protein and DM20 5′ Splice Sites by U1 Small Nuclear RNA Is Regulated by Context and Proximity to the Splice Site
Erming Wang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Frequent pathway mutations of splicing machinery in myelodysplasia
Kenichi Yoshida et al.
NATURE (2011)
Using positional distribution to identify splicing elements and predict pre-mRNA processing defects in human genes
Kian Huat Lim et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Strict 3′ splice site sequence requirements for U2 snRNP recruitment after U2AF binding underlie a genetic defect leading to autoimmune disease
Anna Corrionero et al.
RNA (2011)
The heterogeneous nuclear ribonucleoprotein-R is necessary for axonal β-actin mRNA translocation in spinal motor neurons
Michael Glinka et al.
HUMAN MOLECULAR GENETICS (2010)
Alternative splicing and evolution: diversification, exon definition and function
Hadas Keren et al.
NATURE REVIEWS GENETICS (2010)
HnRNP L-mediated regulation of mammalian alternative splicing by interference with splice site recognition
Monika Heiner et al.
RNA BIOLOGY (2010)
The Spliceosome: Design Principles of a Dynamic RNP Machine
Markus C. Wahl et al.
CELL (2009)
Differential 3′ splice site recognition of SMN1 and SMN2 transcripts by U2AF and U2 snRNP
Mafalda Martins de Araujo et al.
RNA (2009)
The SR protein family
Peter J. Shepard et al.
GENOME BIOLOGY (2009)
A high-throughout screening strategy identifies cardiotonic steroids as alternative splicing modulators
Peter Stoilov et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
hnRNP A1 functions with specificity in repression of SMN2 exon 7 splicing
Tsuyoshi Kashima et al.
HUMAN MOLECULAR GENETICS (2007)
Structural basis for polypyrimidine tract recognition by the essential pre-mRNA splicing factor U2AF65
E. Allen Sickmier et al.
MOLECULAR CELL (2006)
Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2
L Cartegni et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Is spinal muscular atrophy the result of defects in motor neuron processes?
M Briese et al.
BIOESSAYS (2005)
In vivo selection reveals combinatorial controls that define a critical exon in the spinal muscular atrophy genes
NN Singh et al.
RNA (2004)
U2AF homology motifs:: protein recognition in the RRM world
CL Kielkopf et al.
GENES & DEVELOPMENT (2004)
A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy
T Kashima et al.
NATURE GENETICS (2003)
Structural basis for the molecular recognition between human splicing factors U2AF65 and SF1/mBBP
P Selenko et al.
MOLECULAR CELL (2003)
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)
An in vivo reporter system for measuring increased inclusion of exon 7 in SMN2 mRNA: potential therapy of SMA
ML Zhang et al.
GENE THERAPY (2001)
Alternative splicing: increasing diversity in the proteomic world
BR Graveley
TRENDS IN GENETICS (2001)
Alternative pre-mRNA splicing:: the logic of combinatorial control
CWJ Smith et al.
TRENDS IN BIOCHEMICAL SCIENCES (2000)
Share Paper
