Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?
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Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophySurvival motor neuron protein regulates stem cell division, proliferation, and differentiation in DrosophilaIdentification and characterization of Gemin7, a novel component of the survival of motor neuron complexRhythmic serotonin N-acetyltransferase mRNA degradation is essential for the maintenance of its circadian oscillation.Gemin proteins are required for efficient assembly of Sm-class ribonucleoproteins.Dynamics of axonal mRNA transport and implications for peripheral nerve regenerationThe RNA binding protein hnRNP Q modulates the utilization of exon 7 in the survival motor neuron 2 (SMN2) geneA SMN missense mutation complements SMN2 restoring snRNPs and rescuing SMA miceSpinal muscular atrophy: from gene discovery to clinical trialsSplicing therapy for neuromuscular diseaseThe spinal muscular atrophy disease protein SMN is linked to the Golgi networkIn vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation proteinDeterminants of the interaction of the spinal muscular atrophy disease protein SMN with the dimethylarginine-modified box H/ACA small nucleolar ribonucleoprotein GAR1Hyperphosphorylated C-terminal repeat domain-associating proteins in the nuclear proteome link transcription to DNA/chromatin modification and RNA processingA short antisense oligonucleotide masking a unique intronic motif prevents skipping of a critical exon in spinal muscular atrophyHormone response element binding proteins: novel regulators of vitamin D and estrogen signalingThe survival of motor neuron (SMN) protein interacts with the mRNA-binding protein HuD and regulates localization of poly(A) mRNA in primary motor neuron axons.Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneuronsSMN in spinal muscular atrophy and snRNP biogenesisVersatility of MicroRNA biogenesis.The COPI vesicle complex binds and moves with survival motor neuron within axons.Syncrip/hnRNP Q influences synaptic transmission and regulates BMP signaling at the Drosophila neuromuscular synapseMolecular determinants of survival motor neuron (SMN) protein cleavage by the calcium-activated protease, calpainSYNCRIP, a member of the heterogeneous nuclear ribonucleoprotein family, is involved in mouse hepatitis virus RNA synthesisSmall nuclear RNAs and mRNAs: linking RNA processing and transport to spinal muscular atrophy.Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?The Survival of Motor Neuron Protein Acts as a Molecular Chaperone for mRNP AssemblyAssays for the identification and prioritization of drug candidates for spinal muscular atrophyDrug discovery and development for spinal muscular atrophy: lessons from screening approaches and future challenges for clinical development.Drosophila Syncrip modulates the expression of mRNAs encoding key synaptic proteins required for morphology at the neuromuscular junction.A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mouseInfantile spinal muscular atrophy with respiratory distress type 1 (SMARD1).SMN-inducing compounds for the treatment of spinal muscular atrophy.Minute virus of mice small nonstructural protein NS2 interacts and colocalizes with the Smn protein.A feedback loop regulates splicing of the spinal muscular atrophy-modifying gene, SMN2.Subcellular transcriptome alterations in a cell culture model of spinal muscular atrophy point to widespread defects in axonal growth and presynaptic differentiation.Presynaptic localization of Smn and hnRNP R in axon terminals of embryonic and postnatal mouse motoneuronsA multi-exon-skipping detection assay reveals surprising diversity of splice isoforms of spinal muscular atrophy genes.Genome-wide pathway analysis reveals different signaling pathways between secreted lactoferrin and intracellular delta-lactoferrin.Fishing for a mechanism: using zebrafish to understand spinal muscular atrophy.
P2860
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P2860
Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?
description
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2002
@ast
im Januar 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 2002)
@en
vedecký článok (publikovaný 2002/01/01)
@sk
vědecký článek publikovaný v roce 2002
@cs
wetenschappelijk artikel (gepubliceerd op 2002/01/01)
@nl
наукова стаття, опублікована в січні 2002
@uk
مقالة علمية (نشرت عام 2002)
@ar
name
Specific interaction of Smn, t ...... RNA processing in motor axons?
@ast
Specific interaction of Smn, t ...... RNA processing in motor axons?
@en
Specific interaction of Smn, t ...... RNA processing in motor axons?
@nl
type
label
Specific interaction of Smn, t ...... RNA processing in motor axons?
@ast
Specific interaction of Smn, t ...... RNA processing in motor axons?
@en
Specific interaction of Smn, t ...... RNA processing in motor axons?
@nl
prefLabel
Specific interaction of Smn, t ...... RNA processing in motor axons?
@ast
Specific interaction of Smn, t ...... RNA processing in motor axons?
@en
Specific interaction of Smn, t ...... RNA processing in motor axons?
@nl
P2093
P3181
P356
P1476
Specific interaction of Smn, t ...... RNA processing in motor axons?
@en
P2093
Ann-Kathrin Kröning
Sibylle Jablonka
Uta-Maria Ohndorf
Wilfried Rossoll
P304
P3181
P356
10.1093/HMG/11.1.93
P407
P577
2002-01-01T00:00:00Z