Defining early steps in mRNA transport: mutant mRNA in myotonic dystrophy type I is blocked at entry into SC-35 domains.
about
An architectural role for a nuclear noncoding RNA: NEAT1 RNA is essential for the structure of paraspecklesA conserved CCCH-type zinc finger protein regulates mRNA nuclear adenylation and exportMechanistic determinants of MBNL activityStable C0T-1 repeat RNA is abundant and is associated with euchromatic interphase chromosomesSequestration of multiple RNA recognition motif-containing proteins by C9orf72 repeat expansionsGene positioning.Myotonic dystrophies 1 and 2: complex diseases with complex mechanisms.Hsp70 gene association with nuclear speckles is Hsp70 promoter specific.Association between active genes occurs at nuclear speckles and is modulated by chromatin environment.Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy.A multifaceted FISH approach to study endogenous RNAs and DNAs in native nuclear and cell structures.The dynamic pathway of nuclear RNA in eukaryotesA role for TREX components in the release of spliced mRNA from nuclear speckle domains.Large-scale chromatin structure of inducible genes: transcription on a condensed, linear template.Transcriptional changes and developmental abnormalities in a zebrafish model of myotonic dystrophy type 1.Epigenetic changes and non-coding expanded repeats.Perspectives on gene therapy in myotonic dystrophy type 1.Cellular toxicity of expanded RNA repeats: focus on RNA foci.Assembly and mobility of exon-exon junction complexes in living cells.RNA biology of disease-associated microsatellite repeat expansions.Nuclear speckles: molecular organization, biological function and role in disease.Muscleblind-like1 undergoes ectopic relocation in the nuclei of skeletal muscles in myotonic dystrophy and sarcopenia.mRNA nuclear export and human diseaseTranscriptionally correlated subcellular dynamics of MBNL1 during lens development and their implication for the molecular pathology of myotonic dystrophy type 1.Accumulation of poly(A) RNA in nuclear granules enriched in Sam68 in motor neurons from the SMNΔ7 mouse model of SMA.
P2860
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P2860
Defining early steps in mRNA transport: mutant mRNA in myotonic dystrophy type I is blocked at entry into SC-35 domains.
description
2007 nî lūn-bûn
@nan
2007 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Defining early steps in mRNA t ...... ed at entry into SC-35 domains
@nl
Defining early steps in mRNA t ...... d at entry into SC-35 domains.
@ast
Defining early steps in mRNA t ...... d at entry into SC-35 domains.
@en
type
label
Defining early steps in mRNA t ...... ed at entry into SC-35 domains
@nl
Defining early steps in mRNA t ...... d at entry into SC-35 domains.
@ast
Defining early steps in mRNA t ...... d at entry into SC-35 domains.
@en
prefLabel
Defining early steps in mRNA t ...... ed at entry into SC-35 domains
@nl
Defining early steps in mRNA t ...... d at entry into SC-35 domains.
@ast
Defining early steps in mRNA t ...... d at entry into SC-35 domains.
@en
P2093
P2860
P3181
P356
P1476
Defining early steps in mRNA t ...... d at entry into SC-35 domains.
@en
P2093
Carol Johnson
Jeanne B Lawrence
Kelly P Smith
Yigong Xing
P2860
P304
P3181
P356
10.1083/JCB.200706048
P407
P577
2007-09-01T00:00:00Z