Myotonic Dystrophy Type 1 RNA Crystal Structures Reveal Heterogeneous 1 × 1 Nucleotide UU Internal Loop Conformations
about
Structural studies of CNG repeatsUtilizing the GAAA Tetraloop/Receptor To Facilitate Crystal Packing and Determination of the Structure of a CUG RNA HelixA dynamic structural model of expanded RNA CAG repeats: a refined X-ray structure and computational investigations using molecular dynamics and umbrella sampling simulations.Stacking in RNA: NMR of Four Tetramers Benchmark Molecular DynamicsTrinucleotide repeats: a structural perspectiveComputational investigation of RNA CUG repeats responsible for myotonic dystrophy 1Targeting toxic RNAs that cause myotonic dystrophy type 1 (DM1) with a bisamidinium inhibitor.Methods to enable the design of bioactive small molecules targeting RNA.Oligonucleotide-based strategies to combat polyglutamine diseases.MBNL proteins and their target RNAs, interaction and splicing regulation.Induction and reversal of myotonic dystrophy type 1 pre-mRNA splicing defects by small molecules.Features of modularly assembled compounds that impart bioactivity against an RNA target.Structural Insights Reveal the Dynamics of the Repeating r(CAG) Transcript Found in Huntington's Disease (HD) and Spinocerebellar Ataxias (SCAs)RNA Structures as Mediators of Neurological Diseases and as Drug Targets.On the Applicability of Elastic Network Models for the Study of RNA CUG Trinucleotide Repeat Overexpansion.Discovery of the first small-molecule CsrA-RNA interaction inhibitors using biophysical screening technologies.In silico discovery of substituted pyrido[2,3-d]pyrimidines and pentamidine-like compounds with biological activity in myotonic dystrophy models.Crystallographic and Computational Analyses of AUUCU Repeating RNA That Causes Spinocerebellar Ataxia Type 10 (SCA10).Small-molecule-mediated cleavage of RNA in living cells.A Potent Inhibitor of Protein Sequestration by Expanded Triplet (CUG) Repeats that Shows Phenotypic Improvements in a Drosophila Model of Myotonic Dystrophy.Rational design of chemical genetic probes of RNA function and lead therapeutics targeting repeating transcripts.Structural Characteristics of Simple RNA Repeats Associated with Disease and their Deleterious Protein Interactions.An innate twist between Crick's wobble and Watson-Crick base pairs.Structure and Dynamics of RNA Repeat Expansions That Cause Huntington's Disease and Myotonic Dystrophy Type 1.Structures of RNA repeats associated with neurological diseases.Pyrrole-imidazole polyamides distinguish between double-helical DNA and RNA.
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P2860
Myotonic Dystrophy Type 1 RNA Crystal Structures Reveal Heterogeneous 1 × 1 Nucleotide UU Internal Loop Conformations
description
2011 nî lūn-bûn
@nan
2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Myotonic Dystrophy Type 1 RNA ...... UU Internal Loop Conformations
@ast
Myotonic Dystrophy Type 1 RNA ...... UU Internal Loop Conformations
@en
Myotonic Dystrophy Type 1 RNA ...... UU Internal Loop Conformations
@nl
type
label
Myotonic Dystrophy Type 1 RNA ...... UU Internal Loop Conformations
@ast
Myotonic Dystrophy Type 1 RNA ...... UU Internal Loop Conformations
@en
Myotonic Dystrophy Type 1 RNA ...... UU Internal Loop Conformations
@nl
prefLabel
Myotonic Dystrophy Type 1 RNA ...... UU Internal Loop Conformations
@ast
Myotonic Dystrophy Type 1 RNA ...... UU Internal Loop Conformations
@en
Myotonic Dystrophy Type 1 RNA ...... UU Internal Loop Conformations
@nl
P2093
P2860
P3181
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Myotonic dystrophy type 1 RNA ...... UU internal loop conformations
@en
P2093
Amit Kumar
HaJeung Park
Kendall W Nettles
Matthew D Disney
Raman Parkesh
P2860
P304
P3181
P356
10.1021/BI2013068
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P50
P577
2011-10-20T00:00:00Z