Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1.
about
The importance of CELF control: molecular and biological roles of the CUG-BP, Elav-like family of RNA-binding proteinsTherapeutics development in myotonic dystrophy type 1.Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophyMuscleblind-like 1 knockout mice reveal novel splicing defects in the myotonic dystrophy brainA mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition.The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease.Bridging integrator 1 (BIN1) protein expression increases in the Alzheimer's disease brain and correlates with neurofibrillary tangle pathologyDifferences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.Neuropathology does not Correlate with Regional Differences in the Extent of Expansion of CTG Repeats in the Brain with Myotonic Dystrophy Type 1Alternative splicing of the neurofibromatosis type 1 pre-mRNA is regulated by the muscleblind-like proteins and the CUG-BP and ELAV-like factorsDetection of slipped-DNAs at the trinucleotide repeats of the myotonic dystrophy type I disease locus in patient tissues.Regulation of human MAPT gene expression.Neurodegeneration the RNA wayGeneration of neural cells from DM1 induced pluripotent stem cells as cellular model for the study of central nervous system neuropathogenesisCELFish ways to modulate mRNA decay.CUG-BP, Elav-like family (CELF)-mediated alternative splicing regulation in the brain during health and disease.Myotonic dystrophy 1 in the nervous system: from the clinic to molecular mechanisms.Brain MRI abnormalities in the adult form of myotonic dystrophy type 1: A longitudinal case series studyPathogenic RNAs in microsatellite expansion diseaseWidespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy.Aberrant splicing in neurological diseases.Brain pathology in myotonic dystrophy: when tauopathy meets spliceopathy and RNAopathy.Results from an external proficiency testing program: 11 years of molecular genetics testing for myotonic dystrophy type 1.Tau 6D and 6P isoforms inhibit polymerization of full-length tau in vitro.Cerebrospinal fluid biomarkers of neurodegeneration in patients with juvenile and classic myotonic dystrophy type 1.Cerebrospinal fluid tau and amyloid beta42 protein in patients with myotonic dystrophy type 1.Cloning and embryonic expression patterns of the chicken CELF family.
P2860
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P2860
Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1.
@en
type
label
Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1.
@en
prefLabel
Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1.
@en
P2093
P1476
Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1.
@en
P2093
Athena Andreadis
Junning Wang
Marie-Laure Caillet-Boudin
Michel Parent
Nicolas Sergeant
Olivier Leroy
Thomas Cooper
P304
P356
10.1016/J.BBADIS.2005.12.003
P577
2005-12-29T00:00:00Z