Dystrophin is transcribed in brain from a distant upstream promoter.
about
Phosphoglucomutase 1: a gene with two promoters and a duplicated first exonMapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3beta-dystrobrevin, a member of the dystrophin-related protein familySplicing therapy for neuromuscular diseaseTwo different promoters direct expression of two distinct forms of mRNAs of human platelet-activating factor receptorKnockdown of dystrophin Dp71 impairs PC12 cells cycle: localization in the spindle and cytokinesis structures implies a role for Dp71 in cell divisionPhosphorylation of dystrophin Dp71d by Ca2+/calmodulin-dependent protein kinase II modulates the Dp71d nuclear localization in PC12 cellsDetection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophyImpact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry.Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients.Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups.Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients.Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter.The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy.Intron-exon structures of eukaryotic model organisms.Ordered disorder of the astrocytic dystrophin-associated protein complex in the norm and pathologyNegative regulatory elements upstream of a novel exon of the neuronal nicotinic acetylcholine receptor alpha 2 subunit geneSomatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers.Dystrophin in frameshift deletion patients with Becker muscular dystrophyExploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.Recent advances in understanding muscular dystrophyA novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophyA second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophyEnhanced sensitivity of hippocampal pyramidal neurons from mdx mice to hypoxia-induced loss of synaptic transmission.A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues.Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues.Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridization.Quantitative trait loci for aggressive behavior in Drosophila melanogaster.Deposition of beta/A4 immunoreactivity and neuronal pathology in transgenic mice expressing the carboxyl-terminal fragment of the Alzheimer amyloid precursor in the brain.Association between loss of dp140 and cognitive impairment in duchenne and becker dystrophies.Distinct promoters direct neuronal and nonneuronal expression of rat aromatic L-amino acid decarboxylase.Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifs.Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype.Molecular and functional analysis of the utrophin promoterSerum response factor and protein-mediated DNA bending contribute to transcription of the dystrophin muscle-specific promoter.Characterization of gene rearrangements leading to activation of MDR-1.The genetic basis of paediatric heart disease.Dystrophin Dp71 expression is down-regulated during myogenesis: role of Sp1 and Sp3 on the Dp71 promoter activity.A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD).
P2860
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P2860
Dystrophin is transcribed in brain from a distant upstream promoter.
description
1991 nî lūn-bûn
@nan
1991 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Dystrophin is transcribed in brain from a distant upstream promoter.
@ast
Dystrophin is transcribed in brain from a distant upstream promoter.
@en
Dystrophin is transcribed in brain from a distant upstream promoter.
@nl
type
label
Dystrophin is transcribed in brain from a distant upstream promoter.
@ast
Dystrophin is transcribed in brain from a distant upstream promoter.
@en
Dystrophin is transcribed in brain from a distant upstream promoter.
@nl
prefLabel
Dystrophin is transcribed in brain from a distant upstream promoter.
@ast
Dystrophin is transcribed in brain from a distant upstream promoter.
@en
Dystrophin is transcribed in brain from a distant upstream promoter.
@nl
P2093
P2860
P356
P1476
Dystrophin is transcribed in brain from a distant upstream promoter.
@en
P2093
P2860
P304
P356
10.1073/PNAS.88.4.1276
P407
P577
1991-02-01T00:00:00Z