Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
about
Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophyMyotonic dystrophy protein kinase phosphorylates the myosin phosphatase targeting subunit and inhibits myosin phosphatase activityDivergent mitochondrial and endoplasmic reticulum association of DMPK splice isoforms depends on unique sequence arrangements in tail anchors.MKBP, a novel member of the small heat shock protein family, binds and activates the myotonic dystrophy protein kinaseIdentification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophyMyotonic dystrophy protein kinase is critical for nuclear envelope integrityMolecular basis for impaired muscle differentiation in myotonic dystrophyIn vivo co-localisation of MBNL protein with DMPK expanded-repeat transcriptsAltered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout miceIncredible RNA: Dual Functions of Coding and NoncodingMuscle wasting in myotonic dystrophies: a model of premature agingStructure of dystrophia myotonica protein kinaseRNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27)Mice deficient in Six5 develop cataracts: implications for myotonic dystrophyMyofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIbHeterozygous loss of Six5 in mice is sufficient to cause ocular cataractsMyotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal muscle cellsHomodimerization through coiled-coil regions enhances activity of the myotonic dystrophy protein kinaseAge of onset of RNA toxicity influences phenotypic severity: evidence from an inducible mouse model of myotonic dystrophy (DM1).Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy.Myotonic dystrophy protein kinase expressed in rat cardiac muscle is associated with sarcoplasmic reticulum and gap junctions.Role of myotonic dystrophy protein kinase (DMPK) in glucose homeostasis and muscle insulin action.Long tract of untranslated CAG repeats is deleterious in transgenic miceDMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model.Rac-1 and Raf-1 kinases, components of distinct signaling pathways, activate myotonic dystrophy protein kinase.Triplet repeat expansion in neuromuscular disease.Myotonic dystrophy: the role of RNA CUG triplet repeats.Alternative splicing controls myotonic dystrophy protein kinase structure, enzymatic activity, and subcellular localization.RNA-protein interactions in unstable microsatellite diseases.Does (CUG)n repeat in DMPK mRNA 'paint' chromosome 19 to suppress distant genes to create the diverse phenotype of myotonic dystrophy?: A new hypothesis of long-range cis autosomal inactivation.RNase H-mediated degradation of toxic RNA in myotonic dystrophy type 1Expanded CUG repeat RNAs form hairpins that activate the double-stranded RNA-dependent protein kinase PKRLocalization of myotonic dystrophy protein kinase in human and rabbit tissues using a new panel of monoclonal antibodies.Myotonic dystrophy: molecular windows on a complex etiology.Long CTG tracts from the myotonic dystrophy gene induce deletions and rearrangements during recombination at the APRT locus in CHO cells.Hypothesis: neoplasms in myotonic dystrophy.Genome wide identification of aberrant alternative splicing events in myotonic dystrophy type 2.Lens epithelial changes and mutated gene expression in patients with myotonic dystrophy.Myotonic dystrophy: RNA pathogenesis comes into focus.
P2860
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P2860
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh-hant
name
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
@en
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
@nl
type
label
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
@en
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
@nl
prefLabel
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
@en
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
@nl
P2093
P2860
P356
P1433
P1476
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
@en
P2093
Coerwinkel M
Groenen PJ
Hameister H
Molenaar PC
Nederhoff MG
P2860
P2888
P304
P356
10.1038/NG0796-316
P407
P50
P577
1996-07-01T00:00:00Z