Desmosomes in the heart: a review of clinical and mechanistic analyses. - Test2 - elhamkhani - TriplyDB

Desmosomes in the heart: a review of clinical and mechanistic analyses.

Desmosomes in the heart: a review of clinical and mechanistic analyses.

http://www.wikidata.org/entity/Q38206258

about

Striatins as plaque molecules of zonulae adhaerentes in simple epithelia, of tessellate junctions in stratified epithelia, of cardiac composite junctions and of various size classes of lateral adherens junctions in cultures of epithelia- and carcino Transgenic mice overexpressing desmocollin-2 (DSC2) develop cardiomyopathy associated with myocardial inflammation and fibrotic remodeling.Dominant de novo DSP mutations cause erythrokeratodermia-cardiomyopathy syndrome.Accelerated cardiac remodeling in desmoplakin transgenic mice in response to endurance exercise is associated with perturbed Wnt/β-catenin signaling.150th Anniversary Series: Desmosomes and the Hallmarks of Cancer.Cardiomyocytes of the Heart and Pulmonary Veins: Novel Contributors to Asthma?Desmosomes and Intermediate Filaments: Their Consequences for Tissue Mechanics.Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.Molecular insights into cardiomyopathies associated with desmin (DES) mutations

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Desmosomes in the heart: a review of clinical and mechanistic analyses.

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Desmosomes in the heart: a review of clinical and mechanistic analyses.

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Desmosomes in the heart: a review of clinical and mechanistic analyses.

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Desmosomes in the heart: a review of clinical and mechanistic analyses.

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15419061.2014.906533

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Cell Communication & Adhesion

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Desmosomes in the heart: a review of clinical and mechanistic analyses.

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Dipal M Patel

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Kathleen J Green

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P2860

Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma

Differential mechanisms of LEF/TCF family-dependent transcriptional activation by beta-catenin and plakoglobin

Molecular insights into arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 missense mutations

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

LUMA interacts with emerin and influences its distribution at the inner nuclear membrane

Plakophilin 2: a critical scaffold for PKC alpha that regulates intercellular junction assembly

A dysfunctional desmin mutation in a patient with severe generalized myopathy

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109-128

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