Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

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Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

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im Januar 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

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Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

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Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

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Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

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Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

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Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

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P1476

Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

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Andrea Gerbino

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Giuseppe Procino

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Maria Svelto

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Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

Caloric restriction and resveratrol promote longevity through the Sirtuin-1-dependent induction of autophagy

Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy

When lamins go bad: nuclear structure and disease

The nuclear lamina is mechano-responsive to ECM elasticity in mature tissue

Sudden death from genetic and acquired cardiomyopathies

Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy

Regulation of lamin properties and functions: does phosphorylation do it all?

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

LMNA E82K mutation activates FAS and mitochondrial pathways of apoptosis in heart tissue specific transgenic mice

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1356

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scholarly article

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10.3389/FPHYS.2018.01356

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English

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Monica Carmosino

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2018-09-25T00:00:00Z

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30319452

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6167438

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