Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α. - Wikidata - awgldk - TriplyDB

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

http://www.wikidata.org/entity/Q37463359

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The quasi-parallel lives of satellite cells and atrophying muscle The effect of the lamin A and its mutants on nuclear structure, cell proliferation, protein stability, and mobility in embryonic cells MAPK signaling pathways and HDAC3 activity are disrupted during differentiation of emerin-null myogenic progenitor cells.Cellular mechanosensing: getting to the nucleus of it all.Progerin reduces LAP2α-telomere association in Hutchinson-Gilford progeria.Nuclear positioning in muscle development and disease.Lamina-associated polypeptide (LAP)2α and nucleoplasmic lamins in adult stem cell regulation and disease.Lamins at the crossroads of mechanosignaling Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes.Ameliorating pathogenesis by removing an exon containing a missense mutation: a potential exon-skipping therapy for laminopathies.Genetic disruption of Smad7 impairs skeletal muscle growth and regeneration.Laminopathy-causing lamin A mutations reconfigure lamina-associated domains and local spatial chromatin conformation.SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells.The Pathogenesis and Therapies of Striated Muscle Laminopathies Nesprins and Lamins in Health and Diseases of Cardiac and Skeletal Muscles

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Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

http://www.wikidata.org/entity/Q37463359

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article científic

@ca

article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 27 March 2013

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

@en

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

@nl

type

label

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

@en

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

@nl

prefLabel

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

@en

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

@nl

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Human Molecular Genetics

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Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α

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Aditi Phadke

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Colin L Stewart

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Henry Liu

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Jonathan E Cohen

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Juliet A Ellis

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Tatiana V Cohen

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Terence A Partridge

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Viola F Gnocchi

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P2860

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

NIH Image to ImageJ: 25 years of image analysis

Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome

Smad3 signaling is required for satellite cell function and myogenic differentiation of myoblasts

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

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

Cardiomyocyte-specific expression of lamin a improves cardiac function in Lmna-/- mice

A new mathematical model for relative quantification in real-time RT-PCR

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

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

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10.1093/HMG/DDT135

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23535822

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