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BioID-based Identification of Skp Cullin F-box (SCF)β-TrCP1/2 E3 Ligase Substrates.TMEM43 mutation p.S358L alters intercalated disc protein expression and reduces conduction velocity in arrhythmogenic right ventricular cardiomyopathyMuscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organizationNovel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis.Linker of nucleoskeleton and cytoskeleton complex proteins in cardiac structure, function, and disease.Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophyNesprins: tissue-specific expression of epsilon and other short isoforms.A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia.Specific localization of nesprin-1-α2, the short isoform of nesprin-1 with a KASH domain, in developing, fetal and regenerating muscle, using a new monoclonal antibody.A Disulfide Bond Is Required for the Transmission of Forces through SUN-KASH ComplexesGlobal loss of a nuclear lamina component, lamin A/C, and LINC complex components SUN1, SUN2, and nesprin-2 in breast cancer.SUN2 exerts tumor suppressor functions by suppressing the Warburg effect in lung cancerAn Intracellular Arrangement of Histoplasma capsulatum Yeast-Aggregates Generates Nuclear Damage to the Cultured Murine Alveolar Macrophages.Muscle development, regeneration and laminopathies: how lamins or lamina-associated proteins can contribute to muscle development, regeneration and disease.The diverse functional LINCs of the nuclear envelope to the cytoskeleton and chromatinEmery-Dreifuss muscular dystrophy-linked genes and centronuclear myopathy-linked genes regulate myonuclear movement by distinct mechanisms.Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease.SUN1 splice variants, SUN1_888, SUN1_785, and predominant SUN1_916, variably function in directional cell migration.Nesprin-2 mediated nuclear trafficking and its clinical implications.Tissue elasticity bridges cancer stem cells to the tumor microenvironment through microRNAs: Implications for a "watch-and-wait" approach to cancer.Spatial organization of the Schizosaccharomyces pombe genome within the nucleus.Lamin A/C Cardiomyopathies: Current Understanding and Novel Treatment Strategies.Cell Type-Specific Effects of Mutant DISC1: A Proteomics Study.Lamin B Receptor: Interplay between Structure, Function and Localization.Microtubule-actin crosslinking factor 1 (Macf1) domain function in Balbiani body dissociation and nuclear positioning.LINCing defective nuclear-cytoskeletal coupling and DYT1 dystonia.The emerin-binding transcription factor Lmo7 is regulated by association with p130Cas at focal adhesionsDownregulation of SUN2, a novel tumor suppressor, mediates miR-221/222-induced malignancy in central nervous system embryonal tumors.Human tumour viruses and the deregulation of cell polarity in cancer.Molecular Insights into the Mechanisms of SUN1 Oligomerization in the Nuclear Envelope.A Special Topic on Nuclear Mechanobiology
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
The LINC complex and human disease.
@en
The LINC complex and human disease.
@nl
type
label
The LINC complex and human disease.
@en
The LINC complex and human disease.
@nl
prefLabel
The LINC complex and human disease.
@en
The LINC complex and human disease.
@nl
P2093
P2860
P356
P1476
The LINC complex and human disease.
@en
P2093
Manfred S Wehnert
Peter Meinke
Thuy Duong Nguyen
P2860
P304
P356
10.1042/BST20110658
P577
2011-12-01T00:00:00Z