Tissue-Specific Gene Repositioning by Muscle Nuclear Membrane Proteins Enhances Repression of Critical Developmental Genes during Myogenesis.
about
Recent advances in understanding the role of lamins in health and diseaseConstrained release of lamina-associated enhancers and genes from the nuclear envelope during T-cell activation facilitates their association in chromosome compartments.Nuclear bodies reorganize during myogenesis in vitro and are differentially disrupted by expression of FSHD-associated DUX4.Immunohistochemistry on a panel of Emery-Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology.Lamins in the nuclear interior - life outside the lamina.Tissue-specific NETs alter genome organization and regulation even in a heterologous system.Highlight on the dynamic organization of the nucleus.Mechanisms and functions of nuclear envelope remodelling.Dynamic regulation of nuclear architecture and mechanics-a rheostatic role for the nucleus in tailoring cellular mechanosensitivity.Lamina-Associated Domains: Links with Chromosome Architecture, Heterochromatin, and Gene Repression.DNA Methylation, Nuclear Organization, and Cancer.Microinjection of Antibodies Targeting the Lamin A/C Histone-Binding Site Blocks Mitotic Entry and Reveals Separate Chromatin Interactions with HP1, CenpB and PML.Nuclear Pores Regulate Muscle Development and Maintenance by Assembling a Localized Mef2C Complex.Spindle associated membrane protein 1 (Samp1) is required for the differentiation of muscle cells.Expression Profiling of Differentiating Emerin-Null Myogenic Progenitor Identifies Molecular Pathways Implicated in Their Impaired Differentiation.Breaking the scale: how disrupting the karyoplasmic ratio gives cancer cells an advantage for metastatic invasion.Genome-Nuclear Lamina Interactions Regulate Cardiac Stem Cell Lineage Restriction.FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy.Laminopathy-causing lamin A mutations reconfigure lamina-associated domains and local spatial chromatin conformation.Mechanotransduction, nuclear architecture and epigenetics in Emery Dreifuss Muscular Dystrophy: tous pour un, un pour tous.Linker of nucleoskeleton and cytoskeleton complex proteins in cardiomyopathyThe Pathogenesis and Therapies of Striated Muscle LaminopathiesNuclear Envelope Transmembrane Proteins in Myotonic Dystrophy Type 1Nesprins and Lamins in Health and Diseases of Cardiac and Skeletal Muscles
P2860
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P2860
Tissue-Specific Gene Repositioning by Muscle Nuclear Membrane Proteins Enhances Repression of Critical Developmental Genes during Myogenesis.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Tissue-Specific Gene Repositio ...... ental Genes during Myogenesis.
@en
type
label
Tissue-Specific Gene Repositio ...... ental Genes during Myogenesis.
@en
prefLabel
Tissue-Specific Gene Repositio ...... ental Genes during Myogenesis.
@en
P2093
P2860
P50
P1433
P1476
Tissue-Specific Gene Repositio ...... mental Genes during Myogenesis
@en
P2093
David A Kelly
Jose I de Las Heras
Phú Lê Thành
Shaun Webb
P2860
P304
P356
10.1016/J.MOLCEL.2016.04.035
P577
2016-06-02T00:00:00Z