Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation. - sprookjes - yvandenbroek - TriplyDB

Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation.

Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation.

http://www.wikidata.org/entity/Q33778527

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Spatial Genome Organization and Its Emerging Role as a Potential Diagnosis Tool Anchoring a Leviathan: How the Nuclear Membrane Tethers the Genome The nuclear envelope as a chromatin organizer Aging and radiation: bad companions Linker of nucleoskeleton and cytoskeleton complex proteins in cardiac structure, function, and disease.MAPK signaling pathways and HDAC3 activity are disrupted during differentiation of emerin-null myogenic progenitor cells.Constrained release of lamina-associated enhancers and genes from the nuclear envelope during T-cell activation facilitates their association in chromosome compartments.Functional effects of the TMEM43 Ser358Leu mutation in the pathogenesis of arrhythmogenic right ventricular cardiomyopathy Inner nuclear membrane proteins: impact on human disease.The nuclear envelope environment and its cancer connections.Replicative senescence is associated with nuclear reorganization and with DNA methylation at specific transcription factor binding sites Emerin in health and disease.Understanding the roles of nuclear A- and B-type lamins in brain development.Nuclear mechanics in cancer Lmo7 is dispensable for skeletal muscle and cardiac function.Quantitative analysis of the chromatin proteome in disease reveals remodeling principles and identifies high mobility group protein B2 as a regulator of hypertrophic growth.A filtering strategy identifies FOXQ1 as a potential effector of lamin A dysfunction.Chromatin loops, gene positioning, and gene expression.Locus-specific gene repositioning in prostate cancer Genetic mutations and mechanisms in dilated cardiomyopathy Tissue-of-origin-specific gene repositioning in breast and prostate cancer.Emerin and histone deacetylase 3 (HDAC3) cooperatively regulate expression and nuclear positions of MyoD, Myf5, and Pax7 genes during myogenesis.Prp22 and spliceosome components regulate chromatin dynamics in germ-line polyploid cells.Differentiation alters stem cell nuclear architecture, mechanics, and mechano-sensitivity.Nuclear organization: taking a position on gene expression.Hutchinson-Gilford progeria syndrome through the lens of transcription.A Crowdsourced nucleus: understanding nuclear organization in terms of dynamically networked protein function.What Should the Cardiologist know about Lamin Disease?Chromosomal aneuploidies induced upon Lamin B2 depletion are mislocalized in the interphase nucleus Diseases of the Nucleoskeleton.Mechanisms and functions of nuclear envelope remodelling.Perinuclear positioning of the inactive human cystic fibrosis gene depends on CTCF, A-type lamins and an active histone deacetylase.Messenger RNA processing is altered in autosomal dominant leukodystrophy Farnesyltransferase inhibitor treatment restores chromosome territory positions and active chromosome dynamics in Hutchinson-Gilford progeria syndrome cells.Association of LIM Domain 7 Gene Polymorphisms and Plasma Levels of LIM Domain 7 with Dilated Cardiomyopathy in a Chinese Population.Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery.Microinjection of Antibodies Targeting the Lamin A/C Histone-Binding Site Blocks Mitotic Entry and Reveals Separate Chromatin Interactions with HP1, CenpB and PML.Nucleolar tethering mediates pairing between the IgH and Myc loci.Gene expression, chromosome position and lamin A/C mutations.Genome-Nuclear Lamina Interactions Regulate Cardiac Stem Cell Lineage Restriction.

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Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation.

http://www.wikidata.org/entity/Q33778527

description

2010 nî lūn-bûn

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2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Altered chromosomal positionin ...... ith a lamin A/C gene mutation.

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Altered chromosomal positionin ...... ith a lamin A/C gene mutation.

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type

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Altered chromosomal positionin ...... ith a lamin A/C gene mutation.

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Altered chromosomal positionin ...... ith a lamin A/C gene mutation.

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prefLabel

Altered chromosomal positionin ...... ith a lamin A/C gene mutation.

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Altered chromosomal positionin ...... ith a lamin A/C gene mutation.

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JOURNAL.PONE.0014342

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Altered chromosomal positionin ...... ith a lamin A/C gene mutation.

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Christine M Labno

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Elizabeth McNally

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Fida Abuisneineh

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Harinder Singh

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Heather MacLeod

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Karen Reddy

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Lisa Dellefave

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Megan J Puckelwartz

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Peter Pytel

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Sara Selig

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P2860

Bioconductor: open software development for computational biology and bioinformatics

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

Nuclear lamins: building blocks of nuclear architecture

Myne-1, a spectrin repeat transmembrane protein of the myocyte inner nuclear membrane, interacts with lamin A/C

Coupling of the nucleus and cytoplasm: role of the LINC complex

Nesprin-1alpha self-associates and binds directly to emerin and lamin A in vitro

The DNA sequence and analysis of human chromosome 13

Lamin A/C truncation in dilated cardiomyopathy with conduction disease

Detection of chromosomal regions showing differential gene expression in human skeletal muscle and in alveolar rhabdomyosarcoma

SAGA interacting factors confine sub-diffusion of transcribed genes to the nuclear envelope.

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e14342

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scholarly article

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10.1371/JOURNAL.PONE.0014342

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12

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5

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John Fahrenbach

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2010-12-14T00:00:00Z

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49703449

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21179469

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3001866

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