Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
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Fam65b is important for formation of the HDAC6-dysferlin protein complex during myogenic cell differentiationDUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1TDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expressionOsteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-betaThe nuclear envelope LEM-domain protein emerinReduced satellite cell numbers and myogenic capacity in aging can be alleviated by endurance exerciseMicroRNA-206: a potential circulating biomarker candidate for amyotrophic lateral sclerosisLamina-associated polypeptide (LAP)2α and other LEM proteins in cancer biologyEmbryonic senescence and laminopathies in a progeroid zebrafish modelNovel approach to meta-analysis of microarray datasets reveals muscle remodeling-related drug targets and biomarkers in Duchenne muscular dystrophyLamin A/C and emerin are critical for skeletal muscle satellite cell differentiationMonoclonal antibodies specific for disease-associated point-mutants: lamin A/C R453W and R482Wβ-Catenin is central to DUX4-driven network rewiring in facioscapulohumeral muscular dystrophy.Phosphatidylserine receptor BAI1 and apoptotic cells as new promoters of myoblast fusion.Lamin A variants that cause striated muscle disease are defective in anchoring transmembrane actin-associated nuclear lines for nuclear movement.Combining multiple hypothesis testing and affinity propagation clustering leads to accurate, robust and sample size independent classification on gene expression data.VISDA: an open-source caBIG analytical tool for data clustering and beyond.Probe set algorithms: is there a rational best bet?Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2).An emerin "proteome": purification of distinct emerin-containing complexes from HeLa cells suggests molecular basis for diverse roles including gene regulation, mRNA splicing, signaling, mechanosensing, and nuclear architecture.Evidence that proteasome-dependent degradation of the retinoblastoma protein in cells lacking A-type lamins occurs independently of gankyrin and MDM2.Motif-directed network component analysis for regulatory network inference.caBIG VISDA: modeling, visualization, and discovery for cluster analysis of genomic data.The D4Z4 macrosatellite repeat acts as a CTCF and A-type lamins-dependent insulator in facio-scapulo-humeral dystrophy.Network analysis of differential expression for the identification of disease-causing genes.A-MADMAN: annotation-based microarray data meta-analysis tool.Gene module identification from microarray data using nonnegative independent component analysisInterferon-stimulated gene 15 (ISG15) conjugates proteins in dermatomyositis muscle with perifascicular atrophy.MAPK signaling pathways and HDAC3 activity are disrupted during differentiation of emerin-null myogenic progenitor cells.Lamin-binding ProteinsLMNA Sequences of 60,706 Unrelated Individuals Reveal 132 Novel Missense Variants in A-Type Lamins and Suggest a Link between Variant p.G602S and Type 2 DiabetesMeta-analysis of muscle transcriptome data using the MADMuscle database reveals biologically relevant gene patterns.Uncoordinated transcription and compromised muscle function in the lmna-null mouse model of Emery- Emery-Dreyfuss muscular dystrophy.Limb-girdle and congenital muscular dystrophies: current diagnostics, management, and emerging technologies.Alignment of gene expression profiles from test samples against a reference database: New method for context-specific interpretation of microarray data.Statistical Test of Expression Pattern (STEPath): a new strategy to integrate gene expression data with genomic information in individual and meta-analysis studies.A flow cytometry-based screen of nuclear envelope transmembrane proteins identifies NET4/Tmem53 as involved in stress-dependent cell cycle withdrawal.Whole exome sequencing identifies a novel EMD mutation in a Chinese family with dilated cardiomyopathyUpregulation of immunoproteasome subunits in myositis indicates active inflammation with involvement of antigen presenting cells, CD8 T-cells and IFNΓA systems biology approach identifies molecular networks defining skeletal muscle abnormalities in chronic obstructive pulmonary disease
P2860
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P2860
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Nuclear envelope dystrophies s ...... thways in muscle regeneration.
@en
type
label
Nuclear envelope dystrophies s ...... thways in muscle regeneration.
@en
prefLabel
Nuclear envelope dystrophies s ...... thways in muscle regeneration.
@en
P2093
P356
P1433
P1476
Nuclear envelope dystrophies s ...... thways in muscle regeneration.
@en
P2093
Chenguang Fan
Diana Escolar
Elena Pegoraro
Eric P Hoffman
Erynn Gordon
Gisela Melcon
Jianhua Xuan
Jinwook Seo
Lauren M Pachman
Louis Schiltz
P304
P356
10.1093/BRAIN/AWL023
P407
P577
2006-02-14T00:00:00Z