about
Emerin caps the pointed end of actin filaments: evidence for an actin cortical network at the nuclear inner membraneLamin B1 is required for mouse development and nuclear integrityMultiple roles for emerin: implications for Emery-Dreifuss muscular dystrophySun2 is a novel mammalian inner nuclear membrane proteinProteome analysis of a rat liver nuclear insoluble protein fraction and localization of a novel protein, ISP36, to compartments in the interchromatin spaceAccumulation of beta (m), a structural member of X,K-ATPase beta-subunit family, in nuclear envelopes of perinatal myocytesLamin B1 mediates cell-autonomous neuropathology in a leukodystrophy mouse model.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.Keratin mutations and intestinal pathology.TorsinA in the nuclear envelope.Lmo7 is an emerin-binding protein that regulates the transcription of emerin and many other muscle-relevant genes.The muscular dystrophies: from genes to therapies.Nuclear structure in cancer cells.Occurrence of Emery-Dreifuss muscular dystrophy in a rural setting of Cameroon: a case report and review of the literature.Therapy insight: cardiovascular complications associated with muscular dystrophies.The 4q subtelomere harboring the FSHD locus is specifically anchored with peripheral heterochromatin unlike most human telomeresReduced expression of lamin A/C correlates with poor histological differentiation and prognosis in primary gastric carcinoma.Skeletal myopathy in a family with lamin A/C cardiac disease.Nuclear architecture: the cell biology of a laminopathy.Spatial localization of genes determined by intranuclear DNA fragmentation with the fusion proteins lamin KRED and histone KRED und visible light.Proteomic exploration of the impacts of pomegranate fruit juice on the global gene expression of prostate cancer cell.MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-beta signaling.Torn apart: membrane rupture in muscular dystrophies and associated cardiomyopathies.Pleomorphism of the nuclear envelope in breast cancer: a new approach to an old problem.LMNA gene single nucleotide polymorphisms in dilated cardiomyopathy of Han children.The nuclear pore complex protein Tpr is a common autoantigen in sera that demonstrate nuclear envelope staining by indirect immunofluorescence.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Nuclear envelope proteins and neuromuscular diseases.
@ast
Nuclear envelope proteins and neuromuscular diseases.
@en
type
label
Nuclear envelope proteins and neuromuscular diseases.
@ast
Nuclear envelope proteins and neuromuscular diseases.
@en
prefLabel
Nuclear envelope proteins and neuromuscular diseases.
@ast
Nuclear envelope proteins and neuromuscular diseases.
@en
P2860
P356
P1433
P1476
Nuclear envelope proteins and neuromuscular diseases.
@en
P2093
Cecilia Ostlund
Howard J Worman
P2860
P304
P356
10.1002/MUS.10302
P577
2003-04-01T00:00:00Z