Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies.
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Higher order chromatin organization in cancerHP1α mediates defective heterochromatin repair and accelerates senescence in Zmpste24-deficient cells.Genetics of inherited cardiomyopathy.Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria.Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution.Nuclear damages and oxidative stress: new perspectives for laminopathies.Diverse lamin-dependent mechanisms interact to control chromatin dynamics. Focus on laminopathiesHistochemistry through the years, browsing a long-established journal: novelties in traditional subjects.Structural and functional alterations of the cell nucleus in skeletal muscle wasting: the evidence in situ.Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria.
P2860
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P2860
Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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name
Nuclear envelope proteins and ...... c mechanism for laminopathies.
@ast
Nuclear envelope proteins and ...... c mechanism for laminopathies.
@en
type
label
Nuclear envelope proteins and ...... c mechanism for laminopathies.
@ast
Nuclear envelope proteins and ...... c mechanism for laminopathies.
@en
prefLabel
Nuclear envelope proteins and ...... c mechanism for laminopathies.
@ast
Nuclear envelope proteins and ...... c mechanism for laminopathies.
@en
P2093
P50
P1476
Nuclear envelope proteins and ...... ic mechanism for laminopathies
@en
P2093
Columbaro M
Manzoli FA
Maraldi NM
Sabatelli P
P577
2006-01-01T00:00:00Z