Nuclear lamina remodelling and its implications for human disease.
about
Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar AtrophyLamin B1 mediated demyelination: Linking Lamins, Lipids and Leukodystrophies.Bursting the Bubble - Nuclear Envelope Rupture as a Path to Genomic Instability?Junctions in human health and inherited disease.Depletion of nuclear import protein karyopherin alpha 7 (KPNA7) induces mitotic defects and deformation of nuclei in cancer cells.Differential stem cell aging kinetics in Hutchinson-Gilford progeria syndrome and Werner syndrome.
P2860
Nuclear lamina remodelling and its implications for human disease.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Nuclear lamina remodelling and its implications for human disease.
@en
type
label
Nuclear lamina remodelling and its implications for human disease.
@en
prefLabel
Nuclear lamina remodelling and its implications for human disease.
@en
P2093
P2860
P1476
Nuclear lamina remodelling and its implications for human disease.
@en
P2093
Alexandre Chojnowski
Oliver Dreesen
Peh Fern Ong
P2860
P2888
P304
P356
10.1007/S00441-014-2069-4
P577
2014-12-24T00:00:00Z
P6179
1041816443