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Keywords: nucleoskeleton
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Journal Articles
In collection:
Mechanobiology
J Cell Sci (2017) 130 (14): 2243–2250.
Published: 15 July 2017
..., and chromatin in particular, respond to changes in the mechanical microenvironment of the cell, resulting in architectural and transcriptional alterations, and thereby facilitating cellular adaption. Mechanotransduction Nucleus Nuclear lamina Nucleoskeleton Nuclear mechanical response Max...
Journal Articles
J Cell Sci (2014) 127 (18): 3956–3969.
Published: 15 September 2014
.../20.7.1754 Simon   D. N. , Wilson   K. L. (2011). The nucleoskeleton as a genome-associated dynamic ‘network of networks’.   Nat. Rev. Mol. Cell Biol.   12 , 695 – 708 . 10.1038/nrm3207 Simon   D. N. , Zastrow   M. S. , Wilson   K. L. (2010). Direct actin binding to A- and B...
Includes: Supplementary data
Journal Articles
J Cell Sci (2014) 127 (14): 3005–3015.
Published: 15 July 2014
.... Published by The Company of Biologists Ltd 2014 Cell mechanics Mechanotransduction Extra-cellular matrix Nucleus Nucleoskeleton Proteostasis Evolution has likely driven our tissues and organs to fulfill their roles with optimal efficiency and, of course, viability. Mature tissues need...
Journal Articles
J Cell Sci (2009) 122 (10): 1551–1562.
Published: 15 May 2009
... nucleoskeleton as well as a peripheral lamina in human cells. J. Cell Sci. 108 , 635 -644. Jackson, D. A. and Cook, P. R. (1985). Transcription occurs at a nucleoskeleton. EMBO J. 4 , 919 -925. Jackson, D. A. and Cook, P. R. (1988). Visualization of a filamentous nucleoskeleton with a 23 nm...
Includes: Supplementary data
Journal Articles
J Cell Sci (2008) 121 (7): 1014–1024.
Published: 1 April 2008
... of chromosome territories, which relocate towards the nuclear periphery. These results show that a lamin B1-containing nucleoskeleton is required to maintain RNA synthesis and that ongoing synthesis is a fundamental determinant of global nuclear architecture in mammalian cells. ‡ Author for correspondence...
Includes: Supplementary data
Journal Articles
J Cell Sci (2005) 118 (2): 409–420.
Published: 15 January 2005
... myogenesis, Rb was rapidly and progressively dephosphorylated. Underphosphorylated Rb formed complexes with LAP2α in proliferating myoblasts and postmitotic myoblasts. In myoblasts transfected with the mutant lamins, this complex was disrupted. These data suggest that remodelling of the nucleoskeleton...
Journal Articles
J Cell Sci (2003) 116 (9): 1733–1743.
Published: 1 May 2003
... morphology in male meiosis. We propose that EAST constitutes a component of a nucleoskeleton that helps to constrain the mobility of chromosomes in interphase, mitosis and meiosis. * Author for correspondence (e-mail: [email protected]) 21 1 2003 © The Company of Biologists Limited...
Includes: Multimedia, Supplementary data
Journal Articles
J Cell Sci (1998) 111 (24): 3663–3673.
Published: 18 December 1998
...J. Miguel Ortega; Melvin L. DePamphilis ABSTRACT To determine whether or not initiation sites for DNA replication in mammalian cells are defined by association with nuclear structure, attachments between the nucleoskeleton and the hamster DHFR gene initiation zone were examined. Nucleoskeletons...
Journal Articles
J Cell Sci (1995) 1995 (Supplement_19): 59–65.
Published: 1 January 1995
... The Company of Biologists Limited 1995 1995 nucleoskeleton replication transcription repair chromatin loop Compared to the compartmentation found within the cytoplasm, the nucleus has traditionally been viewed as relatively unstructured. However, recent experiments suggest that it also has...
Journal Articles
J Cell Sci (1994) 107 (8): 2191–2202.
Published: 1 August 1994
... sections from which ∼90% chromatin had been removed showed that most DNA synthesis occurs in specific dense structures (replication factories) attached to a diffuse nucleoskeleton. These factories appear at the end of G 1 -phase and quickly become active; as S-phase progresses, they increase in size...
Journal Articles
J Cell Sci (1994) 107 (7): 1745–1752.
Published: 1 July 1994
... nucleoskeleton. After treatment with an endonuclease, most repaired DNA electroeluted from beads with chromatin fragments; this was unlike nascent DNA made during S phase and suggests that repaired DNA is not as closely associated with the skeleton. However, the procedure destroyed repair activity, so repaired...
Journal Articles
J Cell Sci (1994) 107 (3): 469–486.
Published: 1 March 1994
... and nucleosome assembly, and may reflect the attachment of the yeast DNA to the rodent cell nucleoskeleton. The yeast integrant replicates late in S phase at a time when G bands of the mouse chromosomes are being replicated, and participates in sister chromatid exchanges at a high frequency. We discuss...
Journal Articles
J Cell Sci (1994) 107 (2): 639–648.
Published: 1 February 1994
.... These results suggest that the dense fibrillar component is the site of rRNA transcription. After dispersing the granular component and the dense fibrillar component by a hypotonic treatment, removal of most chromatin and preparation of resinless sections, fibrillar centres remained fixed to a nucleoskeleton...
Journal Articles
J Cell Sci (1993) 105 (2): 541–550.
Published: 1 June 1993
... was very stable. Foci remained when ∼90% chromatin was removed, suggesting they were attached to an underlying structure. * Author for correspondence 22 01 1993 24 02 1993 © 1993 by Company of Biologists 1993 replication foci DNA polymerase nucleoskeleton dTTP analogues...
Journal Articles
Journal Articles
J Cell Sci (1988) 90 (3): 365–378.
Published: 1 July 1988
... the gentle deconstruction of the cell and also preserved vital functions. method cytoskeleton nucleoskeleton permeabilize chromatin © 1988 by Company of Biologists 1988 08 02 1988 25 03 1988 * Author for correspondence General methods for assays have been...