相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Heterochromatin Formation Promotes Longevity and Represses Ribosomal RNA Synthesis
Kimberly Larson et al.
PLOS GENETICS (2012)
Osteoblasts from a mandibuloacral dysplasia patient induce human blood precursors to differentiate into active osteoclasts
Sofia Avnet et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2011)
Protein isoprenylation regulates osteogenic differentiation of mesenchymal stem cells: effect of alendronate, and farnesyl and geranylgeranyl transferase inhibitors
G. Duque et al.
BRITISH JOURNAL OF PHARMACOLOGY (2011)
Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle
E. Mattioli et al.
CELL DEATH AND DIFFERENTIATION (2011)
Molecular mechanisms of centrosome and cytoskeleton anchorage at the nuclear envelope
Maria Schneider et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2011)
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria
S Dominici et al.
EUROPEAN JOURNAL OF HISTOCHEMISTRY (2011)
The accumulation of un-repairable DNA damage in laminopathy progeria fibroblasts is caused by ROS generation and is prevented by treatment with N-acetyl cysteine
Shane A. Richards et al.
HUMAN MOLECULAR GENETICS (2011)
Laminopathies and Lamin-Associated Signaling Pathways
Nadir M. Maraldi et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2011)
Lamin A variants that cause striated muscle disease are defective in anchoring transmembrane actin-associated nuclear lines for nuclear movement
Eric S. Folker et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Investigating the purpose of prelamin A processing
Brandon S. J. Davies et al.
NUCLEUS (2011)
TAN lines A novel nuclear envelope structure involved in nuclear positioning
G. W. Gant Luxton et al.
NUCLEUS (2011)
Prelamin A processing and functional effects in restrictive dermopathy
Marta Columbaro et al.
CELL CYCLE (2010)
Mammalian SUN Protein Interaction Networks at the Inner Nuclear Membrane and Their Role in Laminopathy Disease Processes
Farhana Haque et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Lamin A/C-mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy
Alexandre Mejat et al.
JOURNAL OF CELL BIOLOGY (2009)
A nuclear-envelope bridge positions nuclei and moves chromosomes
Daniel A. Starr
JOURNAL OF CELL SCIENCE (2009)
Dysfunctional Connections Between the Nucleus and the Actin and Microtubule Networks in Laminopathic Models
Christopher M. Hale et al.
BIOPHYSICAL JOURNAL (2008)
Chromatin changes induced by lamin A/C deficiency and the histone deacetylase inhibitor trichostatin A
Gabriela Galiova et al.
EUROPEAN JOURNAL OF CELL BIOLOGY (2008)
Effects of prelamin a processing inhibitors on the differentiation and activity of human osteoclasts
Nicoletta Zini et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2008)
Drugs affecting prelamin A processing: Effects on heterochromatin organization
Elisabetta Mattioli et al.
EXPERIMENTAL CELL RESEARCH (2007)
Pre-lamin a processing is linked to heterochromatin organization
Giovanna Lattanzi et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2007)
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type a phenotype
Francesca Lombardi et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2007)
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging
Dale K. Shumaker et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeleton
Farhana Haque et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Coupling of the nucleus and cytoplasm: role of the LINC complex
M Crisp et al.
JOURNAL OF CELL BIOLOGY (2006)
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment
M Columbaro et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2005)
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy
I Filesi et al.
PHYSIOLOGICAL GENOMICS (2005)
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy
C Capanni et al.
HUMAN MOLECULAR GENETICS (2005)
Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome
P Scaffidi et al.
NATURE MEDICINE (2005)
Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C
G Novelli et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)