about
Molecular ageing in progeroid syndromes: Hutchinson-Gilford progeria syndrome as a modelDermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stressThe nuclear envelopathies and human diseasesGenome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathyThe laminopathies: a clinical reviewLamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathyMyopathic lamin mutations cause reductive stress and activate the nrf2/keap-1 pathwayOvercoming functional redundancy to elicit pachyonychia congenita-like nail lesions in transgenic miceLMNA E82K mutation activates FAS and mitochondrial pathways of apoptosis in heart tissue specific transgenic miceImmobility, inheritance and plasticity of shape of the yeast nucleus.A comparative study of Drosophila and human A-type lamins.Nuclear localization signal deletion mutants of lamin A and progerin reveal insights into lamin A processing and emerin targetingDefining the properties of the nonhelical tail domain in type II keratin 5: insight from a bullous disease-causing mutationQuantitative nucleolar proteomics reveals nuclear re-organization during stress- induced senescence in mouse fibroblast.Functions and dysfunctions of the nuclear lamin Ig-fold domain in nuclear assembly, growth, and Emery-Dreifuss muscular dystrophy.Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy.Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionalsEmerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles.Nuclear morphology and deformation in engineered cardiac myocytes and tissues.Nuclear lamins: key regulators of nuclear structure and activitiesHutchinson-Gilford progeria syndrome.Accumulation of the inner nuclear envelope protein Sun1 is pathogenic in progeric and dystrophic laminopathies.Laminopathies.Nuclear envelopathies--raising the nuclear veil.Reversal of laminopathies: the curious case of SUN1For whom the cells pull: Hydrogel and micropost devices for measuring traction forces.Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy.Reduced expression of lamin A/C correlates with poor histological differentiation and prognosis in primary gastric carcinoma.Requirement for Sun1 in the expression of meiotic reproductive genes and piRNA.Bringing KASH under the SUN: the many faces of nucleo-cytoskeletal connections.Skeletal myopathy in a family with lamin A/C cardiac disease.Beyond lamins other structural components of the nucleoskeleton.Lamin A, farnesylation and agingMicrocephalia with mandibular and dental dysplasia in adult Zmpste24-deficient mice.Dynamics and molecular interactions of linker of nucleoskeleton and cytoskeleton (LINC) complex proteins.p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeria.Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference.Proteomic signature of reversine-treated murine fibroblasts by 2-D difference gel electrophoresis and MS: possible associations with cell signalling networks.Lamin A and microtubules collaborate to maintain nuclear morphology.
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
How do mutations in lamins A and C cause disease?
@ast
How do mutations in lamins A and C cause disease?
@en
type
label
How do mutations in lamins A and C cause disease?
@ast
How do mutations in lamins A and C cause disease?
@en
prefLabel
How do mutations in lamins A and C cause disease?
@ast
How do mutations in lamins A and C cause disease?
@en
P2860
P356
P1476
How do mutations in lamins A and C cause disease?
@en
P2093
Howard J Worman
Jean-Claude Courvalin
P2860
P304
P356
10.1172/JCI20832
P407
P577
2004-02-01T00:00:00Z