review Open AccessTop 1% cited
“Laminopathies”: A wide spectrum of human diseases
Experimental Cell Research · 2007 · Vol. 313(10) · pp. 2121–2133
Howard J. Worman✉(Columbia University)Gisèle Bonne(Inserm)
Nuclear Structure and FunctionRNA Research and SplicingSkin and Cellular Biology ResearchLaminLMNABiologyMuscular dystrophyGeneticsEmerinProgeriaLeukodystrophyMutationPhenotype
MeSH terms
AnimalsHumansIntermediate Filament ProteinsMutationNuclear EnvelopeSyndromeNuclear MatrixGenetic Predisposition to DiseaseMuscular Dystrophy, Emery-DreifussActive Transport, Cell NucleusLamins
Funding
- Charcot-Marie-Tooth Association
- National Institutes of Health
Citations
647
FWCI
21.71
field-weighted impact
References
153
Percentile
100%
vs. same field & year
Citations per year
Cited by
Cellular Mechanotransduction: From Tension to Function
Frontiers in Physiology · 2018 · 943 citations
References
The nuclear lamins
Experimental Cell Research · 1986 · 484 citations
Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy
Human Molecular Genetics · 2000 · 656 citations
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)
Human Molecular Genetics · 2000 · 602 citations
Citation Network
How this paper connects to the literature. Drag to explore, click any node to open that paper.