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prelamin A

Known as: lamin A precursor 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Hutchinson‐Gilford progeria syndrome (HGPS) arises when a truncated form of farnesylated prelamin A accumulates at the nuclear… 
2019
2019
Urinary incontinence (UI) is known as a distressing condition particularly among older adults, and negatively associated with… 
2015
2015
CONTEXT Lamin A (LMNA)-linked lipodystrophies belong to a group of clinical disorders characterized by a redistribution of… 
2015
2015
Introduction Mutations in the LMNA gene, which encodes the nuclear intermediate filament proteins lamins A and C, lead to a… 
2013
2013
Hutchinson-Gilford progeria (HGPS) is a rare, genetic progeroid disorder that causes premature ageing, nuclear lamina shape… 
2012
2012
Protein farnesyltransferase (FTase) inhibitors, generally called “FTIs,” block the farnesylation of prelamin A, inhibiting the… 
2010
2010
Laminopathies are an heterogeneous group of human disorders caused by mutations in the lamin A/C gene or in genes coding for… 
2007
2007
Protein farnesylation is required for the activation of multiple proteins involved in cell differentiation and function. In white…