Mutation-agnostic base editing of the progerin farnesylation site rescues Hutchinson-Gilford progeria syndrome phenotypes in neuromuscular organoids. [PDF]
Kim DW +8 more
europepmc +1 more source
TRF2 enriched cytoplasmic chromatin drives cGAS-STAT1-mediated inflammation in senescence. [PDF]
Kandhaya-Pillai R +6 more
europepmc +1 more source
Lamin-ating the genome: quantitative gatekeeping of replication initiation. [PDF]
Parasar B, Moghadami S, Tan L.
europepmc +1 more source
Murine Progeria Model Exhibits Delayed Fracture Healing With Senescent Phenotype and Dysregulated Immune Response. [PDF]
Duke VR +17 more
europepmc +1 more source
Flemming J. Olsen +11 more
doaj +1 more source
In Vivo Base Editing for Neonatal Inborn Errors of Metabolism: Clinical Progress, N-of-1 Therapy, and the Ethics of Bespoke Genetic Medicine. [PDF]
Li OM, Li Y, Li SXT.
europepmc +1 more source
Progeria (Hutchinson-Gilford progeria syndrome) is a rare genetic disorder that offers considerable insight into the biology of premature aging. This review summarizes the clinical characteristics of this disease and the underlying mutation in the lamin ...
Kieran, Mark W.
core
Excessive disulfide bonds in lamin A/C contribute to premature human aging. [PDF]
Ha SG +8 more
europepmc +1 more source
Barrier-to-Autointegration Factor 1: a key regulator of nuclear envelope integrity, genome stability, and disease progression. [PDF]
Shi P +10 more
europepmc +1 more source

