Hutchinson–Gilford progeria syndrome (HGPS) is a progeroid syndrome characterized by
multiple aging-like disease phenotypes. We recently reported that a protein …

Hutchinson-Gilford progeria syndrome (HGPS) is caused by the production of a truncated
prelamin A, called progerin, which is farnesylated at its carboxyl terminus. Progerin is …

Hutchinson-Gilford progeria syndrome (HGPS) is the most dramatic form of human
premature aging. Death occurs at a mean age of 13 years, usually from heart attack or …

Hutchinson-Gilford progeria syndrome (HGPS) is caused by the accumulation of a
farnesylated form of prelamin A (progerin). Previously, we showed that blocking protein …

Hutchinson–Gilford progeria syndrome (HGPS) is an extremely rare, fatal, segmental
premature aging syndrome caused by a mutation in LMNA that produces the farnesylated …

Hutchinson-Gilford progeria syndrome (HGPS), a rare disease that results in what appears
to be premature aging, is caused by the production of a mutant form of prelamin A known as …

Hutchinson–Gilford progeria syndrome (HGPS) is caused by a mutant prelamin A, progerin,
that terminates with a farnesylcysteine. HGPS knock-in mice (Lmna HG/+) develop severe …

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare premature aging disorder caused
by a de novo heterozygous point mutation G608G (GGC> GGT) within exon 11 of LMNA …

Hutchinson–Gilford progeria syndrome (HGPS) is a rare, premature ageing syndrome in
children. HGPS is normally caused by a mutation in the LMNA gene, encoding nuclear lamin …

Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic condition associated with
mutations in the LMNA gene. This disease recapitulates some aspects of normal aging, such …