Potential therapeutic approaches for modulating expression and accumulation of defective lamin A in laminopathies and age-related diseases [PDF]
, 2012 core +1 more source
Author Correction: p300 nucleocytoplasmic shuttling underlies mTORC1 hyperactivation in Hutchinson-Gilford progeria syndrome. [PDF]
Nat Cell BiolSon SM +4 more
europepmc +1 more source
A longevity-associated variant of the human BPIFB4 gene prevents diastolic dysfunction in progeria mice. [PDF]
Signal Transduct Target TherQiu Y +4 more
europepmc +1 more source
Lonafarnib Clinical Trials Demonstrate Uncoupling of the Muscle-Bone Unit in Hutchinson-Gilford Progeria Syndrome. [PDF]
J Bone Miner ResKreienkamp RJ +8 more
europepmc +1 more source
Progeria and Atherosclerosis [PDF]
Archives of Disease in Childhood, 1955 A J, KEAY, M F, OLIVER, G S, BOYD
openaire +2 more sources
A study on the nutritional status and body composition of children with Hutchinson-Gilford progeria syndrome. [PDF]
Orphanet J Rare DisYu Q, Wang J, Fu H, Mao J.
europepmc +1 more source
Genetically Confirmed Familial Case of Nonsyndromic Cardiac Progeria Caused by the <i>LMNA</i> p.Asp300Asn Variant with Presumed Gonadal Mosaicism: Phenotypic Comparison with Previously Reported Patients. [PDF]
Genes (Basel)Nuzhnaya E +5 more
europepmc +1 more source
Generation of Nonintegrative-Induced Pluripotent Stem Cells in Hutchinson-Gilford Progeria Syndrome: Enhancing Aging Research. [PDF]
Aging Med (Milton)Kadiwala J, Shakur R.
europepmc +1 more source
Overexpression of ATase1 and ATase2 disrupts the secretome and causes a progeria phenotype. [PDF]
Life Sci AllianceCheng TL +7 more
europepmc +1 more source
Rare case of longevity in Hutchinson-Gilford progeria syndrome and literature review. [PDF]
Orphanet J Rare DisCai XL +6 more
europepmc +1 more source