TY  - JOUR 
AU  - Cavadas, Cláudia
AU  - Pereira de Almeida, Luís
AU  - Pereira, Dina
AU  - Valero , Jorge
AU  - Cortes, Luísa
AU  - Ferreira-Marques, Marisa
AU  - Aveleira, Célia A
PY  - 2020
SN  - 1079-5006
UR  - http://hdl.handle.net/10366/154684
AB  - Hutchinson-Gilford progeria syndrome (HGPS, or classical progeria) is a rare genetic disorder, characterized by premature aging, and caused by a de novo point mutation (C608G) within the lamin A/C gene (LMNA), producing an abnormal lamin A protein,...
LA  - eng
KW  - Autophagy
KW  - Cellular senescence
KW  - Human aging
KW  - Caloric restriction mimetic
KW  - Neuropeptides
KW  - Phenotype
KW  - Cells
KW  - Progeria
TI  - Neuropeptide Y Enhances Progerin Clearance and Ameliorates the Senescent Phenotype of Human Hutchinson-Gilford Progeria Syndrome Cells
DO  - 10.1093/GERONA/GLZ280
T2  - The Journals of Gerontology: Series A
VL  - 75
M2  - 1073
ER  -