Results 131 to 140 of about 5,892 (251)
Endothelial YAP/TAZ activation promotes atherosclerosis in a mouse model of Hutchinson-Gilford progeria syndrome
The Journal of Clinical InvestigationHutchinson-Gilford progeria syndrome (HGPS) is an extremely rare disease caused by the expression of progerin, an aberrant protein produced by a point mutation in the LMNA gene.Ana Barettino, Cristina González-Gómez, Pilar Gonzalo, María J. Andrés-Manzano, Carlos R. Guerrero, Francisco M. Espinosa, Rosa M. Carmona, Yaazan Blanco, Beatriz Dorado, Carlos Torroja, Fátima Sánchez-Cabo, Ana Quintas, Alberto Benguría, Ana Dopazo, Ricardo García, Ignacio Benedicto, Vicente Andrés +16 moredoaj +1 more sourceDiscordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- and A/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)
, 2011 Martina Plášilová, Chandon Chattopadhyay, Apurba Ghosh, Friedel Wenzel, Philippe Demougin, Christoph Noppen, Nathalie Schaub, Gabor Szinnai, Luigi Terracciano, Karl Heinimann +9 moreopenalex +2 more sourcesComplicações cardiovasculares e os impactos na qualidade de vida dos pacientes portadores da síndrome de Hutchinson-Gilford (HGPS)
, 2020 Pedro Antonio Rodrigues Dias, Maianna Viana Almeida Aguiar, André Rhodes Neves, Gabriela de Matos Reis, Íris Roberta Cruz Andrade, Isabella Pêgo Miranda Netto, Leonardo José Grossi Andrade, Mariane de Matos Reis, Mayra Heringer Motta Costa e Silva, Sara Eduarda Oliveira Da Cruz +9 moreopenalex +2 more sources