Cargando…
Generation and characterization of a novel knockin minipig model of Hutchinson-Gilford progeria syndrome
Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic disorder for which no cure exists. The disease is characterized by premature aging and inevitable death in adolescence due to cardiovascular complications. Most HGPS patients carry a heterozygous de novo LMNA c.1824C > T mut...
Autores principales: | Dorado, Beatriz, Pløen, Gro Grunnet, Barettino, Ana, Macías, Alvaro, Gonzalo, Pilar, Andrés-Manzano, María Jesús, González-Gómez, Cristina, Galán-Arriola, Carlos, Alfonso, José Manuel, Lobo, Manuel, López-Martín, Gonzalo J., Molina, Antonio, Sánchez-Sánchez, Raúl, Gadea, Joaquín, Sánchez-González, Javier, Liu, Ying, Callesen, Henrik, Filgueiras-Rama, David, Ibáñez, Borja, Sørensen, Charlotte Brandt, Andrés, Vicente |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423020/ https://www.ncbi.nlm.nih.gov/pubmed/30911407 http://dx.doi.org/10.1038/s41421-019-0084-z |
Ejemplares similares
-
Metabolic Dysfunction in Hutchinson–Gilford Progeria Syndrome
por: Kreienkamp, Ray, et al.
Publicado: (2020) -
Cardiovascular Progerin Suppression and Lamin A Restoration Rescue Hutchinson-Gilford Progeria Syndrome
por: Sánchez-López, Amanda, et al.
Publicado: (2021) -
Hutchinson-Gilford progeria syndrome
por: Bhukya, Amar Singh, et al.
Publicado: (2015) -
Clonal hematopoiesis is not prevalent in Hutchinson-Gilford progeria syndrome
por: Díez-Díez, Miriam, et al.
Publicado: (2022) -
Hutchinson–Gilford Progeria Syndrome: Clinical and Molecular Characterization
por: Pachajoa, Harry, et al.
Publicado: (2020)