Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Andrea Puebla-Huerta"'
Autor:
Eduardo Silva-Pavez, Elizabeth Mendoza, Pablo Morgado-Cáceres, Ulises Ahumada-Castro, Galdo Bustos, Matías Kangme-Encalada, Amaia Lopez de Arbina, Andrea Puebla-Huerta, Felipe Muñoz, Lucas Cereceda, Manuel Varas-Godoy, Yessia Hidalgo, J. Cesar Cardenas
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract Increasing evidence supports the hypothesis that cancer progression is under mitochondrial control. Mitochondrial fission plays a pivotal role in the maintenance of cancer cell homeostasis. The inhibition of DRP1, the main regulator of mitoc
Externí odkaz:
https://doaj.org/article/17c5a6ac01104de481f2eaf100eee68f
Autor:
Ulises Ahumada-Castro, Galdo Bustos, Eduardo Silva-Pavez, Andrea Puebla-Huerta, Alenka Lovy, César Cárdenas
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
In the last few years, metabolism has been shown to be controlled by cross-organelle communication. The relationship between the endoplasmic reticulum and mitochondria/lysosomes is the most studied; here, inositol 1,4,5-triphosphate (IP3) receptor (I
Externí odkaz:
https://doaj.org/article/b70527f940a24b41b11e74605904d11d
Autor:
Eduardo Silva-Pavez, Cesar Cardenas, Andrea Puebla-Huerta, Ulises Ahumada-Castro, Galdo Bustos, Alenka Lovy
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology
In the last few years, metabolism has been shown to be controlled by cross-organelle communication. The relationship between the endoplasmic reticulum and mitochondria/lysosomes is the most studied; here, inositol 1,4,5-triphosphate (IP3) receptor (I
Autor:
Ulises, Ahumada-Castro, Andrea, Puebla-Huerta, Victor, Cuevas-Espinoza, Alenka, Lovy, J Cesar, Cardenas
Publikováno v:
Biochimica et biophysica acta. Molecular cell research. 1868(11)
Cellular senescence generates a permanent cell cycle arrest, characterized by apoptosis resistance and a pro-inflammatory senescence-associated secretory phenotype (SASP). Physiologically, senescent cells promote tissue remodeling during development