Actn2 defects accelerates H9c2 hypertrophy via ERK phosphorylation under chronic stress
K Wang, Y Wang, H Wan, J Wang, L Hu, S Huang… - Genes & Genomics, 2024 - Springer
Background In humans, ACTN2 mutations are identified as highly relevant to a range of
cardiomyopathies such as DCM and HCM, while their association with sudden cardiac …
cardiomyopathies such as DCM and HCM, while their association with sudden cardiac …
Loss of endogenous estrogen alters mitochondrial metabolism and muscle clock-related protein Rbm20 in female mdx mice
CA Timpani, D Debrincat, S Kourakis, R Boyer… - bioRxiv, 2024 - biorxiv.org
Female carriers of a Duchenne muscular dystrophy (DMD) gene mutation manifest exercise
intolerance and metabolic anomalies that may be exacerbated following menopause due to …
intolerance and metabolic anomalies that may be exacerbated following menopause due to …
Промышленные поллютанты и эпигенетические факторы, ассоциированные с кардиомиопатиями
ДН Нечаев, АА Миролюбов… - Клиническая …, 2023 - clinmedjournal.com
Аннотация В статье представлен обзор современных научных публикаций,
посвященных отдельным аспектам молекулярно-генетического и эпигенетического …
посвященных отдельным аспектам молекулярно-генетического и эпигенетического …