Cargando…
Hacd2 deficiency in mice leads to an early and lethal mitochondrial disease
OBJECTIVE: Mitochondria fuel most animal cells with ATP, ensuring proper energetic metabolism of organs. Early and extensive mitochondrial dysfunction often leads to severe disorders through multiorgan failure. Hacd2 gene encodes an enzyme involved in very long chain fatty acid (C ≥ 18) synthesis, y...
Autores principales: | Khadhraoui, Nahed, Prola, Alexandre, Vandestienne, Aymeline, Blondelle, Jordan, Guillaud, Laurent, Courtin, Guillaume, Bodak, Maxime, Prost, Bastien, Huet, Hélène, Wintrebert, Mélody, Péchoux, Christine, Solgadi, Audrey, Relaix, Frédéric, Tiret, Laurent, Pilot-Storck, Fanny |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986742/ https://www.ncbi.nlm.nih.gov/pubmed/36693621 http://dx.doi.org/10.1016/j.molmet.2023.101677 |
Ejemplares similares
-
HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth
por: Blondelle, Jordan, et al.
Publicado: (2015) -
Cardiolipin content controls mitochondrial coupling and energetic efficiency in muscle
por: Prola, Alexandre, et al.
Publicado: (2021) -
Congenital myopathy is caused by mutation of HACD1
por: Muhammad, Emad, et al.
Publicado: (2013) -
Biallelic LINE insertion mutation in HACD1 causing congenital myopathy
por: Al Amrani, Fatema, et al.
Publicado: (2020) -
Cardiolipin Alterations during Obesity: Exploring Therapeutic Opportunities
por: Prola, Alexandre, et al.
Publicado: (2022)