Cargando…
Phenotypic Characterization of Male Tafazzin-Knockout Mice at 3, 6, and 12 Months of Age
Barth syndrome (BTHS) is an X-linked mitochondrial disease caused by mutations in the gene encoding for tafazzin (TAZ), a key enzyme in the remodeling of cardiolipin. Mice with a germline deficiency in Taz have been generated (Taz-KO) but not yet fully characterized. We performed physiological asses...
Autores principales: | Tomczewski, Michelle V., Chan, John Z., Campbell, Zurie E., Strathdee, Douglas, Duncan, Robin E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953241/ https://www.ncbi.nlm.nih.gov/pubmed/36831174 http://dx.doi.org/10.3390/biomedicines11020638 |
Ejemplares similares
-
Phenotypic Characterization of Female Carrier Mice Heterozygous for Tafazzin Deletion
por: Tomczewski, Michelle V., et al.
Publicado: (2023) -
Mouse Tafazzin Is Required for Male Germ Cell Meiosis and Spermatogenesis
por: Cadalbert, Laurence C., et al.
Publicado: (2015) -
N-oleoylethanolamide treatment of lymphoblasts deficient in Tafazzin improves cell growth and mitochondrial morphology and dynamics
por: Chan, John Z., et al.
Publicado: (2022) -
Role of Tafazzin in Mitochondrial Function, Development and Disease
por: Chin, Michael T., et al.
Publicado: (2020) -
Barth syndrome mutations that cause tafazzin complex lability
por: Claypool, Steven M., et al.
Publicado: (2011)