Cargando…
A neuron‐specific Isca1 knockout rat developments multiple mitochondrial dysfunction syndromes
BACKGROUND: Multiple mitochondrial dysfunction syndromes (MMDS) are rare mitochondrial diseases caused by mutation of mitochondrial iron–sulfur cluster synthesis proteins. This study established a rat model simulating MMDS5 disease in the nervous system to investigate its pathological features and n...
Autores principales: | Sheng, Hanxuan, Lu, Dan, Qi, Xiaolong, Ling, Yahao, Li, Jing, Zhang, Xu, Dong, Wei, Chen, Wei, Gao, Shan, Gao, Xiang, Zhang, Li, Zhang, Lianfeng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158949/ https://www.ncbi.nlm.nih.gov/pubmed/37140997 http://dx.doi.org/10.1002/ame2.12318 |
Ejemplares similares
-
Knockout of ISCA1 causes early embryonic death in rats
por: Yang, Xinlan, et al.
Publicado: (2019) -
Novel rat model of multiple mitochondrial dysfunction syndromes (MMDS) complicated with cardiomyopathy
por: Ling, Yahao, et al.
Publicado: (2021) -
Multiple Mitochondrial Dysfunctions Syndrome 4 Due to ISCA2
Gene Defects: A Review
por: Alfadhel, Majid
Publicado: (2019) -
The human mitochondrial ISCA1, ISCA2, and IBA57 proteins are required for [4Fe-4S] protein maturation
por: Sheftel, Alex D., et al.
Publicado: (2012) -
Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome
por: Shukla, Anju, et al.
Publicado: (2017)