Detecting mitophagy in mitochondrial disease: towards a new type of therapy
<p>Mitochondrial diseases may result from mutations in the maternally-inherited mitochondrial DNA (mtDNA) or from mutations in nuclear genes encoding mitochondrial proteins. Their bi-genomic nature makes mitochondrial diseases a very heterogeneous group of disorders that can present at any age...
Main Author: | Dombi, E |
---|---|
Other Authors: | Poulton, J |
Format: | Thesis |
Published: |
2019
|
Similar Items
-
Modulating mitophagy in mitochondrial disease.
by: Dombi, E, et al.
Published: (2017) -
Mitochondrial dysfunction and mitophagy in Parkinson’s disease: From mechanism to therapy
by: Malpartida, AB, et al.
Published: (2020) -
Mitochondrial Dynamics and Mitophagy in Cardiometabolic Disease
by: Jianguo Lin, et al.
Published: (2022-06-01) -
Targeting Mitochondrial Dysfunction in Lung Diseases: Emphasis on Mitophagy
by: Sureshbabu eAngara, et al.
Published: (2013-12-01) -
Mitochondrial dysfunction and mitophagy in Parkinson's: from familial to sporadic disease.
by: Ryan, B, et al.
Published: (2015)