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Mouse models for mitochondrial diseases
被引:26
|作者:
Ruzzenente, Benedetta
[1
]
Rotig, Agnes
[1
]
Metodiev, Metodi D.
[1
]
机构:
[1] Univ Paris 05, INSERM U1163, Sorbonne Paris Cite, Inst Imagine, 24 Blvd Montparnasse, F-75015 Paris, France
关键词:
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA;
RESPIRATORY-CHAIN DEFICIENCY;
C-OXIDASE DEFICIENCY;
TRANSFER-RNA;
HYPERTROPHIC CARDIOMYOPATHY;
EMBRYONIC LETHALITY;
OXPHOS DEFICIENCIES;
LACTIC-ACIDOSIS;
MODIFIED MICE;
MUTATIONS;
D O I:
10.1093/hmg/ddw176
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Mitochondrial diseases are heterogeneous and incurable conditions typically resulting from deficient ATP production in the cells. Mice, owing to their genetic and physiological similarity to humans as well as their relatively easy maintenance and propagation, are extremely valuable for studying mitochondrial diseases and are also indispensable for the preclinical evaluation of novel therapies for these devastating conditions. Here, we review the recent exciting developments in the field focusing on mouse models for mitochondrial disease genes although models for genes not involved in the pathogenesis of mitochondrial disease and therapeutic proof-of-concept studies using mouse models are also discussed.
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页码:R115 / R122
页数:8
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