NDUFS4: Creation of a mouse model mimicking a Complex I disorder

Mitochondrion

Volumn 9, Issue 3, 2009, Pages 204-210

  Ingraham, Christopher A ^a   Burwell, Lindsay S ^a   Skalska, Jolanta ^a   Brookes, Paul S ^a   Howell, Robert L ^a   Sheu, Shey Shing ^a   Pinkert, Carl A ^a,b  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^b AUBURN UNIVERSITY   (United States)

Author keywords

Gene targeting; Knock in; Leigh syndrome; Leigh's disease

Indexed keywords

GENE PRODUCT; LACTIC ACID; NADH DEHYDROGENASE UBIQUINONE FES 4; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); SUCCINATE DEHYDROGENASE (UBIQUINONE); UNCLASSIFIED DRUG; NDUFS4 PROTEIN, MOUSE;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EMBRYO; ENZYME ACTIVITY; HETEROZYGOTE; HOMOZYGOTE; MOUSE; MUTATIONAL ANALYSIS; NONHUMAN; OXYGEN CONSUMPTION; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DEFECT; ANIMAL; C57BL MOUSE; DEFICIENCY; DISEASE MODEL; FEMALE; GENETICS; INSTITUTE FOR CANCER RESEARCH MOUSE; PATHOLOGY;

ANIMALS; DISEASE MODELS, ANIMAL; ELECTRON TRANSPORT COMPLEX I; FEMALE; HETEROZYGOTE; HOMOZYGOTE; MICE; MICE, INBRED C57BL; MICE, INBRED ICR; MITOCHONDRIAL DISEASES; POINT MUTATION;

ANIMALIA;

EID: 64549117348     PISSN: 15677249     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mito.2009.02.001     Document Type: Article

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