Maternal enzyme masks the phenotype of mouse embryos lacking dihydrolipoamide dehydrogenase

Reproductive BioMedicine Online

Volumn 19, Issue 1, 2009, Pages 79-88

  Johnson, M T ^a,b,f   Vang, P ^c   Filipovits, J ^b,d   Gardner, D K ^b,e  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Fertility Laboratories of Colorado   (United States)

^c VitroLife Inc   (United States)

^d MELBOURNE IVF   (Australia)

^e UNIVERSITY OF MELBOURNE   (Australia)

^f UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

Development; Dihydrolipoamide dehydrogenase; Embryo; Metabolism; Mutation

Indexed keywords

DIHYDROLIPOAMIDE DEHYDROGENASE; LACTIC ACID;

ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; EMBRYO DEVELOPMENT; EMBRYONIC STRUCTURES; ENERGY METABOLISM; ENZYME ACTIVITY; FEMALE; GENOTYPE; GLUCOSE METABOLISM; GLUCOSE TRANSPORT; MITOCHONDRIAL RESPIRATION; MOUSE; NONHUMAN; OOCYTE; PHENOTYPE; PREIMPLANTATION EMBRYO;

EID: 68149180706     PISSN: 14726483     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1472-6483(10)60050-8     Document Type: Article

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