Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of prader-willi syndrome

Clinical and Translational Science

Volumn 6, Issue 5, 2013, Pages 347-355

  Yazdi, Puya G ^a   Su, Hailing ^a   Ghimbovschi, Svetlana ^b   Fan, Weiwei ^a,c,d   Coskun, Pinar E ^a,c   Nalbandian, Angèle ^a   Knoblach, Susan ^b   Resnick, James L ^e   Hoffman, Eric ^b   Wallace, Douglas C ^c,f   Kimonis, Virginia E ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

^e UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

^f UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Differential gene expression; Prader Willi syndrome; PWS IC mouse model

Indexed keywords

2,4 DIENOYL COENZYME A REDUCTASE (NADPH); 3 HYDROXYBUTYRATE DEHYDROGENASE; 5 AMINOLEVULINATE SYNTHASE; ADENYLATE KINASE; AQUAPORIN 1; COPROPORPHYRINOGEN OXIDASE; DIMETHYLANILINE MONOOXYGENASE; GLYCEROL 3 PHOSPHATE DEHYDROGENASE; KINESIN; LONG CHAIN FATTY ACID COENZYME A LIGASE; PALMITOYL COENZYME A HYDROLASE; PHOSPHATIDYLETHANOLAMINE METHYLTRANSFERASE; PYRUVATE DEHYDROGENASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); RETINOIC ACID; RIBOSOME PROTEIN; THIOREDOXIN REDUCTASE 2;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENERGY METABOLISM; ENZYME ACTIVITY; GENE DELETION; GENE EXPRESSION; HEART; LIVER; MITOCHONDRIAL GENE; MOUSE; MUSCLE; NONHUMAN; OXIDATIVE PHOSPHORYLATION; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

MUS;

DIFFERENTIAL GENE EXPRESSION; PRADER-WILLI SYNDROME; PWS-IC MOUSE MODEL;

ANIMALS; BRAIN; DISEASE MODELS, ANIMAL; ELECTRON TRANSPORT CHAIN COMPLEX PROTEINS; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENE REGULATORY NETWORKS; GENOME; GENOMIC IMPRINTING; MICE; MITOCHONDRIA; MUSCLES; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PRADER-WILLI SYNDROME; REPRODUCIBILITY OF RESULTS; RNA, MESSENGER; SEQUENCE DELETION;

EID: 84885848085     PISSN: 17528054     EISSN: 17528062     Source Type: Journal    
DOI: 10.1111/cts.12083     Document Type: Article

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