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Department of Pediatrics
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PDK4 Deficiency Induces Intrinsic Apoptosis in Response to Starvation in Fibroblasts from Doberman Pinschers with Dilated Cardiomyopathy.
BioResearch open access , 2017 | Pubmed ID: 29285418
AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome.
Human gene therapy 02, 2019 | Pubmed ID: 30070157
Infiltrative and drug-resistant slow-cycling cells support metabolic heterogeneity in glioblastoma.
The EMBO journal 12, 2018 | Pubmed ID: 30322894
Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan.
Physiological genomics 11, 2018 | Pubmed ID: 30345904
AAV9- Gene Replacement Ameliorates Cardiac TMT Proteomic Profiles in a Mouse Model of Barth Syndrome.
Molecular therapy. Methods & clinical development Jun, 2019 | Pubmed ID: 30788385
Increased mtDNA Abundance and Improved Function in Human Barth Syndrome Patient Fibroblasts Following AAV- Gene Delivery.
International journal of molecular sciences Jul, 2019 | Pubmed ID: 31336787
Functional Consequences of PDK4 Deficiency in Doberman Pinscher Fibroblasts.
Scientific reports Mar, 2020 | Pubmed ID: 32127618
University of Florida
Silveli Suzuki-Hatano1,
Ang-Chen Tsai1,
Audrey Daugherty1,
Christina A. Pacak1
1Department of Pediatrics, University of Florida
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