Christina A. Pacak Department of Pediatrics University of Florida Biography Publications Institution JoVE Articles Christina A. Pacak has not added a biography. If you are Christina A. Pacak and would like to personalize this page please email our Author Liaison for assistance. Publications Functional Consequences of PDK4 Deficiency in Doberman Pinscher Fibroblasts Scientific Reports. Mar, 2020 | Pubmed ID: 32127618 Noninvasive Tracking of Implanted Cells: Superparamagnetic Iron Oxide Nanoparticles As a Long-Term, Multimodal Imaging Label Methods in Molecular Biology (Clifton, N.J.). 2020 | Pubmed ID: 32112388 The Past, Present, and Future of Modeling Cockayne Syndrome - A Commentary on "Rat Model of Cockayne Syndrome Neurological Disease" DNA Repair. 04, 2020 | Pubmed ID: 32058278 The End of the Beginning: The Journey to Molecular Therapies for Spinal Muscular Atrophy Pediatric Neurology. 01, 2020 | Pubmed ID: 31481328 Myocardial Glucose and Fatty Acid Metabolism is Altered and Associated with Lower Cardiac Function in Young Adults with Barth Syndrome Journal of Nuclear Cardiology : Official Publication of the American Society of Nuclear Cardiology. Nov, 2019 | Pubmed ID: 31705425 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 Selective Serotonin Reuptake Inhibitors Ameliorate MEGF10 Myopathy Human Molecular Genetics. 07, 2019 | Pubmed ID: 31267131 Blunted Fat Oxidation Upon Submaximal Exercise is Partially Compensated by Enhanced Glucose Metabolism in Children, Adolescents, and Young Adults with Barth Syndrome Journal of Inherited Metabolic Disease. 05, 2019 | Pubmed ID: 30924938 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 Identification of a Pathogenic Mutation in ATP2A1 Via in Silico Analysis of Exome Data for Cryptic Aberrant Splice Sites Molecular Genetics & Genomic Medicine. 03, 2019 | Pubmed ID: 30688039 AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome Human Gene Therapy. 02, 2019 | Pubmed ID: 30070157 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 Infiltrative and Drug-resistant Slow-cycling Cells Support Metabolic Heterogeneity in Glioblastoma The EMBO Journal. 12, 2018 | Pubmed ID: 30322894 PDK4 Deficiency Induces Intrinsic Apoptosis in Response to Starvation in Fibroblasts from Doberman Pinschers with Dilated Cardiomyopathy BioResearch Open Access. 2017 | Pubmed ID: 29285418 Consequences of MEGF10 Deficiency on Myoblast Function and Notch1 Interactions Human Molecular Genetics. 08, 2017 | Pubmed ID: 28498977 Impaired Cardiac and Skeletal Muscle Bioenergetics in Children, Adolescents, and Young Adults with Barth Syndrome Physiological Reports. Feb, 2017 | Pubmed ID: 28196853 Transfer of Therapeutic Genes into Fetal Rhesus Monkeys Using Recombinant Adeno-Associated Type I Viral Vectors Human Gene Therapy. Clinical Development. 12, 2016 | Pubmed ID: 27855487 Longitudinal Patterns of Thalidomide Neuropathy in Children and Adolescents The Journal of Pediatrics. Nov, 2016 | Pubmed ID: 27567409 Actin-dependent Mitochondrial Internalization in Cardiomyocytes: Evidence for Rescue of Mitochondrial Function Biology Open. Apr, 2015 | Pubmed ID: 25862247 Superparamagnetic Iron Oxide Nanoparticles Function As a Long-term, Multi-modal Imaging Label for Non-invasive Tracking of Implanted Progenitor Cells PloS One. 2014 | Pubmed ID: 25250622 Growth of Bone Marrow and Skeletal Muscle Side Population Stem Cells in Suspension Culture Methods in Molecular Biology (Clifton, N.J.). 2014 | Pubmed ID: 25173160 Silencing of Drpr Leads to Muscle and Brain Degeneration in Adult Drosophila The American Journal of Pathology. Aug, 2014 | Pubmed ID: 25111228 腺相关病毒载体的心脏基因转移: 实验工具和临床的机会。 Molecular Therapy : the Journal of the American Society of Gene Therapy. Sep, 2011 | Pubmed ID: 21792180 Pompe 病基因治疗。 Human Molecular Genetics. Apr, 2011 | Pubmed ID: 21518733 营养不良性肌腺相关病毒血清型 1 载体基因组的相对持续存在。 Genetic Vaccines and Therapy. 2008 | Pubmed ID: 18854054 组织特定的启动子改善后新生小鼠血管内基因转染的 AAV9 介导的转基因表达的特异性。 Genetic Vaccines and Therapy. 2008 | Pubmed ID: 18811960 背根神经节和较低的运动神经元,换能器的重组腺相关病毒类型 8 新生儿腹腔或静脉注射液。 Human Gene Therapy. Jan, 2008 | Pubmed ID: 18052722 LGMD 2D 的小鼠模型的基因转移后的长期骨骼肌保护。 Molecular Therapy : the Journal of the American Society of Gene Therapy. Oct, 2007 | Pubmed ID: 17653106 腺相关病毒血清型 1 载体的系统性交付 Pompe 病生理修正。 Molecular Therapy : the Journal of the American Society of Gene Therapy. Mar, 2007 | Pubmed ID: 17245350 蛋白质组学设施提交和后续数据分析的TMT样品制备 Silveli Suzuki-Hatano1, Ang-Chen Tsai1, Audrey Daugherty1, Christina A. Pacak1 1Department of Pediatrics, University of Florida JoVE 60970 Biochimie
蛋白质组学设施提交和后续数据分析的TMT样品制备 Silveli Suzuki-Hatano1, Ang-Chen Tsai1, Audrey Daugherty1, Christina A. Pacak1 1Department of Pediatrics, University of Florida JoVE 60970 Biochimie