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 I Vettori Di AAV Per Trasferimento Genico Cardiaco: Strumenti Sperimentali E Cliniche Opportunità Molecular Therapy : the Journal of the American Society of Gene Therapy. Sep, 2011 | Pubmed ID: 21792180 Pompe Malattia Gene Therapy Human Molecular Genetics. Apr, 2011 | Pubmed ID: 21518733 Relativa Persistenza Dei Genomi Di 1 Vettore AAV Sierotipo Distrofica Muscolare Genetic Vaccines and Therapy. 2008 | Pubmed ID: 18854054 Specifici Promotori Tessuto Migliorano La Specificità Dell'espressione Del Transgene AAV9 Mediate Consegna Di Gene Intra-vascular Nei Topi Neonatali Genetic Vaccines and Therapy. 2008 | Pubmed ID: 18811960 Neonatale Iniezioni Per Via Endovenosa O Intraperitoneale Di Recombinant Virus Adeno-associati Tipo 8 Trasducono Gangli Spinali E Neuroni Motori Inferiori Human Gene Therapy. Jan, 2008 | Pubmed ID: 18052722 Protezione a Lungo Termine Del Muscolo Scheletrico Dopo Gene Transfer in Un Modello Murino Di LGMD-2D Molecular Therapy : the Journal of the American Society of Gene Therapy. Oct, 2007 | Pubmed ID: 17653106 Correzione Fisiologica Della Malattia Di Pompe Da Consegna Sistemica Di Vettori Sierotipo 1 Virus Adeno-associati Molecular Therapy : the Journal of the American Society of Gene Therapy. Mar, 2007 | Pubmed ID: 17245350 Preparazione del campione TMT per l'invio di strutture proteomiche e la successiva analisi dei dati Silveli Suzuki-Hatano1, Ang-Chen Tsai1, Audrey Daugherty1, Christina A. Pacak1 1Department of Pediatrics, University of Florida JoVE 60970 Biochemistry
Preparazione del campione TMT per l'invio di strutture proteomiche e la successiva analisi dei dati Silveli Suzuki-Hatano1, Ang-Chen Tsai1, Audrey Daugherty1, Christina A. Pacak1 1Department of Pediatrics, University of Florida JoVE 60970 Biochemistry