Increased mtDNA Abundance and Improved Function in Human Barth Syndrome Patient Fibroblasts Following AAV-TAZ Gene Delivery
出版年份 2019 全文链接
标题
Increased mtDNA Abundance and Improved Function in Human Barth Syndrome Patient Fibroblasts Following AAV-TAZ Gene Delivery
作者
关键词
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出版物
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 20, Issue 14, Pages 3416
出版商
MDPI AG
发表日期
2019-07-11
DOI
10.3390/ijms20143416
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Blunted Fat Oxidation upon Submaximal Exercise is Partially Compensated by Enhanced Glucose Metabolism in Children, Adolescents and Young Adults with Barth Syndrome
- (2019) W. Todd Cade et al. JOURNAL OF INHERITED METABOLIC DISEASE
- AAV9-TAZ Gene Replacement Ameliorates Cardiac TMT Proteomic Profiles in a Mouse Model of Barth Syndrome
- (2019) Silveli Suzuki-Hatano et al. Molecular Therapy-Methods & Clinical Development
- Peak oxygen uptake (VO2peak) across childhood, adolescence and young adulthood in Barth syndrome: Data from cross-sectional and longitudinal studies
- (2018) William Todd Cade et al. PLoS One
- AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome
- (2018) Silveli Suzuki-Hatano et al. HUMAN GENE THERAPY
- Association between mitochondrial DNA copy number and cardiovascular disease: Current evidence based on a systematic review and meta-analysis
- (2018) Peng Yue et al. PLoS One
- A mutation in the TMEM65 gene results in mitochondrial myopathy with severe neurological manifestations
- (2017) Aisha Nazli et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Decreased Peripheral Mitochondrial DNA Copy Number is Associated with the Risk of Heart Failure and Long-term Outcomes
- (2016) Jin Huang et al. MEDICINE
- Evolutionarily conserved intercalated disc protein Tmem65 regulates cardiac conduction and connexin 43 function
- (2015) Parveen Sharma et al. Nature Communications
- Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype
- (2014) Ann Bowron et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies
- (2014) Gang Wang et al. NATURE MEDICINE
- TMEM65 is a mitochondrial inner-membrane protein
- (2014) Naotaka Nishimura et al. PeerJ
- Methods for Detection of Mitochondrial and Cellular Reactive Oxygen Species
- (2012) Sergey I. Dikalov et al. ANTIOXIDANTS & REDOX SIGNALING
- Substrate metabolism during basal and hyperinsulinemic conditions in adolescents and young-adults with Barth syndrome
- (2012) W. Todd Cade et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Impaired cardiac reserve and severely diminished skeletal muscle O2 utilization mediate exercise intolerance in Barth syndrome
- (2011) Carolyn T. Spencer et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- High-Efficiency Transduction of Fibroblasts and Mesenchymal Stem Cells by Tyrosine-Mutant AAV2 Vectors for Their Potential Use in Cellular Therapy
- (2010) Mengxin Li et al. HUMAN GENE THERAPY
- The enigmatic role of tafazzin in cardiolipin metabolism
- (2009) Riekelt H. Houtkooper et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
- Cardiolipin biosynthesis and remodeling enzymes are altered during development of heart failure
- (2008) Harjot K. Saini-Chohan et al. JOURNAL OF LIPID RESEARCH
- Next generation of adeno-associated virus 2 vectors: Point mutations in tyrosines lead to high-efficiency transduction at lower doses
- (2008) L. Zhong et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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