| scholarly article | Q13442814 |
| P356 | DOI | 10.1074/JBC.M201257200 |
| P698 | PubMed publication ID | 11889137 |
| P2093 | author name string | Gordon S Huggins | |
| Richard O Snyder | |||
| Ryuichi Aikawa | |||
| P2860 | cites work | Mutational analysis of the adeno-associated virus type 2 (AAV2) capsid gene and construction of AAV2 vectors with altered tropism | Q24515072 |
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| Midbrain injection of recombinant adeno-associated virus encoding rat glial cell line-derived neurotrophic factor protects nigral neurons in a progressive 6-hydroxydopamine-induced degeneration model of Parkinson's disease in rats | Q33745707 | ||
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| Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons | Q36557727 | ||
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| Regulation of gene expression in vivo following transduction by two separate rAAV vectors | Q42827352 | ||
| Tissue-specific gene expression in medullary thyroid carcinoma cells employing calcitonin regulatory elements and AAV vectors | Q43703255 | ||
| Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors | Q43716886 | ||
| Stable restoration of the sarcoglycan complex in dystrophic muscle perfused with histamine and a recombinant adeno-associated viral vector | Q43783192 | ||
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| Efficient and stable transduction of cardiomyocytes after intramyocardial injection or intracoronary perfusion with recombinant adeno-associated virus vectors | Q45751722 | ||
| Neuron-specific transduction in the rat septohippocampal or nigrostriatal pathway by recombinant adeno-associated virus vectors | Q45756988 | ||
| Long-term gene transfer in porcine myocardium after coronary infusion of an adeno-associated virus vector | Q45765859 | ||
| Long-term correction of canine hemophilia B by gene transfer of blood coagulation factor IX mediated by adeno-associated viral vector | Q45855552 | ||
| Tissue-specific consequences of the anti-adenoviral immune response: implications for cardiac transplants | Q45862470 | ||
| Direct in vivo gene transfer into porcine myocardium using replication-deficient adenoviral vectors | Q45866323 | ||
| Transient expression of genes transferred in vivo into heart using first-generation adenoviral vectors: role of the immune response | Q45876235 | ||
| Immunosuppression prolongs adenoviral mediated transgene expression in cardiac allograft transplantation | Q45884829 | ||
| Adenovirus-mediated gene transfer reconstitutes depressed sarcoplasmic reticulum Ca2+-ATPase levels and shortens prolonged cardiac myocyte Ca2+ transients | Q46403468 | ||
| Effects of growth hormone on cardiac dysfunction and gene expression in genetic murine dilated cardiomyopathy. | Q52542229 | ||
| P433 | issue | 21 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 18979-18985 | |
| P577 | publication date | 2002-03-11 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Cardiomyocyte-specific gene expression following recombinant adeno-associated viral vector transduction | |
| P478 | volume | 277 |
| Q30413864 | A single direct injection into the left ventricular wall of an adeno-associated virus 9 (AAV9) vector expressing extracellular superoxide dismutase from the cardiac troponin-T promoter protects mice against myocardial infarction |
| Q35238264 | AAV vectors for cardiac gene transfer: experimental tools and clinical opportunities |
| Q91970870 | AAV9-Mediated Overexpression of TRPM4 Increases the Incidence of Stress-Induced Ventricular Arrhythmias in Mice |
| Q64062703 | Adeno-Associated Virus Mediated Gene Delivery: Implications for Scalable and Cardiac Optogenetic Models |
| Q37272838 | An emerging adeno-associated viral vector pipeline for cardiac gene therapy |
| Q40445265 | Analysis of angiogenesis induced by local IGF-1 expression after myocardial infarction using microSPECT-CT imaging |
| Q35543526 | Cardiac overexpression of 8-oxoguanine DNA glycosylase 1 protects mitochondrial DNA and reduces cardiac fibrosis following transaortic constriction |
| Q30413287 | Cardiac-selective expression of extracellular superoxide dismutase after systemic injection of adeno-associated virus 9 protects the heart against post-myocardial infarction left ventricular remodeling |
| Q46945604 | Cell type-specific functions of the lysosomal protease cathepsin L in the heart |
| Q36823697 | Current status of cardiovascular gene therapy |
| Q37766126 | Delivery of gene and cellular therapies for heart disease |
| Q64040074 | Development of selective cytotoxic viral vectors for concentration of undifferentiated cells in cardiomyocytes derived from human induced pluripotent stem cells |
| Q36919409 | Factors controlling cardiac myosin-isoform shift during hypertrophy and heart failure |
| Q40119187 | Gene-therapy delivery strategies in cardiology |
| Q73209566 | Lake Tahoe invitation meeting 2002 |
| Q45864538 | Long-term stable expression of human growth hormone by rAAV promotes myocardial protection post-myocardial infarction |
| Q26745822 | MicroRNA-regulated viral vectors for gene therapy |
| Q28576468 | Normal targeting of a tagged Kv1.5 channel acutely transfected into fresh adult cardiac myocytes by a biolistic method |
| Q38298929 | Overt expression of AP-1 reduces alpha myosin heavy chain expression and contributes to heart failure from chronic volume overload |
| Q42176122 | Preservation of cardiac function in left ventricle cardiac hypertrophy using an AAV vector which provides VEGF-A expression in response to p53. |
| Q39356341 | Promise of adeno-associated virus as a gene therapy vector for cardiovascular diseases |
| Q37720225 | Recombinant adeno-associated virus serotype 9 in a mouse model of atherosclerosis: Determination of the optimal expression time in vivo |
| Q30431585 | Robust cardiomyocyte-specific gene expression following systemic injection of AAV: in vivo gene delivery follows a Poisson distribution |
| Q33690970 | Role of cyclic AMP-dependent kinase response element-binding protein in recombinant adeno-associated virus-mediated transduction of heart muscle cells |
| Q30417032 | Systemic delivery of shRNA by AAV9 provides highly efficient knockdown of ubiquitously expressed GFP in mouse heart, but not liver |
| Q35164884 | Targeting the cell cycle machinery for the treatment of cardiovascular disease. |
| Q40738027 | Targeting transgene to the heart and liver with AAV9 by different promoters |
| Q37120438 | The role of the adeno-associated virus capsid in gene transfer |
| Q47574081 | The single-strand DNA/RNA-binding protein, Purbeta, regulates serum response factor (SRF)-mediated cardiac muscle gene expression |
| Q36916955 | Tissue specific promoters improve specificity of AAV9 mediated transgene expression following intra-vascular gene delivery in neonatal mice. |
| Q30442929 | Topoisomerase inhibition accelerates gene expression after adeno-associated virus-mediated gene transfer to the mammalian heart |
| Q39527743 | Utility of vascular endothelial specific peptides for enhancement of adeno-associated virus-mediated gene transfer |
| Q24317565 | Single-stranded DNA-binding proteins PURalpha and PURbeta bind to a purine-rich negative regulatory element of the alpha-myosin heavy chain gene and control transcriptional and translational regulation of the gene expression. Implications in the rep |
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