Home
|
Learning Center
|
中文版
Publications
站内成果搜索:
搜索
AAV-2: how can the capsid be modified to improve the viral vector in gene therapy?
AAV-Mediated Gene Delivery in Adult GM1-Gangliosidosis Mice Corrects Lysosomal Storage in CNS and Improves Survival
AAV-directed muscular dystrophy gene therapy
AAV-mediated chronic over-expression of SNAP-25 in adult rat dorsal hippocampus impairs memory-associated synaptic plasticity
AAV-Mediated Gene Therapy for the Treatment of Retinal Diseases
AAV-Mediated CRISPR/Cas Gene Editing of Retinal Cells In Vivo
AAV-mediated liver-directed gene therapy for Acute Intermittent Porphyria: It is safe but is it effective?
AAV-mediated transduction and targeting of retinal bipolar cells with improved mGluR6 promoters in rodents and primates
AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6 beta-deficient Dogs
AAV-Mediated angiotensin 1-7 overexpression inhibits tumor growth of lung cancer in vitro and in vivo
AAV-Mediated, Optogenetic Ablation of Muller Glia Leads to Structural and Functional Changes in the Mouse Retina
AAV-P125A-endostatin and paclitaxel treatment increases endoreduplication in endothelial cells and inhibits metastasis of breast cancer
AAV-mediated persistent bevacizumab therapy suppresses tumor growth of ovarian cancer
AAV-Mediated Gene Replacement, Either Alone or in Combination with Physical and Pharmacological Agents, Results in Partial and Transient Protection from Photoreceptor Degeneration Associated with beta PDE Deficiency
AAV-Mediated Knock-Down of HRC Exacerbates Transverse Aorta Constriction-Induced Heart Failure
AAV-Directed Persistent Expression of a Gene Encoding Anti-Nicotine Antibody for Smoking Cessation
AAV-mediated gene transfer in the perinatal period results in expression of FVII at levels that protect against fatal spontaneous hemorrhage
AAV-mediated hippocampal expression of short and long Homer 1 proteins differentially affect cognition and seizure activity in adult rats
AAV-mediated gene transfer for the treatment of hemophilia B: problems and prospects
AAV-1-mediated gene transfer to skeletal muscle in humans results in dose-dependent activation of capsid-specific T cells
AAV-mediated knockdown of phosphotamban teads to improved contractitity and catcium handting in cardiomyocytes
AAV-mediated gene targeting methods for human cells
AAV-mediated intramuscular delivery of myotubularin corrects the myotubular myopathy phenotype in targeted murine muscle and suggests a function in plasma membrane homeostasis
AAV-2-Mediated Expression of IGF-1 in Skeletal Myoblasts Stimulates Angiogenesis and Cell Survival
AAV-mediated in vivo knockdown of luciferase using combinatorial RNAi and U1i
AAV-based neonatal gene therapy for hemophilia A: long-term correction and avoidance of immune responses in mice
AAV-mediated Overexpression of Human alpha 7 Integrin Leads to Histological and Functional Improvement in Dystrophic Mice
AAV-MEDIATED GENE DELIVERY ATTENUATES NEUROINFLAMMATION IN FELINE SANDHOFF DISEASE
AAV-mediated delivery of optogenetic constructs to the macaque brain triggers humoral immune responses
AAV-Mediated Anterograde Transsynaptic Tagging: Mapping Corticocollicular Input-Defined Neural Pathways for Defense Behaviors
AAV-Nrf2 Promotes Protection and Recovery in Animal Models of Oxidative Stressle
AAV-based dual-reporter circuit for monitoring cell signaling in living human cells
AAV-mediated expression of anti-tau scFvs decreases tau accumulation in a mouse model of tauopathy
AAV-mediated in vivo functional selection of tissue-protective factors against ischaemia
AAV-8 Is More Efficient than AAV-9 in Transducing Neonatal Dog Heart
AAV-Delivered Antibody Mediates Significant Protective Effects against SIVmac239 Challenge in the Absence of Neutralizing Activity
AAV-mediated expression of anti-tau scFvs decreases tau accumulation in a mouse model of tauopathy (vol 214, pg 2163, 2017)
AAV-ID: A Rapid and Robust Assay for Batch-to-Batch Consistency Evaluation of AAV Preparations
AAV-mediated pancreatic overexpression of Igf1 counteracts progression to autoimmune diabetes in mice
AAV-mediated direct in vivo CRISPR screen identifies functional suppressors in glioblastoma
AAV-mediated transcription factor EB (TFEB) gene delivery ameliorates muscle pathology and function in the murine model of Pompe Disease
AAV-KLF7 Promotes Descending Propriospinal Neuron Axonal Plasticity after Spinal Cord Injury
AAV-mediated Sirt1 overexpression in skeletal muscle activates oxidative capacity but does not prevent insulin resistance
AAV-mediated gene therapy in Dystrophin-Dp71 deficient mouse leads to blood-retinal barrier restoration and oedema reabsorption
AAV-Based RNAi Silencing of NADPH Oxidase gp91(phox) Attenuates Cold-Induced Cardiovascular Dysfunction
AAV-mediated photoreceptor transduction of the pig cone-enriched retina
AAV-Mediated Gene Targeting Is Significantly Enhanced by Transient Inhibition of Nonhomologous End Joining or the Proteasome In Vivo
AAV-mediated transfer of FKRP shows therapeutic efficacy in a murine model but requires control of gene expression
AAV-mediated gene delivery of the calreticulin anti-angiogenic domain inhibits ocular neovascularization
AAV-mediated NT-3 overexpression protects cochleae against noise-induced synaptopathy
AAV-9 mediated phosphatase-1 inhibitor-1 overexpression improves cardiac contractility in unchallenged mice but is deleterious in pressure-overload
AAV-mediated Overexpression of IL-10 Mitigates the Inflammatory Cascade in Stimulated Equine Chondrocyte Pellets
AAV-CRISPR/Cas9-Mediated Depletion of VEGFR2 Blocks Angiogenesis In Vitro
AAV.shRNA-mediated downregulation of ROCK2 attenuates degeneration of dopaminergic neurons in toxin-induced models of Parkinson's disease in vitro and in vivo
AAV.Dysferlin Overlap Vectors Restore Function in Dysferlinopathy Animal Models
AAV/hSTAT3-gene delivery lowers aortic inflammatory cell infiltration in LDLR KO mice on high cholesterol
AAV1/2-mediated CNS Gene Delivery of Dominant-negative CCL2 Mutant Suppresses Gliosis, beta-amyloidosis, and Learning Impairment of APP/PS1 Mice
AAV1.NT-3 Gene Therapy for Charcot-Marie-Tooth Neuropathy
AAV1.NT-3 gene therapy attenuates spontaneous autoimmune peripheral polyneuropathy
AAV1/2-induced overexpression of A53T-alpha-synuclein in the substantia nigra results in degeneration of the nigrostriatal system with Lewy-like pathology and motor impairment: a new mouse model for Parkinson's disease
AAV2-mediated transfer of the human aquaporin-1 cDNA restores fluid secretion from irradiated miniature pig parotid glands
AAV2-GAD gene therapy for advanced Parkinson's disease: a double-blind, sham-surgery controlled, randomised trial
AAV2-Mediated Subretinal Gene Transfer of hIFN-alpha Attenuates Experimental Autoimmune Uveoretinitis in Mice
AAV2-mediated interleukin-12 in the treatment of malignant brain tumors through activation of NK cells
AAV2 mediated retrograde transduction of corticospinal motor neurons reveals initial and selective apical dendrite degeneration in ALS
AAV2-Mediated Subretinal Gene Transfer of mIL-27p28 Attenuates Experimental Autoimmune Uveoretinitis in Mice
AAV2/IL-12 gene delivery into dendritic cells (DC) enhances CTL stimulation above other IL-12 applications Evidence for IL-12 intracrine activity in DC
AAV2-mediated striatum delivery of human CDNF prevents the deterioration of midbrain dopamine neurons in a 6-hydroxydopamine induced parkinsonian rat model
AAV2-neurturin (CERE-120) for Parkinson's disease
AAV2 production with optimized N/P ratio and PEI-mediated transfection results in low toxicity and high titer for in vitro and in vivo applications
AAV2-mediated follistatin overexpression induces ovine primary myoblasts proliferation
AAV2 and Hepatocellular Carcinoma
AAV2 X increases AAV6 rep/cap-driven rAAV production
AAV2 Delivery of Flt23k Intraceptors Inhibits Murine Choroidal Neovascularization
AAV2/8-humanFOXP3 gene therapy shows robust anti-atherosclerosis efficacy in LDLR-KO mice on high cholesterol diet
AAV2/5-mediated NGF gene delivery protects septal cholinergic neurons following axotomy
AAV2/8-mediated Correction of OTC Deficiency Is Robust in Adult but Not Neonatal Spf(ash) Mice
AAV2/8-hSMAD3 gene delivery attenuates aortic atherogenesis, enhances Th2 response without fibrosis, in LDLR-KO mice on high cholesterol diet
AAV2 Gene Therapy Readministration in Three Adults with Congenital Blindness
AAV2/8 Vectors Purified from Culture Medium with a Simple and Rapid Protocol Transduce Murine Liver, Muscle, and Retina Efficiently
AAV2/9介导的PD-L1保护移植物的实验研究
AAV2-mediated GRP78 Transfer Alleviates Retinal Neuronal Injury by Downregulating ER Stress and Tau Oligomer Formation
AAV3-mediated transfer and expression of the pyruvate dehydrogenase E1 alpha subunit gene causes metabolic remodeling and apoptosis of human liver cancer cells