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AAV vectors for in vivo gene transfer or how a small virus becomes large
AAV vector-mediated secretion of chondroitinase provides a sensitive tracer for axonal arborisations
AAV Gene Therapy for MPS1-associated Corneal Blindness
AAV Vector-Mediated Overexpression of CB1 Cannabinoid Receptor in Pyramidal Neurons of the Hippocampus Protects against Seizure-Induced Excitoxicity
AAV Vectors Avoid Inflammatory Signals Necessary to Render Transduced Hepatocyte Targets for Destructive T Cells
AAV serotype influences gene transfer in corneal stroma in vivo
AAV Vectorization of DSB-mediated Gene Editing Technologies
AAV serotype 2/1-mediated gene delivery of anti-inflammatory interleukin-10 enhances neurogenesis and cognitive function in APP+PS1 mice
AAV liver expression of FIX-Padua prevents and eradicates FIX inhibitor without increasing thrombogenicity in hemophilia B dogs and mice
AAV as an immunogen
AAV Vectors for Cardiac Gene Transfer: Experimental Tools and Clinical Opportunities
AAV Recombineering with Single Strand Oligonucleotides
AAV Vector Biology in Primates: Finding the Missing Link?
AAV vectors, insertional mutagenesis, and cancer
AAV vectors transduce hepatocytes in vivo as efficiently in cirrhotic as in healthy rat livers
AAV Transduction of Dopamine Neurons With Constitutively Active Rheb Protects From Neurodegeneration and Mediates Axon Regrowth
AAV Provides an Alternative for Gene Therapy of the Peripheral Sensory Nervous System
AAV for pain: steps towards clinical translation
AAV as a Gene Transfer Vector for the Treatment of Neurological Disorders: Novel Treatment Thoughts for ALS
AAV vector-mediated RNAi of mutant huntingtin expression is neuroprotective in a novel genetic rat model of Huntington's disease
AAV Delivery of Tumor Necrosis Factor-alpha Short Hairpin RNA Attenuates Cold-Induced Pulmonary Hypertension and Pulmonary Arterial Remodeling
AAV gene therapy as a means to increase apolipoprotein (Apo) A-I and high-density lipoprotein-choteslerol levels: correction of murine ApoA-I deficiency
AAV vectors vaccines against infectious diseases
AAV Vector-Mediated Gene Delivery to Substantia Nigra Dopamine Neurons: Implications for Gene Therapy and Disease Models
AAV Capsid Engineering: Zooming in on the Target
AAV gene therapy corrects OTC deficiency and prevents liver fibrosis in aged OTC-knock out heterozygous mice
AAV Infection: Protection from Cancer
AAV vector distribution in the mouse respiratory tract following four different methods of administration
AAV ancestral reconstruction library enables selection of broadly infectious viral variants
AAV gene transfer delays disease onset in a TPP1-deficient canine model of the late infantile form of Batten disease
AAV Gene Therapy for Alcoholism: Inhibition of Mitochondrial Aldehyde Dehydrogenase Enzyme Expression in Hepatoma Cells
AAV Natural Infection Induces Broad Cross-Neutralizing Antibody Responses to Multiple AAV Serotypes in Chimpanzees
AAV shuffles to the liver: commentary on Lisowski et al
AAV Delivery of Wild-Type Rhodopsin Preserves Retinal Function in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa
AAV Mediated GDNF Secretion From Retinal Glia Slows Down Retinal Degeneration in a Rat Model of Retinitis Pigmentosa
AAV Vectors Containing rDNA Homology Display Increased Chromosomal Integration and Transgene Persistence
AAV Vectors for the Nucleolus
AAV Delivery of Endothelin-1 shRNA Attenuates Cold-Induced Hypertension
AAV capsid CD8+T-cell epitopes are highly conserved across AAV serotypes
AAV viral vector delivery to the brain by shape-conforming MR-guided infusions
AAV and Compacted DNA Nanoparticles for the Treatment of Retinal Disorders: Challenges and Future Prospects
AAV vector-meditated expression of HLA-G reduces injury-induced corneal vascularization, immune cell infiltration, and fibrosis
AAV gene delivery to the spinal cord: serotypes, methods, candidate diseases, and clinical trials
AAV delivery of GRP78/BiP promotes adaptation of human RPE cell to ER stress
AAV serotype 8-mediated liver specific GNMT expression delays progression of hepatocellular carcinoma and prevents carbon tetrachloride-induced liver damage
AAV's Anatomy: Roadmap for Optimizing Vectors for Translational Success
AAV's Golden Jubilee
AAV(1/2)-mediated BDNF gene therapy in a transgenic rat model of Huntington's disease
AAV-mediated netrin-1 overexpression increases peri-infarct blood vessel density and improves motor function recovery after experimental stroke
AAV-Mediated Gene Supply for Treatment of Degenerative and Neovascular Retinal Diseases
AAV-mediated gene therapy for liver diseases: the prime candidate for clinical application?
AAV-Mediated Gene Transfer of Human X-Linked Inhibitor of Apoptosis Protects against Oxidative Cell Death in Human RPE Cells
AAV-Mediated Cone Rescue in a Naturally Occurring Mouse Model of CNGA3-Achromatopsia
AAV-Mediated Gene Therapy in Mouse Models of Recessive Retinal Degeneration
AAV-based shRNA silencing of NF-kappa B ameliorates muscle pathologies in mdx mice
AAV-hTGFβ_1体外转染鼠椎间盘再移植的实验研究
AAV-Mediated Lysophosphatidylcholine Acyltransferase 1 (Lpcat1) Gene Replacement Therapy Rescues Retinal Degeneration in rd11 Mice
AAV-Mediated Gene Therapy in the Guanylate Cyclase (RetGC1/RetGC2) Double Knockout Mouse Model of Leber Congenital Amaurosis
AAV-mediated expression of human PRELP inhibits complement activation, choroidal neovascularization and deposition of membrane attack complex in mice
AAV-Mediated Gene Therapy for Choroideremia: Preclinical Studies in Personalized Models
AAV-Mediated Delivery of Zinc Finger Nucleases Targeting Hepatitis B Virus Inhibits Active Replication
AAV-Mediated Administration of Myostatin Pro-Peptide Mutant in Adult Ldlr Null Mice Reduces Diet-Induced Hepatosteatosis and Arteriosclerosis
AAV-Dominant Negative Tumor Necrosis Factor (DN-TNF) Gene Transfer to the Striatum Does Not Rescue Medium Spiny Neurons in the YAC128 Mouse Model of Huntington's Disease
AAV-Mediated Overexpression of Neuroserpin in the Hippocampus Decreases PSD-95 Expression but Does Not Affect Hippocampal-Dependent Learning and Memory
AAV-mediated expression of an ADAMTS13 variant prevents shigatoxin-induced thrombotic thrombocytopenic purpura
AAV-mediated Liver-specific MPV17 Expression Restores mtDNA Levels and Prevents Diet-induced Liver Failure
AAV-Mediated Gene Transfer of the Obesity-Associated Gene Etv5 in Rat Midbrain Does Not Affect Energy Balance or Motivated Behavior
AAV-mediated Gene Delivery in Dp71-null Mouse Model with Compromised Barriers
AAV-encoded OTC activity persisting to adulthood following delivery to newborn spf(ash) mice is insufficient to prevent shRNA-induced hyperammonaemia
AAV-sBTLA facilitates HSP70 vaccine-triggered prophylactic antitumor immunity against a murine melanoma pulmonary metastasis model in vivo
AAV-mediated targeting of gene expression to the peri-infarct region in rat cortical stroke model
AAV-based gene therapy prevents neuropathology and results in normal cognitive development in the hyperargininemic mouse
AAV-ITR单链DNA微载体在小鼠骨骼肌中的表达
AAV-hVEGF_(165)及AAV-TGFβ1转染兔椎间盘纤维环细胞的实验研究
AAV-HGFK1抑制EGFR磷酸化拮抗大肠癌细胞生长
AAV-ITR基因表达微载体在小鼠体内表达
AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy
AAV-IL-22 modifies liver chemokine activity and ameliorates portal inflammation in murine autoimmune cholangitis
AAV-expressed eCD4-Ig provides durable protection from multiple SHIV challenges
AAV-Mediated Gene Delivery in a Feline Model of Sandhoff Disease Corrects Lysosomal Storage in the Central Nervous System
AAV-mediated and pharmacological induction of Hsp70 expression stimulates survival of retinal ganglion cells following axonal injury
AAV-mediated knockdown of Peripherin-2 in vivo using miRNA-based hairpins
AAV-mediated expression of wild-type and ALS-linked mutant VAPB selectively triggers death of motoneurons through a Ca2+-dependent ER-associated pathway