91 results on '"Zolotukhin I"'
Search Results
2. High-titer recombinant adeno-associated virus production utilizing a recombinant herpes simplex virus type I vector expressing AAV-2 Rep and Cap
3. Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield
4. Tight junction protein LSR is a host defense factor against SARS-CoV-2 infection in the small intestine
5. A fast radio burst localized at detection to an edge-on galaxy using very-long-baseline interferometry
6. Pre-clinical evaluation of an enhanced-function factor VIII variant for durable hemophilia A gene therapy in male mice
7. GP64-pseudotyped lentiviral vectors target liver endothelial cells and correct hemophilia A mice
8. Prednisolone and rapamycin reduce the plasma cell gene signature and may improve AAV gene therapy in cynomolgus macaques
9. Successes and challenges in clinical gene therapy
10. Immune profiling of adeno-associated virus response identifies B cell-specific targets that enable vector re-administration in mice
11. Functional two-dimensional high-entropy materials
12. Rational engineering of a functional CpG-free ITR for AAV gene therapy
13. First use of gene therapy to treat growth hormone resistant dwarfism in a mouse model
14. XIAP gene therapy effects on retinal ganglion cell structure and function in a mouse model of glaucoma
15. Transforming gas-rich low-mass disky galaxies into ultra-diffuse galaxies by ram pressure
16. AAV3-miRNA vectors for growth suppression of human hepatocellular carcinoma cells in vitro and human liver tumors in a murine xenograft model in vivo
17. Formation of intermediate-mass planets via magnetically controlled disk fragmentation
18. Parkinson's disease motor symptoms rescue by CRISPRa‐reprogramming astrocytes into GABAergic neurons
19. AAV‐delivered diacylglycerol kinase DGKk achieves long‐term rescue of fragile X syndrome mouse model
20. Antiviral immunity and nucleic acid sensing in haematopoietic stem cell gene engineering
21. Muscle‐directed gene therapy corrects Pompe disease and uncovers species‐specific GAA immunogenicity
22. Characterization and visualization of murine coagulation factor VIII-producing cells in vivo
23. Evaluation of LDL goal achievement in statin consumption, south east of Iran
24. Scalable photonic-based nulling interferometry with the dispersed multi-baseline GLINT instrument
25. Utility of red‐light ultrafast optogenetic stimulation of the auditory pathway
26. Retina transduction by rAAV2 after intravitreal injection: comparison between mouse and rat
27. Superior human hepatocyte transduction with adeno-associated virus vector serotype 7
28. Myeloid cells protect intestinal epithelial barrier integrity through the angiogenin/plexin‐B2 axis
29. Single‐domain antibodies targeting antithrombin reduce bleeding in hemophilic mice with or without inhibitors
30. H1/pHGFK1 nanoparticles exert anti-tumoural and radiosensitising effects by inhibition of MET in glioblastoma
31. Nuclear receptor corepressor 1 represses cardiac hypertrophy
32. In utero delivery of rAAV2/9 induces neuronal expression of the transgene in the brain: towards new models of Parkinson’s disease
33. Optimization of design and production strategies for novel adeno-associated viral display peptide libraries
34. Development of potent class II transactivator gene delivery systems capable of inducing de novo MHC II expression in human cells, in vitro and ex vivo
35. Ultrafast optogenetic stimulation of the auditory pathway by targeting‐optimized Chronos
36. DnaJ/Hsc70 chaperone complexes control the extracellular release of neurodegenerative‐associated proteins
37. A brain microvasculature endothelial cell‐specific viral vector with the potential to treat neurovascular and neurological diseases
38. Reduced retinal transduction and enhanced transgene-directed immunogenicity with intravitreal delivery of rAAV following posterior vitrectomy in dogs
39. Efficacy and safety of myocardial gene transfer of adenovirus, adeno-associated virus and lentivirus vectors in the mouse heart
40. Photoreceptor-targeted gene delivery using intravitreally administered AAV vectors in dogs
41. Development of novel AAV serotype 6 based vectors with selective tropism for human cancer cells
42. Treatment of multifocal breast cancer by systemic delivery of dual-targeted adeno-associated viral vectors
43. AAVrh.10 immunogenicity in mice and humans. Relevance of antibody cross-reactivity in human gene therapy
44. Insulin‐like growth factor 2 reverses memory and synaptic deficits in APP transgenic mice
45. Instrumentation for the detection and characterization of exoplanets
46. Delivering efficient liver-directed AAV-mediated gene therapy
47. The MRI contrast agent gadoteridol enhances distribution of rAAV1 in the rat hippocampus
48. Effective gene therapy for haemophilic mice with pathogenic factor IX antibodies
49. Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus
50. Modulation of feeding by chronic rAAV expression of a relaxin-3 peptide agonist in rat hypothalamus
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