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                             94 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 AAV9-mediated central nervous system–targeted gene delivery via cisterna magna route in mice Lukashchuk, Vera
2016
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2 AAV-mediated Sirt1 overexpression in skeletal muscle activates oxidative capacity but does not prevent insulin resistance Vil, Laia
2016
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3 A comparison of foamy and lentiviral vector genotoxicity in SCID-repopulating cells shows foamy vectors are less prone to clonal dominance Everson, Elizabeth M
2016
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4 All-in-one processing of heterogeneous human cell grafts for gene and cell therapy Lukianova-Hleb, Ekaterina Y
2016
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5 An HSV-based library screen identifies PP1α as a negative TRPV1 regulator with analgesic activity in models of pain Reinhart, Bonnie
2016
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6 A regulatable AAV vector mediating GDNF biological effects at clinically-approved sub-antimicrobial doxycycline doses Chtarto, Abdelwahed
2016
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7 A scalable method for the production of high-titer and high-quality adeno-associated type 9 vectors using the HSV platform Adamson-Small, Laura
2016
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8 Assessment of murine colorectal cancer by micro-ultrasound using three dimensional reconstruction and non-linear contrast imaging Freeling, Jessica L
2016
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9 A targeted controlled force injection of genetic material in vivo Ahlén, Gustaf
2016
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10 A translationally optimized AAV-UGT1A1 vector drives safe and long-lasting correction of Crigler-Najjar syndrome Ronzitti, Giuseppe
2016
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11 Biodistribution studies: understanding international expectations Huang, Ying
2016
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12 Broad HIV-1 inhibition in vitro by vaccine-elicited CD8+ T cells in African adults Mutua, Gaudensia
2016
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13 Clinical development of gene- and cell-based therapies: overview of the European landscape de Wilde, Sofieke
2016
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14 Clinical development of gene therapy: results and lessons from recent successes Kumar, Sandeep RP
2016
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15 Comparative study of human embryonic stem cells (hESC) and human induced pluripotent stem cells (hiPSC) as a treatment for retinal dystrophies Riera, Marina
2016
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16 Constitutively active form of natriuretic peptide receptor 2 ameliorates experimental pulmonary arterial hypertension Nawa, Nobutoshi
2016
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17 Construction of a hybrid β-hexosaminidase subunit capable of forming stable homodimers that hydrolyze GM2 ganglioside in vivo Tropak, Michael B
2016
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18 Corrigendum to “Efficient gene delivery to photoreceptors using AAV2/rh10 and rescue of the Rho–/– mouse” Palfi, Arpad
2016
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19 Design of a titering assay for lentiviral vectors utilizing direct extraction of DNA from transduced cells in microtiter plates Murphy, Michele E
2016
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20 Development of a real-time imaging system for hypoxic cell apoptosis Kagiya, Go
2016
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21 Distribution of AAV8 particles in cell lysates and culture media changes with time and is dependent on the recombinant vector Piras, Bryan A
2016
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22 Dual therapeutic functions of F-5 fragment in burn wounds: preventing wound progression and promoting wound healing in pigs Bhatia, Ayesha
2016
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23 Dynamics of antigen presentation to transgene product-specific CD4+ T cells and of Treg induction upon hepatic AAV gene transfer Perrin, George Q
2016
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24 Effects of FVIII immunity on hepatocyte and hematopoietic stem cell–directed gene therapy of murine hemophilia A Lytle, Allison M
2016
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25 Efficacy and biodistribution analysis of intracerebroventricular administration of an optimized scAAV9-SMN1 vector in a mouse model of spinal muscular atrophy Armbruster, Nicole
2016
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26 Efficient detection of human circulating tumor cells without significant production of false-positive cells by a novel conditionally replicating adenovirus Sakurai, Fuminori
2016
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27 Elimination of proliferating cells from CNS grafts using a Ki67 promoter-driven thymidine kinase Tieng, Vannary
2016
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28 Expression mediated by three partial sequences of the human tyrosine hydroxylase promoter in vivo Rolland, Anne-Sophie
2016
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29 Ex vivo expansion of circulating CD34+ cells enhances the regenerative effect on rat liver cirrhosis Nakamura, Toru
2016
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30 Fbxw7-associated drug resistance is reversed by induction of terminal differentiation in murine intestinal organoid culture Lorenzi, Federica
2016
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31 100-fold but not 50-fold dystrophin overexpression aggravates electrocardiographic defects in the mdx model of Duchenne muscular dystrophy Yue, Yongping
2016
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32 From selection hits to clinical leads: progress in aptamer discovery Maier, Keith E
2016
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33 Functional correction of neurological and somatic disorders at later stages of disease in MPS IIIA mice by systemic scAAV9-hSGSH gene delivery Fu, Haiyan
2016
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34 Helper virus-mediated downregulation of transgene expression permits production of recalcitrant helper-dependent adenoviral vector Palmer, Donna J
2016
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35 Impact of age and vector construct on striatal and nigral transgene expression Polinski, Nicole K
2016
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36 Impact of intravenous infusion time on AAV8 vector pharmacokinetics, safety, and liver transduction in cynomolgus macaques Greig, Jenny A
2016
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37 In utero stem cell transplantation and gene therapy: rationale, history, and recent advances toward clinical application Almeida-Porada, Graça
2016
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38 Investigating the functionality of an OCT4-short response element in human induced pluripotent stem cells Vega-Crespo, Agustin
2016
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39 Manufacturing of AcMNPV baculovirus vectors to enable gene therapy trials Kwang, Timothy Weixin
2016
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40 Manufacturing of recombinant adeno-associated viral vectors for clinical trials Clément, Nathalie
2016
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41 Manufacturing of recombinant adeno-associated viral vectors: new technologies are welcome Ayuso, Eduard
2016
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42 “Marker of Self” CD47 on lentiviral vectors decreases macrophage-mediated clearance and increases delivery to SIRPA-expressing lung carcinoma tumors Sosale, Nisha G
2016
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43 Merging DBS with viral vector or stem cell implantation: “hybrid” stereotactic surgery as an evolution in the surgical treatment of Parkinson's disease Rowland, Nathan C
2016
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44 Methods and clinical development of adenovirus-vectored vaccines against mucosal pathogens Afkhami, Sam
2016
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45 Microglia-specific targeting by novel capsid-modified AAV6 vectors Rosario, Awilda M
2016
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46 Moving oncolytic viruses into the clinic: clinical-grade production, purification, and characterization of diverse oncolytic viruses Ungerechts, Guy
2016
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47 Moving toward a higher efficiency of microcell-mediated chromosome transfer Liskovykh, Mikhail
2016
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48 Multilineage polyclonal engraftment of Cal-1 gene-modified cells and in vivo selection after SHIV infection in a nonhuman primate model of AIDS Peterson, Christopher W.
2016
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49 Multilineage transduction of resident lung cells in vivo by AAV2/8 for α1-antitrypsin gene therapy Payne, Julia G
2016
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50 Multiple mechanisms determine the sensitivity of human-induced pluripotent stem cells to the inducible caspase-9 safety switch Yagyu, Shigeki
2016
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51 Ocular and systemic safety of a recombinant AAV8 vector for X-linked retinoschisis gene therapy: GLP studies in rabbits and Rs1-KO mice Marangoni, Dario
2016
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52 Overexpression of factor VIII after AAV delivery is transiently associated with cellular stress in hemophilia A mice Lange, Amy M
2016
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53 PAX6 MiniPromoters drive restricted expression from rAAV in the adult mouse retina Hickmott, Jack W
2016
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54 Plasma-activated air mediates plasmid DNA delivery in vivo Edelblute, Chelsea M
2016
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55 Potential for cellular stress response to hepatic factor VIII expression from AAV vector Zolotukhin, Irene
2016
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56 Potent spinal parenchymal AAV9-mediated gene delivery by subpial injection in adult rats and pigs Miyanohara, Atsushi
2016
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57 Practical utilization of recombinant AAV vector reference standards: focus on vector genomes titration by free ITR qPCR D'Costa, Susan
2016
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58 Preclinical development and qualification of ZFN-mediated CCR5 disruption in human hematopoietic stem/progenitor cells DiGiusto, David L
2016
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59 Preclinical evaluation of mesenchymal stem cells overexpressing VEGF to treat critical limb ischemia Beegle, Julie R
2016
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60 Preclinical safety, pharmacokinetics, pharmacodynamics, and biodistribution studies with Ad35K++ protein: a novel rituximab cotherapeutic Richter, Maximilian
2016
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61 Preclinical validation: LV/IL-12 transduction of patient leukemia cells for immunotherapy of AML Huang, Ju
2016
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62 Production and clinical development of nanoparticles for gene delivery Chen, Jie
2016
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63 Production and purification of high-titer foamy virus vector for the treatment of leukocyte adhesion deficiency Nasimuzzaman, Md
2016
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64 Production of lentiviral vectors Merten, Otto-Wilhelm
2016
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65 Promise and problems associated with the use of recombinant AAV for the delivery of anti-HIV antibodies Fuchs, Sebastian P
2016
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66 Prophylactic and therapeutic adenoviral vector-based multivirus-specific T-cell immunotherapy for transplant patients Dasari, Vijayendra
2016
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67 Protein transduction therapy into cochleae via the round window niche in guinea pigs Takeda, Hiroki
2016
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68 Purification of baculovirus vectors using heparin affinity chromatography Nasimuzzaman, Md
2016
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69 Quantification of designer nuclease induced mutation rates: a direct comparison of different methods Ehrke-Schulz, Eric
2016
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70 Rapid cloning, expression, and functional characterization of paired αβ and γδ T-cell receptor chains from single-cell analysis Guo, Xi-zhi J
2016
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71 Rapid, scalable, and low-cost purification of recombinant adeno-associated virus produced by baculovirus expression vector system Buclez, Pierre-Olivier
2016
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72 RD-MolPack technology for the constitutive production of self-inactivating lentiviral vectors pseudotyped with the nontoxic RD114-TR envelope Marin, Virna
2016
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73 Retinal pigment epithelial cell expression of active Rap 1a by scAAV2 inhibits choroidal neovascularization Wang, Haibo
2016
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74 Robust generation of transgenic mice by simple hypotonic solution mediated delivery of transgene in testicular germ cells Usmani, Abul
2016
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75 Safety and biodistribution assessment of sc-rAAV2.5IL-1Ra administered via intra-articular injection in a mono-iodoacetate-induced osteoarthritis rat model Wang, Gensheng
2016
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76 Sendai virus, an RNA virus with no risk of genomic integration, delivers CRISPR/Cas9 for efficient gene editing Park, Arnold
2016
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77 Significant changes in endogenous retinal gene expression assessed 1 year after a single intraocular injection of AAV-CNTF or AAV-BDNF LeVaillant, Chrisna J
2016
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78 Strategies to generate high-titer, high-potency recombinant AAV3 serotype vectors Ling, Chen
2016
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79 Tailored transgene expression to specific cell types in the central nervous system after peripheral injection with AAV9 Dashkoff, Jonathan
2016
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80 Targeted approaches to induce immune tolerance for Pompe disease therapy Doerfler, Phillip A
2016
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81 TFEB overexpression promotes glycogen clearance of Pompe disease iPSC-derived skeletal muscle Sato, Yohei
2016
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82 The feasibility of incorporating Vpx into lentiviral gene therapy vectors McAllery, Samantha A
2016
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83 The identification of hematopoietic-specific regulatory elements for WASp gene expression Zhan, Jun
2016
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84 The impact of minimally oversized adeno-associated viral vectors encoding human factor VIII on vector potency in vivo Kyostio-Moore, Sirkka
2016
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85 The superior regenerative potential of muscle-derived stem cells for articular cartilage repair is attributed to high cell survival and chondrogenic potential Li, Hongshuai
2016
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86 Total body irradiation must be delivered at high dose for efficient engraftment and tolerance in a rhesus stem cell gene therapy model Uchida, Naoya
2016
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87 Towards routine manufacturing of gene therapy drugs Merten, Otto-Wilhelm
2016
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88 Transcriptional activity of novel ALDH1L1 promoters in the rat brain following AAV vector-mediated gene transfer Mudannayake, Janitha M
2016
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89 Transcriptionally regulated and nontoxic delivery of the hyperactive Sleeping Beauty Transposase Cocchiarella, Fabienne
2016
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90 Treatment of hypophosphatasia by muscle-directed expression of bone-targeted alkaline phosphatase via self-complementary AAV8 vector Nakamura-Takahashi, Aki
2016
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91 Treatment of osteoarthritis using a helper-dependent adenoviral vector retargeted to chondrocytes Ruan, Merry ZC
2016
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92 Ultracentrifugation-free chromatography-mediated large-scale purification of recombinant adeno-associated virus serotype 1 (rAAV1) Tomono, Taro
2016
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93 Viral-mediated Ntf3 overexpression disrupts innervation and hearing in nondeafened guinea pig cochleae Lee, Min Young
2016
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94 Widespread AAV1- and AAV2-mediated transgene expression in the nonhuman primate brain: implications for Huntington's disease Hadaczek, Piotr
2016
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                             94 gevonden resultaten
 
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