| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adeno-associated Virus Genome Population Sequencing Achieves Full Vector Genome Resolution and Reveals Human-Vector Chimeras
|
Tai, Phillip W.L.
|
|
2018
|
9 |
C |
p. 130-141
|
artikel
|
| 2 |
Amelioration of Muscle and Nerve Pathology in LAMA2 Muscular Dystrophy by AAV9-Mini-Agrin
|
Qiao, Chunping
|
|
2018
|
9 |
C |
p. 47-56
|
artikel
|
| 3 |
An Adeno-Associated Viral Vector Capable of Penetrating the Mucus Barrier to Inhaled Gene Therapy
|
Duncan, Gregg A.
|
|
2018
|
9 |
C |
p. 296-304
|
artikel
|
| 4 |
An Assay that Predicts In Vivo Efficacy for DNA Aptamers that Stimulate Remyelination in a Mouse Model of Multiple Sclerosis
|
Heider, Robin M.
|
|
2018
|
9 |
C |
p. 270-277
|
artikel
|
| 5 |
A New Method for Reactivating and Expanding T Cells Specific for Rhizopus oryzae
|
Castillo, Paul
|
|
2018
|
9 |
C |
p. 305-312
|
artikel
|
| 6 |
An Integrated Approach toward the Biomanufacturing of Engineered Cell Therapy Products in a Stirred-Suspension Bioreactor
|
Hsu, Charlie Y.M.
|
|
2018
|
9 |
C |
p. 376-389
|
artikel
|
| 7 |
A Non-integrating Lentiviral Approach Overcomes Cas9-Induced Immune Rejection to Establish an Immunocompetent Metastatic Renal Cancer Model
|
Hu, Junhui
|
|
2018
|
9 |
C |
p. 203-210
|
artikel
|
| 8 |
A Novel Triple-Mutant AAV6 Capsid Induces Rapid and Potent Transgene Expression in the Muscle and Respiratory Tract of Mice
|
van Lieshout, Laura P.
|
|
2018
|
9 |
C |
p. 323-329
|
artikel
|
| 9 |
A Rationally Engineered Capsid Variant of AAV9 for Systemic CNS-Directed and Peripheral Tissue-Detargeted Gene Delivery in Neonates
|
Wang, Dan
|
|
2018
|
9 |
C |
p. 234-246
|
artikel
|
| 10 |
Biocompatible, Purified VEGF-A mRNA Improves Cardiac Function after Intracardiac Injection 1 Week Post-myocardial Infarction in Swine
|
Carlsson, Leif
|
|
2018
|
9 |
C |
p. 330-346
|
artikel
|
| 11 |
Cre Recombinase Mediates the Removal of Bacterial Backbone to Efficiently Generate rSV40
|
Shi, Xiaoxia
|
|
2018
|
9 |
C |
p. 225-233
|
artikel
|
| 12 |
Delivery of CR2-fH Using AAV Vector Therapy as Treatment Strategy in the Mouse Model of Choroidal Neovascularization
|
Schnabolk, Gloriane
|
|
2018
|
9 |
C |
p. 1-11
|
artikel
|
| 13 |
Detection of Replication Competent Lentivirus Using a qPCR Assay for VSV-G
|
Skrdlant, Lindsey M.
|
|
2018
|
9 |
C |
p. 99
|
artikel
|
| 14 |
Development of Intrathecal AAV9 Gene Therapy for Giant Axonal Neuropathy
|
Bailey, Rachel M.
|
|
2018
|
9 |
C |
p. 160-171
|
artikel
|
| 15 |
Efficacy and Safety of Glycosidic Enzymes for Improved Gene Delivery to the Retina following Intravitreal Injection in Mice
|
Cehajic-Kapetanovic, Jasmina
|
|
2018
|
9 |
C |
p. 192-202
|
artikel
|
| 16 |
Efficient Enrichment of Gene-Modified Primary T Cells via CCR5-Targeted Integration of Mutant Dihydrofolate Reductase
|
Paul, Biswajit
|
|
2018
|
9 |
C |
p. 347-357
|
artikel
|
| 17 |
Engineering PTEN-L for Cell-Mediated Delivery
|
Lavictoire, Sylvie J.
|
|
2018
|
9 |
C |
p. 12-22
|
artikel
|
| 18 |
Enhanced Production of Exosome-Associated AAV by Overexpression of the Tetraspanin CD9
|
Schiller, Lara Timantra
|
|
2018
|
9 |
C |
p. 278-287
|
artikel
|
| 19 |
HDAd5/35++ Adenovirus Vector Expressing Anti-CRISPR Peptides Decreases CRISPR/Cas9 Toxicity in Human Hematopoietic Stem Cells
|
Li, Chang
|
|
2018
|
9 |
C |
p. 390-401
|
artikel
|
| 20 |
Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety
|
Keto, Joni
|
|
2018
|
9 |
C |
p. 109-118
|
artikel
|
| 21 |
Influence of Pre-existing Anti-capsid Neutralizing and Binding Antibodies on AAV Vector Transduction
|
Fitzpatrick, Zachary
|
|
2018
|
9 |
C |
p. 119-129
|
artikel
|
| 22 |
Integrating HDAd5/35++ Vectors as a New Platform for HSC Gene Therapy of Hemoglobinopathies
|
Li, Chang
|
|
2018
|
9 |
C |
p. 142-152
|
artikel
|
| 23 |
Isoliquiritigenin Inhibits IL-1β-Induced Production of Matrix Metalloproteinase in Articular Chondrocytes
|
Zhang, Lei
|
|
2018
|
9 |
C |
p. 153-159
|
artikel
|
| 24 |
Liposome Lipid-Based Formulation Has the Least Influence on rAAV Transduction Compared to Other Transfection Agents
|
Guo, Pengpeng
|
|
2018
|
9 |
C |
p. 367-375
|
artikel
|
| 25 |
Modeling Anti-HIV-1 HSPC-Based Gene Therapy in Humanized Mice Previously Infected with HIV-1
|
Khamaikawin, Wannisa
|
|
2018
|
9 |
C |
p. 23-32
|
artikel
|
| 26 |
Neurturin Gene Therapy Protects Parasympathetic Function to Prevent Irradiation-Induced Murine Salivary Gland Hypofunction
|
Ferreira, Joao N.A.
|
|
2018
|
9 |
C |
p. 172-180
|
artikel
|
| 27 |
Optimizing EphA2-CAR T Cells for the Adoptive Immunotherapy of Glioma
|
Yi, Zhongzhen
|
|
2018
|
9 |
C |
p. 70-80
|
artikel
|
| 28 |
Plastin 3 Promotes Motor Neuron Axonal Growth and Extends Survival in a Mouse Model of Spinal Muscular Atrophy
|
Alrafiah, Aziza
|
|
2018
|
9 |
C |
p. 81-89
|
artikel
|
| 29 |
Platelet-Targeted Gene Therapy for Hemophilia
|
Shi, Qizhen
|
|
2018
|
9 |
C |
p. 100-108
|
artikel
|
| 30 |
Preclinical Development of a Lentiviral Vector for Gene Therapy of X-Linked Severe Combined Immunodeficiency
|
Poletti, Valentina
|
|
2018
|
9 |
C |
p. 257-269
|
artikel
|
| 31 |
Production and Purification of High-Titer Newcastle Disease Virus for Use in Preclinical Mouse Models of Cancer
|
Santry, Lisa A.
|
|
2018
|
9 |
C |
p. 181-191
|
artikel
|
| 32 |
Seizure-Suppressant and Neuroprotective Effects of Encapsulated BDNF-Producing Cells in a Rat Model of Temporal Lobe Epilepsy
|
Falcicchia, Chiara
|
|
2018
|
9 |
C |
p. 211-224
|
artikel
|
| 33 |
Serum-free Erythroid Differentiation for Efficient Genetic Modification and High-Level Adult Hemoglobin Production
|
Uchida, Naoya
|
|
2018
|
9 |
C |
p. 247-256
|
artikel
|
| 34 |
Staurosporine Increases Lentiviral Vector Transduction Efficiency of Human Hematopoietic Stem and Progenitor Cells
|
Lewis, Gretchen
|
|
2018
|
9 |
C |
p. 313-322
|
artikel
|
| 35 |
Target-Cell-Directed Bioengineering Approaches for Gene Therapy of Hemophilia A
|
Brown, Harrison C.
|
|
2018
|
9 |
C |
p. 57-69
|
artikel
|
| 36 |
The Biological Activity of AAV Vectors for Choroideremia Gene Therapy Can Be Measured by In Vitro Prenylation of RAB6A
|
Patrício, Maria I.
|
|
2018
|
9 |
C |
p. 288-295
|
artikel
|
| 37 |
Transduction Patterns of Adeno-associated Viral Vectors in a Laser-Induced Choroidal Neovascularization Mouse Model
|
Lee, Si Hyung
|
|
2018
|
9 |
C |
p. 90-98
|
artikel
|
| 38 |
Treatment of Bone Defects by Transplantation of Genetically Modified Mesenchymal Stem Cell Spheroids
|
Yanagihara, Kayoko
|
|
2018
|
9 |
C |
p. 358-366
|
artikel
|
| 39 |
Universal Method for the Purification of Recombinant AAV Vectors of Differing Serotypes
|
Nass, Shelley A.
|
|
2018
|
9 |
C |
p. 33-46
|
artikel
|
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