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                             28 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 AAV8-Mediated Hepatic Expression of Acid Sphingomyelinase Corrects the Metabolic Defect in the Visceral Organs of a Mouse Model of Niemann–Pick Disease Barbon, Christine M.
2005
12 3 p. 431-440
10 p.
artikel
2 AAV2-mediated ocular gene therapy for infantile neuronal ceroid lipofuscinosis Griffey, Megan
2005
12 3 p. 413-421
9 p.
artikel
3 AAV2/5 vector expressing galactocerebrosidase ameliorates CNS disease in the murine model of globoid-cell leukodystrophy more efficiently than AAV2 Lin, Darshong
2005
12 3 p. 422-430
9 p.
artikel
4 Activation of the Extracellular Signal-Regulated Kinase 1/2 Pathway by AAV Gene Transfer Protects Retinal Ganglion Cells in Glaucoma Zhou, Yu
2005
12 3 p. 402-412
11 p.
artikel
5 Aerosolized nanogram quantities of plasmid DNA mediate highly efficient gene delivery to mouse airway epithelium Rudolph, Carsten
2005
12 3 p. 493-501
9 p.
artikel
6 A picornaviral 2A-like sequence-based tricistronic vector allowing for high-level therapeutic gene expression coupled to a dual-reporter system Osborn, Mark J.
2005
12 3 p. 569-574
6 p.
artikel
7 Author Feedback Program Reveals Satisfaction with the Review Process at Molecular Therapy Frederickson, Robert M.
2005
12 3 p. 375-376
2 p.
artikel
8 Comparison of HIV- and EIAV-Based Vectors on Their Efficiency in Transducing Murine and Human Hematopoietic Repopulating Cells Siapati, Elena K.
2005
12 3 p. 537-546
10 p.
artikel
9 Efficient gene transfer into mouse embryonic stem cells with adenovirus vectors Kawabata, Kenji
2005
12 3 p. 547-554
8 p.
artikel
10 Enhanced Efficacy of Cholesterol-Minus Sonic Hedgehog in Postnatal Skin Lou, Howard
2005
12 3 p. 575-578
4 p.
artikel
11 Erratum to “Sustained Phenotypic Correction of Hemophilia A Mice Following Oncoretroviral-Mediated Expression of a Bioengineered Human Factor VIII Gene in Long-Term Hematopoietic Repopulating Cells” Moayer, Morvarid
2005
12 3 p. 579-580
2 p.
artikel
12 Evaluation of Viral and Mammalian Promoters for Use in Gene Delivery to Salivary Glands Zheng, Changyu
2005
12 3 p. 528-536
9 p.
artikel
13 Factors Influencing Adenovirus-Mediated Airway Transduction in Fetal Mice Buckley, S.M.K.
2005
12 3 p. 484-492
9 p.
artikel
14 Inside this Month 2005
12 3 p. 377-
1 p.
artikel
15 Intrabody applications in neurological disorders: progress and future prospects Miller, Todd W.
2005
12 3 p. 394-401
8 p.
artikel
16 Localized Gene Expression Following Administration of Adeno-associated Viral Vectors via Pancreatic Ducts Loiler, Scott A.
2005
12 3 p. 519-527
9 p.
artikel
17 Phenotypic Improvement of Dystrophic Muscles by rAAV/Microdystrophin Vectors Is Augmented by Igf1 Codelivery Abmayr, Simone
2005
12 3 p. 441-450
10 p.
artikel
18 Plasmid Delivery in Vivo from Porous Tissue-Engineering Scaffolds: Transgene Expression and Cellular Transfection Jang, Jae-Hyung
2005
12 3 p. 475-483
9 p.
artikel
19 Postmitotic Nuclear Retention of Episomal Plasmids Is Altered by DNA Labeling and Detection Methods Gasiorowski, Joshua Z.
2005
12 3 p. 460-467
8 p.
artikel
20 Report from the 2nd Stem Cell Clonality and Genotoxicity Retreat Frederickson, Robert M.
2005
12 3 p. 379-383
5 p.
artikel
21 Research Update 2005
12 3 p. 378-
1 p.
artikel
22 Role of clathrin- and caveolae-mediated endocytosis in gene transfer mediated by lipo- and polyplexes Rejman, Joanna
2005
12 3 p. 468-474
7 p.
artikel
23 Small Hairpin RNAs Efficiently Inhibit Hepatitis C IRES–Mediated Gene Expression in Human Tissue Culture Cells and a Mouse Model Wang, Qian
2005
12 3 p. 562-568
7 p.
artikel
24 Targeted Delivery of Oligodeoxynucleotides to Mouse Lung Endothelial Cells in Vitro and in Vivo Wilson, Annette
2005
12 3 p. 510-518
9 p.
artikel
25 Targeting Viral-Mediated Transduction to the Lung Airway Epithelium with the Anti-inflammatory Cationic Lipid Dexamethasone–Spermine Price, Amber
2005
12 3 p. 502-509
8 p.
artikel
26 The influence of adenovirus fiber structure and function on vector development for gene therapy Nicklin, Stuart A.
2005
12 3 p. 384-393
10 p.
artikel
27 Toward a Gene Therapy for Dominant Disease: Validation of an RNA Interference-Based Mutation-Independent Approach Kiang, Anna-Sophia
2005
12 3 p. 555-561
7 p.
artikel
28 Type I Interferons potently suppress gene expression following gene delivery using liposome–DNA complexes Sellins, Karen
2005
12 3 p. 451-459
9 p.
artikel
                             28 gevonden resultaten
 
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