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                             1118 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 883. AAV-2 Based Gene Therapy Using Novel Anti-VEGF Molecules for Inhibition of Angiogenesis in the Eye Scaria, Abraham
2006
13 S1 p. S340-
1 p.
artikel
2 451. AAV-BDNF Augments Neurogenesis in Both the Normal Adult Rat Brain and the Quinolinic Acid Lesion Model of Huntington's Disease Henry, Rebecca A.
2006
13 S1 p. S174-
1 p.
artikel
3 498. AAV Δ264CFTR Enhances Maturation of ΔF508CFTR and wt CFTR Expression Cebotaru, Liudmila
2006
13 S1 p. S193-
1 p.
artikel
4 253. AAV Delivery of a Trans-Splicing RNA Re-Directs SMN2 Splicing and Results in Increased Full-Length SMN Coady, Tristan H.
2006
13 S1 p. S97-
1 p.
artikel
5 1020. AAV Delivery of Suppression and Replacement Constructs for Rhodopsin-Linked Autosomal Dominant Retinitis Pigmentosa Chadderton, Naomi
2006
13 S1 p. S392-S393
2 p.
artikel
6 745. AAV12, Isolated from Vervet Monkey, Has Unique Tropism and Biological as Well as Neutralization Properties Schmidt, Michael
2006
13 S1 p. S288-
1 p.
artikel
7 712. AAV-Mediated Allele-Specific RNA Interference of a Common Dominant Rhodopsin Mutation Causing Retinitis Pigmentosa Tessitore, Alessandra
2006
13 S1 p. S275-
1 p.
artikel
8 885. AAV-Mediated Gene Transfer of Constitutively and Pharmacologically-Activated Glial Cell-Derived Neurotrophic Factor Receptor To Inhibit Retinal Degeneration Allocca, Mariacarmela
2006
13 S1 p. S341-
1 p.
artikel
9 220. AAV Mediated Gene Transfer of Smad7 in Different Models of Cystic Kidney Diseases Keppler, Andrea
2006
13 S1 p. S85-
1 p.
artikel
10 205. AAV-Mediated Gene Transfer to Muscle and Liver of MPS VI Animal Models Tessitore, Alessandra
2006
13 S1 p. S79-
1 p.
artikel
11 228. AAV Mediated Hypoxia-Inducible VEGF Expression and Neovascular Formation in Ischemic Pig Myocardium Su, Hua
2006
13 S1 p. S87-
1 p.
artikel
12 418. AAV-Mediated sFLT-1 Gene Therapy for Ocular Neovascularization: Longevity, Toxicity and Efficacy Results from Mice and Monkeys Rakoczy, E.P.
2006
13 S1 p. S160-S161
2 p.
artikel
13 886. AAV-Mediated Somatic Gene Transfer as an Approach To Delineate Pathogenic Mechanisms in an Autosomal Dominant Blindness Disorder Resembling Age-Related Macular Degeneration (AMD) Keiser, Nicholas W.
2006
13 S1 p. S341-
1 p.
artikel
14 496. AAV-Mediated, Somatic Gene Transfer to RPE Cells in Order To Study the Pathogenesis of Macular Degeneration: Proteomic and Genomic Analysis Du Bois, Garrett C.
2006
13 S1 p. S192-
1 p.
artikel
15 6. AAV8-Mediated Transgene Expression in Mice and Non-Human Primates Mizukami, Hiroaki
2006
13 S1 p. S3-
1 p.
artikel
16 676. AAV-Rep 78 Mediated Rescue and Integration of a 27kb Transgene Cassette Wang, Hongjie
2006
13 S1 p. S261-
1 p.
artikel
17 1065. AAV2 Vector-Delivered Myostatin Propeptide Improves Muscle Healing after Injury Zhu, Jinhong
2006
13 S1 p. S408-S409
2 p.
artikel
18 344. AAV Vector-Mediated Msx1 Gene Transfer Induces Hematopoietic Stem/Progenitor Cells in Skeletal Muscle Nobuyoshi, Masaharu
2006
13 S1 p. S131-
1 p.
artikel
19 470. ABCB4 P-Glycoprotein Reduces Infectivity of Lentiviral Particles by Increasing Their Phosphatidylcholine Content van Til, Niek P.
2006
13 S1 p. S182-
1 p.
artikel
20 222. Aberrant Striatal Gene Expression in the Striatum of HPRT-Knockout Mouse Song, Shaochun
2006
13 S1 p. S85-
1 p.
artikel
21 987. A Cautionary Tale for Immunotherapy Using Genetically Modified Dendritic Cells; Implications for the Future Design of Vaccines Tan, PengH.
2006
13 S1 p. S380-
1 p.
artikel
22 912. Accelerated Chondrogenesis in Nanofiber Scaffolds Containing BMP-2 Genetically Engineered Chondrocytes Gorsline, Robert T.
2006
13 S1 p. S351-S352
2 p.
artikel
23 869. Accelerated Re-Endothelilization in eNOS Transduced Iliac Artery Following Gene Delivery from an Adenoviral Eluting Stent Sharif, Faisal
2006
13 S1 p. S334-S335
2 p.
artikel
24 565. Acceleration of Fracture Healing with Adenovirally Transduced Human BMP-2 and -6 Genes in Horse Metatarsal Osteotomy and Ostectomy Models Ishihara, Akikazu
2006
13 S1 p. S217-S218
2 p.
artikel
25 47. A Combination Therapy of Selective Intraarterial Gendicine Infusion with Chemotherapy for Locally Advanced Head and Neck Carcinoma Li, Longjiang
2006
13 S1 p. S20-
1 p.
artikel
26 998. A Comparative Analysis of Transgene- Specific Immune Responses Following In Vivo and Ex Vivo Approaches to Gene Therapy Lu, Zhenmei
2006
13 S1 p. S384-S385
2 p.
artikel
27 102. Activation of the LMO2 Gene in Human Lymphoid Cells by rAAV-Mediated Targeted Insertion of a Single LTR Expression Cassette into the First Intron Ryu, Byoung Y.
2006
13 S1 p. S42-
1 p.
artikel
28 609. Acute-Phase Toxicity Following Systemic Administration of Non-Human Primate Derived Adenoviral Vectors to Mice Somanthan, Suryanarayan
2006
13 S1 p. S235-
1 p.
artikel
29 982. Adaptive Immune System Down-Regulates Transgene Expression from Adenovirally Infected Neurons in the Brain In Vivo Zirger, Jeffrey M.
2006
13 S1 p. S378-
1 p.
artikel
30 509. Adeno-Associated Vector Mediated Delivery of Anti-HIV Genes Tamhane, Mayur C.
2006
13 S1 p. S196-
1 p.
artikel
31 48. Adeno-Associated Viral (AAV) Vector- Mediated Systemic Delivery of mda-7/IL24 Inhibits Tumor Growth by Antitumor Bystander Effect Tahara, Ichiro
2006
13 S1 p. S20-
1 p.
artikel
32 488. Adeno-Associated Viral Serotype 2/1 Is a Highly Efficient Vector for In Utero Gene Transfer to Hair Cell Precursors Bedrosian, Jeffrey C.
2006
13 S1 p. S189-
1 p.
artikel
33 709. Adeno-Associated Virus Delivery of siRNAs Leads to a Reduction in Phospholamban Levels Andino, Lourdes M.
2006
13 S1 p. S274-
1 p.
artikel
34 889. Adeno-Associated Virus Gene Therapy of Feline Gangliosidosis Martin, Douglas R.
2006
13 S1 p. S342-
1 p.
artikel
35 8. Adeno-Associated Virus 2-Mediated Gene Transfer: A Complex Interaction between Epidermal Growth Factor Receptor Protein Tyrosine Kinase Signaling and Ubiquitin/Proteasome Pathway in Transgene Expression Zhong, Li
2006
13 S1 p. S3-S4
2 p.
artikel
36 3. Adeno-Associated Virus 2-Mediated Gene Transfer: Identification of a Cellular Protein Serine/Threonine Phosphatase Involved in Augmenting Vector Transduction Efficiency Zhao, Weihong
2006
13 S1 p. S1-S2
2 p.
artikel
37 7. Adeno-Associated Virus Type 2 (AAV2) Contains an Integrin alpha5beta1 Recognition Sequence Essential for Viral Cell Entry Asokan, Aravind
2006
13 S1 p. S3-
1 p.
artikel
38 10. Adeno-Associated Virus Type-1 Vectors Transduce Human Polarized Airway Epithelia without Polarity Preference Yan, Ziying
2006
13 S1 p. S4-S5
2 p.
artikel
39 567. Adeno-Associated Virus Vector 8 (AAV8) Provides Efficient Gene Delivery to Skeletal Muscles In Utero by Systemic Adminstration Koppanati, Bhanu Munil
2006
13 S1 p. S218-
1 p.
artikel
40 337. Adenoviral Delivery of the RheoSwitch® Therapeutic System to Mouse Brain and Liver Potter, David W.
2006
13 S1 p. S128-
1 p.
artikel
41 781. Adenoviral Gene Transfer of Angiopoietin-1 Corrects Post-Pneumonectomy Compensatory Lung Growth in the MMP-9-/- Mice Via Mobilization of Endothelial Progenitor Cells Marwan, A.
2006
13 S1 p. S302-
1 p.
artikel
42 50. Adenoviral-Mediated Gene Transfer of Single Chain Fv 425:sTRAIL Fusion Protein Induces Target Cell Restricted Apoptosis in EGFR- Positive Tumor Cells and a Potent Bystander Effect Haisma, Hidde J.
2006
13 S1 p. S21-
1 p.
artikel
43 429. Adenoviral-Mediated Interleukin-15 Receptor-α Gene Therapy of Murine Breast Cancer Morrison, Brian J.
2006
13 S1 p. S165-
1 p.
artikel
44 289. Adenoviral-Mediated p53 Gene Therapy (Advexin) in a Patient with Li-Fraumeni Syndrome with a Mixed Germ Cell Tumor: Tolerability and Response Senzer, Neil
2006
13 S1 p. S110-
1 p.
artikel
45 942. Adenoviral Mediated Re-Expression of Wnt Antagonist Dkk-1 Induces Apoptosis and Suppresses Tumor Growth in Medulloblastoma Vibhakar, Rajeev
2006
13 S1 p. S363-
1 p.
artikel
46 133. Adenovirus-Light Chain Inhibition of Growth Hormone Release from Pituitary Adenoma Cells Federici, Thais
2006
13 S1 p. S54-
1 p.
artikel
47 281. Adenovirus-Mediated CD40 Ligand Therapy Induces Tumor Cell Apoptosis and Systemic Immunity in the TRAMP-C2 Mouse Prostate Cancer Model Dzojic, Helena
2006
13 S1 p. S107-
1 p.
artikel
48 933. Adenovirus-Mediated Delivery of Secretable Trimeric TRAIL Enhances Apoptosis and Improves Survival Compared with Conventional Chemotherapy for Malignant Gliomas Jeong, Moonsup
2006
13 S1 p. S360-
1 p.
artikel
49 427. Adenovirus Mediated GRP94/gp96 Expression in Treatment of Neuroblastoma Liu, Shanling
2006
13 S1 p. S164-
1 p.
artikel
50 939. Adenovirus-Mediated TA-p73β Gene Transfer Leads to Chemosensitization of Human Malignant Melanoma Tuve, Sebastian
2006
13 S1 p. S362-
1 p.
artikel
51 129. Adenovirus Serotype 35 Vector-Mediated Transduction in Mouse Hematopoietic Stem Cells Isolated from Human CD46-Transgenic Mice Sakurai, Fuminori
2006
13 S1 p. S52-S53
2 p.
artikel
52 121. Adenovirus Titers Determined by Quantitative Real-Time PCR Correlate with Infectious Titers Thomas, Maria A.
2006
13 S1 p. S49-S50
2 p.
artikel
53 674. Administration of rAAV2 and rAAV5 to the Parotid Gland of Non-Human Primates Voutetakis, A.
2006
13 S1 p. S260-
1 p.
artikel
54 241. A Dose-Ranging Study of AAV-hAADC Therapy in Parkinsonian Monkeys Forsayeth, John R.
2006
13 S1 p. S93-
1 p.
artikel
55 644. A Dual-Action Armed Replicating Adenovirus for the Treatment of Bone Metastases of Breast Cancer Cody, James J.
2006
13 S1 p. S248-
1 p.
artikel
56 505. Advances in Large-Scale Production of Recombinant Adeno-Associated Vectors Negrete, Alejandro
2006
13 S1 p. S195-
1 p.
artikel
57 502. Advances in the Application of Combinatorial Technology for the Optimization of Adeno-Associated Virus (AAV) Vectors Perabo, Luca
2006
13 S1 p. S194-
1 p.
artikel
58 387. Advantageous Properties of the piggyBac Transposon System for Gene Transfer in Human Cells Wilson, Matthew H.
2006
13 S1 p. S147-S148
2 p.
artikel
59 692. Aerosol Delivery of Concentrated pDNA/ PEI Formulations to the Murine Lung Davies, Lee A.
2006
13 S1 p. S267-S268
2 p.
artikel
60 435. A Fiber-Modified, Relaxin-Expressing Oncolytic Adenovirus Prolongs Survival of Tumor Bearing Mice Ganesh, Shanthi
2006
13 S1 p. S167-S168
2 p.
artikel
61 375. A Glaucoma Gene Therapy Model: Eighteen Cat Study Revealing Long-Term Targeted Genetic Modification of the Anterior Chamber by Lentiviral Vectors Khare, Pranay D.
2006
13 S1 p. S142-S143
2 p.
artikel
62 693. Airway Pre-Treatment with a Novel Surfactant Compound Improves Standard Enhancement of Lentiviral Gene Transfer In Vivo Cmielewski, Patricia L.
2006
13 S1 p. S268-
1 p.
artikel
63 711. Allele-Specific Silencing of Mutant Huntingtin for Huntington's Disease Therapy Mas-Monteys, Alex
2006
13 S1 p. S274-S275
2 p.
artikel
64 71. Alpha 1 Antitrypsin (AAT) Gene Therapy for the Prevention of Type 1 Diabetes Song, Sihong
2006
13 S1 p. S30-
1 p.
artikel
65 380. Alternative Cellular Receptor for B_Group Adenoviruses: Implications for Gene Therapy Tuve, Sebastian
2006
13 S1 p. S145-
1 p.
artikel
66 134. A Mechanistic and Kinetic Model for the Inactivation of Liquid-Formulated Adenoviral Vectors by the Delayed Onset of a Rapid Period of Penton Disassociation Frey, David
2006
13 S1 p. S54-
1 p.
artikel
67 1067. Amelioration of Arthritis after Local Delivery of an Adeno-Associated Virus Type 6 Expressing a TNF-Blocking Agent under a Disease-Inducible Promoter Khoury, Maroun
2006
13 S1 p. S409-
1 p.
artikel
68 157. A Mutant Type 2 Herpes Simplex Virus Deleted for the Protein Kinase Domain of the ICP10 Gene Is a Potent Oncolytic Virus Fu, Xinping
2006
13 S1 p. S61-S62
2 p.
artikel
69 703. Analysis of the Stability and Functionality of siRNA after Nebulization of siRNA Polyplexes Huth, Stephanie
2006
13 S1 p. S272-
1 p.
artikel
70 524. Analysis of Unique Proteins Bound to Sequentially Injected DOTAP:DNA Vectors Conwell, Christine C.
2006
13 S1 p. S201-
1 p.
artikel
71 107. α2, 3 and α2,6 N-Linked Sialic Acid Facilitate Efficient Binding and Transduction by Adeno-Associated Virus Type 1 and 6 Wu, Zhijian
2006
13 S1 p. S44-
1 p.
artikel
72 437. An E1b-19kD-Deleted p53-Expressing Replicating Adenovirus Markedly Enhances the Induction of Apoptosis When Combined with Cisplatin in Head and Neck Cancer Cells Kutler, David I.
2006
13 S1 p. S168-
1 p.
artikel
73 511. An Enzyme Linked Immunosorbent Assay for the Detection of Herpes Simplex Virus Type 1 Proteins in a Novel rAAV Production and Purification Process Ye, Guo-jie
2006
13 S1 p. S197-
1 p.
artikel
74 19. A New, Plasmid-Based Adenoviral Vectoring System Derived from the Highly Immunogenic, Human Ad4 Strain Hartman, Zachary C.
2006
13 S1 p. S8-
1 p.
artikel
75 221. A New Retroviral Gene Therapy Approach for Cystinuria Research Sagi, Sreedhar
2006
13 S1 p. S85-
1 p.
artikel
76 951. A New Vector Based on Baculovirus Was Effective in Inhibiting Glioma Cell Growth in the Rat Brain Wang, Chaoyang
2006
13 S1 p. S367-
1 p.
artikel
77 961. Angiopoietin-1 Enhances the Effect of Paclitaxel on Breast Cancer Cell Killing in a Mouse Model Qi Huang, Yao
2006
13 S1 p. S370-
1 p.
artikel
78 532. An Inducible Fed-Batch Fermentation Process for Scale-Up and Production of DNA Vaccines and Gene Medicines Carnes, Aaron E.
2006
13 S1 p. S204-
1 p.
artikel
79 176. An Inhibitor of Fumarylacetoacetate Hydrolase (Fah) for Selection of Transplanted Hepatocytes and Gene Correction In Vivo Wursthorn, Karsten
2006
13 S1 p. S68-
1 p.
artikel
80 785. A Novel Adeno Associated Virus Vector That Efficiently Transduces Airway Epithelium In Vivo and Can Be Re-Administered Limberis, Maria
2006
13 S1 p. S304-
1 p.
artikel
81 177. A Novel Class of Cationic Amphiphiles for Airway Gene Delivery Kim, Keun-Sik
2006
13 S1 p. S68-S69
2 p.
artikel
82 1066. A Novel Class of Miniature Stabilized Double-Stranded AAV (msdsAAV) Vectors for the In Vivo Expression of Short Hairpin RNAs Grimm, Dirk
2006
13 S1 p. S409-
1 p.
artikel
83 412. A Novel Friedreich's Ataxia Model and In Vivo Gene Rescue Using HSV-1 Amplicon Vectors in Transgenic Mice Lim, Filip
2006
13 S1 p. S158-
1 p.
artikel
84 153. A Novel Gene Expression System Using Human Artificial Chromosome-HSV-1 Vectors Moralli, Daniela
2006
13 S1 p. S60-
1 p.
artikel
85 778. A Novel Genetically Modified Adenovirus Vector Shows Enhanced Infectivity towards Ex Vivo Pancreatic Cancer van Geer, Michael
2006
13 S1 p. S301-
1 p.
artikel
86 503. A Novel Herpes Simplex Virus Helper Based Production of Adeno- Associated Virus Vectors for Treatment of Retinal Angiogenesis Ye, Guo-jie
2006
13 S1 p. S194-
1 p.
artikel
87 740. A Novel Hybrid System Efficiently Expands AAV Packaging Capacity Ghosh, Arka
2006
13 S1 p. S286-
1 p.
artikel
88 225. A Novel Mechanism between Diabetes Mellitus Complications and Procalcitonin Gene Expression Soylemez, Mehmet A.
2006
13 S1 p. S86-
1 p.
artikel
89 200. A Novel Non-Viral Polymer for Plasmid Delivery to Bone Marrow Stromal Cells (BMSC) Clements, Basak A.
2006
13 S1 p. S78-
1 p.
artikel
90 777. A Novel Pan-Oncolytic Adenovirus Therapeutically Effective in Different Cancer Cell Types Lopez, Maria V.
2006
13 S1 p. S300-S301
2 p.
artikel
91 596. A Novel Replication Incompetent Human Subgroup D Adenoviral Vector Based on Type 49: Manufacture on PER.C6®, Cell Tropism and Immunogenicity Lemckert, Angelique
2006
13 S1 p. S230-
1 p.
artikel
92 334. A Novel Sequence-Specific Anti-Gene LNA Molecule and Its Comparison to Tail-Clamp bisPNA Ge, Rongbin
2006
13 S1 p. S127-
1 p.
artikel
93 302. Anti-Angiogenic Treatment Enhances Anti- Tumor Effects of an Oncolytic Virus in an Experimental Rat Glioma Model Kurozumi, Kazuhiko
2006
13 S1 p. S115-S116
2 p.
artikel
94 263. Antigen-Specific and MHC-Independent Tumor Cell Lysis by Redirected Human CD4+ T Cells Grafted with an Antibody-Type Immunoreceptor Hombach, Andreas
2006
13 S1 p. S101-
1 p.
artikel
95 586. Anti-HIV-1 Neutralizing Antibody Gene Delivery to Rhesus Macaques and Rodents: A Novel Vaccination Approach Clark, K. Reed
2006
13 S1 p. S226-
1 p.
artikel
96 798. Anti-Influenza-Viral Efficacy Attributed to siRNA Formulated as Simple Lipoplex or PEI Polyplexes Is a Result of Their Immunostimulatory Properties Robbins, Marjorie
2006
13 S1 p. S309-
1 p.
artikel
97 884. Anti-Oxidant Gene Delivery to Retinal Epithelial Cells: A Gene Therapy Approach for Macular Degeneration McGinley, Lisa
2006
13 S1 p. S340-S341
2 p.
artikel
98 935. Anti-PI3K/Akt Cell Survival Pathway Gene Therapy Supplemented with Plant Sterol Diet for Prostate Cancer Treatment Zhang, Jun
2006
13 S1 p. S361-
1 p.
artikel
99 721. Antisense Oligonucleotide Therapy for Duchenne Muscular Dystrophy: From Cell Culture to Clinical Trial Ashar, Jignya
2006
13 S1 p. S278-
1 p.
artikel
100 615. Anti-Tumor Activities of IL-12 and IL-23 Are Mediated by Similar, yet Divergent, Effector Mechanisms Ceidro, JaNean C.
2006
13 S1 p. S237-
1 p.
artikel
101 636. Antitumoral Activity Mediated by a Lipid- Based Gene Delivery System Containing Therapeutic Genes Faneca, Henrique
2006
13 S1 p. S245-
1 p.
artikel
102 274. Antitumor Effect of Controlled Expression of Interleukin-12 in a Murine Model of Liver Metastases Mauleon, Itsaso
2006
13 S1 p. S105-
1 p.
artikel
103 310. Antitumor Effect of Telomerase-Specific Virotherapy in Pleural Dissemination of Human Malignant Mesothelioma Watanabe, Yuichi
2006
13 S1 p. S118-
1 p.
artikel
104 841. Anti-Tumor Effect of Tumor Specific Replicating Adenovirus Expressing IL-12 and IL-18 Huang, Jing-Hua
2006
13 S1 p. S325-
1 p.
artikel
105 282. Antitumor Efficacy of Intravenous Administration of Oncolytic Herpes Simplex Virus Expressing Interleukin 12 Guan, Yi
2006
13 S1 p. S108-
1 p.
artikel
106 866. Aortic Disease in Mucopolysaccharidodis I Mice Is Due to Increased Expression of Matrix Metalloproteinase 12 (MMP 12) Can Be Prevented with Neonatal Retroviral Vector-Mediated Gene Therapy Ma, Xiucui
2006
13 S1 p. S333-S334
2 p.
artikel
107 52. A Phase 1 Dose-Escalation Trial of Intravesical CG0070 for Superficial Transitional Cell Carcinoma (TCC) of the Bladder after Bacillus Calmette-Guerin (BCG) Failure Senzer, Neil
2006
13 S1 p. S22-
1 p.
artikel
108 1105. A Phase I Clinical Trial of an IL-12 Gene Plasmid Formulated with a Novel Lipopolymeric Gene Delivery System for Intraperitoneal Treatment of Recurrent Ovarian Cancer Alvarez, Ronald D.
2006
13 S1 p. S425-
1 p.
artikel
109 630. A Phase 2 Randomized Study of GM-CSF Gene-Modified Autologous Tumor Cell Immunotherapy (CG8123) with and without Low- Dose Cyclophosphamide in Advanced Stage Non- Small Cell Lung Cancer (NSCLC) Nemunaitis, John
2006
13 S1 p. S243-
1 p.
artikel
110 447. AP20187-Inducible Insulin-Like Effects in Diabetic Muscle and Liver Transduced with AAV Cotugno, Gabriella
2006
13 S1 p. S172-
1 p.
artikel
111 355. A Platform for Gene Delivery to Embryonic Stem Cells Using HSV Sunyog, April M.
2006
13 S1 p. S135-
1 p.
artikel
112 831. Apoptosis Induced by Oncolytic M Protein Mutant Vesicular Stomatitis Virus Is Dependent on PKR, Fas, and Daxx Gaddy, Daniel F.
2006
13 S1 p. S321-
1 p.
artikel
113 659. Application of HSVtk Suicide Gene to X- SCID Gene Therapy: Ganciclovir Treatment Selectively Elmiinates Gene Corrected Cells In Vitro and In Vivo Uchiyama, Toru
2006
13 S1 p. S254-
1 p.
artikel
114 705. A Practical Approach to siRNA-Based Treatment Design Using Bioluminescent Imaging and Mathematical Modeling Bartlett, Derek W.
2006
13 S1 p. S272-S273
2 p.
artikel
115 559. A Pseudo-Exon Derived from an Intronic Insertion Is Responsible for Duchenne-Like Muscular Dystrophy in the Welsh Corgi Dog Smith, Bruce F.
2006
13 S1 p. S215-
1 p.
artikel
116 103. A Screen for Host Cellular Proteins That Interact with Adeno-Associated Virus Capsid Proteins Reveals Proteins Involved in AAV8 Transduction Akache, Bassel
2006
13 S1 p. S42-S43
2 p.
artikel
117 ASGT 2006 Program 2006
13 S1 p. i-xv
nvt p.
artikel
118 1115. A Simple Method for the Purification of Lentiviral Vectors Using a Combination of Ultrafiltration and Anion Exchange Chromatography Koldej, Rachel M.
2006
13 S1 p. S429-
1 p.
artikel
119 513. A Simple Method To Ensure Titer Conservation of AAV2 Vector Preparations Delivered with Stainless Steel Needles Ketchum, Elias T.
2006
13 S1 p. S197-S198
2 p.
artikel
120 407. A Single Unilateral Injection of AAV1-ASA and AAV1-FGE Vectors into the Hippocampus Results in Bilateral Expression and Widespread Distribution of ASA and Prevention of Sulfatide Storage in the Whole Brain of MLD Model Mice Kurai, Toshiyuki
2006
13 S1 p. S156-
1 p.
artikel
121 844. A Single Vector-Dependent, Doxycycline- Regulatable, Lung Cancer Specific Oncolytic Adenovirus Sipo, Isaac
2006
13 S1 p. S326-
1 p.
artikel
122 1015. Assessment of Zinc Finger-FOKI Chimeric Endonuclease Activity Using a Single Strand Annealing Assay in Mammalian Cells Brondani, Vincent
2006
13 S1 p. S390-S391
2 p.
artikel
123 557. A Study of AAV2/1/SERCA2a Delivered Via the V-Focus Cardiac Delivery System in an Ovine Pacing Model of Heart Failure Byrne, Melissa J.
2006
13 S1 p. S214-S215
2 p.
artikel
124 764. Attenuation of Treg Cells by GITR Ligand Led to Synergistic Enhancement of Treatment Efficacy with Immune-Stimulatory Therapies in Mice Bearing Metastatic 4T1 Breast Carcinoma Chen, Li
2006
13 S1 p. S295-S296
2 p.
artikel
125 1103. Augmentation of Immunity Against AAV- Encoded Transgenes by Use of the Genetic Adjuvants C3d3 and CTLA4 Logan, Grant J.
2006
13 S1 p. S424-
1 p.
artikel
126 650. AU-rich 3′ UTR Elements for Increasing the Specificity of Promoter Regulated Adenoviral Gene Therapy Sarkioja, Merja
2006
13 S1 p. S250-
1 p.
artikel
127 Author Index 2006
13 S1 p. S430-S446
17 p.
artikel
128 326. A Versatile Tool for Conditional Gene Expression and Knockdown Szulc, Jolanta
2006
13 S1 p. S124-
1 p.
artikel
129 732. Avian Sarcoma Leukosis Virus Vectors Can Transduce Rhesus Macaque HSCs and Result in a Potentially Safer Integration Profile Hu, Jingqiong
2006
13 S1 p. S283-
1 p.
artikel
130 699. Bactofection into Airway Epithelial Cells In Vitro and In Vivo Using a Genetically Modified Escherichia coli Larsen, Mia D.B.
2006
13 S1 p. S270-S271
2 p.
artikel
131 163. Baculovirus-Mediated Gene Transfer in New Zealand White Rabbit Skeletal Muscle Heikura, Tommi T.
2006
13 S1 p. S63-
1 p.
artikel
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2006
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133 1087. Balloon Occlusion Catheter-Based Delivery of HDAd into the Nonhuman Primate Liver Results in Stable, High Level Transgene Expression with Minimal Toxicity Brunetti-Pierri, Nicola
2006
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2006
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2006
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2006
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2006
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138 472. Biodistribution of Semliki Forest Virus Vectors and Effect of Preimmunizations in Mice Rodriguez, Juan R.
2006
13 S1 p. S183-
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139 353. Biological Comparison of Mesenchymal Stem Cells Derived from Bone Marrow and Adipose Tissue Izadpanah, Reza
2006
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140 9. Biology of rAAV8 in Mouse Liver Following Vector Administration at Birth Inagaki, Katsuya
2006
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141 162. Bioluminescence Imaging of a Tetanus Toxin C-Terminal Fusion Protein after Vector Delivery Pike, Lisa
2006
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142 739. Bioluminescent Virion Shells: A Novel Tool for Visualization of Viral Vectors in Animal Tissue Asokan, Aravind
2006
13 S1 p. S286-
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143 814. Biomaterial-Mediated Retroviral Gene Delivery Gersbach, Charles A.
2006
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2006
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145 969. Bone Marrow Derived Endothelial Progenitor Cells Engineered by Lentiviral Vectors as Therapeutic Antitumoral Strategy Fernandez, Veronica
2006
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146 452. Bone Marrow Stem Cells Are Potent Targets for Gene Therapy of Epidermolysis Bullosa, a Genetic Blistering Skin Disease Tamai, Katsuto
2006
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2006
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148 920. Bone Regeneration with Xenogeneic BMP-2 Producing Fibroblasts Noh, Moon Jong
2006
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149 182. Branched Chitosan Oligomers Enhance Gene Delivery In Vitro and after Lung Administration In Vivo Issa, Mohamed M.
2006
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2006
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2006
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2006
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2006
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154 30. Cardiac-Specific Gene Expression Using Pseudotyped AAV Vectors and the Cardiac Troponin-T Promoter Prasad, Konkal-Matt R.
2006
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155 23. Catheter-Mediated Local Intramural Delivery of AdEC-SOD Inhibits Oxidative Stress and Reduces In-Stent Neointima by Accelerating Endothelial Cell Recovery in WHHL Rabbits Displaying Complex Human-Like Atherosclerotic Lesions Leppanen, Olli
2006
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2006
13 S1 p. S331-
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157 73. Cats Produce a Potent CTL Response after Neonatal Gene Therapy That Can Be Blocked with CTLA4-Ig Ponder, Katherine P.
2006
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158 352. CD34+ Hematopoietic Stem-Progenitor Cell MicroRNA Expression and Function: The miR Circuit Diagram of Differentiation Control Georgantas, Robert W.
2006
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159 268. CD19-Targeted Normal and CLL Patient T Cells Expanded with Beads Can Eradicate Systemic Tumors In Vivo Stefanski, J.
2006
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2006
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161 83. Cell_Type Specific Delivery of siRNAs with Aptamer_siRNA Chimeras Giangrande, Paloma H.
2006
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162 313. Cell Type Specific Media Optimization for Clinical Retroviral Transduction Protocols Stefanski, J.
2006
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163 548. Cellular Defense Response in Transduced and Transfected Human Tumor and Primary Cell Lines Pellinen, Riikka
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164 812. Cellular Delivery of Gene Therapy Vectors Qiao, Jian
2006
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165 74. Cellular Immunity to Adeno-Associated Virus Capsid Attenuates Transgene Expression in the Liver Murphy, Samuel L.
2006
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2006
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167 340. Cellular Uptake and Subsequent Intracellular of R8-Liposomes Introduced at Low Temperature Iwasa, Akitada
2006
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168 497. Central CART Gene Delivery by Recombinant AAV Vector Decreases Lean Body Mass in Diet-Induced Obese Male Rats Qing, Keyun
2006
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169 938. Ceramide May Have a Role in Sensitizing ACHN Renal Cancer Cells (RCC) to Fas Induced Apoptosis El-Zawahry, Ahmed M.
2006
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170 82. Cftr Gene Targeting in Murine ES Cells Mediated by the SFHR Technique Sangiuolo, Federica
2006
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2006
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2006
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2006
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175 432. Characterization of a Novel Oncolytic Measles Virus Retargeted Against the Urokinase Receptor: In Vitro and In Vivo Studies Merchan, Jaime R.
2006
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2006
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2006
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2006
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2006
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2006
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183 471. Chimeric Lentiviral Vectors with Safety Insurance Kachapati, Kritika
2006
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184 174. Chloroquine and Chloroquine Analogues in Non-Viral Delivery Cheng, Jianjun
2006
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2006
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186 386. Chromosomal Integration Sites of Double-Stranded Linear DNA in Mouse ES Cells Ohbayashi, Fumi
2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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1 p.
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265 566. Delaying the Onset of Diabetes in the NOD Mouse Using Exosomes Derived from Dendritic Cells Transfected with Adenoviral Vectors Ruffner, Melanie A.
2006
13 S1 p. S218-
1 p.
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266 474. Deletion of All Membranous Genes of Recombinant Sendai Virus Results in the Dramatic Reduction of Toxicity for Pulmonary Gene Transfer in Neonatal Mice Tanaka, Sakura
2006
13 S1 p. S184-
1 p.
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267 1082. Delivery of Anti-Oxidative Enzyme Genes Protects Against Ischemia/Reperfusion-Induced Liver Injury in Mice He, Song-Qing
2006
13 S1 p. S415-
1 p.
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268 262. Delivery of CCL21 to Metastatic Disease Improves the Efficacy of Adoptive T Cell Therapy Thanarajasingam, Uma
2006
13 S1 p. S100-S101
2 p.
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269 212. Delivery of Galactocerebrosidase Activity to the Peripheral Nervous System of Mice with Globoid Cell Leukodystrophy (Krabbe Disease) by Intramuscular Injection Rafi, Mohammad A.
2006
13 S1 p. S82-
1 p.
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270 245. Delivery of IGF-1 in the Spinal Cord of a Mouse Model of ALS after Intraparenchymal Injection of an Adeno-Associated Vector Haenggeli, Christine
2006
13 S1 p. S94-
1 p.
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271 752. Delivery of Non-Microparticle Naked DNA Vaccine Using Supersonic Flow by a Low-Pressure Gene Gun Lin, Chi-Chen
2006
13 S1 p. S291-
1 p.
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272 550. Delivery of Oligodeoxynucleotides into Human Saphenous Veins and the Adjunct Effect of Ultrasound and Microbubbles Kodama, Tetsuya
2006
13 S1 p. S212-
1 p.
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273 1072. Delivery of Oncolytic Herpes Simplex Virus to Infiltrative Brain Tumor Sites Via Neuronal Stem Cells Voss, Tyler T.
2006
13 S1 p. S411-
1 p.
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274 175. Delivery Via Non-Viral Options to the Auditory Structures Praetorius, Mark J.
2006
13 S1 p. S68-
1 p.
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275 391. De Novo Human Artificial Chromosome Formation Is Predetermined by Initial Chromatin Assembly and Transcriptional Patterns after Transfection Nakashima, Hiroshi
2006
13 S1 p. S149-
1 p.
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276 523. Deoxyribonuclease I and Endonuclease G Are Host Defense Enzymes Responsible for Inactivation of Foreign DNA in Kidney Tubular Epithelial Cells Buzder, Timea
2006
13 S1 p. S201-
1 p.
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277 1046. Derivation of Functionally Normal Macrophages from Human Embryonic Stem (hES) Cells for HIV-1 Gene Therapy Anderson, Joseph S.
2006
13 S1 p. S401-
1 p.
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278 131. Design and Construction of an Adenovirus Vector Containing Fiber Fibritin/Canine CD40L Fibers Directed to Canine CD40-Expressing Cells Nakayama, Masaharu
2006
13 S1 p. S53-
1 p.
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279 1112. Design and Implementation of VRX496 Phase II Cell Processing for cGMP Production of Multiple Doses of Lentivirally Transduced Autologous HIV Infected CD4+ T Lymphocytes Humeau, Laurent
2006
13 S1 p. S427-
1 p.
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280 908. Design and Optimization of U7snRNAs for Skipping of Exon 51 in DMD: Promising Tools for Future Clinical Trials Goyenvalle, Aurelie
2006
13 S1 p. S350-
1 p.
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281 191. Design, Synthesis, and Characterization of a New Class of Quaternary Ammonium Gemini Amphiphiles for Gene Delivery Li, Qun
2006
13 S1 p. S74-
1 p.
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282 510. Detection and Quantification of rcAAV in rAAV Stocks by Real-Time qPCR Mayfield, Traci L.
2006
13 S1 p. S196-S197
2 p.
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283 145. Detection of the Primary Destabilizing Modification of Liquid-Formulated Adenoviral Vectors by Anion-Exchange High Performance Liquid Chromatography Shu, Cassandra
2006
13 S1 p. S57-
1 p.
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284 830. Determination of the Profile and Site Preference of Lentiviral Vector Integration In Vivo Hacker, Caroline V.
2006
13 S1 p. S321-
1 p.
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285 1010. Developing a Potential Pain Therapy Using Engineered Zinc Finger Protein Repressors of the Sodium Channel PN3 Tan, Siyuan
2006
13 S1 p. S389-
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286 314. Developing Gene Transfer Vectors for Cancer Therapy: Identifying and Overcoming Regulatory Challenges Aurigemma, Rosemarie
2006
13 S1 p. S120-
1 p.
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287 445. Developmental Stage Determines Distribution of Organ Transduction after Intra-Amniotic Injection of Lentiviral Vector Endo, Masayuki
2006
13 S1 p. S171-
1 p.
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288 479. Development and Characterization of a New Noncytopathic Vector Derived from Semliki Forest Virus Casales, Erkuden
2006
13 S1 p. S186-
1 p.
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289 1071. Development and Characterization of HSV-1 Vector-Expressed Dominant Negative PKC epsilon for Pain Therapy Srinivasan, Rahul
2006
13 S1 p. S411-
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290 629. Development and Characterization of Immunotherapy Using SeV/dF-Activated Dendritic Cells Against Squamous Cell Carcinoma Yoneyama, Yasuo
2006
13 S1 p. S242-S243
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291 542. Development and Characterization of Ultrasound Responsive Microbubbles for Gene Delivery Lentacker, Ine
2006
13 S1 p. S208-S209
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292 25. Development and Characterization of Viral Vectors with High Specificity for Atherosclerotic Plaques White, Katie M.
2006
13 S1 p. S11-
1 p.
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293 655. Development of a Human Carboxylesterase That Can Efficiently Metabolize CPT-11 Wierdl, Monika
2006
13 S1 p. S252-
1 p.
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294 516. Development of a Minicircle Vector Free of Plasmid Bacterial DNA Sequences and Capable of øC31-Mediated Site-Specific Integration Chen, Zhi-Ying
2006
13 S1 p. S198-S199
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295 369. Development of an Amplifiable Gene Expression System in Lentivirus Vectors Shaw, Kit L.
2006
13 S1 p. S140-
1 p.
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296 428. Development of an Effective Safety Switch for Selective Elimination of Human T Cells In Vivo after Adoptive Transfer van Meerten, Tom
2006
13 S1 p. S164-S165
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297 591. Development of Anti-JC Virus “Designer T Cells” for Progressive Multifocal Leukoencephalopathy (PML) Immunotherapy Yang, Wen
2006
13 S1 p. S228-S229
2 p.
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298 324. Development of Bioluminescence Tomography for Three-Dimensional Real Time Imaging of Gene Expression Toussaint, Nathalie Y.
2006
13 S1 p. S123-S124
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299 197. Development of Chitosan Nanoparticles for Gene Delivery System Yang, Zhi-Hong
2006
13 S1 p. S76-S77
2 p.
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300 553. Development of Echo-Contrast Gas Entrapping Liposome as Gene and siRNA Delivery Tool Negishi, Yoichi
2006
13 S1 p. S213-
1 p.
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301 820. Development of Efficient Self-Inactive Retroviral Vectors Yoon, Jaehyung
2006
13 S1 p. S318-
1 p.
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302 211. Development of Helper-Dependent Adenovirus (HDAd) Vectors for Gene Therapy in the Mouse Model for Glycogen Storage Disease Type Ia (GSD-Ia) Koeberl, Dwight D.
2006
13 S1 p. S81-S82
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303 873. Development of High Throughput Functional Screening of Cardiovascular Therapeutic Genes Using the HVJ-E Vector Nishikawa, Tomoyuki
2006
13 S1 p. S336-
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304 875. Development of Human Skin Gene Therapy for Systemic In Vivo Delivery of Atrial Natriuretic Peptide (ANP) To Treat Hypertension Therrien, Jean-Philippe
2006
13 S1 p. S337-
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305 696. Development of Lipid/Peptide (Lip/Tide) Vectors for Respiratory Gene Transfer Hart, Stephen L.
2006
13 S1 p. S269-S270
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306 146. Development of Modified Adenovirus Vectors with Reduced Innate Immune Response Mizuguchi, Hiroyuki
2006
13 S1 p. S57-S58
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307 458. Development of Non-Integrating and Site- Specifically Integrating Lentiviral Vectors Apolonia, Luis
2006
13 S1 p. S177-
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308 927. Development of Non-Viral Gene Therapy Targeting Insulin-Like Growth Factor (IGF) System for Treatment of Brain Tumors Villegas, Leah R.
2006
13 S1 p. S358-
1 p.
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309 876. Development of Novel Angiogenic DNA Medicine Using a Genomic/cDNA Hybrid of Hepatocyte Growth Factor Gene Hahn, Woong
2006
13 S1 p. S337-
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310 194. Development of Novel DNA Formulations Based on Polymers and Cyclodextrin for Gene Delivery to the Muscle Roques, Caroline
2006
13 S1 p. S75-S76
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311 529. Development of Novel Systemic Gene Delivery System for Cancer Therapy with Tumor-Specifically Cleavable PEG-Lipid Hatakeyama, Hiroto
2006
13 S1 p. S203-
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312 1007. Development of Nuclear Targeting System of Plasmid DNA; Impact of Sugar Display on the Surface of Lipid Envelope Masuda, Tomoya
2006
13 S1 p. S388-
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313 508. Development of Optimized AAV2 Vector Biosynthesis and Purification Processes To Support High Capacity Production of Clinical Vectors of High Purity and Potency Hauck, Bernd
2006
13 S1 p. S196-
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314 818. Development of Packaging Cell Lines for the Large-Scale Production of High-Titer Clinical Grade Recombinant Retroviruses Ghani, Karim
2006
13 S1 p. S317-S318
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315 907. Development of Recombinant Novel Adeno-Associated Viral (rAAV) Vectors Encoding Optimised Microdystrophin cDNAs for Duchenne Muscular Dystrophy (DMD) Athanasopoulos, Takis
2006
13 S1 p. S349-S350
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316 519. Development of S/MAR Plasmid Vectors for Persistent Expression and Maintenance, In Vivo Argyros, Orestis
2006
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317 143. Development of Telomerase Specific Antineoplastic Adenovirus Telomelysin (OBP-301): Establishment of Useful Assay and Assessment for Antitumor Activity Hashimoto, Yuuri
2006
13 S1 p. S56-
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318 1019. Development of Tissue-Specific RNAi for Gene Therapy Allen, Danny
2006
13 S1 p. S392-
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319 786. Development of Zero-CpG Plasmids with Reduced Inflammatory Responses Following Delivery of Lipid/pDNA Complexes to the Mouse Lung Pringle, Ian A.
2006
13 S1 p. S304-S305
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320 247. Devising Aβ-Specific Passive Immunization Strategies for Alzheimer's Disease Using rAAV Vector-Mediated scFv Antibody Delivery Fowlkes, Kelly L.
2006
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2006
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322 877. Differential Expression of Indoleamine 2,3-dioxygenase (IDO) by Endothelial Cells and Its Overexpression by Gene Transfer: Implications for Cardiovascular Biology Tan, Peng H.
2006
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323 977. Differential Host T Cell Response to the Capsid of AAV2 and 8 in Muscle-Directed Gene Transfer in Murine and Non-Human Primate Models Wang, Lili
2006
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324 996. Direct Comparison of Adeno-Associated Virus (AAV) Serotypes for Muscle Expression of Soluble Anti-Angiogenic Proteins Isotani, Mayu
2006
13 S1 p. S384-
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325 743. Directed Evolution of Adeno-Associated Virus (AAV) by DNA Shuffling Yields Enhanced Gene Delivery Vectors Li, Wuping
2006
13 S1 p. S287-
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326 389. Directed Transposon Integration in Human Cells Yant, StephenR.
2006
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2006
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328 924. D-MAPP Analogue, LCL-204 Sensitizes DU145 Prostate Cancer Cells (PCa) to FasL Gene Therapy through Down-Regulation of Survivin El-Zawahry, Ahmed M.
2006
13 S1 p. S357-
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329 1027. DNase II Knockdown in Human Endothelial Cells Does Not Improve Non-Viral Transfection Efficiency Barker, Gregory A.
2006
13 S1 p. S395-
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330 283. DNA Vaccination with Genes Encoding an Antigenic Protein and Fas Ligand Increased Antigen-Specific Humoral Responses Shimozato, Osamu
2006
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2006
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332 538. DNAvaletTM Transfection Reagent Prata, Carla
2006
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333 214. Dominant-Negative Interference in the Pahenu2 Mouse: Modified Forms of PAH Zori, Andreas
2006
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334 608. Dose Escalation of Recombinant Adenovirus-Based Influenza Virus Vaccine Encoding the Full Length Hemagglutinin (HA) of the A/Vietnam/1203/2004 (H5N1) To Immunize Naïve and Ad-Immune Mice Steitz, Julia
2006
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335 1000. Down-Regulating the Epithelial Glycoprotein-2 Promoter Utilizing Engineered Zinc Finger Protein Transcription Factors Gommans, Willemijn M.
2006
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336 669. Drug Selection of Hematopoietic Cells by Regulated MGMT Activity Verbeek, Barbara
2006
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337 426. dSLIM Immunomodulators Induce Anti- Tumor Responses Both In Vitro and In Vivo Schmidt, Manuel
2006
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338 392. Duration of Expression of the Sleeping Beauty Transposase Gene in Mouse Liver Following Hydrodynamic Delivery Bell, Jason B.
2006
13 S1 p. S150-
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339 31. Dystrophin Expression in Muscles of Duchenne Muscular Dystrophy Patients Following High_Density Injections of Normal Myogenic Cells Tremblay, Jacques P.
2006
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2006
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2006
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2006
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2006
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2006
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345 95. Effective Genetic Engineering of Human Embryonic Stem Cells Using the Sleeping Beauty Transposon System Wilber, Andrew
2006
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346 147. Effective Gene Transfer to Human Glioma Cells Using High Capacity Adenoviral Vectors: Human Glioma Cells Express Substantial Levels of CAR and Integrin Adenoviral Co-Receptors Candolfi, Marianela
2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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388 356. Engineering of Cell Surface Sialic Acids for Polymeric Gene Delivery Loo, Yihua
2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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398 125. Enhancement of Virus Mediated Gene Transfer by Polycationic Compounds Lehmusvaara, Saara
2006
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399 98. Enrichment and Characterization of Ovarian Cancer Stem Cells Li, Zong Yi
2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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2006
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