| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
AAV8-mediated Sirt1 gene transfer to the liver prevents high carbohydrate diet-induced nonalcoholic fatty liver disease
|
Vilà, Laia
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 2 |
AAV shuffles to the liver: commentary on Lisowski et al.
|
Schaffer, David V
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 3 |
Adeno-associated viral vectors do not efficiently target muscle satellite cells
|
Arnett, Andrea LH
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 4 |
Adipose tissue insulin receptor knockdown via a new primate-derived hybrid recombinant AAV serotype
|
Liu, Xianglan
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 5 |
Allogeneic lymphocyte-licensed DCs expand T cells with improved antitumor activity and resistance to oxidative stress and immunosuppressive factors
|
Jin, Chuan
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 6 |
An AAV9 coding for frataxin clearly improved the symptoms and prolonged the life of Friedreich ataxia mouse models
|
Gérard, Catherine
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 7 |
A simplified purification protocol for recombinant adeno-associated virus vectors
|
Potter, Mark
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 8 |
Assessment of toxicity and biodistribution of recombinant AAV8 vector–mediated immunomodulatory gene therapy in mice with Pompe disease
|
Wang, Gensheng
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 9 |
Aurintricarboxylic acid increases yield of HSV-1 vectors
|
Pechan, Peter
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 10 |
B-cell depletion is protective against anti-AAV capsid immune response: a human subject case study
|
Corti, M
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 11 |
Bioengineered coagulation factor VIII enables long-term correction of murine hemophilia A following liver-directed adeno-associated viral vector delivery
|
Brown, Harrison C
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 12 |
Biosafety studies of carrier cells infected with a replication-competent adenovirus introduced by IAI.3B promoter
|
Hamada, Katsuyuki
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 13 |
Bridging the gap: a second open-access sibling joins the MT family of journals
|
Porteus, Matt
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 14 |
Codelivery of antigen and an immune cell adhesion inhibitor is necessary for efficacy of soluble antigen arrays in experimental autoimmune encephalomyelitis
|
Sestak, Joshua O
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 15 |
Comparative analysis of lentiviral vectors and modular protein nanovectors for traumatic brain injury gene therapy
|
Negro-Demontel, María Luciana
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 16 |
Complete restoration of multiple dystrophin isoforms in genetically corrected Duchenne muscular dystrophy patient–derived cardiomyocytes
|
Zatti, Susi
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 17 |
Developmental stage determines efficiency of gene transfer to muscle satellite cells by in utero delivery of adeno-associated virus vector serotype 2/9
|
Stitelman, David H
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 18 |
Development and characterization of an enhanced nonviral expression vector for electroporation cancer treatment
|
Forde, Patrick F
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 19 |
Development of an inducible caspase-9 safety switch for pluripotent stem cell–based therapies
|
Wu, Chuanfeng
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 20 |
Development of gene transfer for induction of antigen-specific tolerance
|
Sack, Brandon K
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 21 |
Differential effects of two MRI contrast agents on the integrity and distribution of rAAV2 and rAAV5 in the rat striatum
|
Osting, Sue
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 22 |
Different protein composition and functional properties of adeno-associated virus-6 vector manufactured from the culture medium and cell lysates
|
Denard, Jerome
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 23 |
Distinct transduction profiles in the CNS via three injection routes of AAV9 and the application to generation of a neurodegenerative mouse model
|
Huda, Fathul
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 24 |
DNA vaccination strategy targets epidermal dendritic cells, initiating their migration and induction of a host immune response
|
Smith, Trevor RF
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 25 |
EC4, a truncation of soluble N-cadherin, reduces vascular smooth muscle cell apoptosis and markers of atherosclerotic plaque instability
|
Lyon, Cressida A
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 26 |
Efficient transduction of LEDGF/p75 mutant cells by complementary gain-of-function HIV-1 integrase mutant viruses
|
Wang, Hao
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 27 |
Empty virions in AAV8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects
|
Gao, Kai
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 28 |
Engineering new mycobacterial vaccine design for HIV–TB pediatric vaccine vectored by lysine auxotroph of BCG
|
Saubi, Narcís
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 29 |
Engraftment potential of dermal fibroblasts following in vivo myogenic conversion in immunocompetent dystrophic skeletal muscle
|
Muir, Lindsey A
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 30 |
Enhancing gene delivery of adeno-associated viruses by cell-permeable peptides
|
Liu, Yarong
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 31 |
Evaluation of gene delivery strategies to efficiently overexpress functional HLA-G on human bone marrow stromal cells
|
Boura, Joana S
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 32 |
Ex vivo expanded autologous polyclonal regulatory T cells suppress inhibitor formation in hemophilia
|
Sarkar, Debalina
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 33 |
Gene electrotransfer enhanced by nanosecond pulsed electric fields
|
Guo, Siqi
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 34 |
Generation and in vivo evaluation of IL10-treated dendritic cells in a nonhuman primate model of AAV-based gene transfer
|
Moreau, Aurélie
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 35 |
Generation of X-CGD cells for vector evaluation from healthy donor CD34+ HSCs by shRNA-mediated knock down of gp91phox
|
Brendel, Christian
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 36 |
Genetic barcode sequencing for screening altered population dynamics of hematopoietic stem cells transduced with lentivirus
|
Zanatta, Daniela B
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 37 |
Genetic rearrangements of variable di-residue (RVD)-containing repeat arrays in a baculoviral TALEN system
|
Lau, Cia-Hin
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 38 |
Hemodynamics of a hydrodynamic injection
|
Kanefuji, Tsutomu
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 39 |
High-titer foamy virus vector transduction and integration sites of human CD34+ cell–derived SCID-repopulating cells
|
Nasimuzzaman, Md
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 40 |
Human fetal liver cells for regulated ex vivo erythropoietin gene therapy
|
El Filali, Ebtisam
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 41 |
In question: the scientific value of preclinical safety pharmacology and toxicology studies with cell-based therapies
|
Broichhausen, Christiane
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 42 |
Intrathecal administration of IGF-I by AAVrh10 improves sensory and motor deficits in a mouse model of diabetic neuropathy
|
Homs, Judit
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 43 |
Introduction of a point mutation into an HLA class I single-chain trimer induces enhancement of CTL priming and antitumor immunity
|
Matsui, Masanori
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 44 |
Kidney-specific expression of GFP by in-utero delivery of pseudotyped adeno-associated virus 9
|
Picconi, Jason L
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 45 |
Lentiviral vectors containing mouse Csf1r control elements direct macrophage-restricted expression in multiple species of birds and mammals
|
Pridans, Clare
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 46 |
Maintaining therapeutic activity in the operating room: compatibility of a gamma-retroviral replicating vector with clinical materials and biofluids
|
Burnett, Ryan
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 47 |
Marmosets as a preclinical model for testing “off-label” use of doxycycline to turn on Flt3L expression from high-capacity adenovirus vectors
|
VanderVeen, Nathan
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 48 |
Optimization of a gene electrotransfer procedure for efficient intradermal immunization with an hTERT-based DNA vaccine in mice
|
Calvet, Christophe Y
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 49 |
Optimizing the production of suspension cells using the G-Rex “M” series
|
Bajgain, Pradip
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 50 |
piggyBac-mediated phenotypic correction of factor VIII deficiency
|
Staber, Janice M
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 51 |
Pigtailed macaques as a model to study long-term safety of lentivirus vector-mediated gene therapy for hemoglobinopathies
|
Kiem, Hans-Peter
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 52 |
Preclinical efficacy and safety of an anti-IL-1β vaccine for the treatment of type 2 diabetes
|
Spohn, Gunther
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 53 |
Preclinical safety and efficacy of an anti–HIV-1 lentiviral vector containing a short hairpin RNA to CCR5 and the C46 fusion inhibitor
|
Wolstein, Orit
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 54 |
Pre-TCRα supports CD3-dependent reactivation and expansion of TCRα-deficient primary human T-cells
|
Galetto, Román
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 55 |
Prevention of adverse events of interferon γ gene therapy by gene delivery of interferon γ-heparin-binding domain fusion protein in mice
|
Ando, Mitsuru
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 56 |
Proof of concept for AAV2/5-mediated gene therapy in iPSC-derived retinal pigment epithelium of a choroideremia patient
|
Cereso, Nicolas
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 57 |
Proteomic profiling of salivary gland after nonviral gene transfer mediated by conventional plasmids and minicircles
|
Geguchadze, Ramaz
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 58 |
Quantitative, noninvasive, in vivo longitudinal monitoring of gene expression in the brain by co-AAV transduction with a PET reporter gene
|
Yoon, Sea Young
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 59 |
Recombinant rabies virus particles presenting botulinum neurotoxin antigens elicit a protective humoral response in vivo
|
Hudacek, Andrew W
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 60 |
Recombination–deletion between homologous cassettes in retrovirus is suppressed via a strategy of degenerate codon substitution
|
Im, Eung Jun
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 61 |
Role of specific endocytic pathways in electrotransfection of cells
|
Chang, Chun-Chi
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 62 |
Safety and tolerability of MRI-guided infusion of AAV2-hAADC into the mid-brain of nonhuman primate
|
Sebastian, Waldy San
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 63 |
Specific tools for targeting and expression in Müller glial cells
|
Pellissier, Lucie P
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 64 |
Suppression of leaky expression of adenovirus genes by insertion of microRNA-targeted sequences in the replication-incompetent adenovirus vector genome
|
Shimizu, Kahori
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 65 |
Systemic gene transfer reveals distinctive muscle transduction profile of tyrosine mutant AAV-1, -6, and -9 in neonatal dogs
|
Hakim, Chady H
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 66 |
Targeted CNS delivery using human MiniPromoters and demonstrated compatibility with adeno-associated viral vectors
|
de Leeuw, Charles N
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 67 |
Type 1 interferon gene transfer enhances host defense against pulmonary Streptococcus pneumoniae infection via activating innate leukocytes
|
Damjanovic, Daniela
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
|
| 68 |
Widespread gene transfer in the central nervous system of cynomolgus macaques following delivery of AAV9 into the cisterna magna
|
Hinderer, Christian
|
|
2014
|
1 |
C |
p. -
1 p.
|
artikel
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