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Short Communication |
Increased oncolytic efficacy for high-grade gliomas by optimal integration of ionizing radiation into the replicative cycle of HSV-1
- S J Advani
- , J M Markert
- & R R Weichselbaum
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Original Article |
Lineage- and stage-restricted lentiviral vectors for the gene therapy of chronic granulomatous disease
- I Barde
- , E Laurenti
- & D Trono
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Enabling Technologies |
Self-inactivating helper virus for the production of high-capacity adenoviral vectors
- M Gonzalez-Aparicio
- , I Mauleon
- & R Hernandez-Alcoceba
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Short Communication |
Peptide affinity reagents for AAV capsid recognition and purification
- N Pulicherla
- & A Asokan
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Original Article |
Investigation of the peak action wavelength of light-activated gene transduction
- M Myakishev-Rempel
- , J Kuper
- & E M Schwarz
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Original Article |
The influence of epileptic neuropathology and prior peripheral immunity on CNS transduction by rAAV2 and rAAV5
- M S Weinberg
- , B L Blake
- & T J McCown
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Original Article |
Differential immune responses mediated by adenovirus- and lentivirus-transduced DCs in a HER-2/neu overexpressing tumor model
- T C Felizardo
- , J C M Wang
- & J A Medin
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Original Article |
Oncolytic adenovirus modified with somatostatin motifs for selective infection of neuroendocrine tumor cells
- J Leja
- , D Yu
- & M Essand
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Original Article
| Open AccessAAV-mediated in vivo knockdown of luciferase using combinatorial RNAi and U1i
- A Koornneef
- , R van Logtenstein
- & T Ritsema
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Original Article |
RNAi-mediated gene silencing in tumour tissue using replication-competent retroviral vectors
- T Schaser
- , C Wrede
- & C J Buchholz
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Short Communication |
Protein transduction by pseudotyped lentivirus-like nanoparticles
- T Aoki
- , K Miyauchi
- & J Komano
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Original Article
| Open AccessOncolytic adenovirus co-expressing IL-12 and IL-18 improves tumor-specific immunity via differentiation of T cells expressing IL-12Rβ2 or IL-18Rα
- I-K Choi
- , J-S Lee
- & C-O Yun
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Original Article
| Open AccessAAV-mediated photoreceptor transduction of the pig cone-enriched retina
- C Mussolino
- , M della Corte
- & E M Surace
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Original Article |
Anti-apoptotic gene therapy prolongs survival of corneal endothelial cells during storage
- T A Fuchsluger
- , U Jurkunas
- & R Dana
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Original Article
| Open AccessLentiviral vectors for induction of self-differentiation and conditional ablation of dendritic cells
- M Pincha
- , G Salguero
- & R Stripecke
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Original Article |
Longevity of rAAV vector and plasmid DNA in blood after intramuscular injection in nonhuman primates: implications for gene doping
- W Ni
- , C Le Guiner
- & R O Snyder
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Original Article |
A bidirectional promoter architecture enhances lentiviral transgenesis in embryonic and extraembryonic stem cells
- M C Golding
- & M R W Mann
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Short Communication |
In vitro and in vivo comparison of viral and cellular internal ribosome entry sites for bicistronic vector expression
- M Licursi
- , S L Christian
- & K Hirasawa
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Original Article |
Risk assessment in skin gene therapy: viral–cellular fusion transcripts generated by proviral transcriptional read-through in keratinocytes transduced with self-inactivating lentiviral vectors
- D Almarza
- , G Bussadori
- & R Murillas
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Original Article |
Innocuous full-length botulinum neurotoxin targets and promotes the expression of lentiviral vectors in central and autonomic neurons
- V B O'Leary
- , S V Ovsepian
- & J O Dolly
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Original Article |
Gene transfer to the rhesus monkey brain using SV40-derived vectors is durable and safe
- J-P Louboutin
- , E Marusich
- & D S Strayer
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Original Article |
Evaluation of the specificity and sensitivity of ferritin as an MRI reporter gene in the mouse brain using lentiviral and adeno-associated viral vectors
- G Vande Velde
- , J R Rangarajan
- & V Baekelandt
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Original Article |
Treatment of experimental autoimmune encephalomyelitis in SJL/J mice with a replicative HSV-1 vector expressing interleukin-5
- M Nygårdas
- , C Aspelin
- & V Hukkanen
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Original Article |
Efficient and stable transduction of dopaminergic neurons in rat substantia nigra by rAAV 2/1, 2/2, 2/5, 2/6.2, 2/7, 2/8 and 2/9
- A Van der Perren
- , J Toelen
- & V Baekelandt
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Original Article |
Adenovirus-mediated delivery of CD46 attenuates the alternative complement pathway on RPE: implications for age-related macular degeneration
- J H Sweigard
- , S M Cashman
- & R Kumar-Singh
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Original Article |
Production and purification of lentiviral vectors generated in 293T suspension cells with baculoviral vectors
- H P Lesch
- , A Laitinen
- & K J Airenne
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Review |
Gene therapy for cancer: bacteria-mediated anti-angiogenesis therapy
- R Gardlik
- , M Behuliak
- & C J Li
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Original Article |
Treatment of canine leukocyte adhesion deficiency by foamy virus vectors expressing CD18 from a PGK promoter
- T R Bauer Jr
- , E M Olson
- & D W Russell
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Short Communication |
APOBEC3-mediated hypermutation of retroviral vectors produced from some retrovirus packaging cell lines
- A D Miller
- & M J Metzger
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Original Article |
Systemic human Netrin-1 gene delivery by adeno-associated virus type 8 alters leukocyte accumulation and atherogenesis in vivo
- J A Khan
- , M Cao
- & P L Hermonat
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Original Article |
Matrix metalloproteinase 14 overexpression reduces corneal scarring
- S D Galiacy
- , P Fournié
- & F Malecaze
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Original Article
| Open AccessQuantification of lentiviral vector copy numbers in individual hematopoietic colony-forming cells shows vector dose-dependent effects on the frequency and level of transduction
- S Charrier
- , M Ferrand
- & A Galy
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Original Article |
Capsid-expressing DNA in AAV vectors and its elimination by use of an oversize capsid gene for vector production
- C L Halbert
- , M J Metzger
- & A D Miller
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Original Article |
Liver-specific microRNA-122 target sequences incorporated in AAV vectors efficiently inhibits transgene expression in the liver
- C Qiao
- , Z Yuan
- & X Xiao
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Original Article |
A tissue-specific, activation-inducible, lentiviral vector regulated by human CD40L proximal promoter sequences
- Z Romero
- , S Torres
- & I J Molina
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Enabling Technologies |
Air-assisted intranasal instillation enhances adenoviral delivery to the olfactory epithelium and respiratory tract
- P Gau
- , S Rodriguez
- & D M Lin
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Short Communication |
10-Year stability of clinical-grade serum-free γ-retroviral vector-containing medium
- F Herbst
- , C R Ball
- & H Glimm
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Short Communication |
CD20-targeted measles virus shows high oncolytic specificity in clinical samples from lymphoma patients independent of prior rituximab therapy
- K-C Yaiw
- , T S Miest
- & R Cattaneo
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Original Article |
microRNA122-regulated transgene expression increases specificity of cardiac gene transfer upon intravenous delivery of AAV9 vectors
- A Geisler
- , A Jungmann
- & O J Müller
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Original Article |
Adenoviral delivery of Tousled kinase for the protection of salivary glands against ionizing radiation damage
- S Palaniyandi
- , Y Odaka
- & G Sunavala-Dossabhoy
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Original Article |
Innovative DNA vaccine for human papillomavirus (HPV)-associated head and neck cancer
- A Wu
- , Q Zeng
- & C-F Hung
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Original Article |
Adenovirus-mediated human paraoxonase1 gene transfer to provide protection against the toxicity of the organophosphorus pesticide toxicant diazoxon
- E G Duysen
- , K Parikh
- & N Chilukuri
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Original Article |
Immune responses to adeno-associated virus type 2 encoding channelrhodopsin-2 in a genetically blind rat model for gene therapy
- E Sugano
- , H Isago
- & H Tomita
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Review |
Physiological and tissue-specific vectors for treatment of inherited diseases
- M G Toscano
- , Z Romero
- & F Martin
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Original Article |
Validation of recombinant Sendai virus in a non-natural host model
- U Griesenbach
- , G McLachlan
- & E W F W Alton
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Original Article |
Development of murine leukemia virus-based retroviral vectors with a minimum possibility of cis-activation
- J Jang
- , J-T Lee
- & S Kim
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Original Article |
AAV2-mediated transfer of the human aquaporin-1 cDNA restores fluid secretion from irradiated miniature pig parotid glands
- R Gao
- , X Yan
- & S Wang
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Original Article |
Readministration of helper-dependent adenoviral vectors to mouse airway mediated via transient immunosuppression
- H Cao
- , T Yang
- & J Hu
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