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| Open AccessMagnetic Nanoparticle Assisted Self-assembly of Cell Penetrating Peptides-Oligonucleotides Complexes for Gene Delivery
- Moataz Dowaidar
- , Hani Nasser Abdelhamid
- & Ülo Langel
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| Open AccessDelivery of large transgene cassettes by foamy virus vector
- Nathan Paul Sweeney
- , Jinhong Meng
- & Myra McClure
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| Open AccessContinual conscious bioluminescent imaging in freely moving somatotransgenic mice
- Rajvinder Karda
- , Dany P. Perocheau
- & Simon N. Waddington
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| Open AccessEngineered HSV vector achieves safe long-term transgene expression in the central nervous system
- Gianluca Verlengia
- , Yoshitaka Miyagawa
- & Joseph C. Glorioso
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| Open AccessKnockdown of toll-like receptor 4 signaling pathways ameliorate bone graft rejection in a mouse model of allograft transplantation
- Jeng-Long Hsieh
- , Po-Chuan Shen
- & Shih-Yao Chen
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| Open AccessPLGA-based dual targeted nanoparticles enhance miRNA transfection efficiency in hepatic carcinoma
- Chenlei Cai
- , Yuexia Xie
- & Peifeng Liu
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| Open AccessCochlear gene therapy with ancestral AAV in adult mice: complete transduction of inner hair cells without cochlear dysfunction
- Jun Suzuki
- , Ken Hashimoto
- & M. Charles Liberman
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| Open AccessExosome-associated AAV2 vector mediates robust gene delivery into the murine retina upon intravitreal injection
- Sarah J. Wassmer
- , Livia S. Carvalho
- & Casey A. Maguire
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| Open AccessLentiviral vectors can be used for full-length dystrophin gene therapy
- John R. Counsell
- , Zeinab Asgarian
- & Olivier Danos
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| Open AccessA Novel Ideal Radionuclide Imaging System for Non-invasively Cell Monitoring built on Baculovirus Backbone by Introducing Sleeping Beauty Transposon
- Jing Lv
- , Yu Pan
- & Yifan Zhang
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| Open AccessLentiviral vectors can be used for full-length dystrophin gene therapy
- John R. Counsell
- , Zeinab Asgarian
- & Olivier Danos
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| Open AccessEfficient genome replication of hepatitis B virus using adenovirus vector: a compact pregenomic RNA-expression unit
- Mariko Suzuki
- , Saki Kondo
- & Yumi Kanegae
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| Open AccessContinuous cell supply from Krt7-expressing hematopoietic stem cells during native hematopoiesis revealed by targeted in vivo gene transfer method
- Yoko Tajima
- , Keiichi Ito
- & Satoshi Yamazaki
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| Open AccessAdenoviral vectors encoding CRISPR/Cas9 multiplexes rescue dystrophin synthesis in unselected populations of DMD muscle cells
- Ignazio Maggio
- , Jin Liu
- & Manuel A. F. V. Gonçalves
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| Open AccessIntraarticular overexpression of Smad7 ameliorates experimental arthritis
- Shih-Yao Chen
- , Ai-Li Shiau
- & Chrong-Reen Wang
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| Open AccessA vector platform for the rapid and efficient engineering of stable complex transgenes
- Carsten Jäckel
- , Melanie Schmitt Nogueira
- & Peter J. Nelson
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| Open AccessImproving protein content and quality by over-expressing artificially synthetic fusion proteins with high lysine and threonine constituent in rice plants
- Shu-Ye Jiang
- , Ali Ma
- & Srinivasan Ramachandran
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Article
| Open AccessA plant 35S CaMV promoter induces long-term expression of luciferase in Atlantic salmon
- Tore Seternes
- , Tom C. Tonheim
- & Roy A. Dalmo
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| Open AccessTranscriptional, epigenetic and retroviral signatures identify regulatory regions involved in hematopoietic lineage commitment
- Oriana Romano
- , Clelia Peano
- & Annarita Miccio
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| Open AccessGenome sequence and plasmid transformation of the model high-yield bacterial cellulose producer Gluconacetobacter hansenii ATCC 53582
- Michael Florea
- , Benjamin Reeve
- & Tom Ellis
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| Open AccessInfluence of cell physiological state on gene delivery to T lymphocytes by chimeric adenovirus Ad5F35
- Wen-feng Zhang
- , Hong-wei Shao
- & Shu-lin Huang
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| Open AccessAAV Gene Therapy for MPS1-associated Corneal Blindness
- Melisa Vance
- , Telmo Llanga
- & Matthew L. Hirsch
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| Open AccessA novel single-chain antibody redirects adenovirus to IL13Rα2-expressing brain tumors
- Julius W. Kim
- , Jacob S. Young
- & Irina V. Balyasnikova
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| Open AccessDelivery of miR-34a by chitosan/PLGA nanoplexes for the anticancer treatment of multiple myeloma
- Donato Cosco
- , Felisa Cilurzo
- & Donatella Paolino
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| Open AccessDevelopment of Endothelial-Specific Single Inducible Lentiviral Vectors for Genetic Engineering of Endothelial Progenitor Cells
- Guanghua Yang
- , M. Gabriela Kramer
- & Cheng Qian
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| Open AccessTAL effectors mediate high-efficiency transposition of the piggyBac transposon in silkworm Bombyx mori L
- Lupeng Ye
- , Zhengying You
- & Boxiong Zhong
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| Open AccessModulation of Macrophage Functional Polarity towards Anti-Inflammatory Phenotype with Plasmid DNA Delivery in CD44 Targeting Hyaluronic Acid Nanoparticles
- Thanh-Huyen Tran
- , Ruchir Rastogi
- & Mansoor M. Amiji
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| Open AccessA geminivirus-based guide RNA delivery system for CRISPR/Cas9 mediated plant genome editing
- Kangquan Yin
- , Ting Han
- & Yule Liu
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| Open AccessA diphtheria toxin resistance marker for in vitro and in vivo selection of stably transduced human cells
- Gabriele Picco
- , Consalvo Petti
- & Enzo Medico
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| Open AccessQuantitative analysis of recombination between YFP and CFP genes of FRET biosensors introduced by lentiviral or retroviral gene transfer
- Akira T. Komatsubara
- , Michiyuki Matsuda
- & Kazuhiro Aoki
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| Open AccessEnzyme replacement in the CSF to treat metachromatic leukodystrophy in mouse model using single intracerebroventricular injection of self-complementary AAV1 vector
- Kohei Hironaka
- , Yoshiyuki Yamazaki
- & Takashi Shimada
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| Open AccessSelf-assembled Messenger RNA Nanoparticles (mRNA-NPs) for Efficient Gene Expression
- Hyejin Kim
- , Yongkuk Park
- & Jong Bum Lee
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| Open AccessRapid generation of endogenously driven transcriptional reporters in cells through CRISPR/Cas9
- Alejandro Rojas-Fernandez
- , Lina Herhaus
- & Gopal P. Sapkota
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| Open AccessEnhanced targeted integration mediated by translocated I-SceI during the Agrobacterium mediated transformation of yeast
- Martijn Rolloos
- , Paul J. J. Hooykaas
- & Bert J. van der Zaal
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| Open AccessAnalysis of the sericin1 promoter and assisted detection of exogenous gene expression efficiency in the silkworm Bombyx mori L.
- Lupeng Ye
- , Qiujie Qian
- & Boxiong Zhong
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| Open AccessNovel codon-optimized mini-intronic plasmid for efficient, inexpensive and xeno-free induction of pluripotency
- Sebastian Diecke
- , Jiamiao Lu
- & Joseph C. Wu
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| Open AccessIn-vivo RGB marking and multicolour single-cell tracking in the adult brain
- Diego Gomez-Nicola
- , Kristoffer Riecken
- & V. Hugh Perry
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| Open AccessVector modifications to eliminate transposase expression following piggyBac-mediated transgenesis
- Syandan Chakraborty
- , HaYeun Ji
- & Kam W. Leong
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| Open AccessNovel Adeno-associated Viruses Derived From Pig Tissues Transduce Most Major Organs in Mice
- Alexander Bello
- , Allan Chand
- & Gary P. Kobinger
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| Open AccessNovel lentiviral vectors with mutated reverse transcriptase for mRNA delivery of TALE nucleases
- Ulrike Mock
- , Kristoffer Riecken
- & Boris Fehse
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| Open AccessDown syndrome-associated haematopoiesis abnormalities created by chromosome transfer and genome editing technologies
- Yasuhiro Kazuki
- , Yuwna Yakura
- & Mitsuo Oshimura
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| Open AccessTargeted gene transfer into ependymal cells through intraventricular injection of AAV1 vector and long-term enzyme replacement via the CSF
- Yoshiyuki Yamazaki
- , Yukihiko Hirai
- & Takashi Shimada
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| Open AccessAdenoviral vector delivery of RNA-guided CRISPR/Cas9 nuclease complexes induces targeted mutagenesis in a diverse array of human cells
- Ignazio Maggio
- , Maarten Holkers
- & Manuel A. F. V. Gonçalves
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| Open AccessTranscription activator-like effector nuclease-mediated transduction of exogenous gene into IL2RG locus
- Yohei Matsubara
- , Tomoki Chiba
- & Hiroshi Asahara
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| Open AccessViability of Long-Term Gene Therapy in the Cochlea
- Patrick J. Atkinson
- , Andrew K. Wise
- & Rachael T. Richardson
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| Open AccessNon-integrating gamma-retroviral vectors as a versatile tool for transient zinc-finger nuclease delivery
- Sylwia Bobis-Wozowicz
- , Melanie Galla
- & Toni Cathomen
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| Open AccessImproved site-specific recombinase-based method to produce selectable marker- and vector-backbone-free transgenic cells
- Yuan Yu
- , Qi Tong
- & Yong Zhang
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| Open AccessAdenovirus vectors lacking virus-associated RNA expression enhance shRNA activity to suppress hepatitis C virus replication
- Zheng Pei
- , Guoli Shi
- & Yumi Kanegae
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| Open AccessContinuous DOPA synthesis from a single AAV: dosing and efficacy in models of Parkinson's disease
- Erik Cederfjäll
- , Nathalie Nilsson
- & Deniz Kirik