标题
AAV vector-mediated in vivo reprogramming into pluripotency
作者
关键词
-
出版物
Nature Communications
Volume 9, Issue 1, Pages -
出版商
Springer Nature
发表日期
2018-07-03
DOI
10.1038/s41467-018-05059-x
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- In Vivo Transient and Partial Cell Reprogramming to Pluripotency as a Therapeutic Tool for Neurodegenerative Diseases
- (2018) S. Tamanini et al. MOLECULAR NEUROBIOLOGY
- A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear
- (2017) Lukas D Landegger et al. NATURE BIOTECHNOLOGY
- Identification of liver-specific enhancer–promoter activity in the 3′ untranslated region of the wild-type AAV2 genome
- (2017) Grant J Logan et al. NATURE GENETICS
- GENE-IS: Time-Efficient and Accurate Analysis of Viral Integration Events in Large-Scale Gene Therapy Data
- (2017) Saira Afzal et al. Molecular Therapy-Nucleic Acids
- Common Telomere Changes during In Vivo Reprogramming and Early Stages of Tumorigenesis
- (2017) Rosa M. Marión et al. Stem Cell Reports
- Bursts of Reprogramming: A Path to Extend Lifespan?
- (2016) Salah Mahmoudi et al. CELL
- In Vivo Amelioration of Age-Associated Hallmarks by Partial Reprogramming
- (2016) Alejandro Ocampo et al. CELL
- Molecular Obstacles to Clinical Translation of iPSCs
- (2016) Natalia Tapia et al. Cell Stem Cell
- Mending a Faltering Heart
- (2016) Mo Li et al. CIRCULATION RESEARCH
- Development of Patient-specific AAV Vectors After Neutralizing Antibody Selection for Enhanced Muscle Gene Transfer
- (2016) Chengwen Li et al. MOLECULAR THERAPY
- In Situ Pluripotency Factor Expression Promotes Functional Recovery From Cerebral Ischemia
- (2016) Jung Hwa Seo et al. MOLECULAR THERAPY
- Recombinant AAV Integration Is Not Associated With Hepatic Genotoxicity in Nonhuman Primates and Patients
- (2016) Irene Gil-Farina et al. MOLECULAR THERAPY
- Cre-dependent selection yields AAV variants for widespread gene transfer to the adult brain
- (2016) Benjamin E Deverman et al. NATURE BIOTECHNOLOGY
- Looking to the future following 10 years of induced pluripotent stem cell technologies
- (2016) Mo Li et al. Nature Protocols
- Tissue damage and senescence provide critical signals for cellular reprogramming in vivo
- (2016) Lluc Mosteiro et al. SCIENCE
- Directed Dedifferentiation Using Partial Reprogramming Induces Invasive Phenotype in Melanoma Cells
- (2016) Nathalie Knappe et al. STEM CELLS
- A regulatable AAV vector mediating GDNF biological effects at clinically-approved sub-antimicrobial doxycycline doses
- (2016) Abdelwahed Chtarto et al. Molecular Therapy-Methods & Clinical Development
- Adeno-Associated Virus Type 2 and Hepatocellular Carcinoma?
- (2015) Kenneth I. Berns et al. HUMAN GENE THERAPY
- E Pluribus Unum: 50 Years of Research, Millions of Viruses, and One Goal—Tailored Acceleration of AAV Evolution
- (2015) Dirk Grimm et al. MOLECULAR THERAPY
- Riboswitch-mediated Attenuation of Transgene Cytotoxicity Increases Adeno-associated Virus Vector Yields in HEK-293 Cells
- (2015) Benjamin Strobel et al. MOLECULAR THERAPY
- Adeno-associated Vector Toxicity—To Be or Not to Be?
- (2015) Hildegard Büning et al. MOLECULAR THERAPY
- Lineage conversion induced by pluripotency factors involves transient passage through an iPSC stage
- (2015) Ori Bar-Nur et al. NATURE BIOTECHNOLOGY
- Recurrent AAV2-related insertional mutagenesis in human hepatocellular carcinomas
- (2015) Jean-Charles Nault et al. NATURE GENETICS
- Alleviation of off-target effects from vector-encoded shRNAs via codelivered RNA decoys
- (2015) Stefan Mockenhaupt et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Generation of induced pluripotent stem cells from virus-free in vivo reprogramming of BALB/c mouse liver cells
- (2014) Irene de Lázaro et al. BIOMATERIALS
- CRISPR/Cas9-mediated genome engineering: An adeno-associated viral (AAV) vector toolbox
- (2014) Elena Senís et al. Biotechnology Journal
- Premature Termination of Reprogramming In Vivo Leads to Cancer Development through Altered Epigenetic Regulation
- (2014) Kotaro Ohnishi et al. CELL
- Efficient transduction and optogenetic stimulation of retinal bipolar cells by a synthetic adeno-associated virus capsid and promoter
- (2014) T. Cronin et al. EMBO Molecular Medicine
- Exit from Pluripotency Is Gated by Intracellular Redistribution of the bHLH Transcription Factor Tfe3
- (2013) Joerg Betschinger et al. CELL
- Smooth Muscle Cells Differentiated From Reprogrammed Embryonic Lung Fibroblasts Through DKK3 Signaling Are Potent for Tissue Engineering of Vascular Grafts
- (2013) Eirini Karamariti et al. CIRCULATION RESEARCH
- Reprogramming in vivo produces teratomas and iPS cells with totipotency features
- (2013) María Abad et al. NATURE
- A largely random AAV integration profile after LPLD gene therapy
- (2013) Christine Kaeppel et al. NATURE MEDICINE
- Robust RNAi enhancement via human Argonaute-2 overexpression from plasmids, viral vectors and cell lines
- (2013) Kathleen Börner et al. NUCLEIC ACIDS RESEARCH
- In Vivo Cell Reprogramming towards Pluripotency by Virus-Free Overexpression of Defined Factors
- (2013) Açelya Yilmazer et al. PLoS One
- Effect of in vivo administration of reprogramming factors in the mouse liver
- (2013) AKIRA TOMOKUNI et al. Oncology Letters
- The ROSA26-iPSC Mouse: A Conditional, Inducible, and Exchangeable Resource for Studying Cellular (De)Differentiation
- (2013) Lieven Haenebalcke et al. Cell Reports
- Enhancing the Utility of Adeno-Associated Virus Gene Transfer through Inducible Tissue-Specific Expression
- (2013) Shu-Jen Chen et al. Human Gene Therapy Methods
- Reprogramming Adipose Tissue-Derived Mesenchymal Stem Cells into Pluripotent Stem Cells by a Mutant Adeno-Associated Viral Vector
- (2013) Mong-Jen Chen et al. Human Gene Therapy Methods
- Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells
- (2012) Marc Thier et al. Cell Stem Cell
- Induced Pluripotent Stem Cell Clones Reprogrammed via Recombinant Adeno-Associated Virus-Mediated Transduction Contain Integrated Vector Sequences
- (2012) J. Weltner et al. JOURNAL OF VIROLOGY
- Integration Frequency and Intermolecular Recombination of rAAV Vectors in Non-human Primate Skeletal Muscle and Liver
- (2012) Ali Nowrouzi et al. MOLECULAR THERAPY
- Conversion of human fibroblasts to angioblast-like progenitor cells
- (2012) Leo Kurian et al. NATURE METHODS
- Direct reprogramming of fibroblasts into endothelial cells capable of angiogenesis and reendothelialization in tissue-engineered vessels
- (2012) A. Margariti et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Fate tracing of mature hepatocytes in mouse liver homeostasis and regeneration
- (2011) Yann Malato et al. JOURNAL OF CLINICAL INVESTIGATION
- Lentiviral Vector Design and Imaging Approaches to Visualize the Early Stages of Cellular Reprogramming
- (2011) Eva Warlich et al. MOLECULAR THERAPY
- Methods for making induced pluripotent stem cells: reprogramming à la carte
- (2011) Federico González et al. NATURE REVIEWS GENETICS
- Direct reprogramming of mouse fibroblasts to neural progenitors
- (2011) J. Kim et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Assessing the potential for AAV vector genotoxicity in a murine model
- (2010) H. Li et al. BLOOD
- Argonaute proteins are key determinants of RNAi efficacy, toxicity, and persistence in the adult mouse liver
- (2010) Dirk Grimm et al. JOURNAL OF CLINICAL INVESTIGATION
- MicroRNA-regulated, Systemically Delivered rAAV9: A Step Closer to CNS-restricted Transgene Expression
- (2010) Jun Xie et al. MOLECULAR THERAPY
- Visualization of omics data for systems biology
- (2010) Nils Gehlenborg et al. NATURE METHODS
- Transgenic mice with defined combinations of drug-inducible reprogramming factors
- (2009) Styliani Markoulaki et al. NATURE BIOTECHNOLOGY
- Comprehensive genomic access to vector integration in clinical gene therapy
- (2009) Richard Gabriel et al. NATURE MEDICINE
- A reprogrammable mouse strain from gene-targeted embryonic stem cells
- (2009) Matthias Stadtfeld et al. NATURE METHODS
- A myocardium tropic adeno-associated virus (AAV) evolved by DNA shuffling and in vivo selection
- (2009) L. Yang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Feeder-free derivation of induced pluripotent stem cells from adult human adipose stem cells
- (2009) N. Sun et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- In Vitro and In Vivo Gene Therapy Vector Evolution via Multispecies Interbreeding and Retargeting of Adeno-Associated Viruses
- (2008) D. Grimm et al. JOURNAL OF VIROLOGY
- Self-complementary AAV Vectors; Advances and Applications
- (2008) Douglas M McCarty MOLECULAR THERAPY
- Next generation of adeno-associated virus 2 vectors: Point mutations in tyrosines lead to high-efficiency transduction at lower doses
- (2008) L. Zhong et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Tyrosine-phosphorylation of AAV2 vectors and its consequences on viral intracellular trafficking and transgene expression
- (2008) Li Zhong et al. VIROLOGY
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