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7. High-Throughput Sequencing of AAV Proviral Libraries from the Human Population Reveals Novel Variants with Unprecedented Intra-and Inter-Tissue Diversity

Molecular therapy, 2016-05, Vol.24, p.S4-S4

2016

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733. Somatically Repairing Compound Heterozygous Recessive Mutations by Chromosomal Cut-and-Paste for In Vivo Gene Therapy

Molecular therapy, 2016-05, Vol.24, p.S289-S289

2016

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739. rAAV Delivered MicroRNA Therapeutics Towards Efficacious Treatment of Corneal Neovascularization

Molecular therapy, 2016-05, Vol.24, p.S291-S291

2016

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9. rAAV Designs Harboring DNA Secondary Structures with High Thermal Stabilities Produce Heterogenic Viral Genome Populations

Molecular therapy, 2016-05, Vol.24, p.S5-S5

2016

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AAV-Genome Population Sequencing of Vectors Packaging CRISPR Components Reveals Design-Influenced Heterogeneity

Molecular therapy. Methods & clinical development, 2020-09, Vol.18, p.639-651

2020

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The AAV2.7m8 capsid packages a higher degree of heterogeneous vector genomes than AAV2

Gene therapy, 2024-08

2024

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Activation of Cyclic Adenosine Monophosphate Pathway Increases the Sensitivity of Cancer Cells to the Oncolytic Virus M1

Molecular therapy, 2016-01, Vol.24 (1), p.156-165

2016

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Adeno-associated Virus Genome Population Sequencing Achieves Full Vector Genome Resolution and Reveals Human-Vector Chimeras

Molecular therapy. Methods & clinical development, 2018-06, Vol.9, p.130-141

2018

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Adeno-associated virus vector as a platform for gene therapy delivery

Nature reviews. Drug discovery, 2019-05, Vol.18 (5), p.358-378

2019

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Bone-Targeting AAV-Mediated Gene Silencing in Osteoclasts for Osteoporosis Therapy

Molecular therapy. Methods & clinical development, 2020-06, Vol.17, p.922-935

2020

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Bone-targeting AAV-mediated silencing of Schnurri-3 prevents bone loss in osteoporosis

Nature communications, 2019-07, Vol.10 (1), p.2958-13, Article 2958

2019

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Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice

Nature biotechnology, 2018-10, Vol.36 (9), p.839-842

2018

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Cell Extract–Derived Differentiation of Embryonic Stem Cells

Stem cells (Dayton, Ohio), 2005-06, Vol.23 (6), p.712-718

2005

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Characterization of adenoviral transduction profile in prostate cancer cells and normal prostate tissue

The Prostate, 2017-09, Vol.77 (12), p.1265-1270

2017

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Characterization of human fetal osteoblasts by microarray analysis following stimulation with 58S bioactive gel-glass ionic dissolution products

Journal of biomedical materials research. Part B, Applied biomaterials, 2006-05, Vol.77B (2), p.431-446

2006

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Circumventing cellular immunity by miR142-mediated regulation sufficiently supports rAAV-delivered OVA expression without activating humoral immunity

JCI insight, 2019-07, Vol.5 (13)

2019

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Comparative Quantification of the Surfaceome of Human Multipotent Mesenchymal Progenitor Cells

Stem cell reports, 2015-03, Vol.4 (3), p.473-488

2015

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Could co-transplantation of iPS cells derived hepatocytes and MSCs cure end-stage liver disease?

Cell biology international, 2009-11, Vol.33 (11), p.1180-1183

2009

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Cytokeratin 15 marks basal epithelia in developing ureters and is upregulated in a subset of urothelial cell carcinomas

PloS one, 2013-11, Vol.8 (11), p.e81167-e81167

2013

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Differentiation of Osteoblasts from Murine Embryonic Stem Cells by Overexpression of the Transcriptional Factor Osterix

Tissue engineering, 2004-09, Vol.10 (9-10), p.1456-1466

2004

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Differentiation of osteoblasts from murine embryonic stem cells by overexpression of the transcriptional factor osterix

Tissue engineering, 2004-09, Vol.10 (9-10), p.1456-1466

2004

Volltextzugriff (PDF)

Direct ITR-to-ITR Nanopore Sequencing of AAV Vector Genomes

Human gene therapy, 2022-11, Vol.33 (21-22), p.1187

2022

Volltextzugriff (PDF)

Diseases caused by different mutations in the two alleles of a gene are treated in mice by Cas-9-induced allelic exchange: Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice

Nature biotechnology, 2018-08, Vol.36 (9), p.839-842

2018

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Dose- and time-dependent effect of bioactive gel-glass ionic-dissolution products on human fetal osteoblast-specific gene expression

Journal of biomedical materials research, 2005-07, Vol.74B (1), p.529-537

2005

Volltextzugriff (PDF)

Effective and Accurate Gene Silencing by a Recombinant AAV-Compatible MicroRNA Scaffold

Molecular therapy, 2020-02, Vol.28 (2), p.422-430

2020

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7. High-Throughput Sequencing of AAV Proviral Libraries from the Human Population Reveals Novel Variants with Unprecedented Intra-and Inter-Tissue Diversity

733. Somatically Repairing Compound Heterozygous Recessive Mutations by Chromosomal Cut-and-Paste for In Vivo Gene Therapy

739. rAAV Delivered MicroRNA Therapeutics Towards Efficacious Treatment of Corneal Neovascularization

9. rAAV Designs Harboring DNA Secondary Structures with High Thermal Stabilities Produce Heterogenic Viral Genome Populations

AAV-Genome Population Sequencing of Vectors Packaging CRISPR Components Reveals Design-Influenced Heterogeneity

The AAV2.7m8 capsid packages a higher degree of heterogeneous vector genomes than AAV2

Activation of Cyclic Adenosine Monophosphate Pathway Increases the Sensitivity of Cancer Cells to the Oncolytic Virus M1

Adeno-associated Virus Genome Population Sequencing Achieves Full Vector Genome Resolution and Reveals Human-Vector Chimeras

Adeno-associated virus vector as a platform for gene therapy delivery

Bone-Targeting AAV-Mediated Gene Silencing in Osteoclasts for Osteoporosis Therapy

Bone-targeting AAV-mediated silencing of Schnurri-3 prevents bone loss in osteoporosis

Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice

Cell Extract–Derived Differentiation of Embryonic Stem Cells

Characterization of adenoviral transduction profile in prostate cancer cells and normal prostate tissue

Characterization of human fetal osteoblasts by microarray analysis following stimulation with 58S bioactive gel-glass ionic dissolution products

Circumventing cellular immunity by miR142-mediated regulation sufficiently supports rAAV-delivered OVA expression without activating humoral immunity

Comparative Quantification of the Surfaceome of Human Multipotent Mesenchymal Progenitor Cells

Could co-transplantation of iPS cells derived hepatocytes and MSCs cure end-stage liver disease?

Cytokeratin 15 marks basal epithelia in developing ureters and is upregulated in a subset of urothelial cell carcinomas

Differentiation of Osteoblasts from Murine Embryonic Stem Cells by Overexpression of the Transcriptional Factor Osterix

Differentiation of osteoblasts from murine embryonic stem cells by overexpression of the transcriptional factor osterix

Direct ITR-to-ITR Nanopore Sequencing of AAV Vector Genomes

Diseases caused by different mutations in the two alleles of a gene are treated in mice by Cas-9-induced allelic exchange: Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice

Dose- and time-dependent effect of bioactive gel-glass ionic-dissolution products on human fetal osteoblast-specific gene expression

Effective and Accurate Gene Silencing by a Recombinant AAV-Compatible MicroRNA Scaffold

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