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Adenovirus vectors in hematopoietic stem cell genome editing

FEBS letters, 2019-12, Vol.593 (24), p.3623-3648

2019

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In Vivo HSC Gene Therapy Using a Bi-modular HDAd5/35++ Vector Cures Sickle Cell Disease in a Mouse Model

Molecular therapy, 2021-02, Vol.29 (2), p.822-837

2021

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Adenovirus Binding to Blood Factors Results in Liver Cell Infection and Hepatotoxicity

Journal of Virology, 2005-06, Vol.79 (12), p.7478-7491

2005

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CryoEM structure of adenovirus type 3 fibre with desmoglein 2 shows an unusual mode of receptor engagement

Nature communications, 2019-03, Vol.10 (1), p.1181-1181, Article 1181

2019

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CD46 and CD59 inhibitors enhance complement-dependent cytotoxicity of anti-CD38 monoclonal antibodies daratumumab and isatuximab in multiple myeloma and other B-cell malignancy cells

Cancer biology & therapy, 2024-12, Vol.25 (1), p.2314322-2314322

2024

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Prospects and challenges of in vivo hematopoietic stem cell genome editing for hemoglobinopathies

Molecular therapy, 2023-10, Vol.31 (10), p.2823-2825

2023

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Reactivation of γ-globin in adult β-YAC mice after ex vivo and in vivo hematopoietic stem cell genome editing

Blood, 2018-06, Vol.131 (26), p.2915-2928

2018

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Incomplete Description

Deutsches Ärzteblatt international, 2021-09, Vol.118I processed the file.I'm waiting for feedback tomorrow (35-36), p.604-604

2021

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In vivo HSC prime editing rescues sickle cell disease in a mouse model

Blood, 2023-04, Vol.141 (17), p.2085-2099

2023

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Adenovirus-Platelet Interaction in Blood Causes Virus Sequestration to the Reticuloendothelial System of the Liver

Journal of Virology, 2007-05, Vol.81 (9), p.4866-4871

2007

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Protein engineering to target complement evasion in cancer

FEBS letters, 2014-01, Vol.588 (2), p.334-340

2014

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HDAd5/35 ++ Adenovirus Vector Expressing Anti-CRISPR Peptides Decreases CRISPR/Cas9 Toxicity in Human Hematopoietic Stem Cells

Molecular therapy. Methods & clinical development, 2018-06, Vol.9, p.390-401

2018

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Novel Group C Oncolytic Adenoviruses Carrying a miRNA Inhibitor Demonstrate Enhanced Oncolytic Activity In Vitro and In Vivo

Molecular cancer therapeutics, 2022-03, Vol.21 (3), p.460-470

2022

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Targeted Integration and High-Level Transgene Expression in AAVS1 Transgenic Mice after In Vivo HSC Transduction with HDAd5/35++ Vectors

Molecular therapy, 2019-12, Vol.27 (12), p.2195-2212

2019

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Role of Fiber Shaft Length in Tumor Targeting with Ad5/3 Vectors

Genes, 2022-11, Vol.13 (11), p.2056

2022

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Desmoglein-2 as a prognostic and biomarker in ovarian cancer

Cancer biology & therapy, 2020-12, Vol.21 (12), p.1154-1162

2020

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Analysis of epithelial and mesenchymal markers in ovarian cancer reveals phenotypic heterogeneity and plasticity

PloS one, 2011-01, Vol.6 (1), p.e16186-e16186

2011

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Enhanced HbF reactivation by multiplex mutagenesis of thalassemic CD34+ cells in vitro and in vivo

Blood, 2021-10, Vol.138 (17), p.1540-1553

2021

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In vivo hematopoietic stem cell gene therapy ameliorates murine thalassemia intermedia

The Journal of clinical investigation, 2019-02, Vol.129 (2), p.598-615

2019

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In vivo HSPC gene therapy with base editors allows for efficient reactivation of fetal γ-globin in β-YAC mice

Blood advances, 2021-02, Vol.5 (4), p.1122-1135

2021

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Studies on the Correct Length of Nasopharyngeal Airways in Adults: A Literature Review

Journal of special operations medicine, 2021, Vol.21 (3), p.45

2021

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Desmoglein 2 is a receptor for adenovirus serotypes 3, 7, 11 and 14

Nature medicine, 2011-01, Vol.17 (1), p.96-104

2011

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HDAd6/35++ - A new helper-dependent adenovirus vector platform for in vivo transduction of hematopoietic stem cells

Molecular therapy. Methods & clinical development, 2023-06, Vol.29, p.213-226

2023

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Analysis of Adenovirus Sequestration in the Liver, Transduction of Hepatic Cells, and Innate Toxicity after Injection of Fiber-Modified Vectors

Journal of Virology, 2004-05, Vol.78 (10), p.5368-5381

2004

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CD46 is a cellular receptor for group B adenoviruses

Nature medicine, 2003-11, Vol.9 (11), p.1408-1412

2003

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Adenovirus vectors in hematopoietic stem cell genome editing

In Vivo HSC Gene Therapy Using a Bi-modular HDAd5/35++ Vector Cures Sickle Cell Disease in a Mouse Model

Adenovirus Binding to Blood Factors Results in Liver Cell Infection and Hepatotoxicity

CryoEM structure of adenovirus type 3 fibre with desmoglein 2 shows an unusual mode of receptor engagement

CD46 and CD59 inhibitors enhance complement-dependent cytotoxicity of anti-CD38 monoclonal antibodies daratumumab and isatuximab in multiple myeloma and other B-cell malignancy cells

Prospects and challenges of in vivo hematopoietic stem cell genome editing for hemoglobinopathies

Reactivation of γ-globin in adult β-YAC mice after ex vivo and in vivo hematopoietic stem cell genome editing

Incomplete Description

In vivo HSC prime editing rescues sickle cell disease in a mouse model

Adenovirus-Platelet Interaction in Blood Causes Virus Sequestration to the Reticuloendothelial System of the Liver

Protein engineering to target complement evasion in cancer

HDAd5/35 ++ Adenovirus Vector Expressing Anti-CRISPR Peptides Decreases CRISPR/Cas9 Toxicity in Human Hematopoietic Stem Cells

Novel Group C Oncolytic Adenoviruses Carrying a miRNA Inhibitor Demonstrate Enhanced Oncolytic Activity In Vitro and In Vivo

Targeted Integration and High-Level Transgene Expression in AAVS1 Transgenic Mice after In Vivo HSC Transduction with HDAd5/35++ Vectors

Role of Fiber Shaft Length in Tumor Targeting with Ad5/3 Vectors

Desmoglein-2 as a prognostic and biomarker in ovarian cancer

Analysis of epithelial and mesenchymal markers in ovarian cancer reveals phenotypic heterogeneity and plasticity

Enhanced HbF reactivation by multiplex mutagenesis of thalassemic CD34+ cells in vitro and in vivo

In vivo hematopoietic stem cell gene therapy ameliorates murine thalassemia intermedia

In vivo HSPC gene therapy with base editors allows for efficient reactivation of fetal γ-globin in β-YAC mice

Studies on the Correct Length of Nasopharyngeal Airways in Adults: A Literature Review

Desmoglein 2 is a receptor for adenovirus serotypes 3, 7, 11 and 14

HDAd6/35++ - A new helper-dependent adenovirus vector platform for in vivo transduction of hematopoietic stem cells

Analysis of Adenovirus Sequestration in the Liver, Transduction of Hepatic Cells, and Innate Toxicity after Injection of Fiber-Modified Vectors

CD46 is a cellular receptor for group B adenoviruses

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