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Lista de obras de Dan Wang

A Rationally Engineered Capsid Variant of AAV9 for Systemic CNS-Directed and Peripheral Tissue-Detargeted Gene Delivery in Neonates.

artículo científico publicado en 2018

A Single Injection of Recombinant Adeno-Associated Virus into the Lumbar Cistern Delivers Transgene Expression Throughout the Whole Spinal Cord.

artículo científico publicado en 2015

AAV9 delivering a modified human Mullerian inhibiting substance as a gene therapy in patient-derived xenografts of ovarian cancer

artículo científico publicado en 2015

AMH/MIS as a contraceptive that protects the ovarian reserve during chemotherapy

artículo científico publicado en 2017

Adeno-Associated Virus Neutralizing Antibodies in Large Animals and Their Impact on Brain Intraparenchymal Gene Transfer

article

Adeno-associated Virus Serotype Vectors Efficiently Transduce Normal Prostate Tissue and Prostate Cancer Cells.

artículo científico publicado en 2015

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

article

Adenovirus-Mediated Somatic Genome Editing of Pten by CRISPR/Cas9 in Mouse Liver in Spite of Cas9-Specific Immune Responses.

artículo científico publicado en 2015

Attenuation of nonsense-mediated mRNA decay enhances in vivo nonsense suppression

artículo científico publicado en 2013

Base editing rescue of spinal muscular atrophy in cells and in mice

artículo científico publicado en 2023

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

scientific article published on 04 July 2019

CNS-restricted Transduction and CRISPR/Cas9-mediated Gene Deletion with an Engineered AAV Vector

artículo científico publicado en 2016

Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutation.

artículo científico publicado en 2010

Gene Delivery to Nonhuman Primate Preimplantation Embryos Using Recombinant Adeno-Associated Virus

artículo científico publicado en 2019

In vivo genome editing partially restores alpha1-antitrypsin in a murine model of AAT deficiency.

artículo científico publicado en 2018

Intrathecal Adeno-Associated Virus Vector-mediated Gene Delivery for Adrenomyeloneuropathy

article

Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo

artículo científico publicado en 2021

Short DNA Hairpins Compromise Recombinant Adeno-Associated Virus Genome Homogeneity.

artículo científico publicado en 2017

Slow Infusion of Recombinant Adeno-Associated Viruses into the Mouse Cerebrospinal Fluid Space.

artículo científico publicado en 2018

Slow intrathecal injection of rAAVrh10 enhances its transduction of spinal cord and therapeutic efficacy in a mutant SOD1 model of ALS.

artículo científico publicado en 2017

Streamlined ex vivo and in vivo genome editing in mouse embryos using recombinant adeno-associated viruses.

artículo científico publicado en 2018

Suppression of premature termination codons as a therapeutic approach.

artículo científico publicado en 2012

Taking a Hint from Structural Biology: To Better Understand AAV Transport across the BBB.

artículo científico publicado en 2018

The designer aminoglycoside NB84 significantly reduces glycosaminoglycan accumulation associated with MPS I-H in the Idua-W392X mouse ⬇️

artículo científico publicado el 19 de octubre de 2011

The potential of adeno-associated viral vectors for gene delivery to muscle tissue

artículo científico publicado en 2014

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