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Martine Aubert

Fred Hutchinson Cancer Research Center

28

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1145

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CRISPR/Cas9 gene editing of hepatitis B virus in chronically infected humanized mice

2020 Molecular therapy. Methods & clinical development
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Gene transfer in AAV seropositive rhesus macaques following rapamycin treatment and subcutaneous delivery of AAV6 but not retargeted AAV6 vectors.

2020 Human Gene Therapy
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Gene editing and elimination of latent herpes simplex virus in vivo.

2020 Nature Communications
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Rapamycin immune tolerization enables gene transfer following subcutaneous delivery of AAV6 but not CD4-retargeted AAV6 vectors in AAV-seropositive rhesus macaques

2019 Journal of virus eradication
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CRISPR/Cas9 and Genome Editing for Viral Disease—Is Resistance Futile?

2018 ACS Infectious Diseases
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In vivo dynamics of AAV-mediated gene delivery to sensory neurons of the trigeminal ganglia

2017 Scientific Reports
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Detection of treatment-resistant infectious HIV after genome-directed antiviral endonuclease therapy

2016 Antiviral Research
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765. Detection of Treatment-Resistant Infectious HIV After Genome-Directed Antiviral Endonuclease Therapy

2016 Molecular Therapy
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In vivo disruption of latent HSV by designer endonuclease therapy

2016 JCI insight
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DNA cleavage enzymes for treatment of persistent viral infections: recent advances and the pathway forward.

2014 Virology
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Citations (27)