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Ascending Vaginal Infection Using Bioluminescent Bacteria Evokes Intrauterine Inflammation, Preterm Birth, and Neonatal Brain Injury in Pregnant Mice

The American journal of pathology, 2018-10, Vol.188 (10), p.2164-2176

2018

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Production of lentiviral vectors using novel, enzymatically produced, linear DNA

Gene therapy, 2019-04, Vol.26 (3-4), p.86-92

2019

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Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease

EMBO molecular medicine, 2023-10, Vol.15 (10), p.e17393-e17393

2023

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Argininosuccinic aciduria fosters neuronal nitrosative stress reversed by Asl gene transfer

Nature communications, 2018-08, Vol.9 (1), p.3505-14, Article 3505

2018

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Cervical Gene Delivery of the Antimicrobial Peptide, Human β-Defensin (HBD)-3, in a Mouse Model of Ascending Infection-Related Preterm Birth

Frontiers in immunology, 2020-02, Vol.11, p.106

2020

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A Broad Overview and Review of CRISPR-Cas Technology and Stem Cells

Current stem cell reports, 2016-03, Vol.2 (1), p.9-20

2016

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Re-structuring lentiviral vectors to express genomic RNA via cap-dependent translation

Molecular therapy. Methods & clinical development, 2021-03, Vol.20, p.357-365

2021

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A Broad Overview and Review of CRISPR-Cas Technology and Stem Cells

Current stem cell reports, 2016, Vol.2 (1), p.9-20

2016

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Foamy Virus Vectors Transduce Visceral Organs and Hippocampal Structures following In Vivo Delivery to Neonatal Mice

Molecular therapy. Nucleic acids, 2018-09, Vol.12, p.626-634

2018

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Genetic therapeutic advancements for Dravet Syndrome

Epilepsy & behavior, 2022-07, Vol.132, p.108741-108741, Article 108741

2022

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Rapid and inexpensive purification of adenovirus vectors using an optimised aqueous two-phase technology

Journal of virological methods, 2022-01, Vol.299, p.114305-114305, Article 114305

2022

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Eliminating HIV-1 Packaging Sequences from Lentiviral Vector Proviruses Enhances Safety and Expedites Gene Transfer for Gene Therapy

Molecular therapy, 2017-08, Vol.25 (8), p.1790-1804

2017

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Gene Therapy with Adeno-associated Virus for Cystic Fibrosis

American journal of respiratory and critical care medicine, 2016-02, Vol.193 (3), p.234-236

2016

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181. Real-Time Monitoring of Transcription Factor Activity Using In Vitro and In Vivo Models of Cholestasis

Molecular therapy, 2015-05, Vol.23, p.S72-S72

2015

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In vivo bioimaging with tissue-specific transcription factor activated luciferase reporters

Scientific reports, 2015-07, Vol.5 (1), p.11842-11842, Article 11842

2015

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380. Use of Somatotransgenic Bioimaging as a Platform for Studying NFkB Pathway in a Tissue-Specific Manner in Two Mouse Models of Inflammation: Rheumatoid Arthritis and Contact Dermatitis

Molecular therapy, 2015-05, Vol.23, p.S151-S151

2015

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437. A Light-Producing Model of Infection-Related Preterm Birth

Molecular therapy, 2016-05, Vol.24, p.S173-S173

2016

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609. Transduction of the Central Nervous System with the LTR1 Lentiviral Backbone

Molecular therapy, 2016-05, Vol.24, p.S241-S241

2016

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Longitudinal in vivo bioimaging of hepatocyte transcription factor activity following cholestatic liver injury in mice

Scientific reports, 2017-02, Vol.7 (1), p.41874-41874, Article 41874

2017

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392. Evaluating Promoter Regulated Dopaminergic Neuron Targeting with AAV9 Delivered To the Neonatal Mouse

Molecular therapy, 2015-05, Vol.23, p.S155-S156

2015

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305. Generation of Light-Producing, Somatic-Transgenic Mice Using Lentivirus and Adeno-Associated Virus Vectors

Molecular therapy, 2016-05, Vol.24, p.S123-S123

2016

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Bioluminescence Monitoring of Promoter Activity In Vitro and In Vivo

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1651, p.49

2017

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134. Generation of Light-Emitting Somatic-Transgenic Mice for Disease Modelling of Hypoxic Ischaemic Encephalopathy

Molecular therapy, 2015-05, Vol.23, p.S55-S55

2015

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529. Novel LTR-1 Lentiviral Vectors Are Fully Functional Following the Removal of HIV-1 Gag-RRE Sequences

Molecular therapy, 2015-05, Vol.23, p.S212-S212

2015

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Ascending Vaginal Infection Using Bioluminescent Bacteria Evokes Intrauterine Inflammation, Preterm Birth, and Neonatal Brain Injury in Pregnant Mice

Production of lentiviral vectors using novel, enzymatically produced, linear DNA

Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease

Argininosuccinic aciduria fosters neuronal nitrosative stress reversed by Asl gene transfer

Cervical Gene Delivery of the Antimicrobial Peptide, Human β-Defensin (HBD)-3, in a Mouse Model of Ascending Infection-Related Preterm Birth

A Broad Overview and Review of CRISPR-Cas Technology and Stem Cells

Re-structuring lentiviral vectors to express genomic RNA via cap-dependent translation

A Broad Overview and Review of CRISPR-Cas Technology and Stem Cells

Foamy Virus Vectors Transduce Visceral Organs and Hippocampal Structures following In Vivo Delivery to Neonatal Mice

Genetic therapeutic advancements for Dravet Syndrome

Rapid and inexpensive purification of adenovirus vectors using an optimised aqueous two-phase technology

Gene therapy restores dopamine transporter expression and ameliorates pathology in iPSC and mouse models of infantile parkinsonism

Eliminating HIV-1 Packaging Sequences from Lentiviral Vector Proviruses Enhances Safety and Expedites Gene Transfer for Gene Therapy

Gene Therapy with Adeno-associated Virus for Cystic Fibrosis

181. Real-Time Monitoring of Transcription Factor Activity Using In Vitro and In Vivo Models of Cholestasis

In vivo bioimaging with tissue-specific transcription factor activated luciferase reporters

380. Use of Somatotransgenic Bioimaging as a Platform for Studying NFkB Pathway in a Tissue-Specific Manner in Two Mouse Models of Inflammation: Rheumatoid Arthritis and Contact Dermatitis

437. A Light-Producing Model of Infection-Related Preterm Birth

609. Transduction of the Central Nervous System with the LTR1 Lentiviral Backbone

Longitudinal in vivo bioimaging of hepatocyte transcription factor activity following cholestatic liver injury in mice

392. Evaluating Promoter Regulated Dopaminergic Neuron Targeting with AAV9 Delivered To the Neonatal Mouse

305. Generation of Light-Producing, Somatic-Transgenic Mice Using Lentivirus and Adeno-Associated Virus Vectors

Bioluminescence Monitoring of Promoter Activity In Vitro and In Vivo

134. Generation of Light-Emitting Somatic-Transgenic Mice for Disease Modelling of Hypoxic Ischaemic Encephalopathy

529. Novel LTR-1 Lentiviral Vectors Are Fully Functional Following the Removal of HIV-1 Gag-RRE Sequences

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