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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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The Future of SCN1A Gene-targeting Research for the Treatment of Dravet Syndrome

US neurology, 2023, Vol.19 (2), p.1

Karda, Rajvinder

2023

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Generation of light-producing somatic-transgenic mice using adeno-associated virus vectors

Scientific reports, 2020-02, Vol.10 (1), p.2121-2121, Article 2121

2020

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Continual conscious bioluminescent imaging in freely moving somatotransgenic mice

Scientific reports, 2017-07, Vol.7 (1), p.6374-13, Article 6374

2017

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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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Creation of de novo cryptic splicing for ALS and FTD precision medicine

Science (American Association for the Advancement of Science), 2024-10, Vol.386 (6717), p.61-69

2024

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

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

2016

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Gene transfer to the neonatal cns

Karda, Rajvinder

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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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

The Future of SCN1A Gene-targeting Research for the Treatment of Dravet Syndrome

Generation of light-producing somatic-transgenic mice using adeno-associated virus vectors

Continual conscious bioluminescent imaging in freely moving somatotransgenic mice

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

Creation of de novo cryptic splicing for ALS and FTD precision medicine

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

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

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

Gene transfer to the neonatal cns

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

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