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Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria

The Journal of clinical investigation, 2011-01, Vol.121 (1), p.446-453

2011

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Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

The Journal of clinical investigation, 2008-12, Vol.118 (12), p.3881-3892

2008

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Long-Term Follow-Up of the First in Human Intravascular Delivery of AAV for Gene Transfer: AAV2-hFIX16 for Severe Hemophilia B

Molecular therapy, 2020-09, Vol.28 (9), p.2073-2082

2020

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The next wave of cellular immunotherapies in pancreatic cancer

Molecular therapy. Oncolytics, 2022-03, Vol.24, p.561-576

2022

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Cell and gene therapy manufacturing capabilities in Australia and New Zealand

Cytotherapy (Oxford, England), 2019-12, Vol.21 (12), p.1258-1273

2019

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Autologous transplantation of endothelial progenitor cells genetically modified by adeno-associated viral vector delivering insulin-like growth factor-1 gene after myocardial infarction

Human gene therapy, 2010-10, Vol.21 (10), p.1327-1334

2010

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Production, safety and efficacy of iPSC-derived mesenchymal stromal cells in acute steroid-resistant graft versus host disease: a phase I, multicenter, open-label, dose-escalation study

Nature medicine, 2020-11, Vol.26 (11), p.1720-1725

2020

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Journey to the Center of the Cell: Tracing the Path of AAV Transduction

Trends in molecular medicine, 2021-02, Vol.27 (2), p.172-184

2021

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Marketing of unproven stem cell-based interventions: A call to action

Science translational medicine, 2017-07, Vol.9 (397)

2017

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Anti-Mesothelin CAR T cell therapy for malignant mesothelioma

Biomarker research, 2021-02, Vol.9 (1), p.11-11, Article 11

2021

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Two-year safety outcomes of iPS cell-derived mesenchymal stromal cells in acute steroid-resistant graft-versus-host disease

Nature medicine, 2024-06, Vol.30 (6), p.1556-1558

2024

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Establishing a robust chimeric antigen receptor T-cell therapy program in Australia: the Royal Prince Alfred Hospital experience

Cytotherapy (Oxford, England), 2022-01, Vol.24 (1), p.45-48

2022

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Mesothelin antigen density influences anti-mesothelin chimeric antigen receptor T cell cytotoxicity

Cytotherapy (Oxford, England), 2024-04, Vol.26 (4), p.325-333

2024

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Understanding AAV vector immunogenicity: from particle to patient

Theranostics, 2024-01, Vol.14 (3), p.1260-1288

2024

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International Society for Cell & Gene Therapy Position Paper: Key considerations to support evidence-based cell and gene therapies and oppose marketing of unproven products

Cytotherapy (Oxford, England), 2023-09, Vol.25 (9), p.920-929

2023

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Splice and Dice: Intronic microRNAs, Splicing and Cancer

Biomedicines, 2021-09, Vol.9 (9), p.1268

2021

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Potential Use of Gene Transfer in Athletic Performance Enhancement

Molecular therapy, 2007-10, Vol.15 (10), p.1751-1766

2007

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Developing strategies for detection of gene doping

The journal of gene medicine, 2008-01, Vol.10 (1), p.3-20

2008

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Biodistribution of the RD114/mammalian type D retrovirus receptor, RDR

The journal of gene medicine, 2004-03, Vol.6 (3), p.249-259

2004

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Specific adeno-associated virus serotypes facilitate efficient gene transfer into human and non-human primate mesenchymal stromal cells

The journal of gene medicine, 2007-01, Vol.9 (1), p.22-32

2007

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Rapid screening for high-titer retroviral packaging cell lines using an in situ fluorescence assay

Human gene therapy, 2002-06, Vol.13 (9), p.1005-1013

2002

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Ex vivo selection for oncoretrovirally transduced green fluorescent protein-expressing CD34-enriched cells increases short-term engraftment of transduced cells in baboons

Human gene therapy, 2002-05, Vol.13 (8), p.891-899

2002

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Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

Long-Term Follow-Up of the First in Human Intravascular Delivery of AAV for Gene Transfer: AAV2-hFIX16 for Severe Hemophilia B

The next wave of cellular immunotherapies in pancreatic cancer

Cell and gene therapy manufacturing capabilities in Australia and New Zealand

Autologous transplantation of endothelial progenitor cells genetically modified by adeno-associated viral vector delivering insulin-like growth factor-1 gene after myocardial infarction

Production, safety and efficacy of iPSC-derived mesenchymal stromal cells in acute steroid-resistant graft versus host disease: a phase I, multicenter, open-label, dose-escalation study

Journey to the Center of the Cell: Tracing the Path of AAV Transduction

Marketing of unproven stem cell-based interventions: A call to action

Anti-Mesothelin CAR T cell therapy for malignant mesothelioma

Two-year safety outcomes of iPS cell-derived mesenchymal stromal cells in acute steroid-resistant graft-versus-host disease

Establishing a robust chimeric antigen receptor T-cell therapy program in Australia: the Royal Prince Alfred Hospital experience

Mesothelin antigen density influences anti-mesothelin chimeric antigen receptor T cell cytotoxicity

Understanding AAV vector immunogenicity: from particle to patient

International Society for Cell & Gene Therapy Position Paper: Key considerations to support evidence-based cell and gene therapies and oppose marketing of unproven products

Splice and Dice: Intronic microRNAs, Splicing and Cancer

Potential Use of Gene Transfer in Athletic Performance Enhancement

Developing strategies for detection of gene doping

Biodistribution of the RD114/mammalian type D retrovirus receptor, RDR

Specific adeno-associated virus serotypes facilitate efficient gene transfer into human and non-human primate mesenchymal stromal cells

Rapid screening for high-titer retroviral packaging cell lines using an in situ fluorescence assay

Ex vivo selection for oncoretrovirally transduced green fluorescent protein-expressing CD34-enriched cells increases short-term engraftment of transduced cells in baboons

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