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Robert A. Kaiser

Mayo Clinic

14

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48

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Development of a porcine model of phenylketonuria with a humanized R408W mutation for gene editing

2021 PLOS ONE
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Use of an AAV serotype Anc80 to provide durable cure of phenylketonuria in a mouse model.

2021 Journal of Inherited Metabolic Disease
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Comparison of BNT162b2 (Pfizer-BioNtech) and mRNA-1273 (Moderna) SARS-CoV-2 mRNA vaccine immunogenicity in dialysis patients.

2021 Kidney International
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In vivo lentiviral vector gene therapy to cure hereditary tyrosinemia type 1 and prevent development of precancerous and cancerous lesions

2021 bioRxiv
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Comparison of BNT162b2 (BioNTech/Pfizer) and mRNA-1273 (Moderna) SARS-CoV-2 mRNA vaccine immunogenicity in dialysis patients.

2021 Kidney International
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The future of gene-targeted therapy for hereditary tyrosinemia type 1 as a lead indication among the inborn errors of metabolism

2020 Expert opinion on orphan drugs
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Ex vivo cell therapy by ectopic hepatocyte transplantation treats the porcine tyrosinemia model of acute liver failure

2020 Molecular therapy. Methods & clinical development
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Ectopic hepatocyte transplantation cures the pig model of tyrosinemia

2019
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Ectopic hepatocyte transplantation cures the pig model of tyrosinemia

2019 bioRxiv
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Lentiviral Vector-mediated Gene Therapy of Hepatocytes Ex Vivo for Autologous Transplantation in Swine

2018 Journal of Visualized Experiments
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