CH
Claus Hallwirth
Children's Medical Research Institute, Victor Chang Cardiac Research Institute, University of KwaZulu-Natal - Pietermaritzburg Campus, University of KwaZulu-Natal, Molecular Diagnostic Services
Research areas: Biochemistry, Genetics and Molecular Biology · Molecular Biology · Virus-based gene therapy research · RNA Interference and Gene Delivery · CRISPR and Genetic Engineering
Employment
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Children's Medical Research Institute Senior Research Officer2009 - Present
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Victor Chang Cardiac Research Institute Post-doctoral scientist2006 - 2009
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Molecular Diagnostic Services Molecular biological research scientist2005 - 2006
Education
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University of KwaZulu-Natal - Pietermaritzburg Campus B.Sc.Agric1994 - 1997
- ? - 2008
Projects & Funding
Projects & funding information is unavailable.
Publications (14)
- Restoring the natural tropism of AAV2 vectors for human liver Save
- Efficient in vivo editing of OTC-deficient patient-derived primary human hepatocytes Save
- Codon-Optimization of Wild-Type Adeno-Associated Virus Capsid Sequences Enhances DNA Family Shuffling while Conserving Functionality. Save
- Identification of liver-specific enhancer-promoter activity in the 3' untranslated region of the wild-type AAV2 genome. Save
- Ub-ISAP: a streamlined UNIX pipeline for mining unique viral vector integration sites from next generation sequencing data. Save
- Limiting Thymic Precursor Supply Increases the Risk of Lymphoid Malignancy in Murine X-Linked Severe Combined Immunodeficiency. Save
- Germline viral "fossils" guide in silico reconstruction of a mid-Cenozoic era marsupial adeno-associated virus. Save
- Modeling correction of severe urea cycle defects in the growing murine liver using a hybrid recombinant adeno-associated virus/piggyBac transposase gene delivery system. Save
- Coherence analysis discriminates between retroviral integration patterns in CD34(+) cells transduced under differing clinical trial conditions. Save
- Probing the closed-loop model of mRNA translation in living cells. Save
- Impact of next-generation sequencing error on analysis of barcoded plasmid libraries of known complexity and sequence. Save
- A Moloney murine leukemia virus driven by the Jaagsiekte sheep retrovirus enhancers shows enhanced specificity for infectivity in lung epithelial cells. Save
- Variable regions 1 and 2 (VR1 and VR2) in JSRV gag are not responsible for the endogenous JSRV particle release defect. Save
- Molecular cloning and functional analysis of three type D endogenous retroviruses of sheep reveal a different cell tropism from that of the highly related exogenous jaagsiekte sheep retrovirus. Save