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Dr Amanda Kijas
Dr

Amanda Kijas

Email: 
Phone: 
+61 7 334 64178

Overview

Background

I am a passionate research scientist who joined Professor Alan Rowans group in 2017 to develop novel wound management agents and investigate the interface between material science and cellular responses. These projects focus on studying cellular responses within 3D matrices of defined properties where we can investigate the role of biophysical and biochemical interactions in real time and with applied mechanical force using a confocal rheometer. Extracellular matrices are a large focus, acting as dynamic platforms not only providing a physical scaffold with defined mechanical properties but also act as a repository for biochemical based signalling molecules and interaction domains, orchestrating biological responses. Matrices composed of synthetic or naturally derived material, offer different and overlapping array of advantageous in the context of cell behaviour. We are exploring both types in isolation and as composite and hybrid materials to tailor the biophysical aspects to the specific applications. By combining these matrices with bioactive components we are empowering the materials to bring about the biochemical responses in defined ways, enabling the investigation of both fundamental biological processes as well as development of clinically relevant agents.

Availability

Dr Amanda Kijas is:
Available for supervision

Qualifications

  • Bachelor (Honours), Flinders University
  • Doctor of Philosophy, Uppsala University

Works

Search Professor Amanda Kijas’s works on UQ eSpace

34 works between 1998 and 2024

21 - 34 of 34 works

2009

Journal Article

Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder.

Waltes, R, Kalb, R, Gatei, M, Kijas, AW, Stumm, M, Sobeck, A, Wieland, B, Varon, R, Lerenthal Y, Lavin, Martin F., Schindler, D and Dörk, T (2009). Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder.. American Journal of Human Genetics, 84 (5), 605-616. doi: 10.1016/j.ajhg.2009.04.010

Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder.

2007

Journal Article

A subgroup of spinocerebellar ataxias defective in DNA damage responses

Gueven, N., Chen, P., Nakamura, J., Becherel, O.J., Kijas, A.W., Grattan-Smith, P. and Lavin, M.F. (2007). A subgroup of spinocerebellar ataxias defective in DNA damage responses. Neuroscience, 145 (4), 1418-1425. doi: 10.1016/j.neuroscience.2006.12.010

A subgroup of spinocerebellar ataxias defective in DNA damage responses

2006

Journal Article

Aprataxin forms a discrete branch in the HIT (Histidine Triad) superfamily of proteins with both DNA/RNA binding and nucleotide hydrolase activities

Kijas, Amanda W., Harris, Janelle L., Harris, Jonathan M. and Lavin, Martin F. (2006). Aprataxin forms a discrete branch in the HIT (Histidine Triad) superfamily of proteins with both DNA/RNA binding and nucleotide hydrolase activities. Journal of Biological Chemistry, 281 (20), 13939-13948. doi: 10.1074/jbc.M507946200

Aprataxin forms a discrete branch in the HIT (Histidine Triad) superfamily of proteins with both DNA/RNA binding and nucleotide hydrolase activities

2003

Journal Article

msh2 separation of function mutations confer defects in the initiation steps of mismatch repair

Kijas, Amanda Wraith, Studamire, Barbara and Alani, Eric (2003). msh2 separation of function mutations confer defects in the initiation steps of mismatch repair. Journal of Molecular Biology, 331 (1), 123-138. doi: 10.1016/S0022-2836(03)00694-6

msh2 separation of function mutations confer defects in the initiation steps of mismatch repair

2003

Journal Article

Crystal structure and biochemical analysis of the MutS dot ADP dot beryllium fluoride complex suggests a conserved mechanism for ATP interactions in mismatch repair

Alani, Eric, Lee, Jae Young, Schofield, Mark J., Kijas, Amanda W., Hsieh, Peggy and Yang, Wei (2003). Crystal structure and biochemical analysis of the MutS dot ADP dot beryllium fluoride complex suggests a conserved mechanism for ATP interactions in mismatch repair. Journal of Biological Chemistry, 278 (18), 16088-16094. doi: 10.1074/jbc.M213193200

Crystal structure and biochemical analysis of the MutS dot ADP dot beryllium fluoride complex suggests a conserved mechanism for ATP interactions in mismatch repair

2003

Journal Article

Systematic mutagenesis of the Saccharomyces cerevisiae MLH1 gene reveals distinct roles for Mlh1p in meiotic crossing over and in vegetative and meiotic mismatch repair

Argueso, Juan Lucas, Kijas, Amanda Wraith, Sarin, Sumeet, Heck, Julie, Waase, Marc and Alani, Eric (2003). Systematic mutagenesis of the Saccharomyces cerevisiae MLH1 gene reveals distinct roles for Mlh1p in meiotic crossing over and in vegetative and meiotic mismatch repair. Molecular and Cellular Biology, 23 (3), 873-886. doi: 10.1128/MCB.23.3.873-886.2003

Systematic mutagenesis of the Saccharomyces cerevisiae MLH1 gene reveals distinct roles for Mlh1p in meiotic crossing over and in vegetative and meiotic mismatch repair

2001

Journal Article

Origins of the many NPY-family receptors in mammals

Larhammar, Dan, Wraith, Amanda, Berglund, Magnus M., Holmberg, Sara K. S. and Lundell, Ingrid (2001). Origins of the many NPY-family receptors in mammals. Peptides, 22 (3), 295-307. doi: 10.1016/S0196-9781(01)00331-X

Origins of the many NPY-family receptors in mammals

2000

Journal Article

Zebrafish genes for neuropeptide Y and peptide YY reveal origin by chromosome duplication from an ancestral gene linked to the homeobox cluster

Söderberg, Charlotte, Wraith, Amanda, Ringvall, Maria, Yan, Yi-Lin, Postlethwait, John H., Brodin, Lennart and Larhammar, Dan (2000). Zebrafish genes for neuropeptide Y and peptide YY reveal origin by chromosome duplication from an ancestral gene linked to the homeobox cluster. Journal of Neurochemistry, 75 (3), 908-918. doi: 10.1046/j.1471-4159.2000.0750908.x

Zebrafish genes for neuropeptide Y and peptide YY reveal origin by chromosome duplication from an ancestral gene linked to the homeobox cluster

2000

Journal Article

Evolution of the neuropeptide Y receptor family: gene and chromosome duplications deduced from the cloning and mapping of the five receptor subtype genes in pig

Wraith, Amanda, Törnsten, Anna, Chardon, Patrick, Harbitz, Ingrid, Chowdhary, Bhanu P., Andersson, Leif, Lundin, Lars-Gustav and Larhammar, Dan (2000). Evolution of the neuropeptide Y receptor family: gene and chromosome duplications deduced from the cloning and mapping of the five receptor subtype genes in pig. Genome Research, 10 (3), 302-310. doi: 10.1101/gr.10.3.302

Evolution of the neuropeptide Y receptor family: gene and chromosome duplications deduced from the cloning and mapping of the five receptor subtype genes in pig

1999

Journal Article

Characterization of the cloned Atlantic cod neuropeptide Y-Yb receptor: peptide-binding requirements distinct from known mammalian Y receptors

Sharma, Parul, Arvidsson, Ann-Kristin, Wraith, Amanda, Beck-Sickinger, Annette G., Jönsson-Rylander, Ann-Cathrine and Larhammar, Dan (1999). Characterization of the cloned Atlantic cod neuropeptide Y-Yb receptor: peptide-binding requirements distinct from known mammalian Y receptors. General and Comparative Endocrinology, 115 (3), 422-428. doi: 10.1006/gcen.1999.7332

Characterization of the cloned Atlantic cod neuropeptide Y-Yb receptor: peptide-binding requirements distinct from known mammalian Y receptors

1999

Journal Article

Neuropeptide Y receptor subtype with unique properties cloned in the zebrafish: the zYa receptor

Starbäck, P., Lundell, I., Fredriksson, R., Berglund, M. M., Yan, Y. L., Wraith, A., Söderberg, C., Postlethwait, J. H. and Larhammar, D. (1999). Neuropeptide Y receptor subtype with unique properties cloned in the zebrafish: the zYa receptor. Molecular Brain Research, 70 (2), 242-252. doi: 10.1016/S0169-328X(99)00152-7

Neuropeptide Y receptor subtype with unique properties cloned in the zebrafish: the zYa receptor

1998

Journal Article

Cloning of a neuropeptide Y/peptide YY receptor from the Atlantic cod: the Yb receptor

Arvidsson, Ann-Kristin, Wraith, Amanda, Jönsson-Rylander, Ann-Cathrine and Larhammar, Dan (1998). Cloning of a neuropeptide Y/peptide YY receptor from the Atlantic cod: the Yb receptor. Regulatory Peptides, 75-76, 39-43. doi: 10.1016/S0167-0115(98)00051-2

Cloning of a neuropeptide Y/peptide YY receptor from the Atlantic cod: the Yb receptor

1998

Journal Article

Neutrophils induce damage to respiratory epithelial cells infected with respiratory syncytial virus.

Wang, S. Z., Xu, H., Wraith, A., Bowden, J. J., Alpers, J. H. and Forsyth, K. D. (1998). Neutrophils induce damage to respiratory epithelial cells infected with respiratory syncytial virus.. European Respiratory Journal, 12 (3), 612-618. doi: 10.1183/09031936.98.12030612

Neutrophils induce damage to respiratory epithelial cells infected with respiratory syncytial virus.

1998

Journal Article

FISH mapping of the porcine NPY5 gene to chromosome 8p11

Törnsten, A., Wraith, A., Larhammar, D. and Chowdhary, B. P. (1998). FISH mapping of the porcine NPY5 gene to chromosome 8p11. Mammalian Genome, 9 (3), 262-263. doi: 10.1007/s003359900742

FISH mapping of the porcine NPY5 gene to chromosome 8p11

Funding

Current funding

  • 2024 - 2027
    Motor Accident Insurance Commission Research Fellowship
    Motor Accident Insurance Commission
    Open grant
  • 2023 - 2025
    Venom driven wound healing
    Metro North Hospital and Health Service
    Open grant
  • 2023 - 2025
    Unveiling the modulators of scarless wound healing
    NHMRC IDEAS Grants
    Open grant
  • 2022 - 2026
    Expediting wound repair for burns and trauma patients with biomaterials conducive to issue driven repair.
    Metro North Hospital and Health Service
    Open grant

Past funding

  • 2023 - 2024
    Biobandage CUREator
    UniQuest Pty Ltd
    Open grant

Supervision

Availability

Dr Amanda Kijas is:
Available for supervision

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Supervision history

Current supervision

Completed supervision

Media

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