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Insititute of Infection Immunity and Inflammation
Papalazarou, V., Drew, J., Juin, A., Spence, H. J., Whitelaw, J., Nixon, C., Salmeron-Sanchez, M. and Machesky, L. M. (2022) Collagen VI expression is negatively mechanosensitive in pancreatic cancer cells and supports the metastatic niche. Journal of Cell Science, 135(24), jcs259978. (doi: 10.1242/jcs.259978)
Zickus, V. et al. (2020) Fluorescence lifetime imaging with a megapixel SPAD camera and neural network lifetime estimation. Scientific Reports, 10, 20986. (doi: 10.1038/s41598-020-77737-0) (PMID:33268900) (PMCID:PMC7710711)
Del Rosario, M. et al. (2019) Apicomplexan F-actin is required for efficient nuclear entry during host cell invasion. EMBO Reports, 20(12), e48896. (doi: 10.15252/embr.201948896) (PMID:31584242) (PMCID:PMC6893294)
Fort, L. et al. (2018) Fam49/CYRI interacts with Rac1 and locally suppresses protrusions. Nature Cell Biology, 20(10), pp. 1159-1171. (doi: 10.1038/s41556-018-0198-9) (PMID:30250061) (PMCID:PMC6863750)
Gras, S., Jackson, A., Woods, S., Pall, G., Whitelaw, J., Leung, J. M., Ward, G. E., Roberts, C. W. and Meissner, M. (2017) Parasites lacking the micronemal protein MIC2 are deficient in surface attachment and host cell egress, but remain virulent in vivo. Wellcome Open Research, 2, 32. (doi: 10.12688/wellcomeopenres.11594.2) (PMID:28630943) (PMCID:PMC5473411)
Periz, J. et al. (2017) Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation. eLife, 6, e24119. (doi: 10.7554/eLife.24119) (PMID:28322189) (PMCID:PMC5375643)
Whitelaw, J. A. et al. (2017) Surface attachment, promoted by the actomyosin system of Toxoplasma gondii is important for efficient gliding motility and invasion. BMC Biology, 15, 1. (doi: 10.1186/s12915-016-0343-5) (PMID:28100223) (PMCID:PMC5242020)
Papalazarou, V., Drew, J., Juin, A., Spence, H. J., Whitelaw, J., Nixon, C., Salmeron-Sanchez, M. and Machesky, L. M. (2022) Collagen VI expression is negatively mechanosensitive in pancreatic cancer cells and supports the metastatic niche. Journal of Cell Science, 135(24), jcs259978. (doi: 10.1242/jcs.259978)
Zickus, V. et al. (2020) Fluorescence lifetime imaging with a megapixel SPAD camera and neural network lifetime estimation. Scientific Reports, 10, 20986. (doi: 10.1038/s41598-020-77737-0) (PMID:33268900) (PMCID:PMC7710711)
Del Rosario, M. et al. (2019) Apicomplexan F-actin is required for efficient nuclear entry during host cell invasion. EMBO Reports, 20(12), e48896. (doi: 10.15252/embr.201948896) (PMID:31584242) (PMCID:PMC6893294)
Fort, L. et al. (2018) Fam49/CYRI interacts with Rac1 and locally suppresses protrusions. Nature Cell Biology, 20(10), pp. 1159-1171. (doi: 10.1038/s41556-018-0198-9) (PMID:30250061) (PMCID:PMC6863750)
Gras, S., Jackson, A., Woods, S., Pall, G., Whitelaw, J., Leung, J. M., Ward, G. E., Roberts, C. W. and Meissner, M. (2017) Parasites lacking the micronemal protein MIC2 are deficient in surface attachment and host cell egress, but remain virulent in vivo. Wellcome Open Research, 2, 32. (doi: 10.12688/wellcomeopenres.11594.2) (PMID:28630943) (PMCID:PMC5473411)
Periz, J. et al. (2017) Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation. eLife, 6, e24119. (doi: 10.7554/eLife.24119) (PMID:28322189) (PMCID:PMC5375643)
Whitelaw, J. A. et al. (2017) Surface attachment, promoted by the actomyosin system of Toxoplasma gondii is important for efficient gliding motility and invasion. BMC Biology, 15, 1. (doi: 10.1186/s12915-016-0343-5) (PMID:28100223) (PMCID:PMC5242020)
Nikolaou, S. , Juin, A., Whitelaw, J., Paul, N., Fort, L., Nixon, C., Spence, H., Bryson, S. and Machesky, L. (2022) CYRI-B mediated macropinocytosis drives metastasis via lysophosphatidic acid receptor uptake. [Data Collection]