Dr Charles Bailey
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Research Fellow
C39 - Royal Prince Alfred Hospital |
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Publications
2008
Bröer, S., Bailey, C., Kowalczuk, S., Ng, C., Vanslambrouck, J., Rodgers, H., Auray-Blais, C., Cavanaugh, J., Bröer, A., Rasko, J. Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. Journal of Clinical Investigation. 2008; 0:0. [Abstract]
2007
Horan, K., Watanabe, K., Kong, A., Bailey, C., Rasko, J., Sasaki, T., Mitchell, C. Regulation of FcgammaR-stimulated phagocytosis by the 72-kDa inositol polyphosphate 5-phosphatase: SHIP1, but not the 72-kDa 5-phosphatase, regulates complement receptor 3 mediated phagocytosis by differential recruitment of these 5-phosphatases to the phagocytic cup. Blood. 2007; 110:4480-4491. [Abstract]
Azmanov, D., Rodgers, H., Auray-Blais, C., Giguère, R., Bailey, C., Bröer, S., Rasko, J., Cavanaugh, J. Persistence of the common Hartnup disease D173N allele in populations of European origin. Annals of human genetics. 2007; 71:755-761. [Abstract]
2006
Tsoutsman, T., Chung, J., Doolan, A., Nguyen, L., Williams, I., Tu, E., Lam, L., Bailey, C., Rasko, J., Allen, D., Semsarian, C. Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathy. Journal of molecular and cellular cardiology. 2006; 41:623-32. [Abstract]