Dr Cherie Stayner

Bowden, S. A., Rodger, E. J., Bates, M., Chatterjee, A., Eccles, M. R., & Stayner, C. (2018). Genome-scale single nucleotide resolution analysis of DNA methylation in human autosomal dominant polycystic kidney disease. American Journal of Nephrology, 48(6), 415-424. doi: 10.1159/000494739 Journal - Research Article

Kaur, G., Li, C. G., Chantry, A., Stayner, C., Horsfield, J., & Eccles, M. R. (2018). SMAD proteins directly suppress PAX2 transcription downstream of transforming growth factor-beta 1 (TGF-β1) signalling in renal cell carcinoma. Oncotarget, 9(42), 26852-26867. doi: 10.18632/oncotarget.25516 Journal - Research Article

de Bruin, W. E., Stayner, C., de Lange, M., & Taylor, R. W. (2018). Who are the key players involved with shaping public opinion and policies on obesity and diabetes in New Zealand? Nutrients, 10(11), 1592. doi: 10.3390/nu10111592 Journal - Research Article

Stayner, C., Poole, C. A., McGlashan, S. R., Pilanthananond, M., Brauning, R., Markie, D., … Slobbe, L., … Parker, K., Wiles, A., … Leichter, A., Leask, M., … Jennings, M., Horsfield, J. A., Walker, R. J., & Eccles, M. R. (2017). An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutations. Scientific Reports, 7, 1601. doi: 10.1038/s41598-017-01519-4 Journal - Research Article

Pinnapureddy, A. R., Stayner, C., McEwan, J., Baddeley, O., Forman, J., & Eccles, M. R. (2015). Large animal models of rare genetic disorders: Sheep as phenotypically relevant models of human genetic disease. Orphanet Journal of Rare Diseases, 10, 107. doi: 10.1186/s13023-015-0327-5 Journal - Research Article

Stayner, C., & Davidson, A. J. (2015). Report on the 2nd Asia-Pacific Kidney Development Workshop. Nephrology, 20(7), 443. doi: 10.1111/nep.12516 Journal - Professional & Other Non-Research Articles

Eccles, M. R., & Stayner, C. A. (2014). Polycystic kidney disease: Where gene dosage counts. F1000Prime Reports, 6, 24. doi: 10.12703/p6-24 Journal - Research Article

Stayner, C., Shields, J., Slobbe, L., Shillingford, J. M., Weimbs, T., & Eccles, M. R. (2012). Rapamycin-mediated suppression of renal cyst expansion in del34 Pkd1^-/- mutant mouse embryos: An investigation of the feasibility of renal cyst prevention in the foetus. Nephrology, 17(8), 739-747. doi: 10.1111/j.1440-1797.2012.01639.x Journal - Research Article

Ineson, J., Stayner, C., Hazlett, J., Slobbe, L., Robson, E., Legge, M., & Eccles, M. R. (2012). Somatic reactivation of expression of the silent maternal Mest allele and acquisition of normal reproductive behaviour in a colony of Peg1/Mest mutant mice. Journal of Reproduction & Development, 58(4), 490-500. Journal - Research Article

Stayner, C., Iglesias, D. M., Goodyer, P. R., Ellis, L., Germino, G., Zhou, J., & Eccles, M. R. (2006). Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease. Human Molecular Genetics, 15(24), 3520-3528. Journal - Research Article

Stayner, C., Lett, B., Slobbe, L., Wiles, A., Markie, D., McEwan, J., … Walker, R. J., Poole, C. A., & Eccles, M. (2011, September). Novel missense mutations in an ovine model of Meckel-Gruber Syndrome. Verbal presentation at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand. Conference Contribution - Verbal presentation and other Conference outputs

Stayner, C., Shields, J., Shillingford, J. M., Weimbs, T., & Eccles, M. R. (2010, November-December). Rapamycin treatment suppresses renal cyst formation in PKD1^-/- embryos. Verbal presentation at the Medical Sciences Congress: A New Decade of Discovery (MedSciNZ), Queenstown, New Zealand. Conference Contribution - Verbal presentation and other Conference outputs

Poole, C. A., Stayner, C., McGlashan, S. R., Parker, K., Wiles, A., Jennings, M., … Johnstone, A. C., Walker, R. J., & Eccles, M. R. (2011, June-July). Primary cilia defects in an ovine model of Meckel Gruber syndrome. Poster session presented at the FASEB Summer Research Conference: Polycystic Kidney Disease: From Bench to Bedside, Saxtons River, Vermont. Conference Contribution - Poster Presentation (not in published proceedings)

Stayner, C., Shields, J., Ellis, L., Goodyer, P., Germino, G., Zhou, J., & Eccles, M. (2008, August-September). The role of PAX2 in polycystic kidney disease. Verbal presentation at the Queenstown Molecular Biology Meetings, Queenstown, New Zealand. Conference Contribution - Verbal presentation and other Conference outputs

Lett, B., Stayner, C., Mahon, C., Markie, D., McEwan, J., & Eccles, M. R. (2009). Searching for a mutation in the Meckel-Gruber syndrome gene, TMEM67, in a sheep model of autosomal recessive polycystic kidney disease. Proceedings of the ComBio2009 Conference. [CD-ROM] [Abstract] Conference Contribution - Published proceedings: Abstract

Wiles, A., Lett, B., Stayner, C., Slobbe, L., Markie, D., McEwan, J., Johnstone, A. C., Walker, R. J., Poole, C. A., & Eccles, M. (2011, June-July). A large animal ciliopathy: Genetic characterization of an ovine model of Meckel-Gruber syndrome. Poster session presented at the FASEB Summer Research Conference: Polycystic Kidney Disease: From Bench to Bedside, Saxtons River, Vermont. Conference Contribution - Poster Presentation (not in published proceedings)

Eccles, M. R., Lett, B., Stayner, C., Wiles, A., Slobbe, L., Parker, K., Johnstone, A. C., Walker, R. J., … Markie, D. (2011, October). Genetic and phenotypic characterization of an ovine large animal model of the MKS/JBTS/NPHP ciliopathy, Meckel-Gruber syndrome. Poster session presented at the 12th International Congress of Human Genetics (ICHG) and 61st Annual Meeting of the American Society of Human Genetics (ASHG), Montreal, Canada. Conference Contribution - Poster Presentation (not in published proceedings)

Poole, C. A., McGlashan, S. R., Jensen, C. G., Eccles, M. R., Lett, B., Stayner, C., Johnstone, A. C., Jennings, M., Wiles, A., & Walker, R. J. (2010, July). Primary cilia defects on an ovine model of Meckel-Gruber Syndrome. Poster session presented at the FASEB Summer Research Conference: The Biology of Cilia and Flagella, Saxtons River, Vermont. Conference Contribution - Poster Presentation (not in published proceedings)

Sun, Y., Zhou, J., Stayner, C., Munasinghe, J., Shen, X., Beier, D. R., & Albert, M. S. (2002). Magnetic resonance imaging assessment of a murine model of recessive polycystic kidney disease. Comparative Medicine, 52(5), 433-438. Journal - Research Article

Basora, N., Nomura, H., Berger, U. V., Stayner, C.-A. K., Guo, L., Shen, X., & Zhou, J. (2002). Tissue and cellular localization of a novel polycystic kidney disease-like gene product, polycystin-L. Journal of the American Society of Nephrology, 13, 293-301. Journal - Research Article

Stayner, C.-A. K., & Zhou, J. (2001). Polycystin channels and kidney disease. Trends in Pharmacological Sciences, 22(11), 543-546. Journal - Research Article

Stayner, C. K., Cunliffe, H. E., Ward, T. A., & Eccles, M. R. (1998). Cloning and characterization of the human PAX2 promoter. Journal of Biological Chemistry, 273(39), 25472-25479. Journal - Research Article