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Number of items: 12.

Grigorieva, Irina, Woods, Emma L., Steadman, Robert ORCID:, Bowen, Timothy ORCID: and Meran, Soma ORCID: 2023. Hyaluronan in kidney fibrosis. Passi, Alberto, ed. Hyaluronan: Structure, Biology and Biotechnology, Vol. 14. Biology of Extracellular Matrix, Springer, pp. 77-97. (10.1007/978-3-031-30300-5_5)

Lu, Yueh-An, Liao, Chia-Te, Raybould, Rachel, Talabani, Bnar, Grigorieva, Irina, Szomolay, Barbara ORCID:, Bowen, Timothy ORCID:, Andrews, Robert, Taylor, Philip R. ORCID: and Fraser, Donald ORCID: 2021. Single-nucleus RNA sequencing identifies new classes of proximal tubular epithelial cells in kidney fibrosis. Journal of the American Society of Nephrology 32 (10) , pp. 2501-2516. 10.1681/ASN.2020081143

Woods, Emma L., Grigorieva, Irina V., Midgley, Adam C., Brown, Charlotte V.M., Lu, Yueh-an, Phillips, Aled O. ORCID:, Bowen, Timothy ORCID:, Meran, Soma ORCID: and Steadman, Robert ORCID: 2021. CD147 mediates the CD44s-dependent differentiation of myofibroblasts driven by transforming growth factor-β1. Journal of Biological Chemistry 297 (3) , 100987. 10.1016/j.jbc.2021.100987

Lines, K. E., Stevenson, M., Mihai, R., Grigorieva, Irina V., Shariq, O. A., Gaynor, K. U., Jeyabalan, J., Javid, M. and Thakker, R. V. 2021. Hypoxia stimulates angiogenesis and a metabolic switch in human parathyroid adenoma cells. Endocrine Oncology 1 (1) , pp. 23-32. 10.1530/EO-21-0014

Gaynor, Katherine U., Grigorieva, Irina V., Mirczuk, Samantha M., Piret, Sian E., Kooblall, Kreepa G., Stevenson, Mark, Rizzoti, Karine, Bowl, Michael R., Nesbit, M. Andrew, Christie, Paul T., Fraser, William D., Hough, Tertius, Whyte, Michael P., Lovell-Badge, Robin and Thakker, Rajesh V. 2020. Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism. Endocrine Connections 9 (2) , pp. 173-186. 10.1530/EC-19-0478

Grigorieva, Irina V., Oszwald, Andre, Grigorieva, Elena F., Schachner, Helga, Neudert, Barbara, Ostendorf, Tammo, Floege, Jürgen, Lindenmeyer, Maja T., Cohen, Clemens D., Panzer, Ulf, Aigner, Christof, Schmidt, Alice, Grosveld, Frank, Thakker, Rajesh V., Rees, Andrew Jackson and Kain, Renate 2019. A novel role for GATA3 in mesangial cells in glomerular development and injury. Journal of the American Society of Nephrology 30 (9) , pp. 1641-1658. 10.1681/ASN.2018111143

Gaynor, Katherine U., Grigorieva, Irina V., Allen, Michael D., Esapa, Christopher T., Head, Rosemary A., Gopinath, Preethi, Christie, Paul T., Nesbit, M. Andrew, Jones, J. Louise and Thakker, Rajesh V. 2013. GATA3 mutations found in breast cancers may be associated with aberrant nuclear localization, reduced transactivation and cell invasiveness. Hormones and Cancer 4 (3) , pp. 123-139. 10.1007/s12672-013-0138-x

Grigorieva, Irina V. and Thakker, Rajesh V. 2011. Transcription factors in parathyroid development: lessons from hypoparathyroid disorders. Annals of the New York Academy of Sciences 1237 (1) , pp. 24-38. 10.1111/j.1749-6632.2011.06221.x

Grigorieva, Irina V., Mirczuk, Samantha, Gaynor, Katherine U., Nesbit, M. Andrew, Grigorieva, Elena F., Wei, Qiaozhi, Ali, Asif, Fairclough, Rebecca J., Stacey, Joanna M., Stechman, Michael J., Mihai, Radu, Kurek, Dorota, Fraser, William D., Hough, Tertius, Condie, Brian G., Manley, Nancy, Grosveld, Frank and Thakker, Rajesh V. 2010. Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2. Journal of Clinical Investigation 120 (6) , pp. 2144-2155. 10.1172/JCI42021

Bowl, M. R., Mirczuk, S. M., Grigorieva, I. V., Piret, S. E., Cranston, T., Southam, L., Allgrove, J., Bahl, S., Brain, C., Loughlin, J., Mughal, Z., Ryan, F., Shaw, N., Thakker, Y. V., Tiosano, D., Nesbit, M. A. and Thakker, R. V. 2010. Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism. Human Molecular Genetics 19 (10) , pp. 2028-2038. 10.1093/hmg/ddq084

Gaynor, Katherine U., Grigorieva, Irina V., Nesbit, M. Andrew, Cranston, Treena, Gomes, Thushari, Gortner, Ludwig and Thakker, Rajesh V. 2009. A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome. Journal of Clinical Endocrinology and Metabolism 94 (10) , pp. 3897-3904. 10.1210/jc.2009-0717

Ali, A., Christie, P. T., Grigorieva, I. V., Harding, B., Van Esch, H., Ahmed, S. F., Bitner-Glindzicz, M., Blind, E., Bloch, C., Christin, P., Clayton, P., Gecz, J., Gilbert-Dussardier, B., Guillen-Navarro, E., Hackett, A., Halac, I., Hendy, G. N., Lalloo, F., Mache, C. J., Mughal, Z., Ong, A. C.M., Rinat, C., Shaw, N., Smithson, S. F., Tolmie, J., Weill, J., Nesbit, M. A. and Thakker, R. V. 2007. Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor. Human Molecular Genetics 16 (3) , pp. 265-275. 10.1093/hmg/ddl454

This list was generated on Mon Jul 22 12:29:07 2024 BST.