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Number of items: 14.

Lu, Yueh-An, Smith, Tanya, Deshpande, Sumukh, Liao, Chia-Te, Talabani, Bnar, Grigorieva, Irina, Mason, Anna, Andrews, Robert, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Taylor, Philip R. ORCID: https://orcid.org/0000-0003-0163-1421 and Fraser, Donald ORCID: https://orcid.org/0000-0003-0102-9342 2024. Sex-specific proximal tubular cell differentiation pathways identified by single-nucleus RNA sequencing. Scientific Reports 14 (1) , 24041. 10.1038/s41598-024-73102-7
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Brown, Charlotte V. M., Pino-Chavez, Gilda, Zaidi, Aeliya, Grigorieva, Irina, Woods, Emma, Steadman, Robert ORCID: https://orcid.org/0000-0002-1303-2496, Chavez, Rafael, Meran, Soma ORCID: https://orcid.org/0000-0003-3408-3978 and Khalid, Usman 2024. Protective effect of ischaemic preconditioning on acute and chronic renal damage following ischaemia reperfusion injury: characterisation of fibrosis development after inflammation resolution. International Journal of Clinical and Experimental Pathology 17 (4) , pp. 151-164. 10.62347/MFJG1164
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Grigorieva, Irina, Woods, Emma L., Steadman, Robert ORCID: https://orcid.org/0000-0002-1303-2496, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435 and Meran, Soma ORCID: https://orcid.org/0000-0003-3408-3978 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: https://orcid.org/0000-0002-5375-5533, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Andrews, Robert, Taylor, Philip R. ORCID: https://orcid.org/0000-0003-0163-1421 and Fraser, Donald ORCID: https://orcid.org/0000-0003-0102-9342 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
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Woods, Emma L., Grigorieva, Irina V., Midgley, Adam C., Brown, Charlotte V.M., Lu, Yueh-an, Phillips, Aled O. ORCID: https://orcid.org/0000-0001-9744-7113, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Meran, Soma ORCID: https://orcid.org/0000-0003-3408-3978 and Steadman, Robert ORCID: https://orcid.org/0000-0002-1303-2496 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
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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
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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
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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 Sat Nov 23 07:43:48 2024 GMT.


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