Cyhoeddiad
2023
- Grigorieva, I., Woods, E. L., Steadman, R., Bowen, T. and Meran, S. 2023. Hyaluronan in kidney fibrosis. In: Passi, A. ed. Hyaluronan: Structure, Biology and Biotechnology., Vol. 14. Biology of Extracellular Matrix Springer, pp. 77-97., (10.1007/978-3-031-30300-5_5)
2021
- Lu, Y. et al. 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, E. L. et al. 2021. CD147 mediates the CD44s-dependent differentiation of myofibroblasts driven by transforming growth factor-β1. Journal of Biological Chemistry 297(3), article number: 100987. (10.1016/j.jbc.2021.100987)
- Lines, K. E. et al. 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)
2020
- Gaynor, K. U. et al. 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)
2019
- Grigorieva, I. V. et al. 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)
2013
- Gaynor, K. U. et al. 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)
2011
- Grigorieva, I. V. and Thakker, R. 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)
2010
- Grigorieva, I. V. et al. 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. et al. 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)
2009
- Gaynor, K. U., Grigorieva, I. V., Nesbit, M. A., Cranston, T., Gomes, T., Gortner, L. and Thakker, R. 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)
2007
- Ali, A. et al. 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)
Adrannau llyfrau
- Grigorieva, I., Woods, E. L., Steadman, R., Bowen, T. and Meran, S. 2023. Hyaluronan in kidney fibrosis. In: Passi, A. ed. Hyaluronan: Structure, Biology and Biotechnology., Vol. 14. Biology of Extracellular Matrix Springer, pp. 77-97., (10.1007/978-3-031-30300-5_5)
Erthyglau
- Lu, Y. et al. 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, E. L. et al. 2021. CD147 mediates the CD44s-dependent differentiation of myofibroblasts driven by transforming growth factor-β1. Journal of Biological Chemistry 297(3), article number: 100987. (10.1016/j.jbc.2021.100987)
- Lines, K. E. et al. 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, K. U. et al. 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, I. V. et al. 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, K. U. et al. 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, I. V. and Thakker, R. 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, I. V. et al. 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. et al. 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, K. U., Grigorieva, I. V., Nesbit, M. A., Cranston, T., Gomes, T., Gortner, L. and Thakker, R. 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. et al. 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)