Chapple, J Paul
Queen Mary University of London · William Harvey Research Institute
6 papers on CoChatORCID 0000-0003-1876-1505
Most cited papers
- Verified
Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
Metherell, L. A., Chapple, J. P., Cooray, S., David, A., Becker, C., Rüschendorf, F., Naville, D., Begeot, M., Khoo, B., Nürnberg, P., et al. (2005) · Nature Genetics
Adrenal Hormones and DisordersStress Responses and Cortisol
Cited by 437
- Verified
Deficiency of ferritin heavy-chain nuclear import in Triple A syndrome implies nuclear oxidative damage as the primary disease mechanism
Storr, H. L., Kind, B., Parfitt, D. A., Chapple, J. P., Lorenz, M., Koehler, K., Huebner, A., & Clark, A. J. L. (2009) · Molecular Endocrinology
Nuclear Structure and FunctionNeurological diseases and metabolism
Cited by 84
- Verified
The majority of adrenocorticotropin receptor (melanocortin 2 receptor) mutations found in familial glucocorticoid deficiency type 1 lead to defective trafficking of the receptor to the cell surface
Chung, T. T., Webb, T. R., Chan, L. F., Cooray, S. N., Metherell, L. A., King, P. J., Chapple, J. P., & Clark, A. J. L. (2008) · The Journal of Clinical Endocrinology & Metabolism
Adrenal Hormones and DisordersReceptor Mechanisms and Signaling
Cited by 82
- Verified
The melanocortin 2 receptor accessory protein exists as a homodimer and is essential for the function of the melanocortin 2 receptor in the mouse y1 cell line
Cooray, S. N., Almiro Do Vale, I., Leung, K.-Y., Webb, T. R., Chapple, J. P., Egertová, M., Cheetham, M. E., Elphick, M. R., & Clark, A. J. L. (2008) · Endocrinology
Receptor Mechanisms and SignalingAdrenal Hormones and Disorders
Cited by 73
- Verified
The primary cilium influences interleukin-1β-induced NFκB signalling by regulating IKK activity
Wann, A. K. T., Chapple, J. P., & Knight, M. M. (2014) · Cellular Signalling
Genetic and Kidney Cyst DiseasesNF-κB Signaling Pathways
Cited by 53
- Verified
Interleukin-1β sequesters hypoxia inducible factor 2α to the primary cilium
Wann, A. K., Thompson, C. L., Chapple, J. P., & Knight, M. M. (2013) · Cilia
Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances
Cited by 38
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