Clark, Adrian J. L.
Queen Mary University of London · William Harvey Research Institute
8 papers on CoChat
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
Loss of function of the melanocortin 2 receptor accessory protein 2 is associated with mammalian obesity
Asai, M., Ramachandrappa, S., Joachim, M., Shen, Y., Zhang, R., Nuthalapati, N., Ramanathan, V., Strochlic, D. E., Ferket, P., Linhart, K., et al. (2013) · Science
Regulation of Appetite and ObesityHypothalamic control of reproductive hormones
Cited by 290
- Verified
Adrenocorticotropin insensitivity syndromes
Clark, A. J. L., & Weber, A. (1998) · Endocrine Reviews
Adrenal Hormones and DisordersMetabolism and Genetic Disorders
Cited by 234
- Verified
Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency
Metherell, L. A., Naville, D., Halaby, G., Begeot, M., Huebner, A., Nürnberg, G., Nürnberg, P., Green, J., Tomlinson, J. W., Krone, N. P., et al. (2009) · The Journal of Clinical Endocrinology & Metabolism
Adrenal Hormones and DisordersSexual Differentiation and Disorders
Cited by 162
- Verified
The melanocortin receptors and their accessory proteins
Ramachandrappa, S., Gorrigan, R. J., Clark, A. J. L., & Chan, L. F. (2013) · Frontiers in Endocrinology
Receptor Mechanisms and SignalingRegulation of Appetite and Obesity
Cited by 87
- Verified
Inherited ACTH insensitivity illuminates the mechanisms of ACTH action
Clark, A. J. L., Metherell, L. A., Cheetham, M. E., & Huebner, A. (2005) · Trends in Endocrinology & Metabolism
Adrenal Hormones and DisordersReceptor Mechanisms and Signaling
Cited by 82
- 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
ACTH Antagonists
Clark, A. J., Forfar, R., Hussain, M., Jerman, J., McIver, E., Taylor, D., & Chan, L. (2016) · Frontiers in Endocrinology
Adrenal Hormones and DisordersPituitary Gland Disorders and Treatments
Cited by 49
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