Deficiency of ALADIN Impairs Redox Homeostasis in Human Adrenal Cells and Inhibits Steroidogenesis

por Prasad, R., Metherell, L. A., Clark, A. J., Storr, H. L.
Publicado 2013

Oxidative stress and adrenocortical insufficiency

por Prasad, R, Kowalczyk, J C, Meimaridou, E, Storr, H L, Metherell, L A
Publicado 2014

Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency

por Dias, R P, Chan, L F, Metherell, L A, Pearce, S H S, Clark, A J L
Publicado 2010

Identification and characterisation of a novel GHR defect disrupting the polypyrimidine tract and resulting in GH insensitivity

por David, A, Miraki-Moud, F, Shaw, N J, Savage, M O, Clark, A J L, Metherell, L A
Publicado 2010

NNT is a key regulator of adrenal redox homeostasis and steroidogenesis in male mice

por Meimaridou, E, Goldsworthy, M, Chortis, V, Fragouli, E, Foster, P A, Arlt, W, Cox, R, Metherell, L A
Publicado 2017

Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction

por Maharaj, A., Williams, J., Bradshaw, T., Güran, T., Braslavsky, D., Casas, J., Chan, L.F., Metherell, L.A., Prasad, R.
Publicado 2020

Neonatal presentation of familial glucocorticoid deficiency resulting from a novel splice mutation in the melanocortin 2 receptor accessory protein

por Jain, V, Metherell, L A, David, A, Sharma, R, Sharma, P K, Clark, A J L, Chan, L F
Publicado 2011