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Featured researches published by Peter King.


Archive | 2003

The ACTH Receptor and Its Mutations

Adrian Clark; Peter King

ACTH stimulates steroidogenesis by acting on a single highly specific cell surface receptor in the adrenal cortex. ACTH also has weaker affinity for all the other four members of the melanocortin receptor family, which are expressed in a variety of tissues. The principal endogenous agonists for these other receptors are α- and γ- melanocyte stimulating hormones (α -and γ- MSH), but these peptides are unable to bind to the ACTH receptor. This chapter aims to describe the characterization of this receptor prior to its cloning in 1992 and the subsequent studies of receptor regulation and function. Finally, the defects of this receptor in human disease are described.


18th European Congress of Endocrinology | 2016

Adrenal pigmentation in PPNAD is a result of melanin deposition and associated with upregulation of the melanocortin 1 receptor

Dominic Cavlan; Chris Evagora; Daniel Berney; Helen L. Storr; W. Drake; Peter King


Society for Endocrinology BES 2015 | 2015

Unveiling the complexity of the undifferentiated zone in the human adrenal cortex

Irene Hadjidemetriou; Gerard Ruiz-Babot; Celso Gomez-Sanchez; Peter King; Leonardo Guasti


Society for Endocrinology BES 2015 | 2015

Molecular and immunohistochemical analysis of aldosterone producing adenomas

Rea Ganatra; Lewis Saunders; Candy Sze; Ashley Parker; Philip Hall; Dominic Cavlan; Peter King


42nd Meeting of the British Society for Paediatric Endocrinology and Diabetes | 2014

Expression of Sonic hedgehog signalling components in the developing human adrenal cortex

Writaja Halder; Rea Ganatra; Leo Dunkel; Helen L. Storr; Leonardo Guasti; Peter King


40th Meeting of the British Society for Paediatric Endocrinology and Diabetes | 2012

A homozygous glutathione peroxidase 1 mutation, p. Arg130-Leu133del, in a patient with familial glucocorticoid deficiency

Julia Kowalczyk; Eirini Meimaridou; Leonardo Guasti; Peter Nurnberg; Philippe Touraine; Peter King; Lou Metherell


39th Meeting of the British Society for Paediatric Endocrinology and Diabetes | 2011

Twenty novel mutations in nicotinamide nucleotide transhydrogenase (NNT) causing FGD

Lou Metherell; Eirini Meimaridou; Julia Kowalczyk; Leo Guasti; Claire Hughes; Nicholas Mann; Ritwik Banerjee; Peter King; Adrian Clark


39th Meeting of the British Society for Paediatric Endocrinology and Diabetes | 2011

MCM4 mutation causes a novel DNA replication disorder associated with short stature and adrenal failure

Claire Hughes; Leonardo Guasti; Eirini Meimaridou; Chen-Hua Chaung; John Schimenti; Peter King; Colm Costigan; Adrian Clark; Louise Metherell


Society for Endocrinology BES 2009 | 2009

Glucocorticoid effects on the programming of AT1b angiotensin receptor expression in the rat fetus

Irina Bogdarina; Peter King; Simon C. Langley-Evans; Adrian Clark


Society for Endocrinology BES 2008 | 2008

The cell surface expression of MC2R mutations found in familial glucocorticoid deficiency

Teng-Teng Ll Chung; Sadani N. Cooray; Tom R. Webb; Lou Metherell; Peter King; Paul Chapple; Adrian Clark

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Adrian Clark

St Bartholomew's Hospital

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Leonardo Guasti

Queen Mary University of London

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Eirini Meimaridou

Queen Mary University of London

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Lou Metherell

Queen Mary University of London

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Claire Hughes

Queen Mary University of London

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Dominic Cavlan

Queen Mary University of London

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Helen L. Storr

Queen Mary University of London

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Julia Kowalczyk

Queen Mary University of London

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Gerard Ruiz-Babot

Queen Mary University of London

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