Challenges past, present and future for Endocrine Connections

por Clark, Adrian J L
Publicado 2023

Stability and Turnover of the ACTH Receptor Complex

por Clark, Adrian J. L., Chan, Li
Publicado 2019

Fake science for sale? How Endocrine Connections is tackling paper mills

por Clark, Adrian J L, Buckmaster, Simon
Publicado 2021

Characterization of the angiotensin (AT1b) receptor promoter and its regulation by glucocorticoids

por Bogdarina, Irina G, King, Peter J, Clark, Adrian J L
Publicado 2009

Glucocorticoid Effects on the Programming of AT1b Angiotensin Receptor Gene Methylation and Expression in the Rat

por Bogdarina, Irina, Haase, Andrea, Langley-Evans, Simon, Clark, Adrian J. L.
Publicado 2010

The melanocortin receptors and their accessory proteins

por Ramachandrappa, Shwetha, Gorrigan, Rebecca J., Clark, Adrian J. L., Chan, Li F.
Publicado 2013

Bioluminescence Resonance Energy Transfer Reveals the Adrenocorticotropin (ACTH)-Induced Conformational Change of the Activated ACTH Receptor Complex in Living Cells

por Cooray, Sadani N., Chung, Teng-Teng, Mazhar, Khansa, Szidonya, Laszlo, Clark, Adrian J. L.
Publicado 2011

Genome-Wide Methylation and Gene Expression Changes in Newborn Rats following Maternal Protein Restriction and Reversal by Folic Acid

por Altobelli, Gioia, Bogdarina, Irina G., Stupka, Elia, Clark, Adrian J. L., Langley-Evans, Simon
Publicado 2013

Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2

por Chung, Teng-Teng L L, Chan, Li F, Metherell, Louise A, Clark, Adrian J L
Publicado 2010

Functional consequence of a novel Y129C mutation in a patient with two contradictory melanocortin-2-receptor mutations

por Chan, Li F, Chung, Teng-Teng, Massoud, Ahmed F, Metherell, Louise A, Clark, Adrian J L
Publicado 2009

Whole-Exome Sequencing in the Differential Diagnosis of Primary Adrenal Insufficiency in Children

por Chan, Li F., Campbell, Daniel C., Novoselova, Tatiana V., Clark, Adrian J. L., Metherell, Louise A.
Publicado 2015

ACTH signalling and adrenal development: lessons from mouse models

por Novoselova, Tatiana V, King, Peter J, Guasti, Leonardo, Metherell, Louise A, Clark, Adrian J L, Chan, Li F
Publicado 2019

An Atypical Case of Familial Glucocorticoid Deficiency without Pigmentation Caused by Coexistent Homozygous Mutations in MC2R (T152K) and MC1R (R160W)

por Turan, Serap, Hughes, Claire, Atay, Zeynep, Guran, Tulay, Haliloglu, Belma, Clark, Adrian J. L., Bereket, Abdullah, Metherell, Louise A.
Publicado 2012

MRAP deficiency impairs adrenal progenitor cell differentiation and gland zonation

por Novoselova, Tatiana V., Hussain, Mashal, King, Peter J., Guasti, Leonardo, Metherell, Louise A., Charalambous, Marika, Clark, Adrian J. L., Chan, Li F.
Publicado 2018

Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasia

por Lin, Lin, Hindmarsh, Peter C, Metherell, Louise A, Alzyoud, Mahmoud, Al-Ali, Maryam, Brain, Caroline E, Clark, Adrian J L, Dattani, Mehul T, Achermann, John C
Publicado 2007

Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid defi...

por Chan, Li F, Metherell, Louise A, Krude, Heiko, Ball, Colin, O'Riordan, Stephen M P, Costigan, Colm, Lynch, Sally A, Savage, Martin O, Cavarzere, Paolo, Clark, Adrian J L
Publicado 2009

Thioredoxin Reductase 2 (TXNRD2) Mutation Associated With Familial Glucocorticoid Deficiency (FGD)

por Prasad, Rathi, Chan, Li F., Hughes, Claire R., Kaski, Juan P., Kowalczyk, Julia C., Savage, Martin O., Peters, Catherine J., Nathwani, Nisha, Clark, Adrian J. L., Storr, Helen L., Metherell, Louise A.
Publicado 2014

Mutations in Nicotinamide Nucleotide Transhydrogenase (NNT) cause familial glucocorticoid deficiency

por Meimaridou, Eirini, Kowalczyk, Julia, Guasti, Leonardo, Hughes, Claire R., Wagner, Florian, Frommolt, Peter, Nürnberg, Peter, Mann, Nicholas P., Banerjee, Ritwik, Saka, H. Nurcin, Chapple, J. Paul, King, Peter J., Clark, Adrian J.L., Metherell, Louise A.
Publicado 2012