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

Por Bogdarina, Irina G, King, Peter J, Clark, Adrian J L
Publicado em 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 em 2010

The melanocortin receptors and their accessory proteins

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

Epigenetic modification of the renin-angiotensin system in the fetal programming of hypertension

Por Bogdarina, Irina, Welham, Simon, King, Peter J., Burns, Shamus P., Clark, Adrian J.L.
Publicado em 2007

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 em 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 em 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 em 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 em 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 no Front Endocrinol (Lausanne) (2015)

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 em 2012

Ligand-specific conformational change of the G-protein–coupled receptor ALX/FPR2 determines proresolving functional responses

Por Cooray, Sadani N., Gobbetti, Thomas, Montero-Melendez, Trinidad, McArthur, Simon, Thompson, Dawn, Clark, Adrian J. L., Flower, Roderick J., Perretti, Mauro
Publicado em 2013

Pseudoexon Activation as a Novel Mechanism for Disease Resulting in Atypical Growth-Hormone Insensitivity

Por Metherell, Louise A., Akker, Scott A., Munroe, Patricia B, Rose, Stephen J, Caulfield, Mark, Savage, Martin O., Chew, Shern L., Clark, Adrian J. L.
Publicado em 2001

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 em 2007

MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans

Por Hughes, Claire R., Guasti, Leonardo, Meimaridou, Eirini, Chuang, Chen-Hua, Schimenti, John C., King, Peter J., Costigan, Colm, Clark, Adrian J.L., Metherell, Louise A.
Publicado em 2012

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 em 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 em 2014

MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family

Por Chan, Li F., Webb, Tom R., Chung, Teng-Teng, Meimaridou, Eirini, Cooray, Sadani N., Guasti, Leonardo, Chapple, J. Paul, Egertová, Michaela, Elphick, Maurice R., Cheetham, Michael E., Metherell, Louise A., Clark, Adrian J. L.
Publicado em 2009

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 em 2012

Nonclassic Lipoid Congenital Adrenal Hyperplasia Masquerading as Familial Glucocorticoid Deficiency

Por Metherell, Louise A., Naville, Danielle, Halaby, George, Begeot, Martine, Huebner, Angela, Nürnberg, Gudrun, Nürnberg, Peter, Green, Jane, Tomlinson, Jeremy W., Krone, Nils P., Lin, Lin, Racine, Michael, Berney, Dan M., Achermann, John C., Arlt, Wiebke, Clark, Adrian J. L.
Publicado em 2009