Minireview: The Melanocortin 2 Receptor Accessory Proteins

Por Webb, Tom R., Clark, Adrian J. L.
Publicado no Mol Endocrinol (2010)

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

Melanocortin receptor accessory proteins in adrenal disease and obesity

Por Jackson, David S., Ramachandrappa, Shwetha, Clark, Adrian J., Chan, Li F.
Publicado no Front Neurosci (2015)

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

Localisation of the melanocortin-2-receptor and its accessory proteins in the developing and adult adrenal gland

Por Gorrigan, Rebecca J, Guasti, Leonardo, King, Peter, Clark, Adrian J, Chan, Li F
Publicado em 2011

Repair of Aberrant Splicing in Growth Hormone Receptor by Antisense Oligonucleotides Targeting the Splice Sites of a Pseudoexon

Por David, Alessia, Srirangalingam, Umasuthan, Metherell, Louise A., Khoo, Bernard, Clark, Adrian J. L.
Publicado no Mol Endocrinol (2010)

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)

The Cytosolic Chaperone Hsc70 Promotes Traffic to the Cell Surface of Intracellular Retained Melanocortin-4 Receptor Mutants

Por Meimaridou, Eirini, Gooljar, Sakina B., Ramnarace, Nalini, Anthonypillai, Lucia, Clark, Adrian J. L., Chapple, J. Paul
Publicado no Mol Endocrinol (2011)

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

Deficiency of Ferritin Heavy-Chain Nuclear Import in Triple A Syndrome Implies Nuclear Oxidative Damage as the Primary Disease Mechanism

Por Storr, Helen L., Kind, Barbara, Parfitt, David A., Chapple, J. Paul, Lorenz, M., Koehler, Katrin, Huebner, Angela, Clark, Adrian J. L.
Publicado no Mol Endocrinol (2009)

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

Melanocortin 4 Receptor Becomes an ACTH Receptor by Coexpression of Melanocortin Receptor Accessory Protein 2

Por Josep Agulleiro, Maria, Cortés, Raúl, Fernández-Durán, Begoña, Navarro, Sandra, Guillot, Raúl, Meimaridou, Eirini, Clark, Adrian J.L., Cerdá-Reverter, José Miguel
Publicado no Mol Endocrinol (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