Hakutulokset - Adrian J. L. Clark

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  1. 1
    Minireview: The Melanocortin 2 Receptor Accessory Proteins

    Minireview: The Melanocortin 2 Receptor Accessory Proteins Tekijä Tom R. Webb, Adrian J. L. Clark

    Julkaistu 2009
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  2. 2
    Cloning and expression of a novel angiotensin II receptor subtype.

    Cloning and expression of a novel angiotensin II receptor subtype. Tekijä Kathryn Sandberg, H Ji, Adrian J. L. Clark, Hagit Shapira, Kevin Catt

    Julkaistu 1992
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  3. 3
    Localisation of the melanocortin-2-receptor and its accessory proteins in the developing and adult adrenal gland

    Localisation of the melanocortin-2-receptor and its accessory proteins in the developing and adult adrenal gland Tekijä Rebecca Gorrigan, Leonardo Guasti, Peter King, Adrian J. L. Clark, Li Chan

    Julkaistu 2011
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  4. 4
    Epigenetic Modification of the Renin-Angiotensin System in the Fetal Programming of Hypertension

    Epigenetic Modification of the Renin-Angiotensin System in the Fetal Programming of Hypertension Tekijä Irina Bogdarina, Simon Welham, Peter King, S. P. Burns, Adrian J. L. Clark

    Julkaistu 2007
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  5. 5
    Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene

    Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene Tekijä Katrin Handschug, Silke Sperling, Sungjoo Kim Yoon, Steffen Hennig, Adrian J. L. Clark, Angela Huebner

    Julkaistu 2001
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  6. 6
    Severe loss‐of‐function mutations in the adrenocorticotropin receptor (ACTHR, <i>MC2R</i>) can be found in patients diagnosed with salt‐losing adrenal hypoplasia

    Severe loss‐of‐function mutations in the adrenocorticotropin receptor (ACTHR, <i>MC2R</i>) can be found in patients diagnosed with salt‐losing adrenal hypoplasia Tekijä Lin Lin, Peter C. Hindmarsh, Lou Metherell, Mahmoud Alzyoud, Maryam Alali, Caroline Brain, Adrian J. L. Clark, Mehul Dattani, John C. Achermann

    Julkaistu 2006
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  7. 7
    Deficiency of Ferritin Heavy-Chain Nuclear Import in Triple A Syndrome Implies Nuclear Oxidative Damage as the Primary Disease Mechanism

    Deficiency of Ferritin Heavy-Chain Nuclear Import in Triple A Syndrome Implies Nuclear Oxidative Damage as the Primary Disease Mechanism Tekijä Helen L. Storr, Barbara Kind, David A. Parfitt, J. Paul Chapple, Michael G. Lorenz, Katrin Koehler, Angela Huebner, Adrian J. L. Clark

    Julkaistu 2009
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  8. 8
    Ligand-specific conformational change of the G-protein–coupled receptor ALX/FPR2 determines proresolving functional responses

    Ligand-specific conformational change of the G-protein–coupled receptor ALX/FPR2 determines proresolving functional responses Tekijä Sadani N. Cooray, Thomas Gobbetti, Trinidad Montero‐Melendez, Simon McArthur, Dawn Thompson, Adrian J. L. Clark, Roderick J. Flower, Mauro Perretti

    Julkaistu 2013
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  9. 9
    The Melanocortin 2 Receptor Accessory Protein Exists as a Homodimer and Is Essential for the Function of the Melanocortin 2 Receptor in the Mouse Y1 Cell Line

    The Melanocortin 2 Receptor Accessory Protein Exists as a Homodimer and Is Essential for the Function of the Melanocortin 2 Receptor in the Mouse Y1 Cell Line Tekijä Sadani N. Cooray, Isabel Almiro Do Vale, Kit‐Yi Leung, Tom R. Webb, J. Paul Chapple, Michaela Egertová, Michael E. Cheetham, Maurice R. Elphick, Adrian J. L. Clark

    Julkaistu 2007
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  10. 10
    Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency

    Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency Tekijä Eirini Meimaridou, Julia Kowalczyk, Leonardo Guasti, Claire Hughes, Florian Wagner, Peter Frommolt, Peter Nürnberg, Nicholas P. Mann, Ritwik Banerjee, Hami Saka, J. Paul Chapple, Peter King, Adrian J. L. Clark, Lou Metherell

    Julkaistu 2012
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  11. 11
    MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family

    MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family Tekijä Li Chan, Tom R. Webb, Teng‐Teng Chung, Eirini Meimaridou, Sadani N. Cooray, Leonardo Guasti, J. Paul Chapple, Michaela Egertová, Maurice R. Elphick, Michael E. Cheetham, Lou Metherell, Adrian J. L. Clark

    Julkaistu 2009
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  12. 12
    Luteinizing Hormone (LH)-Responsive Cushing’s Syndrome: The Demonstration of LH Receptor Messenger Ribonucleic Acid in Hyperplastic Adrenal Cells, which Respond to Chorionic Gonadotropin and Serotonin Agonists<i>in Vitro</i>

    Luteinizing Hormone (LH)-Responsive Cushing’s Syndrome: The Demonstration of LH Receptor Messenger Ribonucleic Acid in Hyperplastic Adrenal Cells, which Respond to Chorionic Gonado... Tekijä Richard A. Feelders, Steven W. J. Lamberts, Leo J. Hofland, Peter M. van Koetsveld, Miriam Verhoef‐Post, Axel P. N. Themmen, Frank H. de Jong, H. Jaap Bonjer, Adrian J. L. Clark, Aart‐Jan van der Lely, Wouter W. de Herder

    Julkaistu 2003
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  13. 13
    Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years’ Experience in the UK

    Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years’ Experience in the UK Tekijä Federica Buonocore, Avinaash Maharaj, Younus Qamar, Katrin Koehler, Jenifer P. Suntharalingham, Li Chan, Bruno Ferraz‐de‐Souza, Claire Hughes, Lin Lin, Rathi Prasad, Jeremy Allgrove, Edward Andrews, Charles Buchanan, Tim Cheetham, Elizabeth Crowne, Justin H. Davies, John W Gregory, Peter C. Hindmarsh, Tony Hulse, Nils Krone, Pratik Shah, M Guftar Shaikh, Catherine Roberts, Peter Clayton, Mehul Dattani, N. Simon Thomas, Angela Huebner, Adrian J. L. Clark, Lou Metherell, John C. Achermann

    Julkaistu 2021
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