Hasil Pencarian - Sian E. Piret

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  1. 1
    A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress

    A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress oleh Sian E. Piret, Eric Olinger, Anita A. C. Reed, M. Andrew Nesbit, Tertius A. Hough, Liz Bentley, Olivier Devuyst, Roger D. Cox, Rajesh V. Thakker

    Diterbitkan 2017-06-01
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  2. 2
    Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway.

    Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Sig... oleh Christopher T Esapa, Sian E Piret, M Andrew Nesbit, Nellie Y Loh, Gethin Thomas, Peter I Croucher, Matthew A Brown, Steve D M Brown, Roger D Cox, Rajesh V Thakker

    Diterbitkan 2016-01-01
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  3. 3
    A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation.

    A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation. oleh Sian E Piret, Christopher T Esapa, Caroline M Gorvin, Rosie Head, Nellie Y Loh, Olivier Devuyst, Gethin Thomas, Steve D M Brown, Matthew Brown, Peter Croucher, Roger Cox, Rajesh V Thakker

    Diterbitkan 2012-01-01
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  4. 4
    Genetic background influences tumour development in heterozygous Men1 knockout mice

    Genetic background influences tumour development in heterozygous Men1 knockout mice oleh Kate E Lines, Mahsa Javid, Anita A C Reed, Gerard V Walls, Mark Stevenson, Michelle Simon, Kreepa G Kooblall, Sian E Piret, Paul T Christie, Paul J Newey, Ann-Marie Mallon, Rajesh V Thakker

    Diterbitkan 2020-05-01
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  5. 5
    Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism

    Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism oleh Katherine U Gaynor, Irina V Grigorieva, Samantha M Mirczuk, Sian E Piret, Kreepa G Kooblall, Mark Stevenson, Karine Rizzoti, Michael R Bowl, M Andrew Nesbit, Paul T Christie, William D Fraser, Tertius Hough, Michael P Whyte, Robin Lovell-Badge, Rajesh V Thakker

    Diterbitkan 2020-02-01
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  6. 6
    Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5.

    Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5. oleh Nellie Y Loh, Liz Bentley, Henrik Dimke, Sjoerd Verkaart, Paolo Tammaro, Caroline M Gorvin, Michael J Stechman, Bushra N Ahmad, Fadil M Hannan, Sian E Piret, Holly Evans, Ilaria Bellantuono, Tertius A Hough, William D Fraser, Joost G J Hoenderop, Frances M Ashcroft, Steve D M Brown, René J M Bindels, Roger D Cox, Rajesh V Thakker

    Diterbitkan 2013-01-01
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