Resultats de la cerca - David G. Brownstein
- Mostrar 1 - 14 resultats de 14
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Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume per Tom Van Agtmael, Matthew A. Bailey, Ursula Schlötzer‐Schrehardt, Eilidh Craigie, Ian J. Jackson, David G. Brownstein, Ian L. Megson, John J. Mullins
Publicat 2010Artigo -
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Haploinsufficiency of the murine Col3a1 locus causes aortic dissection: a novel model of the vascular type of Ehlers–Danlos syndrome per Lee B. Smith, Patrick W. F. Hadoke, Emma Dyer, Martin A. Denvir, David G. Brownstein, Eileen Miller, Nancy A. Nelson, Sara Wells, Michael Cheeseman, Andy Greenfield
Publicat 2010Artigo -
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11β-Hydroxysteroid Dehydrogenase Type 1, But Not Type 2, Deficiency Worsens Acute Inflammation and Experimental Arthritis in Mice per Agnes E. Coutinho, Mohini Gray, David G. Brownstein, Donald M. Salter, Deborah A. Sawatzky, Spike Clay, James S. Gilmour, Jonathan R. Seckl, John Savill, Karen E. Chapman
Publicat 2011Artigo -
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Enhanced Hippocampal Long-Term Potentiation and Spatial Learning in Aged 11β-Hydroxysteroid Dehydrogenase Type 1 Knock-Out Mice per Joyce L.W. Yau, Kara McNair, June Noble, David G. Brownstein, Carina Hibberd, Nik Morton, John J. Mullins, Richard Morris, Stuart Cobb, Jonathan R. Seckl
Publicat 2007Artigo -
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11β-Hydroxysteroid Dehydrogenase Type 2 Deficiency Accelerates Atherogenesis and Causes Proinflammatory Changes in the Endothelium in Apoe−/− Mice per Graeme A. Deuchar, Danielle L. McLean, Patrick W. F. Hadoke, David G. Brownstein, David R. Webb, John J. Mullins, Karen E. Chapman, Jonathan R. Seckl, Yuri Kotelevtsev
Publicat 2010Artigo -
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ER stress and basement membrane defects combine to cause glomerular and tubular renal disease resulting from <i>Col4a1</i> mutations in mice per Frances E. Jones, Matthew A. Bailey, Lydia Murray, Yinhui Lu, Sarah McNeilly, Ursula Schlötzer‐Schrehardt, Rachel Lennon, Yoshikazu Sado, David G. Brownstein, John J. Mullins, Karl E. Kadler, Tom Van Agtmael
Publicat 2016Artigo -
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A Wt1-Controlled Chromatin Switching Mechanism Underpins Tissue-Specific Wnt4 Activation and Repression per Abdelkader Essafi, Anna Webb, Rachel L. Berry, Joan Slight, Sally F. Burn, Lee Spraggon, Víctor Velecela, Ofelia M. Martínez-Estrada, John H. Wiltshire, Stefan G. E. Roberts, David G. Brownstein, Jamie A. Davies, N D Hastie, Peter Hohenstein
Publicat 2011Carta -
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A novel mouse model of Warburg Micro Syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton per Sarah M. Carpanini, Lisa McKie, Derek Thomson, Ann K. Wright, Sarah L. Gordon, Sarah L. Roche, Mark T. Handley, Harris Morrison, David G. Brownstein, Thomas M. Wishart, Michael A. Cousin, Thomas H. Gillingwater, Irene A. Aligianis, Ian J. Jackson
Publicat 2014Artigo -
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Glucocorticoid receptor is required for foetal heart maturation per Eva A. Rog‐Zielinska, Adrian Thomson, Christopher J. Kenyon, David G. Brownstein, Carmel M. Moran, Dorota Szumska, Zoi Michailidou, Jennifer Richardson, Elizabeth Owen, Alistair J. Watt, Harris Morrison, Lesley M. Forrester, Shoumo Bhattacharya, Megan C. Holmes, Karen E. Chapman
Publicat 2013Artigo -
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Acute Multiple Organ Failure in Adult Mice Deleted for the Developmental Regulator Wt1 per You-Ying Chau, David G. Brownstein, Heidi K. Mjoseng, Wen‐Chin Lee, Natalija Buza-Vidas, Claus Nerlov, Sten Eirik W. Jacobsen, Paul Perry, Rachel L. Berry, Anna Thornburn, David Sexton, Nik Morton, Peter Hohenstein, Elisabeth Freyer, Kay Samuel, Rob van’t Hof, Nicholas D. Hastie
Publicat 2011Artigo
Eines de cerca:
Matèries relacionades
Biology
Internal medicine
Medicine
Cell biology
Endocrinology
Gene
Chemistry
Genetics
Biochemistry
Phenotype
Aldosterone
Chromatin
Endothelium
Glucocorticoid
Immunology
Inflammation
Kidney
Mineralocorticoid
Mineralocorticoid receptor
Mutant
Neuroscience
Pathology
Smooth muscle
Vascular smooth muscle
11β-hydroxysteroid dehydrogenase type 1
Anatomy
Anemia
Animal science
Aorta
Aortic dissection