검색어 : 통합검색[Robson Anthony.]
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401
- Point-of-Care Cluster Randomized Trial in Stroke Secondary Prevention Using Electronic Health Records
- Dregan, Alex; van Staa, Tjeerd P.; McDermott, Lisa; McCann, Gerard; Ashworth, Mark; Charlton, Judith; Wolfe, Charles D.A.; Rudd, Anthony; Yardley, Lucy; Gulliford, Martin C.; Meredith, Sarah; Kerry, Sally; Murray, Elizabeth; Mant, Jonathan; Robson, John; Haywood, Andrew; Pursani, Nanik; From the Department of Primary Care and Public Health Sciences, King’s College London, London, United Kingdom (A.D., L.M., M.A., J.C., C.D.A.W., A.R., M.C.G.); NIHR Biomedical Research Centre at Guy’s and St Thomas’ Hospital London, London, United Kingdom (A.D., C.D.A.W., A.R., M.C.G.); Clinical Practice Research Datalink (CPRD), Medicines and Healthcare Products Regulatory Agency, London, United Kingdom (T.P.v.S., G.M.); London School of Hygiene & Tropical Medicine, London, United Kingdom (T.P.v.S.); and Division of Community Clinical Sciences, University of Southampton, Southampton, United Kingdom (L.M., L.Y.).; From the Department of Primary Care and Public Health Sciences, King’s College London, London, United Kingdom (A.D., L.M., M.A., J.C., C.D.A.W., A.R., M.C.G.); NIHR Biomedical Research Centre at Guy’s and St Thomas’ Hospital London, London, United Kingdom (A.D., C.D.A.W., A.R., M.C.G.); Clinical Practice Research Datalink (CPRD), Medicines and Healthcare Products; (Stroke, v.45, 2014, pp.2066-2071)
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402
- Sarcomere function activates a p53-dependent DNA damage response that promotes polyploidization and limits <i>in vivo</i> cell engraftment
- Pettinato, Anthony M.; Yoo, Dasom; VanOudenhove, Jennifer; Chen, Yu-Sheng; Cohn, Rachel; Ladha, Feria A.; Yang, Xiulan; Thakar, Ketan; Romano, Robert; Legere, Nicolas; Meredith, Emily; Robson, Paul; Regnier, Michael; Cotney, Justin L.; Murry, Charles E.; Hinson, J. Travis; Department of Genetics and Genome Sciences, UConn Health; Department of Bioengineering, University of Washington; Department of Genetics and Genome Sciences, UConn Health; The Jackson Laboratory for Genomic Medicine; The Jackson Laboratory for Genomic Medicine; Department of Genetics and Genome Sciences, UConn Health; Center for Cardiovascular Biology and Institute for Stem Cell and Regenerative Medicine, University of Washington; The Jackson Laboratory for Genomic Medicine; The Jackson Laboratory for Genomic Medicine; The Jackson Laboratory for Genomic Medicine; The Jackson Laboratory for Genomic Medicine; The Jackson Laboratory for Genomic Medicine; Department of Bioengineering, University of Washingt; (Cell reports, v.35, 2021, pp.109088)
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403
- HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1<sup>-/-</sup> Mice
- Webb, Bryn D.; Shaaban, S.; Gaspar, H.; Cunha, Luis F.; Schubert, Christian R.; Hao, K.; Robson, Caroline D.; Chan, W.M.; Andrews, C.; MacKinnon, S.; Oystreck, Darren T.; Hunter, David G.; Iacovelli, Anthony J.; Ye, X.; Camminady, A.; Engle, Elizabeth C.; Jabs, E.; ; (American journal of human genetics, v.91, 2012, pp.171-179)
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404
- WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression
- Majander, Anna; Jurkute, Neringa; Burté , Florence; Brock, Kristian; Joã o, Catarina; Huang, Houbin; Neveu, Magella M.; Chan, Choi Mun; Duncan, Holly J.; Kelly, Simon; Burkitt-Wright, Emma; Khoyratty, Fadil; Lai, Yoon Tse; Subash, Mala; Chinnery, Patrick F.; Bitner-Glindzicz, Maria; Arno, Gavin; Webster, Andrew R.; Moore, Anthony T.; Michaelides, Michel; Stockman, Andrew; Robson, Anthony G.; Yu-Wai-Man, Patrick; ; (American journal of ophthalmology, v.241, 2022, pp.9-27)
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405
- INNV-27. BT-LIFE (BRAIN TUMOURS, LIFESTYLE INTERVENTIONS, AND FATIGUE EVALUATION): LESSONS LEARNED FROM RUNNING A NOVEL MULTI-SECTORAL RESEARCH TRIAL
- G Rooney, Alasdair; Hewins, William; Walker, Amie; Withington, Lisa; Mackinnon, Mairi; Robson, Sara; Green, Aimee; Anderson, Garry; Bulbeck, Helen; Torrens, Claire; Emerson, Julie; Dunlop, Jo; Welsh, Michelle; McEleney, Tracy; Hopcroft, Lisa; Wells, Mary; McBain, Catherine; Chalmers, Anthony; Grant, Robin; NHS Lothian, Edinburgh, United Kingdom; University of Edinburgh, Edinburgh, United Kingdom; University of Edinburgh, Glasgow, United Kingdom; Christie NHS Foundation Trust, Manchester, United Kingdom; NHS Greater Glasgow and Clyde, Glasgow, United Kingdom; Christie NHS Foundation Trust, Manchester, United Kingdom; Christie NHS Foundation Trust, Manchester, United Kingdom; EH3 Performance, Edinburgh, United Kingdom; brainstrust, Edinburgh, United Kingdom; University of Stirling, Stirling, United Kingdom; Christie NHS Foundation Trust, Manchester, United Kingdom; Public Health Scotland, Edinburgh, United Kingdom; Public Health Scotland, Edinburgh, United Kingdom; Public Health Scotland, Edinburgh, United Kingdom; Public Health Scotland, Edinburgh, United Kingdom; Imperial College Healthcare NHS Trust, London, United Kingdom; The Christie NHS Foundation Trust, Manchester, United Kingdom; University of Glasgow, Glasgow, United Kingdom; NHS Lothian, Edinburgh, United Kingd; (Neuro-oncology, v.22, 2020, pp.ii122-ii122)
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406
- Clinicopathological Case Series of Four Patients with Inherited Macular Disease
- Wickham, Louisa; Chen, Fred K.; Lewis, Geoffrey P.; Uppal, Germit S.; Neveu, Magella M.; Wright, Genevieve A.; Robson, Anthony G.; Webster, Andrew R.; Grierson, Iain; Hiscott, Paul; Coffey, Peter J.; Holder, Graham E.; Fisher, Steven K.; Da Cruz, Lyndon; From the Departments of Vitreoretinal Surgery and; From the Departments of Vitreoretinal Surgery and2Department of Cellular Therapy, UCL Institute of Ophthalmology, London, United Kingdom; the; Neuroscience Research Institute, University of California, Santa Barbara, California; and the; From the Departments of Vitreoretinal Surgery and; Electrophysiology, Moorfields Eye Hospital, London, United Kingdom; the; From the Departments of Vitreoretinal Surgery and; Electrophysiology, Moorfields Eye Hospital, London, United Kingdom; the; Department of Cellular Therapy, UCL Institute of Ophthalmology, London, United Kingdom; the; Unit of Ophthalmology, Department of Medicine, University of Liverpool, Liverpool, United Kingdom.; Unit of Ophthalmology, Department of Medicine, University of Liverpool, Liverpool, United Kingdom.; Department of Cellular Therapy, UCL Institute of Ophthalmology, London, United Kingdom; the; Electrophysiology, Moorfields Eye Hospital, London, United Kingdom; (Investigative ophthalmology & visual science, v.50, 2009, pp.3553)
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407
- Effects of high-intensity interval training on physical performance, systolic blood pressure, oxidative stress and inflammatory markers in skeletal muscle of spontaneously hypertensive rats
- D’Almeida, Thaynara Zanoni; Gomes, Mariana Janini; Engel, Leticia Estevam; Giometti, Ines Cristina; Ferreira, Natalia Zamberlan; Stuani, Rafael; Corrê a, Camila Renata; Castoldi, Robson Chacon; Nunes, Sarah Gomes; Aguiar, Andreo Fernando; Castilho, Anthony Cé sar; Okoshi, Marina Politi; Pacagnelli, Francis Lopes; ; (PLoS ONE, v.20, 2025, pp.e0316441)
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408
- <i>SSBP1</i> mutations in dominant optic atrophy with variable retinal degeneration
- Jurkute, Neringa; Leu, Costin; Pogoda, Hans‐ Martin; Arno, Gavin; Robson, Anthony G.; Nü rnberg, Gudrun; Altmü ller, Janine; Thiele, Holger; Motameny, Susanne; Toliat, Mohammad Reza; Powell, Kate; Hö hne, Wolfgang; Michaelides, Michel; Webster, Andrew R.; Moore, Anthony T.; Hammerschmidt, Matthias; Nü rnberg, Peter; Yu‐ Wai‐ Man, Patrick; Votruba, Marcela; Moorfields Eye Hospital National Health Service Foundation Trust, London, United Kingdom; Cologne Center for Genomics, University of Cologne, Cologne, Germany; Institute for Zoology, Developmental Biology Unit, University of Cologne, Cologne, Germany; Moorfields Eye Hospital National Health Service Foundation Trust, London, United Kingdom; Moorfields Eye Hospital National Health Service Foundation Trust, London, United Kingdom; Cologne Center for Genomics, University of Cologne, Cologne, Germany; Cologne Center for Genomics, University of Cologne, Cologne, Germany; Cologne Center for Genomics, University of Cologne, Cologne, Germany; Cologne Center for Genomics, University of; (Annals of neurology, v.86, 2019, pp.368-383)
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409
- X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development
- Webb, Tom R.; Matarin, M.; Gardner, Jessica C.; Kelberman, D.; Hassan, H.; Ang, W.; Michaelides, M.; Ruddle, Jonathan B.; Pennell, Craig E.; Yazar, S.; Khor, Chiea C.; Aung, T.; Yogarajah, M.; Robson, Anthony G.; Holder, Graham E.; Cheetham, Michael E.; Traboulsi, Elias I.; Moore, Anthony T.; Sowden, Jane C.; Sisodiya, Sanjay M.; Mackey, David A.; Tuft, Stephen J.; Hardcastle, Alison J.; ; (American journal of human genetics, v.90, 2012, pp.247-259)
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410
- Abstract C114: Androstenedione levels in postmenopausal women with resected early-stage breast cancer are associated with SNPs in CYP11B1 and CYP11B2 identified by a genome-wide association study (GWAS).
- Ibrahim-zada, Irada; Ingle, James N.; Fridley, Brooke L.; Buzdar, Aman; Robson, Mark E.; Kubo, Michiaki; Batzler, Anthony; Jenkins, Gregory D.; Goetz, Matthew P.; Northfelt, Donald W.; Perez, Edith A.; Williard, Clark V.; Wang, Liewei; Schaid, Daniel J.; Nakamura, Yusuke; Weinshilboum, Richard M.; ; (Molecular cancer therapeutics, v.10, 2011, pp.C114-C114)
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