Zobrazeno 1 - 10
of 130
pro vyhledávání: '"Hirst RA"'
Autor:
Shoemark, A, Moya, E, Hirst, RA, Patel, MP, Robson, EA, Hayward, J, Scully, J, Fassad, MR, Lamb, W, Schmidts, M, Dixon, M, Patel-King, RS, Rogers, AV, Rutman, A, Jackson, CL, Goggin, P, Rubbo, B, Ollosson, S, Carr, S, Walker, W, Adler, B, Loebinger, MR, Wilson, R, Bush, A, Williams, H, Boustred, C, Jenkins, L, Sheridan, E, Chung, EMK, Watson, CM, Cullup, T, Lucas, JS, Kenia, P, O’Callaghan, C, King, SM, Hogg, C, Mitchison, HM
Rationale Primary ciliary dyskinesia is a genetically heterogeneous inherited condition characterised by progressive lung disease arising from abnormal cilia function. Approximately half of patients have situs inversus. The estimated prevalence of pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::191a9da350332b1bfc465837cb943101
https://eprints.whiterose.ac.uk/146744/1/nihms931245.pdf
https://eprints.whiterose.ac.uk/146744/1/nihms931245.pdf
Autor:
Lucas, Jane, Evans, HJ, Haarman, EG, Hirst, RA, Hogg, C, Jackson, Claire, Nielsen, KG, Omran, H, Papon, J-F, Robinson, P, Shoemark, A, Walker, WT
Publikováno v:
Lucas, J S, Evans, H J, Haarman, E G, Hirst, R A, Hogg, C, Jackson, C L, Nielsen, K G, Omran, H, Papon, J F, Robinson, P, Shoemark, A & Walker, W T 2017, ' Exploring the Art of Ciliary Beating : The Benefits of High-Speed Video Analysis ', Chest, vol. 152, no. 6, pp. 1348-1349 . https://doi.org/10.1016/j.chest.2017.06.053
Chest, 152(6), 1348-1349. American College of Chest Physicians
Chest, 152(6), 1348-1349. American College of Chest Physicians
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c644759540569d9eb497319758985cd9
https://research.vumc.nl/en/publications/2178b878-a525-49cd-bc14-14de6e337c34
https://research.vumc.nl/en/publications/2178b878-a525-49cd-bc14-14de6e337c34
Autor:
Munye, MM, Shoemark, A, Hirst, RA, Delhove, JM, Sharp, TV, McKay, TR, O'Callaghan, C, Baines, DL, Howe, SJ, Hart, SL
Air-liquid interface (ALI) culture of primary airway epithelial cells enables mucociliary differentiation providing an in vitro model of the human airway but their proliferative potential is limited. To extend proliferation, these cells were previous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::7f9570a3e6124aa2a9aa124fff2971f1
Autor:
Lucas, JS, Barbato, A, Collins, SA, Goutaki, M, Behan, L, Caudri, D, Dell, S, Eber, E, Escudier, E, Hirst, RA, Hogg, C, Jorissen, M, Latzin, P, Legendre, M, Leigh, MW, Midulla, F, Nielsen, KG, Omran, H, Papon, JF, Pohunek, P, Redfern, B, Rigau, D, Rindlisbacher, B, Santamaria, F, Shoemark, A, Snijders, D, Tonia, T, Titieni, A, Walker, WT, Werner, C, Bush, A, Kuehni, CE
The diagnosis of primary ciliary dyskinesia is often confirmed with standard, albeit complex and expensive, tests. In many cases, however, the diagnosis remains difficult despite the array of sophisticated diagnostic tests. There is no "gold standard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4caf28e82c3949a4aa599c0228e8e57a
https://europepmc.org/articles/PMC6054534/
https://europepmc.org/articles/PMC6054534/
Autor:
Hoenderdos, K, Lodge, KM, Hirst, RA, Chen, C, Palazzo, SGC, Emerenciana, A, Summers, C, Angyal, A, Porter, L, Juss, JK, O'Callaghan, C, Chilvers, ER, Condliffe, AM
Background: The inflamed bronchial mucosal surface is a profoundly hypoxic environment. Neutrophilic airway inflammation and neutrophil-derived proteases have been linked to disease progression in conditions such as COPD and cystic fibrosis, but the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::29d6c97899a662403a9a544ef3e1ef43
http://hdl.handle.net/10044/1/64553
http://hdl.handle.net/10044/1/64553
Autor:
Onoufriadis, A, Shoemark, A, Schmidts, M, Patel, M, Jimenez, G, Liu, H, Thomas, B, Dixon, M, Hirst, RA, Rutman, A, Burgoyne, T, Williams, C, Scully, J, Bolard, F, Lafitte, J-J, Beales, PL, Hogg, C, Yang, P, Chung, EMK, Emes, RD, O'Callaghan, C, Bouvagnet, P, Mitchison, HM
Publikováno v:
Human Molecular Genetics
Primary ciliary dyskinesia (PCD) is an inherited chronic respiratory obstructive disease with randomized body laterality and infertility, resulting from cilia and sperm dysmotility. PCD is characterized by clinical variability and extensive genetic h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fee3bfa3b324d094a59b4859e7a9af79
https://nottingham-repository.worktribe.com/file/723289/1/ddu046.pdf
https://nottingham-repository.worktribe.com/file/723289/1/ddu046.pdf
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Akademický článek
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