Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jane Lambie"'
Autor:
Mahmood F. Bhutta, Jane Lambie, Lindsey Hobson, Debbie Williams, Hayley E. Tyrer, George Nicholson, Steve D.M. Brown, Helen Brown, Chiara Piccinelli, Guillaume Devailly, James Ramsden, Michael T. Cheeseman
Publikováno v:
Frontiers in Genetics, Vol 10 (2020)
Chronic otitis media with effusion (COME) is the most common cause of childhood hearing loss in the developed world. Underlying pathophysiology is not well understood, and in particular the factors that lead to the transition from acute to chronic in
Externí odkaz:
https://doaj.org/article/7b5273a54c93410c993a1cda268e80f9
Autor:
Mahmood F. Bhutta, Jane Lambie, Lindsey Hobson, Anuj Goel, Lena Hafrén, Elisabet Einarsdottir, Petri S. Mattila, Martin Farrall, Steve Brown, Martin J. Burton
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Abstract Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and known to have high heritability. Mutant mouse models have identified Fbxo11, Evi1, Tgif1, and Nisch as potential risk loci. We recruited chil
Externí odkaz:
https://doaj.org/article/4e3ad4f89c544c7ca34f1dfdf0d95724
Autor:
George Nicholson, James D. Ramsden, Hayley E. Tyrer, Guillaume Devailly, Chiara Piccinelli, Helen Brown, Mahmood F. Bhutta, Michael Cheeseman, Debbie Williams, Steve D. M. Brown, Lindsey Hobson, Jane Lambie
Publikováno v:
Bhutta, M F, Lambie, J, Hobson, L, Williams, D, Tyrer, H E, Nicholson, G, Brown, S, Brown, H, Piccinelli, C, Devailly, G, Ramsden, J & Cheeseman, M 2020, ' Transcript analysis reveals a hypoxic inflammatory environment in human chronic otitis media with effusion ', Frontiers in genetics, vol. 10, 1327 . https://doi.org/10.3389/fgene.2019.01327
Frontiers in Genetics
Frontiers in Genetics, Frontiers, 2020, 10, Non paginé. ⟨10.3389/fgene.2019.01327⟩
Frontiers in Genetics, Vol 10 (2020)
Frontiers in Genetics
Frontiers in Genetics, Frontiers, 2020, 10, Non paginé. ⟨10.3389/fgene.2019.01327⟩
Frontiers in Genetics, Vol 10 (2020)
Chronic otitis media with effusion (COME) is the most common cause of childhood hearing loss in the developed world. Underlying pathophysiology is not well understood, and in particular the factors that lead to the transition from acute to chronic in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d825f257f328286fb9848996bd8126ae
https://hdl.handle.net/20.500.11820/a00b6cae-9dff-4504-bea7-7779e9a30be5
https://hdl.handle.net/20.500.11820/a00b6cae-9dff-4504-bea7-7779e9a30be5
Autor:
Lindsey Hobson, Petri S. Mattila, Martin J. Burton, Elisabet Einarsdottir, Jane Lambie, Anuj Goel, Mahmood F. Bhutta, Lena Hafrén, Steve D.M. Brown, Martin Farrall
Publikováno v:
Scientific Reports
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and known to have high heritability. Mutant mouse models have identified Fbxo11, Evi1, Tgif1, and Nisch as potential risk loci. We recruited children aged
Autor:
Dominic Furniss, Henk Giele, Lindsey Hobson, Elizabeth S. H. Scaman, Jane Lambie, Sarra E. Jamieson, Mahmood F. Bhutta, Martin J. Burton
Publikováno v:
Annals of Human Genetics. 77:244-250
Summary Collection of saliva for DNA extraction has created new opportunities to recruit participants from the community for genetic association studies. However, sample return rates are variable. No prior study has specifically addressed how study d