Zobrazeno 1 - 10
of 175
pro vyhledávání: '"Anne E. Hughes"'
Autor:
Hackett, Charles W.
Publikováno v:
The Southwestern Historical Quarterly, 1914 Oct 01. 18(2), 222-225.
Externí odkaz:
https://www.jstor.org/stable/30234638
Publikováno v:
The Mississippi Valley Historical Review, 1914 Dec 01. 1(3), 474-475.
Externí odkaz:
https://www.jstor.org/stable/1897632
Autor:
Declan T Bradley, Thomas W Bourke, Derek J Fairley, Raymond Borrow, Michael D Shields, Peter F Zipfel, Anne E Hughes
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120757 (2015)
Neisseria meningitidis can cause severe infection in humans. Polymorphism of Complement Factor H (CFH) is associated with altered risk of invasive meningococcal disease (IMD). We aimed to find whether polymorphism of other complement genes altered ri
Externí odkaz:
https://doaj.org/article/a132c76cb3814764850efb788597a855
Autor:
Anne E Hughes, Nick Orr, Chris Patterson, Hossein Esfandiary, Ruth Hogg, Vivienne McConnell, Giuliana Silvestri, Usha Chakravarthy
Publikováno v:
PLoS Medicine, Vol 4, Iss 12, p e355 (2007)
BackgroundAge-related macular degeneration (AMD) is the major cause of blindness in the elderly. Those with the neovascular end-stage of disease have irreversible loss of central vision. AMD is a complex disorder in which genetic and environmental fa
Externí odkaz:
https://doaj.org/article/c37a638b67d04842aeb0062674c372c4
Autor:
Peter F Zipfel, Matthew Edey, Stefan Heinen, Mihály Józsi, Heiko Richter, Joachim Misselwitz, Bernd Hoppe, Danny Routledge, Lisa Strain, Anne E Hughes, Judith A Goodship, Christoph Licht, Timothy H J Goodship, Christine Skerka
Publikováno v:
PLoS Genetics, Vol 3, Iss 3, p e41 (2007)
Atypical hemolytic uremic syndrome (aHUS) is associated with defective complement regulation. Disease-associated mutations have been described in the genes encoding the complement regulators complement factor H, membrane cofactor protein, factor B, a
Externí odkaz:
https://doaj.org/article/5dbab60a997e4d30ae0bf040891b6ada
Autor:
C., I. J.
Publikováno v:
Journal of American History; December 1914, Vol. 1 Issue: 3 p474-474, 1p
Autor:
Weihua Meng, Declan Bradley, Dwight Stambolian, Mingyao Li, Christine A. Curcio, Anne E. Hughes, Stephen Bridgett
Publikováno v:
Hughes, A E, Bridgett, S, Meng, W, Li, M, Curcio, C A, Stambolian, D & Bradley, D T 2016, ' Sequence and expression of complement factor H gene cluster variants and their roles in age-related macular degeneration risk ', Investigative Ophthalmology and Visual Science, vol. 57, no. 6, pp. 2763-2769 . https://doi.org/10.1167/iovs.15-18744
Investigative Ophthalmology & Visual Science
Investigative Ophthalmology & Visual Science
Purpose: To investigate how potentially functional genetic variants are coinherited on each of four common complement factor H (CFH) and CFH-related gene haplotypes and to measure expression of these genes in eye and liver tissues.Methods: We sequenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40c3b7681322c91ba559cd18028193dc
https://pure.qub.ac.uk/en/publications/sequence-and-expression-of-complement-factor-h-gene-cluster-variants-and-their-roles-in-agerelated-macular-degeneration-risk(83356758-1280-4a78-90e3-fb43285c72f0).html
https://pure.qub.ac.uk/en/publications/sequence-and-expression-of-complement-factor-h-gene-cluster-variants-and-their-roles-in-agerelated-macular-degeneration-risk(83356758-1280-4a78-90e3-fb43285c72f0).html
Autor:
Derek Fairley, Declan Bradley, Peter F. Zipfel, Thomas Bourke, Ian S. Young, Ray Borrow, Anne E. Hughes, Michael D. Shields
Publikováno v:
International Journal of Immunogenetics. 39:328-337
Invasive infection caused by Neisseria meningitidis is a worldwide public health problem. Previous reports have indicated that carriage of common 'defective' structural polymorphisms of the host mannose-binding lectin gene (MBL2) greatly increases an
Publikováno v:
Eye. 25:683-693
Age-related macular degeneration (AMD) is an inflammatory disease, which causes visual impairment and blindness in older people. The proteins of the complement system are central to the development of this disease. Local and systemic inflammation in
Publikováno v:
International Journal of Immunogenetics. 38:243-248
Summary Variants in the genes of the alternative complement pathway are associated with risk of numerous inflammatory diseases. Abdominal aortic aneurysm is associated with inflammation and is a common cause of illness and death among European popula