Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration

By Spencer Kylee L.   Hauser Michael A.   Olson Lana M.   Schmidt Silke   Scott William K.   Gallins Paul   Agarwal Anita   Postel Eric A.   Pericak-Vance Margaret A.   Haines Jonathan L.  

Human Molecular Genetics, Vol. 16, Iss. 16, 2007-08 ,pp. : 1986-1992

Oxford University Press

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Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease

By Caprioli Jessica   Castelletti Federica   Bucchioni Sara   Bettinaglio Paola   Bresin Elena   Pianetti Gaia   Gamba Sara   Brioschi Simona   Daina Erica   Remuzzi Giuseppe   for the International Registry of Recurrent and Familial HUS/TTP  

Human Molecular Genetics, Vol. 12, Iss. 24, 2003-12 ,pp. : 3385-3395

Oxford University Press

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Two cDNAs from the purple sea urchin, Strongylocentrotus purpuratus, encoding mosaic proteins with domains found in factor H, factor I, and complement components C6 and C7

By Multerer Keri   Smith L.  

Immunogenetics, Vol. 56, Iss. 2, 2004-05 ,pp. : 89-106

Springer Publishing Company

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Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

By Rivera Andrea  

Human Molecular Genetics, Vol. 14, Iss. 21, 2005-11 ,pp. : 3227-3236

Oxford University Press

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The −14010*C variant associated with lactase persistence is located between an Oct-1 and HNF1α binding site and increases lactase promoter activity

By Jensen Tine   Liebert Anke   Lewinsky Rikke   Swallow Dallas   Olsen Jørgen   Troelsen Jesper  

Human Genetics, Vol. 130, Iss. 4, 2011-10 ,pp. : 483-493

Springer Publishing Company

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