-
2
-
-
38449106206
-
Genetic susceptibility to age-related macular degeneration: a paradigm for dissecting complex disease traits
-
Swaroop A., Branham K., Chen W., and Abecasis G. Genetic susceptibility to age-related macular degeneration: a paradigm for dissecting complex disease traits. Hum Mol Genet 16 (2007) R174-R182
-
(2007)
Hum Mol Genet
, vol.16
-
-
Swaroop, A.1
Branham, K.2
Chen, W.3
Abecasis, G.4
-
3
-
-
33750201885
-
CFH, ELOVL4, PLEKHA1, and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses
-
Conley Y.P., Jakobsdottir J., Mah T., et al. CFH, ELOVL4, PLEKHA1, and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses. Hum Mol Genet 15 (2006) 3206-3218
-
(2006)
Hum Mol Genet
, vol.15
, pp. 3206-3218
-
-
Conley, Y.P.1
Jakobsdottir, J.2
Mah, T.3
-
4
-
-
33645419787
-
Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration
-
Gold B., Merriam J.E., Zernant J., et al. Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration. Nat Genet 38 (2006) 458-462
-
(2006)
Nat Genet
, vol.38
, pp. 458-462
-
-
Gold, B.1
Merriam, J.E.2
Zernant, J.3
-
5
-
-
34547764305
-
Complement C3 variant and the risk of age-related macular degeneration
-
Yates J.R., Sepp T., Matharu B.K., et al. Complement C3 variant and the risk of age-related macular degeneration. N Engl J Med 357 (2007) 553-561
-
(2007)
N Engl J Med
, vol.357
, pp. 553-561
-
-
Yates, J.R.1
Sepp, T.2
Matharu, B.K.3
-
6
-
-
33750300013
-
Association between apolipoprotein E polymorphisms and age-related macular degeneration: a HuGe review and meta-analysis
-
Thakkinstian A., Bowe S., McEvoy M., Smith W., and Attia J. Association between apolipoprotein E polymorphisms and age-related macular degeneration: a HuGe review and meta-analysis. Am J Epidemiol 67 (2006) 813-822
-
(2006)
Am J Epidemiol
, vol.67
, pp. 813-822
-
-
Thakkinstian, A.1
Bowe, S.2
McEvoy, M.3
Smith, W.4
Attia, J.5
-
7
-
-
56249123595
-
Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study
-
10.1016/S0140-6736(08)61348-3 published online Oct 7.
-
Ennis S., Jomary C., Mullins R., et al. Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study. Lancet (2008) 10.1016/S0140-6736(08)61348-3 published online Oct 7.
-
(2008)
Lancet
-
-
Ennis, S.1
Jomary, C.2
Mullins, R.3
-
8
-
-
0034832029
-
An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and age-related macular degeneration
-
Hageman G.S., Luthert P.J., Chong N.V., Johnson L.V., Anderson D.H., and Mullins R.F. An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and age-related macular degeneration. Prog Retin Eye Res 20 (2001) 705-732
-
(2001)
Prog Retin Eye Res
, vol.20
, pp. 705-732
-
-
Hageman, G.S.1
Luthert, P.J.2
Chong, N.V.3
Johnson, L.V.4
Anderson, D.H.5
Mullins, R.F.6
-
9
-
-
49749150467
-
Systemic complement activation in age-related macular degeneration
-
Scholl H.P., Issa P.C., Walier M., et al. Systemic complement activation in age-related macular degeneration. PLoS ONE 3 (2008) e2593
-
(2008)
PLoS ONE
, vol.3
-
-
Scholl, H.P.1
Issa, P.C.2
Walier, M.3
-
10
-
-
34748845718
-
Comparison of human RPE gene expression in macula and periphery highlights potential topographic differences in Bruch's membrane
-
van Soest S., de Wit G.J.M., Essing A., et al. Comparison of human RPE gene expression in macula and periphery highlights potential topographic differences in Bruch's membrane. Mol Vis 13 (2007) 1608-1617
-
(2007)
Mol Vis
, vol.13
, pp. 1608-1617
-
-
van Soest, S.1
de Wit, G.J.M.2
Essing, A.3
-
11
-
-
50849141120
-
Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedema
-
Gosswein T., Kocot A., Emmert G., et al. Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedema. Cytogenet Genome Res 121 (2008) 181-188
-
(2008)
Cytogenet Genome Res
, vol.121
, pp. 181-188
-
-
Gosswein, T.1
Kocot, A.2
Emmert, G.3
-
12
-
-
33746661188
-
Functional analysis of splicing mutations and of an exon 2 polymorphic variant of SERPING1/C1NH
-
Duponchel C., Djenouhat K., Fremeaux-Bacchi V., Monnier N., Drouet C., and Tosi M. Functional analysis of splicing mutations and of an exon 2 polymorphic variant of SERPING1/C1NH. Hum Mut 27 (2006) 295-296
-
(2006)
Hum Mut
, vol.27
, pp. 295-296
-
-
Duponchel, C.1
Djenouhat, K.2
Fremeaux-Bacchi, V.3
Monnier, N.4
Drouet, C.5
Tosi, M.6
-
13
-
-
34447291329
-
Association between nasal carriage of Staphylococcus aureus and the human complement cascade activator serine protease C1 inhibitor (C1INH) valine vs. Methionine polymorphism at amino acid position 480
-
Emonts M., de Jongh C.E., Houwing-Duistermaat J.J., et al. Association between nasal carriage of Staphylococcus aureus and the human complement cascade activator serine protease C1 inhibitor (C1INH) valine vs. Methionine polymorphism at amino acid position 480. FEMS Immunol Med Microbiol 50 (2007) 330-332
-
(2007)
FEMS Immunol Med Microbiol
, vol.50
, pp. 330-332
-
-
Emonts, M.1
de Jongh, C.E.2
Houwing-Duistermaat, J.J.3
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