Detalhe da pesquisa
1.
Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration.
Hum Mol Genet
; 25(23): 5276-5285, 2016 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28011711
2.
Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degeneration.
Retina
; 33(9): 1815-27, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23584701
3.
Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG.
Acta Ophthalmol
; 101(2): 215-221, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36128853
4.
Lack of complement inhibitors in the outer intracranial artery aneurysm wall associates with complement terminal pathway activation.
Am J Pathol
; 177(6): 3224-32, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20971742
5.
Vascular endothelial growth factor gene variation and the response to photodynamic therapy in age-related macular degeneration.
Ophthalmology
; 117(1): 103-8, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19896188
6.
[Properdin mutations a risk factor for meningitis]. / Properdiinigeenin mutaatio meningiitin taustalla.
Duodecim
; 126(9): 1071-5, 2010.
Artigo
em Fi
| MEDLINE | ID: mdl-20593630
7.
Single nucleotide polymorphisms of the tenomodulin gene (TNMD) in age-related macular degeneration.
Mol Vis
; 15: 762-70, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19381347
8.
The IL-8, VEGF, and CFH polymorphisms and bevacizumab in age-related macular degeneration.
Ophthalmology
; 121(4): 973-973.e1, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24534755
9.
[Identification of susceptibility genes for age-related macular degeneration--a success story of molecular genetics]. / Silmänpohjan ikärappeuman alttiusgeenien tunnistaminen--molekyyligenetiikan menestystarina.
Duodecim
; 125(21): 2360-4, 2009.
Artigo
em Fi
| MEDLINE | ID: mdl-19999660
10.
[Pathogenesis of age-related macular degeneration]. / Silmänpohjan ikärappeuman patogeneesi.
Duodecim
; 125(2): 145-53, 2009.
Artigo
em Fi
| MEDLINE | ID: mdl-19341030
11.
A founder mutation in CERKL is a major cause of retinal dystrophy in Finland.
Acta Ophthalmol
; 96(2): 183-191, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29068140
12.
Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population.
Mol Vis
; 12: 796-801, 2006 Jul 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-16885922
13.
The genetic variant rs4073 AâT of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degeneration.
Acta Ophthalmol
; 93(8): 726-33, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26154559
14.
Leucocyte telomere length in age-related macular degeneration.
Acta Ophthalmol
; 91(5): 453-6, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22551349
15.
Adiponectin receptor 1 gene (ADIPOR1) variant is associated with advanced age-related macular degeneration in Finnish population.
Neurosci Lett
; 513(2): 233-7, 2012 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-22387454
16.
Screening of DNA-variants in the properdin gene (CFP) in age-related macular degeneration (AMD).
Mol Immunol
; 47(6): 1334-6, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20122735
17.
Complement factor H Y402H polymorphism and characteristics of exudative age-related macular degeneration lesions.
Acta Ophthalmol
; 86(4): 390-4, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17995985
18.
Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration.
PLoS One
; 3(12): e3833, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-19048105
19.
Y402H polymorphism of complement factor H affects binding affinity to C-reactive protein.
J Immunol
; 178(6): 3831-6, 2007 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17339482