188 related articles for article (PubMed ID: 18464802)
1. Q455V mutation in COL8A2 is associated with Fuchs' corneal dystrophy in Korean patients.
Mok JW; Kim HS; Joo CK
Eye (Lond); 2009 Apr; 23(4):895-903. PubMed ID: 18464802
[TBL] [Abstract][Full Text] [Related]
2. Analysis of COL8A2 gene mutation in Japanese patients with Fuchs' endothelial dystrophy and posterior polymorphous dystrophy.
Kobayashi A; Fujiki K; Murakami A; Kato T; Chen LZ; Onoe H; Nakayasu K; Sakurai M; Takahashi M; Sugiyama K; Kanai A
Jpn J Ophthalmol; 2004; 48(3):195-8. PubMed ID: 15175909
[TBL] [Abstract][Full Text] [Related]
3. No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy.
Aldave AJ; Rayner SA; Salem AK; Yoo GL; Kim BT; Saeedian M; Sonmez B; Yellore VS
Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3787-90. PubMed ID: 16936088
[TBL] [Abstract][Full Text] [Related]
4. Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy.
Tang H; Zhang W; Yan XM; Wang LP; Dong H; Shou T; Lei H; Guo Q
Int J Mol Med; 2016 Jun; 37(6):1487-500. PubMed ID: 27121161
[TBL] [Abstract][Full Text] [Related]
5. Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.
Biswas S; Munier FL; Yardley J; Hart-Holden N; Perveen R; Cousin P; Sutphin JE; Noble B; Batterbury M; Kielty C; Hackett A; Bonshek R; Ridgway A; McLeod D; Sheffield VC; Stone EM; Schorderet DF; Black GC
Hum Mol Genet; 2001 Oct; 10(21):2415-23. PubMed ID: 11689488
[TBL] [Abstract][Full Text] [Related]
6. Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.
Minear MA; Li YJ; Rimmler J; Balajonda E; Watson S; Allingham RR; Hauser MA; Klintworth GK; Afshari NA; Gregory SG
Mol Vis; 2013; 19():2508-16. PubMed ID: 24348007
[TBL] [Abstract][Full Text] [Related]
7. Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India.
Hemadevi B; Srinivasan M; Arunkumar J; Prajna NV; Sundaresan P
BMC Ophthalmol; 2010 Feb; 10():3. PubMed ID: 20144242
[TBL] [Abstract][Full Text] [Related]
8. L450W and Q455K Col8a2 knock-in mouse models of Fuchs endothelial corneal dystrophy show distinct phenotypes and evidence for altered autophagy.
Meng H; Matthaei M; Ramanan N; Grebe R; Chakravarti S; Speck CL; Kimos M; Vij N; Eberhart CG; Jun AS
Invest Ophthalmol Vis Sci; 2013 Mar; 54(3):1887-97. PubMed ID: 23422828
[TBL] [Abstract][Full Text] [Related]
9. An alpha 2 collagen VIII transgenic knock-in mouse model of Fuchs endothelial corneal dystrophy shows early endothelial cell unfolded protein response and apoptosis.
Jun AS; Meng H; Ramanan N; Matthaei M; Chakravarti S; Bonshek R; Black GC; Grebe R; Kimos M
Hum Mol Genet; 2012 Jan; 21(2):384-93. PubMed ID: 22002996
[TBL] [Abstract][Full Text] [Related]
10. Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India.
Gupta R; Kumawat BL; Paliwal P; Tandon R; Sharma N; Sen S; Kashyap S; Nag TC; Vajpayee RB; Sharma A
Mol Vis; 2015; 21():1252-60. PubMed ID: 26622166
[TBL] [Abstract][Full Text] [Related]
11. Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of fuchs corneal dystrophy.
Gottsch JD; Sundin OH; Liu SH; Jun AS; Broman KW; Stark WJ; Vito EC; Narang AK; Thompson JM; Magovern M
Invest Ophthalmol Vis Sci; 2005 Jun; 46(6):1934-9. PubMed ID: 15914606
[TBL] [Abstract][Full Text] [Related]
12.
Moschos MM; Diamantopoulou A; Gouliopoulos N; Droutsas K; Bagli E; Chatzistefanou K; Kitsos G; Kroupis C
In Vivo; 2019; 33(3):963-971. PubMed ID: 31028223
[TBL] [Abstract][Full Text] [Related]
13. Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy.
Soumittra N; Loganathan SK; Madhavan D; Ramprasad VL; Arokiasamy T; Sumathi S; Karthiyayini T; Rachapalli SR; Kumaramanickavel G; Casey JR; Rajagopal R
J Hum Genet; 2014 Aug; 59(8):444-53. PubMed ID: 25007886
[TBL] [Abstract][Full Text] [Related]
14. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.
Lechner J; Dash DP; Muszynska D; Hosseini M; Segev F; George S; Frazer DG; Moore JE; Kaye SB; Young T; Simpson DA; Churchill AJ; Héon E; Willoughby CE
Invest Ophthalmol Vis Sci; 2013 May; 54(5):3215-23. PubMed ID: 23599324
[TBL] [Abstract][Full Text] [Related]
15. Screening of the COL8A2 gene in an Australian family with early-onset Fuchs' endothelial corneal dystrophy.
Kuot A; Mills R; Craig JE; Sharma S; Burdon KP
Clin Exp Ophthalmol; 2014 Mar; 42(2):198-200. PubMed ID: 23601356
[No Abstract] [Full Text] [Related]
16. Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy.
Igo RP; Kopplin LJ; Joseph P; Truitt B; Fondran J; Bardenstein D; Aldave AJ; Croasdale CR; Price MO; Rosenwasser M; Lass JH; Iyengar SK;
PLoS One; 2012; 7(10):e46742. PubMed ID: 23110055
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide linkage scan in fuchs endothelial corneal dystrophy.
Afshari NA; Li YJ; Pericak-Vance MA; Gregory S; Klintworth GK
Invest Ophthalmol Vis Sci; 2009 Mar; 50(3):1093-7. PubMed ID: 18502986
[TBL] [Abstract][Full Text] [Related]
18. British family with early-onset Fuchs' endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene.
Liskova P; Prescott Q; Bhattacharya SS; Tuft SJ
Br J Ophthalmol; 2007 Dec; 91(12):1717-8. PubMed ID: 18024822
[No Abstract] [Full Text] [Related]
19. A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.
Kelliher C; Chakravarti S; Vij N; Mazur S; Stahl PJ; Engler C; Matthaei M; Yu SM; Jun AS
Exp Eye Res; 2011 Dec; 93(6):880-8. PubMed ID: 22020132
[TBL] [Abstract][Full Text] [Related]
20. Transethnic replication of association of CTG18.1 repeat expansion of TCF4 gene with Fuchs' corneal dystrophy in Chinese implies common causal variant.
Xing C; Gong X; Hussain I; Khor CC; Tan DT; Aung T; Mehta JS; Vithana EN; Mootha VV
Invest Ophthalmol Vis Sci; 2014 Oct; 55(11):7073-8. PubMed ID: 25298419
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]