344 related articles for article (PubMed ID: 17558846)
1. Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.
Aldave AJ; Sonmez B; Bourla N; Schultz G; Papp JC; Salem AK; Rayner SA; Yellore VS
Ophthalmic Genet; 2007 Jun; 28(2):57-67. PubMed ID: 17558846
[TBL] [Abstract][Full Text] [Related]
2. Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.
Aldave AJ; Rosenwasser GO; Yellore VS; Papp JC; Sobel EM; Pham MN; Chen MC; Dandekar S; Sripracha R; Rayner SA; Sassani JW; Gorin MB
Invest Ophthalmol Vis Sci; 2010 Aug; 51(8):4006-12. PubMed ID: 20357198
[TBL] [Abstract][Full Text] [Related]
3. Targeted expression of a lumican transgene rescues corneal deficiencies in lumican-null mice.
Meij JT; Carlson EC; Wang L; Liu CY; Jester JV; Birk DE; Kao WW
Mol Vis; 2007 Oct; 13():2012-8. PubMed ID: 17982425
[TBL] [Abstract][Full Text] [Related]
4. A novel keratocan mutation causing autosomal recessive cornea plana.
Lehmann OJ; El-ashry MF; Ebenezer ND; Ocaka L; Francis PJ; Wilkie SE; Patel RJ; Ficker L; Jordan T; Khaw PT; Bhattacharya SS
Invest Ophthalmol Vis Sci; 2001 Dec; 42(13):3118-22. PubMed ID: 11726611
[TBL] [Abstract][Full Text] [Related]
5. Case report: a novel KERA mutation associated with cornea plana and its predicted effect on protein function.
Roos L; Bertelsen B; Harris P; Bygum A; Jensen H; Grønskov K; Tümer Z
BMC Med Genet; 2015 Jun; 16():40. PubMed ID: 26099342
[TBL] [Abstract][Full Text] [Related]
6. A new autosomal dominant Peters' anomaly phenotype expanding the anterior segment dysgenesis spectrum.
Berker N; Alanay Y; Elgin U; Volkan-Salanci B; Simsek T; Akarsu N; Alikasifoglu M
Acta Ophthalmol; 2009 Feb; 87(1):52-7. PubMed ID: 18616618
[TBL] [Abstract][Full Text] [Related]
7. Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12.
Kim MJ; Frausto RF; Rosenwasser GO; Bui T; Le DJ; Stone EM; Aldave AJ
PLoS One; 2014; 9(4):e95037. PubMed ID: 24759697
[TBL] [Abstract][Full Text] [Related]
8. Exclusion of lumican and fibromodulin as candidate genes in MYP3 linked high grade myopia.
Paluru PC; Scavello GS; Ganter WR; Young TL
Mol Vis; 2004 Nov; 10():917-22. PubMed ID: 15592176
[TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular characterization of a family with autosomal recessive cornea plana.
Ebenezer ND; Patel CB; Hariprasad SM; Chen LL; Patel RJ; Hardcastle AJ; Allen RC
Arch Ophthalmol; 2005 Sep; 123(9):1248-53. PubMed ID: 16157807
[TBL] [Abstract][Full Text] [Related]
10. Keratocan-deficient mice display alterations in corneal structure.
Liu CY; Birk DE; Hassell JR; Kane B; Kao WW
J Biol Chem; 2003 Jun; 278(24):21672-7. PubMed ID: 12665512
[TBL] [Abstract][Full Text] [Related]
11. Mutations in KERA, encoding keratocan, cause cornea plana.
Pellegata NS; Dieguez-Lucena JL; Joensuu T; Lau S; Montgomery KT; Krahe R; Kivelä T; Kucherlapati R; Forsius H; de la Chapelle A
Nat Genet; 2000 May; 25(1):91-5. PubMed ID: 10802664
[TBL] [Abstract][Full Text] [Related]
12. The association of haplotype at the lumican gene with high myopia susceptibility in Taiwanese patients.
Chen ZT; Wang IJ; Shih YF; Lin LL
Ophthalmology; 2009 Oct; 116(10):1920-7. PubMed ID: 19616852
[TBL] [Abstract][Full Text] [Related]
13. Genes encoding proteoglycans are associated with the risk of anterior cruciate ligament ruptures.
Mannion S; Mtintsilana A; Posthumus M; van der Merwe W; Hobbs H; Collins M; September AV
Br J Sports Med; 2014 Dec; 48(22):1640-6. PubMed ID: 24552666
[TBL] [Abstract][Full Text] [Related]
14. Keratocan and lumican regulate neutrophil infiltration and corneal clarity in lipopolysaccharide-induced keratitis by direct interaction with CXCL1.
Carlson EC; Lin M; Liu CY; Kao WW; Perez VL; Pearlman E
J Biol Chem; 2007 Dec; 282(49):35502-9. PubMed ID: 17911102
[TBL] [Abstract][Full Text] [Related]
15. A novel KERA mutation associated with autosomal recessive cornea plana.
Khan A; Al-Saif A; Kambouris M
Ophthalmic Genet; 2004 Jun; 25(2):147-52. PubMed ID: 15370545
[TBL] [Abstract][Full Text] [Related]
16. Keratocan, a cornea-specific keratan sulfate proteoglycan, is regulated by lumican.
Carlson EC; Liu CY; Chikama T; Hayashi Y; Kao CW; Birk DE; Funderburgh JL; Jester JV; Kao WW
J Biol Chem; 2005 Jul; 280(27):25541-7. PubMed ID: 15849191
[TBL] [Abstract][Full Text] [Related]
17. A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.
Micheal S; Siddiqui SN; Zafar SN; Villanueva-Mendoza C; Cortés-González V; Khan MI; den Hollander AI
PLoS One; 2016; 11(7):e0160016. PubMed ID: 27463523
[TBL] [Abstract][Full Text] [Related]
18. Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma.
Cella W; de Vasconcellos JP; de Melo MB; Kneipp B; Costa FF; Longui CA; Costa VP
Invest Ophthalmol Vis Sci; 2006 May; 47(5):1803-9. PubMed ID: 16638984
[TBL] [Abstract][Full Text] [Related]
19. Evaluation of proteoglycan gene polymorphisms as risk factors in the genetic susceptibility to high myopia.
Yip SP; Leung KH; Ng PW; Fung WY; Sham PC; Yap MK
Invest Ophthalmol Vis Sci; 2011 Aug; 52(9):6396-403. PubMed ID: 21743019
[TBL] [Abstract][Full Text] [Related]
20. Genomic characterization of human DSPG3.
Deere M; Dieguez JL; Yoon SJ; Hewett-Emmett D; de la Chapelle A; Hecht JT
Genome Res; 1999 May; 9(5):449-56. PubMed ID: 10330124
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]