302 related articles for article (PubMed ID: 19005574)
1. The EPHA2 gene is associated with cataracts linked to chromosome 1p.
Shiels A; Bennett TM; Knopf HL; Maraini G; Li A; Jiao X; Hejtmancik JF
Mol Vis; 2008; 14():2042-55. PubMed ID: 19005574
[TBL] [Abstract][Full Text] [Related]
2. CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20q.
Shiels A; Bennett TM; Knopf HL; Yamada K; Yoshiura K; Niikawa N; Shim S; Hanson PI
Am J Hum Genet; 2007 Sep; 81(3):596-606. PubMed ID: 17701905
[TBL] [Abstract][Full Text] [Related]
3. Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family.
Kaul H; Riazuddin SA; Shahid M; Kousar S; Butt NH; Zafar AU; Khan SN; Husnain T; Akram J; Hejtmancik JF; Riazuddin S
Mol Vis; 2010 Mar; 16():511-7. PubMed ID: 20361013
[TBL] [Abstract][Full Text] [Related]
4. Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract.
Bennett TM; Maraini G; Jin C; Sun W; Hejtmancik JF; Shiels A
Mol Vis; 2013; 19():835-44. PubMed ID: 23592921
[TBL] [Abstract][Full Text] [Related]
5. X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7.
Shiels A; Bennett TM; Prince JB; Tychsen L
Mol Vis; 2007 Nov; 13():2233-41. PubMed ID: 18087240
[TBL] [Abstract][Full Text] [Related]
6. A recurrent missense mutation in GJA3 associated with autosomal dominant cataract linked to chromosome 13q.
Bennett TM; Shiels A
Mol Vis; 2011; 17():2255-62. PubMed ID: 21897748
[TBL] [Abstract][Full Text] [Related]
7. Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts.
Li F; Wang S; Gao C; Liu S; Zhao B; Zhang M; Huang S; Zhu S; Ma X
Mol Vis; 2008 Mar; 14():378-86. PubMed ID: 18334953
[TBL] [Abstract][Full Text] [Related]
8. A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
Bennett TM; Mackay DS; Knopf HL; Shiels A
Mol Vis; 2004 Jun; 10():376-82. PubMed ID: 15208569
[TBL] [Abstract][Full Text] [Related]
9. A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts.
Ma X; Li FF; Wang SZ; Gao C; Zhang M; Zhu SQ
Mol Vis; 2008; 14():1906-11. PubMed ID: 18958306
[TBL] [Abstract][Full Text] [Related]
10. EPHA2 is associated with age-related cortical cataract in mice and humans.
Jun G; Guo H; Klein BE; Klein R; Wang JJ; Mitchell P; Miao H; Lee KE; Joshi T; Buck M; Chugha P; Bardenstein D; Klein AP; Bailey-Wilson JE; Gong X; Spector TD; Andrew T; Hammond CJ; Elston RC; Iyengar SK; Wang B
PLoS Genet; 2009 Jul; 5(7):e1000584. PubMed ID: 19649315
[TBL] [Abstract][Full Text] [Related]
11. Association of EPHA2 polymorphisms and age-related cortical cataract in a Han Chinese population.
Tan W; Hou S; Jiang Z; Hu Z; Yang P; Ye J
Mol Vis; 2011; 17():1553-8. PubMed ID: 21686326
[TBL] [Abstract][Full Text] [Related]
12. Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract.
Zhang T; Hua R; Xiao W; Burdon KP; Bhattacharya SS; Craig JE; Shang D; Zhao X; Mackey DA; Moore AT; Luo Y; Zhang J; Zhang X
Hum Mutat; 2009 May; 30(5):E603-11. PubMed ID: 19306328
[TBL] [Abstract][Full Text] [Related]
13. Functional analysis of deleterious
Li D; Han X; Zhao Z; Lu Y; Yang J
Mol Vis; 2021; 27():384-395. PubMed ID: 34220184
[TBL] [Abstract][Full Text] [Related]
14. A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract.
Berry V; Francis PJ; Prescott Q; Waseem NH; Moore AT; Bhattacharya SS
Mol Vis; 2011; 17():1249-53. PubMed ID: 21633712
[TBL] [Abstract][Full Text] [Related]
15. Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts.
Li FF; Zhu SQ; Wang SZ; Gao C; Huang SZ; Zhang M; Ma X
Mol Vis; 2008 Apr; 14():750-5. PubMed ID: 18449377
[TBL] [Abstract][Full Text] [Related]
16. A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea.
Zhang L; Fu S; Ou Y; Zhao T; Su Y; Liu P
Mol Vis; 2009; 15():276-82. PubMed ID: 19204787
[TBL] [Abstract][Full Text] [Related]
17. Functional analysis of deleterious
Li D; Han X; Zhao Z; Lu Y; Yang J
Mol Vis; 2021; 27():403-414. PubMed ID: 34267496
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel C-terminal extension mutation in EPHA2 in a family affected with congenital cataract.
Reis LM; Tyler RC; Semina EV
Mol Vis; 2014; 20():836-42. PubMed ID: 24940039
[TBL] [Abstract][Full Text] [Related]
19. Congenital anterior polar cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.
Zhang L; Zhang Y; Liu P; Cao W; Tang X; Su S
Mol Vis; 2011; 17():2693-7. PubMed ID: 22065922
[TBL] [Abstract][Full Text] [Related]
20. A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q.
Mackay DS; Andley UP; Shiels A
Mol Vis; 2004 Mar; 10():155-62. PubMed ID: 15041957
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]