BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 26900323)

  • 1. EPHA2 MUTATIONS CONTRIBUTE TO CONGENITAL CATARACT THROUGH DIVERSE MECHANISMS.
    Dave A; Martin S; Kumar R; Craig JE; Burdon KP; Sharma S
    Mol Vis; 2016; 22():18-30. PubMed ID: 26900323
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Novel Human Congenital Cataract Mutation in EPHA2 Kinase Domain (p.G668D) Alters Receptor Stability and Function.
    Zhai Y; Zhu S; Li J; Yao K
    Invest Ophthalmol Vis Sci; 2019 Nov; 60(14):4717-4726. PubMed ID: 31725171
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The status of intercellular junctions in established lens epithelial cell lines.
    Dave A; Craig JE; Sharma S
    Mol Vis; 2012; 18():2937-46. PubMed ID: 23288986
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Human cataract mutations in EPHA2 SAM domain alter receptor stability and function.
    Park JE; Son AI; Hua R; Wang L; Zhang X; Zhou R
    PLoS One; 2012; 7(5):e36564. PubMed ID: 22570727
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia.
    Dave A; Laurie K; Staffieri SE; Taranath D; Mackey DA; Mitchell P; Wang JJ; Craig JE; Burdon KP; Sharma S
    PLoS One; 2013; 8(8):e72518. PubMed ID: 24014202
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mutation of the EPHA2 Tyrosine-Kinase Domain Dysregulates Cell Pattern Formation and Cytoskeletal Gene Expression in the Lens.
    Zhou Y; Bennett TM; Ruzycki PA; Shiels A
    Cells; 2021 Sep; 10(10):. PubMed ID: 34685586
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Abnormal function of
    Zhang JJ; Cao ZF; Zhou BT; Yang JH; Li Z; Lin S; Chen XL; Zhang NW; Ye Q; Ma X; Zhu YH
    Int J Ophthalmol; 2024; 17(6):1007-1017. PubMed ID: 38895685
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epha2 genotype influences ultraviolet radiation induced cataract in mice.
    Dave A; Craig JE; Skrzypiec K; Quinn S; Barnes M; Di Girolamo N; Mackey DA; Burdon KP; de Iongh RU; Sharma S
    Exp Eye Res; 2019 Nov; 188():107806. PubMed ID: 31539542
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structural investigation of a C-terminal EphA2 receptor mutant: Does mutation affect the structure and interaction properties of the Sam domain?
    Mercurio FA; Costantini S; Di Natale C; Pirone L; Guariniello S; Scognamiglio PL; Marasco D; Pedone EM; Leone M
    Biochim Biophys Acta Proteins Proteom; 2017 Sep; 1865(9):1095-1104. PubMed ID: 28602916
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel splice donor site mutation in EPHA2 caused congenital cataract in a Chinese family.
    Bu J; He S; Wang L; Li J; Liu J; Zhang X
    Indian J Ophthalmol; 2016 May; 64(5):364-8. PubMed ID: 27380975
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Epha2 and Efna5 participate in lens cell pattern-formation.
    Zhou Y; Shiels A
    Differentiation; 2018; 102():1-9. PubMed ID: 29800803
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract.
    Berry V; Pontikos N; Albarca-Aguilera M; Plagnol V; Massouras A; Prescott D; Moore AT; Arno G; Cheetham ME; Michaelides M
    Ophthalmic Genet; 2018 Apr; 39(2):236-241. PubMed ID: 29039721
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. EPHA2 Polymorphisms in Estonian Patients with Age-Related Cataract.
    Celojevic D; Abramsson A; Seibt Palmér M; Tasa G; Juronen E; Zetterberg H; Zetterberg M
    Ophthalmic Genet; 2016; 37(1):14-8. PubMed ID: 24673449
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Germ-line and somatic EPHA2 coding variants in lens aging and cataract.
    Bennett TM; M'Hamdi O; Hejtmancik JF; Shiels A
    PLoS One; 2017; 12(12):e0189881. PubMed ID: 29267365
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Biallelic Variants in
    Jarwar P; Sheikh SA; Waryah YM; Ujjan IU; Riazuddin S; Waryah AM; Ahmed ZM
    Int J Mol Sci; 2021 Sep; 22(19):. PubMed ID: 34638995
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.