BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 19649315)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. 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]  

  • 26. Mapping the Universe of Eph Receptor and Ephrin Ligand Transcripts in Epithelial and Fiber Cells of the Eye Lens.
    Vu MP; Cheng C
    Cells; 2022 Oct; 11(20):. PubMed ID: 36291158
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Further analysis of the lens of ephrin-A5-/- mice: development of postnatal defects.
    Son AI; Cooper MA; Sheleg M; Sun Y; Kleiman NJ; Zhou R
    Mol Vis; 2013; 19():254-66. PubMed ID: 23401654
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Association of the ephreceptor tyrosinekinase-type A2 (EPHA2) gene polymorphism rs3754334 with age-related cataract risk: a meta-analysis.
    Yang J; Luo J; Zhou P; Fan Q; Luo Y; Lu Y
    PLoS One; 2013; 8(8):e71003. PubMed ID: 23976972
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular characterization of mouse lens epithelial cell lines and their suitability to study RNA granules and cataract associated genes.
    Terrell AM; Anand D; Smith SF; Dang CA; Waters SM; Pathania M; Beebe DC; Lachke SA
    Exp Eye Res; 2015 Feb; 131():42-55. PubMed ID: 25530357
    [TBL] [Abstract][Full Text] [Related]  

  • 31. p62 expression and autophagy in αB-crystallin R120G mutant knock-in mouse model of hereditary cataract.
    Wignes JA; Goldman JW; Weihl CC; Bartley MG; Andley UP
    Exp Eye Res; 2013 Oct; 115():263-73. PubMed ID: 23872361
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. Microphakia and congenital cataract formation in a novel Lim2(C51R) mutant mouse.
    Puk O; Ahmad N; Wagner S; de Angelis MH; Graw J
    Mol Vis; 2011; 17():1164-71. PubMed ID: 21617753
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Targeted deletion of the murine Lgr4 gene decreases lens epithelial cell resistance to oxidative stress and induces age-related cataract formation.
    Zhu J; Hou Q; Dong XD; Wang Z; Chen X; Zheng D; Zhou L; He C; Liu M; Tu L; Qu J
    PLoS One; 2015; 10(3):e0119599. PubMed ID: 25811370
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic Factors.
    Lhussiez V; Dubus E; Cesar Q; Acar N; Nandrot EF; Simonutti M; Audo I; Lizé E; Nguyen S; Geissler A; Bouchot A; Ansar M; Picaud S; Thauvin-Robinet C; Olivier-Faivre L; Duplomb L; Da Costa R
    Invest Ophthalmol Vis Sci; 2020 Sep; 61(11):18. PubMed ID: 32915983
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Age-related retention of fiber cell nuclei and nuclear fragments in the lens cortices of multiple species.
    Pendergrass W; Zitnik G; Urfer SR; Wolf N
    Mol Vis; 2011; 17():2672-84. PubMed ID: 22065920
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Loss of EphA2 receptor tyrosine kinase reduces ApcMin/+ tumorigenesis.
    Bogan C; Chen J; O'Sullivan MG; Cormier RT
    Int J Cancer; 2009 Mar; 124(6):1366-71. PubMed ID: 19089910
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    Harding P; Toms M; Schiff E; Owen N; Bell S; Lloyd IC; Moosajee M
    Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33671840
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.