BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 33729517)

  • 21. Screening the visual system homeobox 1 gene in keratoconus and posterior polymorphous dystrophy cohorts identifies a novel variant.
    Vincent AL; Jordan C; Sheck L; Niederer R; Patel DV; McGhee CN
    Mol Vis; 2013; 19():852-60. PubMed ID: 23592923
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Multi-level consistent changes of the ECM pathway identified in a typical keratoconus twin's family by multi-omics analysis.
    Hao XD; Chen XN; Zhang YY; Chen P; Wei C; Shi WY; Gao H
    Orphanet J Rare Dis; 2020 Aug; 15(1):227. PubMed ID: 32867823
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya Angiopathy.
    Grangeon L; Guey S; Schwitalla JC; Bergametti F; Arnould M; Corpechot M; Hadjadj J; Riant F; Aloui C; Drunat S; Vidaud D; Tournier-Lasserve E; Kraemer M
    Stroke; 2019 Apr; 50(4):789-796. PubMed ID: 30908154
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Expression of type XII collagen and hemidesmosome-associated proteins in keratoconus corneas.
    Cheng EL; Maruyama I; SundarRaj N; Sugar J; Feder RS; Yue BY
    Curr Eye Res; 2001 May; 22(5):333-40. PubMed ID: 11600933
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification.
    Karolak JA; Polakowski P; Szaflik J; Szaflik JP; Gajecka M
    Ophthalmic Genet; 2016; 37(1):37-43. PubMed ID: 24940934
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Evidence against ZNF469 being causative for keratoconus in Polish patients.
    Karolak JA; Gambin T; Rydzanicz M; Szaflik JP; Polakowski P; Frajdenberg A; Mrugacz M; Podfigurna-Musielak M; Stankiewicz P; Gajecka M
    Acta Ophthalmol; 2016 May; 94(3):289-94. PubMed ID: 26806788
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The synthesis of glycosaminoglycans by cultures of corneal stromal cells from patients with keratoconus.
    Yue BY; Baum JL; Silbert JE
    J Clin Invest; 1979 Apr; 63(4):545-51. PubMed ID: 438319
    [TBL] [Abstract][Full Text] [Related]  

  • 28. WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness.
    Cuellar-Partida G; Springelkamp H; Lucas SE; Yazar S; Hewitt AW; Iglesias AI; Montgomery GW; Martin NG; Pennell CE; van Leeuwen EM; Verhoeven VJ; Hofman A; Uitterlinden AG; Ramdas WD; Wolfs RC; Vingerling JR; Brown MA; Mills RA; Craig JE; Klaver CC; van Duijn CM; Burdon KP; MacGregor S; Mackey DA
    Hum Mol Genet; 2015 Sep; 24(17):5060-8. PubMed ID: 26049155
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Identification of seven novel
    Yu X; Chen B; Zhang X; Shentu X
    Mol Vis; 2017; 23():296-305. PubMed ID: 28484309
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology.
    Baschal EE; Terhune EA; Wethey CI; Baschal RM; Robinson KD; Cuevas MT; Pradhan S; Sutphin BS; Taylor MRG; Gowan K; Pearson CG; Niswander LA; Jones KL; Miller NH
    G3 (Bethesda); 2018 Jul; 8(8):2663-2672. PubMed ID: 29930198
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Heterogeneity of type I collagen expression in human corneal keratoconus fibroblasts.
    Peters DP; Harrison DA; Brandt CR
    Ophthalmic Res; 1993; 25(5):273-9. PubMed ID: 7505054
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.
    Burdon KP; Coster DJ; Charlesworth JC; Mills RA; Laurie KJ; Giunta C; Hewitt AW; Latimer P; Craig JE
    Hum Genet; 2008 Nov; 124(4):379-86. PubMed ID: 18795334
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.
    Hardcastle AJ; Liskova P; Bykhovskaya Y; McComish BJ; Davidson AE; Inglehearn CF; Li X; Choquet H; Habeeb M; Lucas SEM; Sahebjada S; Pontikos N; Lopez KER; Khawaja AP; Ali M; Dudakova L; Skalicka P; Van Dooren BTH; Geerards AJM; Haudum CW; Faro VL; Tenen A; Simcoe MJ; Patasova K; Yarrand D; Yin J; Siddiqui S; Rice A; Farraj LA; Chen YI; Rahi JS; Krauss RM; Theusch E; Charlesworth JC; Szczotka-Flynn L; Toomes C; Meester-Smoor MA; Richardson AJ; Mitchell PA; Taylor KD; Melles RB; Aldave AJ; Mills RA; Cao K; Chan E; Daniell MD; Wang JJ; Rotter JI; Hewitt AW; MacGregor S; Klaver CCW; Ramdas WD; Craig JE; Iyengar SK; O'Brart D; Jorgenson E; Baird PN; Rabinowitz YS; Burdon KP; Hammond CJ; Tuft SJ; Hysi PG
    Commun Biol; 2021 Mar; 4(1):266. PubMed ID: 33649486
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of differentially expressed genes in keratoconus epithelium analyzed on microarrays.
    Nielsen K; Birkenkamp-Demtröder K; Ehlers N; Orntoft TF
    Invest Ophthalmol Vis Sci; 2003 Jun; 44(6):2466-76. PubMed ID: 12766045
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Variants in SKP1, PROB1, and IL17B genes at keratoconus 5q31.1-q35.3 susceptibility locus identified by whole-exome sequencing.
    Karolak JA; Gambin T; Pitarque JA; Molinari A; Jhangiani S; Stankiewicz P; Lupski JR; Gajecka M
    Eur J Hum Genet; 2017 Jan; 25(1):73-78. PubMed ID: 27703147
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Corneal Perforation After Corneal Cross-Linking in Keratoconus Associated With Potentially Pathogenic ZNF469 Mutations.
    Zhang W; Margines JB; Jacobs DS; Rabinowitz YS; Hanser EM; Chauhan T; Chung D; Bykhovskaya Y; Gaster RN; Aldave AJ
    Cornea; 2019 Aug; 38(8):1033-1039. PubMed ID: 31107761
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Enhanced expression of a transmembrane phosphotyrosine phosphatase (LAR) in keratoconus cultures and corneas.
    Chiplunkar S; Chamblis K; Chwa M; Rosenberg S; Kenney MC; Brown DJ
    Exp Eye Res; 1999 Mar; 68(3):283-93. PubMed ID: 10079136
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mitochondrial complex 1 gene analysis in keratoconus.
    Pathak D; Nayak B; Singh M; Sharma N; Tandon R; Sinha R; Titiyal JS; Dada R
    Mol Vis; 2011; 17():1514-25. PubMed ID: 21691575
    [TBL] [Abstract][Full Text] [Related]  

  • 39. EMMPRIN and MMP-1 in keratoconus.
    Seppälä HP; Määttä M; Rautia M; Mackiewicz Z; Tuisku I; Tervo T; Konttinen YT
    Cornea; 2006 Apr; 25(3):325-30. PubMed ID: 16633034
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Variant c.2262A>C in DOCK9 Leads to Exon Skipping in Keratoconus Family.
    Karolak JA; Rydzanicz M; Ginter-Matuszewska B; Pitarque JA; Molinari A; Bejjani BA; Gajecka M
    Invest Ophthalmol Vis Sci; 2015 Dec; 56(13):7687-90. PubMed ID: 26641546
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.