BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 27845061)

  • 1. Major review: Exfoliation syndrome; advances in disease genetics, molecular biology, and epidemiology.
    Aboobakar IF; Johnson WM; Stamer WD; Hauser MA; Allingham RR
    Exp Eye Res; 2017 Jan; 154():88-103. PubMed ID: 27845061
    [TBL] [Abstract][Full Text] [Related]  

  • 2. From epidemiology to lysyl oxidase like one (LOXL1) polymorphisms discovery: phenotyping and genotyping exfoliation syndrome and exfoliation glaucoma in Iceland.
    Jonasson F
    Acta Ophthalmol; 2009 Aug; 87(5):478-87. PubMed ID: 19664108
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The role of lysyl oxidase-like 1 (LOXL1) in exfoliation syndrome and glaucoma.
    Schlötzer-Schrehardt U; Zenkel M
    Exp Eye Res; 2019 Dec; 189():107818. PubMed ID: 31563608
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Expression and regulation of LOXL1 and elastin-related genes in eyes with exfoliation syndrome.
    Zenkel M; Schlötzer-Schrehardt U
    J Glaucoma; 2014; 23(8 Suppl 1):S48-50. PubMed ID: 25275906
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevalence of high-risk alleles in the LOXL1 gene and its association with pseudoexfoliation syndrome and exfoliation glaucoma in a Latin American population.
    Jaimes M; Rivera-Parra D; Miranda-Duarte A; Valdés G; Zenteno JC
    Ophthalmic Genet; 2012 Mar; 33(1):12-7. PubMed ID: 21970694
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exfoliation syndrome: beyond glaucoma.
    Ritch R
    Arch Ophthalmol; 2008 Jun; 126(6):859-61. PubMed ID: 18541854
    [No Abstract]   [Full Text] [Related]  

  • 7. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
    Aung T; Ozaki M; Lee MC; Schlötzer-Schrehardt U; Thorleifsson G; Mizoguchi T; Igo RP; Haripriya A; Williams SE; Astakhov YS; Orr AC; Burdon KP; Nakano S; Mori K; Abu-Amero K; Hauser M; Li Z; Prakadeeswari G; Bailey JNC; Cherecheanu AP; Kang JH; Nelson S; Hayashi K; Manabe SI; Kazama S; Zarnowski T; Inoue K; Irkec M; Coca-Prados M; Sugiyama K; Järvelä I; Schlottmann P; Lerner SF; Lamari H; Nilgün Y; Bikbov M; Park KH; Cha SC; Yamashiro K; Zenteno JC; Jonas JB; Kumar RS; Perera SA; Chan ASY; Kobakhidze N; George R; Vijaya L; Do T; Edward DP; de Juan Marcos L; Pakravan M; Moghimi S; Ideta R; Bach-Holm D; Kappelgaard P; Wirostko B; Thomas S; Gaston D; Bedard K; Greer WL; Yang Z; Chen X; Huang L; Sang J; Jia H; Jia L; Qiao C; Zhang H; Liu X; Zhao B; Wang YX; Xu L; Leruez S; Reynier P; Chichua G; Tabagari S; Uebe S; Zenkel M; Berner D; Mossböck G; Weisschuh N; Hoja U; Welge-Luessen UC; Mardin C; Founti P; Chatzikyriakidou A; Pappas T; Anastasopoulos E; Lambropoulos A; Ghosh A; Shetty R; Porporato N; Saravanan V; Venkatesh R; Shivkumar C; Kalpana N; Sarangapani S; Kanavi MR; Beni AN; Yazdani S; Lashay A; Naderifar H; Khatibi N; Fea A; Lavia C; Dallorto L; Rolle T; Frezzotti P; Paoli D; Salvi E; Manunta P; Mori Y; Miyata K; Higashide T; Chihara E; Ishiko S; Yoshida A; Yanagi M; Kiuchi Y; Ohashi T; Sakurai T; Sugimoto T; Chuman H; Aihara M; Inatani M; Miyake M; Gotoh N; Matsuda F; Yoshimura N; Ikeda Y; Ueno M; Sotozono C; Jeoung JW; Sagong M; Park KH; Ahn J; Cruz-Aguilar M; Ezzouhairi SM; Rafei A; Chong YF; Ng XY; Goh SR; Chen Y; Yong VHK; Khan MI; Olawoye OO; Ashaye AO; Ugbede I; Onakoya A; Kizor-Akaraiwe N; Teekhasaenee C; Suwan Y; Supakontanasan W; Okeke S; Uche NJ; Asimadu I; Ayub H; Akhtar F; Kosior-Jarecka E; Lukasik U; Lischinsky I; Castro V; Grossmann RP; Sunaric Megevand G; Roy S; Dervan E; Silke E; Rao A; Sahay P; Fornero P; Cuello O; Sivori D; Zompa T; Mills RA; Souzeau E; Mitchell P; Wang JJ; Hewitt AW; Coote M; Crowston JG; Astakhov SY; Akopov EL; Emelyanov A; Vysochinskaya V; Kazakbaeva G; Fayzrakhmanov R; Al-Obeidan SA; Owaidhah O; Aljasim LA; Chowbay B; Foo JN; Soh RQ; Sim KS; Xie Z; Cheong AWO; Mok SQ; Soo HM; Chen XY; Peh SQ; Heng KK; Husain R; Ho SL; Hillmer AM; Cheng CY; Escudero-Domínguez FA; González-Sarmiento R; Martinon-Torres F; Salas A; Pathanapitoon K; Hansapinyo L; Wanichwecharugruang B; Kitnarong N; Sakuntabhai A; Nguyn HX; Nguyn GTT; Nguyn TV; Zenz W; Binder A; Klobassa DS; Hibberd ML; Davila S; Herms S; Nöthen MM; Moebus S; Rautenbach RM; Ziskind A; Carmichael TR; Ramsay M; Álvarez L; García M; González-Iglesias H; Rodríguez-Calvo PP; Fernández-Vega Cueto L; Oguz Ç; Tamcelik N; Atalay E; Batu B; Aktas D; Kasım B; Wilson MR; Coleman AL; Liu Y; Challa P; Herndon L; Kuchtey RW; Kuchtey J; Curtin K; Chaya CJ; Crandall A; Zangwill LM; Wong TY; Nakano M; Kinoshita S; den Hollander AI; Vesti E; Fingert JH; Lee RK; Sit AJ; Shingleton BJ; Wang N; Cusi D; Qamar R; Kraft P; Pericak-Vance MA; Raychaudhuri S; Heegaard S; Kivelä T; Reis A; Kruse FE; Weinreb RN; Pasquale LR; Haines JL; Thorsteinsdottir U; Jonasson F; Allingham RR; Milea D; Ritch R; Kubota T; Tashiro K; Vithana EN; Micheal S; Topouzis F; Craig JE; Dubina M; Sundaresan P; Stefansson K; Wiggs JL; Pasutto F; Khor CC
    Nat Genet; 2017 Jul; 49(7):993-1004. PubMed ID: 28553957
    [TBL] [Abstract][Full Text] [Related]  

  • 8. LOXL1 gene polymorphisms are associated with exfoliation syndrome/exfoliation glaucoma risk: An updated meta-analysis.
    Li X; He J; Sun J
    PLoS One; 2021; 16(4):e0250772. PubMed ID: 33909695
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exfoliation syndrome: assembling the puzzle pieces.
    Pasquale LR; Borrás T; Fingert JH; Wiggs JL; Ritch R
    Acta Ophthalmol; 2016 Sep; 94(6):e505-12. PubMed ID: 26648185
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.
    Bernstein AM; Ritch R; Wolosin JM
    J Glaucoma; 2018 Jul; 27 Suppl 1(Suppl 1):S44-S53. PubMed ID: 29547474
    [TBL] [Abstract][Full Text] [Related]  

  • 11. LOXL1 Gene Polymorphism With Exfoliation Syndrome/Exfoliation Glaucoma: A Meta-Analysis.
    Wang L; Yu Y; Fu S; Zhao W; Liu P
    J Glaucoma; 2016 Jan; 25(1):62-94. PubMed ID: 25304275
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus.
    Hauser MA; Aboobakar IF; Liu Y; Miura S; Whigham BT; Challa P; Wheeler J; Williams A; Santiago-Turla C; Qin X; Rautenbach RM; Ziskind A; Ramsay M; Uebe S; Song L; Safi A; Vithana EN; Mizoguchi T; Nakano S; Kubota T; Hayashi K; Manabe S; Kazama S; Mori Y; Miyata K; Yoshimura N; Reis A; Crawford GE; Pasutto F; Carmichael TR; Williams SE; Ozaki M; Aung T; Khor CC; Stamer WD; Ashley-Koch AE; Allingham RR
    Hum Mol Genet; 2015 Nov; 24(22):6552-63. PubMed ID: 26307087
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.
    Thorleifsson G; Magnusson KP; Sulem P; Walters GB; Gudbjartsson DF; Stefansson H; Jonsson T; Jonasdottir A; Jonasdottir A; Stefansdottir G; Masson G; Hardarson GA; Petursson H; Arnarsson A; Motallebipour M; Wallerman O; Wadelius C; Gulcher JR; Thorsteinsdottir U; Kong A; Jonasson F; Stefansson K
    Science; 2007 Sep; 317(5843):1397-400. PubMed ID: 17690259
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recent advances in risk factors associated with ocular exfoliation syndrome.
    Ghaffari Sharaf M; Damji KF; Unsworth LD
    Acta Ophthalmol; 2020 Mar; 98(2):113-120. PubMed ID: 31736276
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Regulation of lysyl oxidase-like 1 (LOXL1) and elastin-related genes by pathogenic factors associated with pseudoexfoliation syndrome.
    Zenkel M; Krysta A; Pasutto F; Juenemann A; Kruse FE; Schlötzer-Schrehardt U
    Invest Ophthalmol Vis Sci; 2011 Oct; 52(11):8488-95. PubMed ID: 21948647
    [TBL] [Abstract][Full Text] [Related]  

  • 16. LOXL1 expression in lens capsule tissue specimens from individuals with pseudoexfoliation syndrome and glaucoma.
    Khan TT; Li G; Navarro ID; Kastury RD; Zeil CJ; Semchyshyn TM; Moya FJ; Epstein DL; Gonzalez P; Challa P
    Mol Vis; 2010 Nov; 16():2236-41. PubMed ID: 21139690
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of LOXL1 gene with Finnish exfoliation syndrome patients.
    Lemmelä S; Forsman E; Onkamo P; Nurmi H; Laivuori H; Kivelä T; Puska P; Heger M; Eriksson A; Forsius H; Järvelä I
    J Hum Genet; 2009 May; 54(5):289-97. PubMed ID: 19343041
    [TBL] [Abstract][Full Text] [Related]  

  • 18. LOXL1 folding in exfoliation glaucoma.
    Bernstein AM; Ritch R; Wolosin JM
    Adv Protein Chem Struct Biol; 2019; 118():273-288. PubMed ID: 31928728
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome.
    Hirbo JB; Pasutto F; Gamazon ER; Evans P; Pawar P; Berner D; Sealock J; Tao R; Straub PS; Konkashbaev AI; Breyer MA; Schlötzer-Schrehardt U; Reis A; Brantley MA; Khor CC; Joos KM; Cox NJ
    BMC Genomics; 2023 Feb; 24(1):75. PubMed ID: 36797672
    [TBL] [Abstract][Full Text] [Related]  

  • 20. LOXL1 gene sequence variants and vascular disease in exfoliation syndrome and exfoliative glaucoma.
    Holló G; Gál A; Kóthy P; Molnár JM
    J Glaucoma; 2011 Mar; 20(3):143-7. PubMed ID: 20436359
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.