BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 30523160)

  • 21. From organ to cell: Multi-level telomere length assessment in patients with idiopathic pulmonary fibrosis.
    van Batenburg AA; Kazemier KM; van Oosterhout MFM; van der Vis JJ; van Es HW; Grutters JC; Goldschmeding R; van Moorsel CHM
    PLoS One; 2020; 15(1):e0226785. PubMed ID: 31910222
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Pulmonary Fibrosis and a TERT Founder Mutation With a Latency Period of 300 Years.
    van der Vis JJ; van der Smagt JJ; Hennekam FAM; Grutters JC; van Moorsel CHM
    Chest; 2020 Aug; 158(2):612-619. PubMed ID: 32315675
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features.
    Fernandez BA; Fox G; Bhatia R; Sala E; Noble B; Denic N; Fernandez D; Duguid N; Dohey A; Kamel F; Edwards L; Mahoney K; Stuckless S; Parfrey PS; Woods MO
    Respir Res; 2012 Aug; 13(1):64. PubMed ID: 22853774
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prevalence and characteristics of TERT and TERC mutations in suspected genetic pulmonary fibrosis.
    Borie R; Tabèze L; Thabut G; Nunes H; Cottin V; Marchand-Adam S; Prevot G; Tazi A; Cadranel J; Mal H; Wemeau-Stervinou L; Bergeron Lafaurie A; Israel-Biet D; Picard C; Reynaud Gaubert M; Jouneau S; Naccache JM; Mankikian J; Ménard C; Cordier JF; Valeyre D; Reocreux M; Grandchamp B; Revy P; Kannengiesser C; Crestani B
    Eur Respir J; 2016 Dec; 48(6):1721-1731. PubMed ID: 27836952
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Telomere shortening in familial and sporadic pulmonary fibrosis.
    Cronkhite JT; Xing C; Raghu G; Chin KM; Torres F; Rosenblatt RL; Garcia CK
    Am J Respir Crit Care Med; 2008 Oct; 178(7):729-37. PubMed ID: 18635888
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation.
    Gutierrez-Rodrigues F; Masri N; Chouery E; Diamond C; Jalkh N; Vicente A; Kajigaya S; Abillama F; Bejjani N; Serhal W; Calado RT; Young NS; Farhat H; Coussa ML
    Hum Genet; 2019 Dec; 138(11-12):1323-1330. PubMed ID: 31677132
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Subclinical lung disease, macrocytosis, and premature graying in kindreds with telomerase (TERT) mutations.
    Diaz de Leon A; Cronkhite JT; Yilmaz C; Brewington C; Wang R; Xing C; Hsia CCW; Garcia CK
    Chest; 2011 Sep; 140(3):753-763. PubMed ID: 21349926
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Interstitial pneumonia with autoimmune features and undifferentiated connective tissue disease: Our interdisciplinary rheumatology-pneumology experience, and review of the literature.
    Ferri C; Manfredi A; Sebastiani M; Colaci M; Giuggioli D; Vacchi C; Della Casa G; Cerri S; Torricelli P; Luppi F
    Autoimmun Rev; 2016 Jan; 15(1):61-70. PubMed ID: 26384526
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Adult-onset pulmonary fibrosis caused by mutations in telomerase.
    Tsakiri KD; Cronkhite JT; Kuan PJ; Xing C; Raghu G; Weissler JC; Rosenblatt RL; Shay JW; Garcia CK
    Proc Natl Acad Sci U S A; 2007 May; 104(18):7552-7. PubMed ID: 17460043
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders.
    Trotta L; Norberg A; Taskinen M; Béziat V; Degerman S; Wartiovaara-Kautto U; Välimaa H; Jahnukainen K; Casanova JL; Seppänen M; Saarela J; Koskenvuo M; Martelius T
    Orphanet J Rare Dis; 2018 Aug; 13(1):139. PubMed ID: 30115091
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Pulmonary surfactant protein adenosine triphosphate-binding-cassette-A3 gene composite mutations in infant congenital interstitial lung disease: report of a case and review of literature].
    Xie N; Chen DH; Lin YN; Wu SZ; Gu YY; Zeng QS; Zhai YY; Yang LY; Xu JX
    Zhonghua Er Ke Za Zhi; 2016 Oct; 54(10):761-766. PubMed ID: 27784479
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Rare Protein-Altering Telomere-related Gene Variants in Patients with Chronic Hypersensitivity Pneumonitis.
    Ley B; Torgerson DG; Oldham JM; Adegunsoye A; Liu S; Li J; Elicker BM; Henry TS; Golden JA; Jones KD; Dressen A; Yaspan BL; Arron JR; Noth I; Hoffmann TJ; Wolters PJ
    Am J Respir Crit Care Med; 2019 Nov; 200(9):1154-1163. PubMed ID: 31268371
    [No Abstract]   [Full Text] [Related]  

  • 33. Integrating Genomics Into Management of Fibrotic Interstitial Lung Disease.
    Adegunsoye A; Vij R; Noth I
    Chest; 2019 May; 155(5):1026-1040. PubMed ID: 30660786
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Nintedanib in patients with progressive fibrosing interstitial lung diseases-subgroup analyses by interstitial lung disease diagnosis in the INBUILD trial: a randomised, double-blind, placebo-controlled, parallel-group trial.
    Wells AU; Flaherty KR; Brown KK; Inoue Y; Devaraj A; Richeldi L; Moua T; Crestani B; Wuyts WA; Stowasser S; Quaresma M; Goeldner RG; Schlenker-Herceg R; Kolb M;
    Lancet Respir Med; 2020 May; 8(5):453-460. PubMed ID: 32145830
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Telomerase mutations in families with idiopathic pulmonary fibrosis.
    Armanios MY; Chen JJ; Cogan JD; Alder JK; Ingersoll RG; Markin C; Lawson WE; Xie M; Vulto I; Phillips JA; Lansdorp PM; Greider CW; Loyd JE
    N Engl J Med; 2007 Mar; 356(13):1317-26. PubMed ID: 17392301
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder.
    Bergantini L; Baldassarri M; d'Alessandro M; Brunelli G; Fabbri G; Zguro K; Degl'Innocenti A; ; Fallerini C; Bargagli E; Renieri A
    Respir Res; 2023 Jun; 24(1):158. PubMed ID: 37328761
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Role of Telomerase and Telomeres in Interstitial Lung Diseases: From Molecules to Clinical Implications.
    Arish N; Petukhov D; Wallach-Dayan SB
    Int J Mol Sci; 2019 Jun; 20(12):. PubMed ID: 31248154
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Telomerase-related monogenic lung fibrosis presenting with subacute onset: a case report and review of literature.
    Planté-Bordeneuve T; Haouas H; Vanderheyde K; Froidure A
    Acta Clin Belg; 2019 Dec; 74(6):445-450. PubMed ID: 30451599
    [No Abstract]   [Full Text] [Related]  

  • 39. Novel heterozygous mutation of RTEL1 in interstitial pneumonia with autoimmune feature.
    Yuan ZZ; Fan LL; Wang CY; Luo H; Liu L
    QJM; 2022 Apr; 115(4):253-255. PubMed ID: 34894270
    [No Abstract]   [Full Text] [Related]  

  • 40. Prevalence and prognosis of unclassifiable interstitial lung disease.
    Ryerson CJ; Urbania TH; Richeldi L; Mooney JJ; Lee JS; Jones KD; Elicker BM; Koth LL; King TE; Wolters PJ; Collard HR
    Eur Respir J; 2013 Sep; 42(3):750-7. PubMed ID: 23222877
    [TBL] [Abstract][Full Text] [Related]  

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