761 related articles for article (PubMed ID: 17460043)
1. 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]
2. Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations.
Diaz de Leon A; Cronkhite JT; Katzenstein AL; Godwin JD; Raghu G; Glazer CS; Rosenblatt RL; Girod CE; Garrity ER; Xing C; Garcia CK
PLoS One; 2010 May; 5(5):e10680. PubMed ID: 20502709
[TBL] [Abstract][Full Text] [Related]
3. Telomerase gene mutations and telomere length shortening in patients with idiopathic pulmonary fibrosis in a Chinese population.
Dai J; Cai H; Zhuang Y; Wu Y; Min H; Li J; Shi Y; Gao Q; Yi L
Respirology; 2015 Jan; 20(1):122-8. PubMed ID: 25346280
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. A Rare Missense Variant in Telomerase Reverse Transcriptase is Associated with Idiopathic Pulmonary Fibrosis in a Chinese Han Family.
Zheng CM; Zhan X; Yang YH; Jiang T; Ye Q; Lu Y
Chin Med J (Engl); 2018 Sep; 131(18):2205-2209. PubMed ID: 30203795
[TBL] [Abstract][Full Text] [Related]
8. Functional characterization of novel telomerase RNA (TERC) mutations in patients with diverse clinical and pathological presentations.
Marrone A; Sokhal P; Walne A; Beswick R; Kirwan M; Killick S; Williams M; Marsh J; Vulliamy T; Dokal I
Haematologica; 2007 Aug; 92(8):1013-20. PubMed ID: 17640862
[TBL] [Abstract][Full Text] [Related]
9. Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis.
Alder JK; Cogan JD; Brown AF; Anderson CJ; Lawson WE; Lansdorp PM; Phillips JA; Loyd JE; Chen JJ; Armanios M
PLoS Genet; 2011 Mar; 7(3):e1001352. PubMed ID: 21483807
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Investigation of telomere related gene mutations in idiopathic pulmonary fibrosis.
Yildirim H; Yildiz P; Coskunpinar E
Mol Biol Rep; 2020 Oct; 47(10):7851-7860. PubMed ID: 33006015
[TBL] [Abstract][Full Text] [Related]
12. Telomerase deficiency does not alter bleomycin-induced fibrosis in mice.
Degryse AL; Xu XC; Newman JL; Mitchell DB; Tanjore H; Polosukhin VV; Jones BR; McMahon FB; Gleaves LA; Phillips JA; Cogan JD; Blackwell TS; Lawson WE
Exp Lung Res; 2012 Apr; 38(3):124-34. PubMed ID: 22394286
[TBL] [Abstract][Full Text] [Related]
13. Telomerase mutations in smokers with severe emphysema.
Stanley SE; Chen JJ; Podlevsky JD; Alder JK; Hansel NN; Mathias RA; Qi X; Rafaels NM; Wise RA; Silverman EK; Barnes KC; Armanios M
J Clin Invest; 2015 Feb; 125(2):563-70. PubMed ID: 25562321
[TBL] [Abstract][Full Text] [Related]
14. Short telomeres in pulmonary fibrosis: from genetics to clinical significance.
Trăilă D; Mlădinescu OF; Oancea C; Tudorache V
Pneumologia; 2015; 64(1):8, 11-3. PubMed ID: 26016050
[TBL] [Abstract][Full Text] [Related]
15. Clinical mutations in the TERT and TERC genes coding for telomerase components induced oxidative stress, DNA damage at telomeres and cell apoptosis besides decreased telomerase activity.
Fernández-Varas B; Manguan-García C; Rodriguez-Centeno J; Mendoza-Lupiáñez L; Calatayud J; Perona R; Martín-Martínez M; Gutierrez-Rodriguez M; Benítez-Buelga C; Sastre L
Hum Mol Genet; 2024 Apr; 33(9):818-834. PubMed ID: 38641551
[TBL] [Abstract][Full Text] [Related]
16. Short telomeres are a risk factor for idiopathic pulmonary fibrosis.
Alder JK; Chen JJ; Lancaster L; Danoff S; Su SC; Cogan JD; Vulto I; Xie M; Qi X; Tuder RM; Phillips JA; Lansdorp PM; Loyd JE; Armanios MY
Proc Natl Acad Sci U S A; 2008 Sep; 105(35):13051-6. PubMed ID: 18753630
[TBL] [Abstract][Full Text] [Related]
17. Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study.
Dressen A; Abbas AR; Cabanski C; Reeder J; Ramalingam TR; Neighbors M; Bhangale TR; Brauer MJ; Hunkapiller J; Reeder J; Mukhyala K; Cuenco K; Tom J; Cowgill A; Vogel J; Forrest WF; Collard HR; Wolters PJ; Kropski JA; Lancaster LH; Blackwell TS; Arron JR; Yaspan BL
Lancet Respir Med; 2018 Aug; 6(8):603-614. PubMed ID: 29891356
[TBL] [Abstract][Full Text] [Related]
18. Idiopathic pulmonary fibrosis: update on genetic discoveries.
Garcia CK
Proc Am Thorac Soc; 2011 May; 8(2):158-62. PubMed ID: 21543794
[TBL] [Abstract][Full Text] [Related]
19. Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia.
Yamaguchi H; Calado RT; Ly H; Kajigaya S; Baerlocher GM; Chanock SJ; Lansdorp PM; Young NS
N Engl J Med; 2005 Apr; 352(14):1413-24. PubMed ID: 15814878
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]