159 related articles for article (PubMed ID: 35419815)
21. Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
Stuart BD; Choi J; Zaidi S; Xing C; Holohan B; Chen R; Choi M; Dharwadkar P; Torres F; Girod CE; Weissler J; Fitzgerald J; Kershaw C; Klesney-Tait J; Mageto Y; Shay JW; Ji W; Bilguvar K; Mane S; Lifton RP; Garcia CK
Nat Genet; 2015 May; 47(5):512-7. PubMed ID: 25848748
[TBL] [Abstract][Full Text] [Related]
22. [A concise review of telomere and telomerase-related genetic markers in fibrotic lung diseases].
Fan YL; Ye Q
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi; 2020 Dec; 38(12):952-956. PubMed ID: 33406566
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Utility of whole genome sequencing in assessing risk and clinically relevant outcomes for pulmonary fibrosis.
Zhang D; Newton CA; Wang B; Povysil G; Noth I; Martinez FJ; Raghu G; Goldstein D; Garcia CK
Eur Respir J; 2022 Dec; 60(6):. PubMed ID: 36028256
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Lung transplant recipients with telomere-mediated pulmonary fibrosis have increased risk for hematologic complications.
Hannan SJ; Iasella CJ; Sutton RM; Popescu ID; Koshy R; Burke R; Chen X; Zhang Y; Pilewski JM; Hage CA; Sanchez PG; Im A; Farah R; Alder JK; McDyer JF
Am J Transplant; 2023 Oct; 23(10):1590-1602. PubMed ID: 37392813
[TBL] [Abstract][Full Text] [Related]
28. Genotype-Phenotype Relationships in Inheritable Idiopathic Pulmonary Fibrosis: A Greek National Cohort Study.
Manali ED; Kannengiesser C; Borie R; Ba I; Bouros D; Markopoulou A; Antoniou K; Kolilekas L; Papaioannou AI; Tzilas V; Tzouvelekis A; Daniil Z; Fouka E; Papakosta D; Xyfteri A; Karakatsani A; Loukides S; Korbila I; Tomos IP; Konstantinidis AK; Gogali A; Steiropoulos P; Papanikolaou IC; Bazaka C; Haritou A; Vassilakopoulos T; Maniati M; Kagouridis K; Markozannes E; Bouros E; Rampiadou C; Kounti G; Trachalaki A; Dimeas I; Karampitsakos T; Lyberopoulos P; Malamadakis N; Spyropoulou S; Revy P; Lainey E; Dieudé P; Rebah K; Ménard C; Oudin C; Masson C; Plessier A; Legendre M; Nathan N; Coulomb-L'Hermine A; Clement A; Amselem S; Boileau C; Crestani B; Papiris S;
Respiration; 2022; 101(6):531-543. PubMed ID: 35078193
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Telomerase treatment prevents lung profibrotic pathologies associated with physiological aging.
Piñeiro-Hermida S; Autilio C; Martínez P; Bosch F; Pérez-Gil J; Blasco MA
J Cell Biol; 2020 Oct; 219(10):. PubMed ID: 32777016
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Telomerase and telomere length in pulmonary fibrosis.
Liu T; Ullenbruch M; Young Choi Y; Yu H; Ding L; Xaubet A; Pereda J; Feghali-Bostwick CA; Bitterman PB; Henke CA; Pardo A; Selman M; Phan SH
Am J Respir Cell Mol Biol; 2013 Aug; 49(2):260-8. PubMed ID: 23526226
[TBL] [Abstract][Full Text] [Related]
33. Lung transplant recipients with idiopathic pulmonary fibrosis have impaired alloreactive immune responses.
Wang P; Leung J; Lam A; Lee S; Calabrese DR; Hays SR; Golden JA; Kukreja J; Singer JP; Wolters PJ; Tang Q; Greenland JR
J Heart Lung Transplant; 2022 May; 41(5):641-653. PubMed ID: 34924263
[TBL] [Abstract][Full Text] [Related]
34. Impact of age and telomere length on circulating T cells and rejection risk after lung transplantation for idiopathic pulmonary fibrosis.
Snyder ME; Anderson MR; Benvenuto LJ; Sutton RM; Bondonese A; Koshy R; Burke R; Clifford S; Craig A; Iasella CJ; Hannan SJ; Popescu I; Zhang Y; Sanchez PG; Alder JK; McDyer JF
J Heart Lung Transplant; 2023 Dec; 42(12):1666-1677. PubMed ID: 37544465
[TBL] [Abstract][Full Text] [Related]
35. Genomic Fingerprint Associated with Familial Idiopathic Pulmonary Fibrosis: A Review.
Ding D; Gao R; Xue Q; Luan R; Yang J
Int J Med Sci; 2023; 20(3):329-345. PubMed ID: 36860670
[TBL] [Abstract][Full Text] [Related]
36. Pulmonary phenotypes associated with genetic variation in telomere-related genes.
Hoffman TW; van Moorsel CHM; Borie R; Crestani B
Curr Opin Pulm Med; 2018 May; 24(3):269-280. PubMed ID: 29474209
[TBL] [Abstract][Full Text] [Related]
37. MMP19 Variants in Familial and Sporadic Idiopathic Pulmonary Fibrosis.
Fan Y; Zheng C; Ma R; Wang J; Yang S; Ye Q
Lung; 2023 Dec; 201(6):571-580. PubMed ID: 37971547
[TBL] [Abstract][Full Text] [Related]
38. An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis.
Petrovski S; Todd JL; Durheim MT; Wang Q; Chien JW; Kelly FL; Frankel C; Mebane CM; Ren Z; Bridgers J; Urban TJ; Malone CD; Finlen Copeland A; Brinkley C; Allen AS; O'Riordan T; McHutchison JG; Palmer SM; Goldstein DB
Am J Respir Crit Care Med; 2017 Jul; 196(1):82-93. PubMed ID: 28099038
[TBL] [Abstract][Full Text] [Related]
39. Telomere Abnormalities in the Pathobiology of Idiopathic Pulmonary Fibrosis.
Bilgili H; Białas AJ; Górski P; Piotrowski WJ
J Clin Med; 2019 Aug; 8(8):. PubMed ID: 31426295
[TBL] [Abstract][Full Text] [Related]
40. Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis.
Peljto AL; Zhang Y; Fingerlin TE; Ma SF; Garcia JG; Richards TJ; Silveira LJ; Lindell KO; Steele MP; Loyd JE; Gibson KF; Seibold MA; Brown KK; Talbert JL; Markin C; Kossen K; Seiwert SD; Murphy E; Noth I; Schwarz MI; Kaminski N; Schwartz DA
JAMA; 2013 Jun; 309(21):2232-9. PubMed ID: 23695349
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
