251 related articles for article (PubMed ID: 31488579)
1.
Gable DL; Gaysinskaya V; Atik CC; Talbot CC; Kang B; Stanley SE; Pugh EW; Amat-Codina N; Schenk KM; Arcasoy MO; Brayton C; Florea L; Armanios M
Genes Dev; 2019 Oct; 33(19-20):1381-1396. PubMed ID: 31488579
[TBL] [Abstract][Full Text] [Related]
2. Synonymous Mutation in DKC1 Causes Telomerase RNA Insufficiency Manifesting as Familial Pulmonary Fibrosis.
Gaysinskaya V; Stanley SE; Adam S; Armanios M
Chest; 2020 Dec; 158(6):2449-2457. PubMed ID: 32710892
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. hTERT mutations associated with idiopathic pulmonary fibrosis affect telomerase activity, telomere length, and cell growth by distinct mechanisms.
Tsang AR; Wyatt HD; Ting NS; Beattie TL
Aging Cell; 2012 Jun; 11(3):482-90. PubMed ID: 22364217
[TBL] [Abstract][Full Text] [Related]
6. Expression of telomerase RNA template, but not telomerase reverse transcriptase, is limiting for telomere length maintenance in vivo.
Chiang YJ; Hemann MT; Hathcock KS; Tessarollo L; Feigenbaum L; Hahn WC; Hodes RJ
Mol Cell Biol; 2004 Aug; 24(16):7024-31. PubMed ID: 15282303
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.
Kannengiesser C; Borie R; Ménard C; Réocreux M; Nitschké P; Gazal S; Mal H; Taillé C; Cadranel J; Nunes H; Valeyre D; Cordier JF; Callebaut I; Boileau C; Cottin V; Grandchamp B; Revy P; Crestani B
Eur Respir J; 2015 Aug; 46(2):474-85. PubMed ID: 26022962
[TBL] [Abstract][Full Text] [Related]
9. Nuclear Exosome Targeting Complex Core Factor Zcchc8 Regulates the Degradation of LINE1 RNA in Early Embryos and Embryonic Stem Cells.
Wu Y; Liu W; Chen J; Liu S; Wang M; Yang L; Chen C; Qi M; Xu Y; Qiao Z; Yan R; Kou X; Zhao Y; Shen B; Yin J; Wang H; Gao Y; Gao S
Cell Rep; 2019 Nov; 29(8):2461-2472.e6. PubMed ID: 31747613
[TBL] [Abstract][Full Text] [Related]
10. Structural basis for MTR4-ZCCHC8 interactions that stimulate the MTR4 helicase in the nuclear exosome-targeting complex.
Puno MR; Lima CD
Proc Natl Acad Sci U S A; 2018 Jun; 115(24):E5506-E5515. PubMed ID: 29844170
[TBL] [Abstract][Full Text] [Related]
11. A new variant in the
Groen K; van der Vis JJ; van Batenburg AA; Kazemier KM; de Bruijn MJW; Stadhouders R; Arp P; Verkerk AJMH; Schoemaker AE; de Bie CI; Massink MPG; van Beek FT; Grutters JC; Vergouw LJM; van Moorsel CHM
ERJ Open Res; 2024 Jan; 10(1):. PubMed ID: 38375433
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita.
Parry EM; Alder JK; Lee SS; Phillips JA; Loyd JE; Duggal P; Armanios M
J Med Genet; 2011 May; 48(5):327-33. PubMed ID: 21415081
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Familial forms of nonspecific interstitial pneumonia/idiopathic pulmonary fibrosis: clinical course and genetic background.
Borie R; Kannengiesser C; Crestani B
Curr Opin Pulm Med; 2012 Sep; 18(5):455-61. PubMed ID: 22781209
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A spectrum of severe familial liver disorders associate with telomerase mutations.
Calado RT; Regal JA; Kleiner DE; Schrump DS; Peterson NR; Pons V; Chanock SJ; Lansdorp PM; Young NS
PLoS One; 2009 Nov; 4(11):e7926. PubMed ID: 19936245
[TBL] [Abstract][Full Text] [Related]
19. Identification of a Nuclear Exosome Decay Pathway for Processed Transcripts.
Meola N; Domanski M; Karadoulama E; Chen Y; Gentil C; Pultz D; Vitting-Seerup K; Lykke-Andersen S; Andersen JS; Sandelin A; Jensen TH
Mol Cell; 2016 Nov; 64(3):520-533. PubMed ID: 27871484
[TBL] [Abstract][Full Text] [Related]
20. Dyskeratosis congenita: the diverse clinical presentation of mutations in the telomerase complex.
Vulliamy TJ; Dokal I
Biochimie; 2008 Jan; 90(1):122-30. PubMed ID: 17825470
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
