392 related articles for article (PubMed ID: 22079513)
1. Telomerase and idiopathic pulmonary fibrosis.
Armanios M
Mutat Res; 2012 Feb; 730(1-2):52-8. PubMed ID: 22079513
[TBL] [Abstract][Full Text] [Related]
2. Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase.
Parry EM; Alder JK; Qi X; Chen JJ; Armanios M
Blood; 2011 May; 117(21):5607-11. PubMed ID: 21436073
[TBL] [Abstract][Full Text] [Related]
3. Syndromes of telomere shortening.
Armanios M
Annu Rev Genomics Hum Genet; 2009; 10():45-61. PubMed ID: 19405848
[TBL] [Abstract][Full Text] [Related]
4. Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita.
Armanios M; Chen JL; Chang YP; Brodsky RA; Hawkins A; Griffin CA; Eshleman JR; Cohen AR; Chakravarti A; Hamosh A; Greider CW
Proc Natl Acad Sci U S A; 2005 Nov; 102(44):15960-4. PubMed ID: 16247010
[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. 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]
7. Human diseases of telomerase dysfunction: insights into tissue aging.
Garcia CK; Wright WE; Shay JW
Nucleic Acids Res; 2007; 35(22):7406-16. PubMed ID: 17913752
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. The molecular genetics of the telomere biology disorders.
Bertuch AA
RNA Biol; 2016 Aug; 13(8):696-706. PubMed ID: 26400640
[TBL] [Abstract][Full Text] [Related]
11. Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes.
Arias-Salgado EG; Galvez E; Planas-Cerezales L; Pintado-Berninches L; Vallespin E; Martinez P; Carrillo J; Iarriccio L; Ruiz-Llobet A; Catalá A; Badell-Serra I; Gonzalez-Granado LI; Martín-Nalda A; Martínez-Gallo M; Galera-Miñarro A; Rodríguez-Vigil C; Bastos-Oreiro M; Perez de Nanclares G; Leiro-Fernández V; Uria ML; Diaz-Heredia C; Valenzuela C; Martín S; López-Muñiz B; Lapunzina P; Sevilla J; Molina-Molina M; Perona R; Sastre L
Orphanet J Rare Dis; 2019 Apr; 14(1):82. PubMed ID: 30995915
[TBL] [Abstract][Full Text] [Related]
12. [Idiopathic pulmonary fibrosis--telomerase mutation in the familial form].
Herrmann M
Pneumologie; 2008 Mar; 62(3):121. PubMed ID: 18370353
[No Abstract] [Full Text] [Related]
13. Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC.
Vulliamy T; Marrone A; Szydlo R; Walne A; Mason PJ; Dokal I
Nat Genet; 2004 May; 36(5):447-9. PubMed ID: 15098033
[TBL] [Abstract][Full Text] [Related]
14. Structural Analysis Reveals the Deleterious Effects of Telomerase Mutations in Bone Marrow Failure Syndromes.
Hoffman H; Rice C; Skordalakes E
J Biol Chem; 2017 Mar; 292(11):4593-4601. PubMed ID: 28154186
[TBL] [Abstract][Full Text] [Related]
15. Telomerase RNA mutated in autosomal dyskeratosis congenita reconstitutes a weakly active telomerase enzyme defective in telomere elongation.
Cerone MA; Ward RJ; Londoño-Vallejo JA; Autexier C
Cell Cycle; 2005 Apr; 4(4):585-9. PubMed ID: 15753647
[TBL] [Abstract][Full Text] [Related]
16. Recent progress in dyskeratosis congenita.
Nishio N; Kojima S
Int J Hematol; 2010 Oct; 92(3):419-24. PubMed ID: 20882440
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Dyskeratosis congenita -- a disease of dysfunctional telomere maintenance.
Mason PJ; Wilson DB; Bessler M
Curr Mol Med; 2005 Mar; 5(2):159-70. PubMed ID: 15974869
[TBL] [Abstract][Full Text] [Related]
20. Understanding telomere diseases through analysis of patient-derived iPS cells.
Batista LF; Artandi SE
Curr Opin Genet Dev; 2013 Oct; 23(5):526-33. PubMed ID: 23993228
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
