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Volumn 196, Issue 11, 2017, Pages 1481-1484

Rare genetic variants in PARN are associated with pulmonary fibrosis in families

Author keywords

[No Author keywords available]

Indexed keywords

GENETIC VARIATION; GENETICS; HUMAN; LUNG FIBROSIS;

EID: 85038108300     PISSN: 1073449X     EISSN: 15354970     Source Type: Journal    
DOI: 10.1164/rccm.201703-0635LE     Document Type: Letter
Times cited : (30)

References (13)
  • 10
    • 84949101798 scopus 로고    scopus 로고
    • Poly(A)-specific ribonuclease (PARN) mediates 39-end maturation of the telomerase RNA component
    • Moon DH, Segal M, Boyraz B, Guinan E, Hofmann I, Cahan P, Tai AK, Agarwal S. Poly(A)-specific ribonuclease (PARN) mediates 39-end maturation of the telomerase RNA component. Nat Genet 2015;47:1482–1488.
    • (2015) Nat Genet , vol.47 , pp. 1482-1488
    • Moon, D.H.1    Segal, M.2    Boyraz, B.3    Guinan, E.4    Hofmann, I.5    Cahan, P.6    Tai, A.K.7    Agarwal, S.8
  • 13
    • 84960172419 scopus 로고    scopus 로고
    • Inhibition of telomerase RNA decay rescues telomerase deficiency caused by dyskerin or PARN defects
    • Shukla S, Schmidt JC, Goldfarb KC, Cech TR, Parker R. Inhibition of telomerase RNA decay rescues telomerase deficiency caused by dyskerin or PARN defects. Nat Struct Mol Biol 2016;23:286–292.
    • (2016) Nat Struct Mol Biol , vol.23 , pp. 286-292
    • Shukla, S.1    Schmidt, J.C.2    Goldfarb, K.C.3    Cech, T.R.4    Parker, R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.