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Volumn 160, Issue 4, 2012, Pages

Rapid and progressive pulmonary fibrosis in 2 families with DNA repair deficiencies of undetermined etiology

Author keywords

[No Author keywords available]

Indexed keywords

ATM PROTEIN; IMMUNOGLOBULIN; METHYLPREDNISOLONE;

EID: 84858340689     PISSN: 00223476     EISSN: 10976833     Source Type: Journal    
DOI: 10.1016/j.jpeds.2011.12.001     Document Type: Article
Times cited : (7)

References (10)
  • 1
    • 78049384356 scopus 로고    scopus 로고
    • Genetic basis of children's interstitial lung disease
    • L.M. Nogee Genetic basis of children's interstitial lung disease Pediatr Allergy Immunol Pulmonol 23 2010 15 24
    • (2010) Pediatr Allergy Immunol Pulmonol , vol.23 , pp. 15-24
    • Nogee, L.M.1
  • 2
  • 3
    • 70350771055 scopus 로고    scopus 로고
    • DNA double-strand break repair defects, primary immunodeficiency disorders, and "radiosensitivity"
    • S.A. Nahas, and R.A. Gatti DNA double-strand break repair defects, primary immunodeficiency disorders, and "radiosensitivity" Curr Opin Allergy Clin Immunol 9 2009 510 516
    • (2009) Curr Opin Allergy Clin Immunol , vol.9 , pp. 510-516
    • Nahas, S.A.1    Gatti, R.A.2
  • 5
    • 18844385980 scopus 로고    scopus 로고
    • Interstitial lung disease in patients with ataxia-telangiectasia
    • S.A. Schroeder, M. Swift, C. Sandoval, and C. Langston Interstitial lung disease in patients with ataxia-telangiectasia Pediatr Pulmonol 39 2005 537 543
    • (2005) Pediatr Pulmonol , vol.39 , pp. 537-543
    • Schroeder, S.A.1    Swift, M.2    Sandoval, C.3    Langston, C.4
  • 6
    • 0036085557 scopus 로고    scopus 로고
    • Early diagnosis of ataxia-telangiectasia using radiosensitivity testing
    • X. Sun, S. Becker-Catania, H.H. Chun, M.J. Hwang, Y. Huo, and Z. Wang Early diagnosis of ataxia-telangiectasia using radiosensitivity testing J Pediatr 40 2002 724 731
    • (2002) J Pediatr , vol.40 , pp. 724-731
    • Sun, X.1    Becker-Catania, S.2    Chun, H.H.3    Hwang, M.J.4    Huo, Y.5    Wang, Z.6
  • 7
    • 59049103900 scopus 로고    scopus 로고
    • The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage
    • G.S. Stewart, S. Panier, K. Townsend, A.K. Al-Hakim, N.K. Kolas, and E.S. Miller The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage Cell 136 2009 420 434
    • (2009) Cell , vol.136 , pp. 420-434
    • Stewart, G.S.1    Panier, S.2    Townsend, K.3    Al-Hakim, A.K.4    Kolas, N.K.5    Miller, E.S.6
  • 8
    • 66849138419 scopus 로고    scopus 로고
    • Solving the RIDDLE of 53BP1 recruitment to sites of damage
    • G.S. Stewart Solving the RIDDLE of 53BP1 recruitment to sites of damage Cell Cycle 8 2009 1532 1538
    • (2009) Cell Cycle , vol.8 , pp. 1532-1538
    • Stewart, G.S.1
  • 9
    • 59049091728 scopus 로고    scopus 로고
    • RNF168 binds and amplifies ubiquitin conjugates on damaged chromosomes to allow accumulation of repair proteins
    • C. Doil, N. Mailand, S. Bekker-Jensen, P. Menard, D.H. Larsen, and R. Pepperkok RNF168 binds and amplifies ubiquitin conjugates on damaged chromosomes to allow accumulation of repair proteins Cell 136 2009 435 446
    • (2009) Cell , vol.136 , pp. 435-446
    • Doil, C.1    Mailand, N.2    Bekker-Jensen, S.3    Menard, P.4    Larsen, D.H.5    Pepperkok, R.6
  • 10
    • 80051717220 scopus 로고    scopus 로고
    • Homozygous deficiency of ubiquitin-ligase ring-finger protein RNF168 mimics the radiosensitivity syndrome of ataxia-telangiectasia
    • S. Devgan, O. Sanal, C. Doil, K. Nakamura, S.A. Nahas, and K. Pettijohn Homozygous deficiency of ubiquitin-ligase ring-finger protein RNF168 mimics the radiosensitivity syndrome of ataxia-telangiectasia Cell Death Differ 18 2011 1500 1506
    • (2011) Cell Death Differ , vol.18 , pp. 1500-1506
    • Devgan, S.1    Sanal, O.2    Doil, C.3    Nakamura, K.4    Nahas, S.A.5    Pettijohn, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.