BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

249 related articles for article (PubMed ID: 20371530)

  • 1. Identification of early interstitial lung disease in an individual with genetic variations in ABCA3 and SFTPC.
    Crossno PF; Polosukhin VV; Blackwell TS; Johnson JE; Markin C; Moore PE; Worrell JA; Stahlman MT; Phillips JA; Loyd JE; Cogan JD; Lawson WE
    Chest; 2010 Apr; 137(4):969-73. PubMed ID: 20371530
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation.
    Bullard JE; Nogee LM
    Pediatr Res; 2007 Aug; 62(2):176-9. PubMed ID: 17597647
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort.
    van Moorsel CH; van Oosterhout MF; Barlo NP; de Jong PA; van der Vis JJ; Ruven HJ; van Es HW; van den Bosch JM; Grutters JC
    Am J Respir Crit Care Med; 2010 Dec; 182(11):1419-25. PubMed ID: 20656946
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Similarities and differences of interstitial lung disease associated with pathogenic variants in SFTPC and ABCA3 in adults.
    Diesler R; Legendre M; Si-Mohamed S; Brillet PY; Wemeau L; Manali ED; Gagnadoux F; Hirschi S; Lorillon G; Reynaud-Gaubert M; Bironneau V; Blanchard E; Bourdin A; Dominique S; Justet A; Macey J; Marchand-Adam S; Morisse-Pradier H; Nunes H; Papiris SA; Traclet J; Traore I; Crestani B; Amselem S; Nathan N; Borie R; Cottin V;
    Respirology; 2024 Apr; 29(4):312-323. PubMed ID: 38345107
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Pulmonary surfactant protein adenosine triphosphate-binding-cassette-A3 gene composite mutations in infant congenital interstitial lung disease: report of a case and review of literature].
    Xie N; Chen DH; Lin YN; Wu SZ; Gu YY; Zeng QS; Zhai YY; Yang LY; Xu JX
    Zhonghua Er Ke Za Zhi; 2016 Oct; 54(10):761-766. PubMed ID: 27784479
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A non-BRICHOS SFTPC mutant (SP-CI73T) linked to interstitial lung disease promotes a late block in macroautophagy disrupting cellular proteostasis and mitophagy.
    Hawkins A; Guttentag SH; Deterding R; Funkhouser WK; Goralski JL; Chatterjee S; Mulugeta S; Beers MF
    Am J Physiol Lung Cell Mol Physiol; 2015 Jan; 308(1):L33-47. PubMed ID: 25344067
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inherited pulmonary surfactant metabolism disorders in Argentina: Differences between patients with SFTPC and ABCA3 variants.
    Balinotti JE; Mallie C; Maffey A; Colom A; Epaud R; de Becdelievre A; Fanen P; Delestrain C; Medín M; Teper A
    Pediatr Pulmonol; 2023 Feb; 58(2):540-549. PubMed ID: 36324278
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Usual interstitial pneumonia in an adolescent with ABCA3 mutations.
    Young LR; Nogee LM; Barnett B; Panos RJ; Colby TV; Deutsch GH
    Chest; 2008 Jul; 134(1):192-5. PubMed ID: 18628224
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetics of pediatric interstitial lung disease.
    Nogee LM
    Curr Opin Pediatr; 2006 Jun; 18(3):287-92. PubMed ID: 16721150
    [TBL] [Abstract][Full Text] [Related]  

  • 10. ABCA3 mutations associated with pediatric interstitial lung disease.
    Bullard JE; Wert SE; Whitsett JA; Dean M; Nogee LM
    Am J Respir Crit Care Med; 2005 Oct; 172(8):1026-31. PubMed ID: 15976379
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Population-based frequency of surfactant dysfunction mutations in a native Chinese cohort.
    Chen YJ; Wambach JA; DePass K; Wegner DJ; Chen SK; Zhang QY; Heins H; Cole FS; Hamvas A
    World J Pediatr; 2016 May; 12(2):190-5. PubMed ID: 26547207
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and genetic spectrum of interstitial lung disease in Chinese children associated with surfactant protein C mutations.
    Hong D; Dai D; Liu J; Zhang C; Jin T; Shi Y; Jiang G; Mei M; Wang L; Qian L
    Ital J Pediatr; 2019 Aug; 45(1):117. PubMed ID: 31462320
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary interstitial lung diseases manifesting in early childhood in Japan.
    Akimoto T; Cho K; Hayasaka I; Morioka K; Kaneshi Y; Furuta I; Yamada M; Ariga T; Minakami H
    Pediatr Res; 2014 Nov; 76(5):453-8. PubMed ID: 25105258
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Surfactant dysfunction mutations in children's interstitial lung disease and beyond.
    Deterding R; Fan LL
    Am J Respir Crit Care Med; 2005 Oct; 172(8):940-1. PubMed ID: 16216835
    [No Abstract]   [Full Text] [Related]  

  • 15. Surfactant Protein C-associated interstitial lung disease; three different phenotypes of the same SFTPC mutation.
    Salerno T; Peca D; Menchini L; Schiavino A; Boldrini R; Esposito F; Danhaive O; Cutrera R
    Ital J Pediatr; 2016 Feb; 42():23. PubMed ID: 26925580
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New surfactant protein C gene mutations associated with diffuse lung disease.
    Guillot L; Epaud R; Thouvenin G; Jonard L; Mohsni A; Couderc R; Counil F; de Blic J; Taam RA; Le Bourgeois M; Reix P; Flamein F; Clement A; Feldmann D
    J Med Genet; 2009 Jul; 46(7):490-4. PubMed ID: 19443464
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical, radiological and pathological features of ABCA3 mutations in children.
    Doan ML; Guillerman RP; Dishop MK; Nogee LM; Langston C; Mallory GB; Sockrider MM; Fan LL
    Thorax; 2008 Apr; 63(4):366-73. PubMed ID: 18024538
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease.
    Tredano M; Griese M; Brasch F; Schumacher S; de Blic J; Marque S; Houdayer C; Elion J; Couderc R; Bahuau M
    Am J Med Genet A; 2004 Apr; 126A(1):18-26. PubMed ID: 15039969
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic basis for childhood interstitial lung disease among Japanese infants and children.
    Hayasaka I; Cho K; Akimoto T; Ikeda M; Uzuki Y; Yamada M; Nakata K; Furuta I; Ariga T; Minakami H
    Pediatr Res; 2018 Feb; 83(2):477-483. PubMed ID: 29569581
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinical analysis of heterozygous ABCA3 mutations in children].
    Xu X; Liu E; Luo Z; Luo J; Fu Z
    Zhonghua Er Ke Za Zhi; 2014 Apr; 52(4):244-7. PubMed ID: 24915907
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.