BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 2240828)

  • 1. The role of mucous glycoproteins in the rheologic properties of cystic fibrosis sputum.
    Lethem MI; James SL; Marriott C
    Am Rev Respir Dis; 1990 Nov; 142(5):1053-8. PubMed ID: 2240828
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Is cystic fibrosis mucus abnormal?
    King M
    Pediatr Res; 1981 Feb; 15(2):120-2. PubMed ID: 7254936
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Revisited physicochemical and transport properties of respiratory mucus in genotyped cystic fibrosis patients.
    Deneuville E; Perrot-Minot C; Pennaforte F; Roussey M; Zahm JM; Clavel C; Puchelle E; de Bentzmann S
    Am J Respir Crit Care Med; 1997 Jul; 156(1):166-72. PubMed ID: 9230742
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chemical markers of mucous and serum glycoproteins and their relation to viscosity in mucoid and purulent sputum from various hypersecretory diseases.
    Lopez-Vidriero MT; Reid L
    Am Rev Respir Dis; 1978 Mar; 117(3):465-77. PubMed ID: 629481
    [TBL] [Abstract][Full Text] [Related]  

  • 5. MUC5AC and MUC5B Mucins Are Decreased in Cystic Fibrosis Airway Secretions.
    Henke MO; Renner A; Huber RM; Seeds MC; Rubin BK
    Am J Respir Cell Mol Biol; 2004 Jul; 31(1):86-91. PubMed ID: 14988081
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Improved clearability of cystic fibrosis sputum with dextran treatment in vitro.
    Feng W; Garrett H; Speert DP; King M
    Am J Respir Crit Care Med; 1998 Mar; 157(3 Pt 1):710-4. PubMed ID: 9517580
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Physical and transport properties of sputum from children with idiopathic bronchiectasis.
    Redding GJ; Kishioka C; Martinez P; Rubin BK
    Chest; 2008 Dec; 134(6):1129-1134. PubMed ID: 18753467
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Effect of chondroitinase ABC on purulent sputum from cystic fibrosis and other patients.
    Khatri IA; Bhaskar KR; Lamont JT; Sajjan SU; Ho CK; Forstner J
    Pediatr Res; 2003 Apr; 53(4):619-27. PubMed ID: 12612214
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The effect of a first-generation antihistamine on sputum viscoelasticity in cystic fibrosis.
    Homnick DN; Marks JH; Rubin BK
    J Aerosol Med; 2007; 20(1):45-9. PubMed ID: 17388752
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chondroitin sulfate in sputum from patients with cystic fibrosis and chronic bronchitis.
    Rahmoune H; Lamblin G; Lafitte JJ; Galabert C; Filliat M; Roussel P
    Am J Respir Cell Mol Biol; 1991 Oct; 5(4):315-20. PubMed ID: 1910815
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Physical and functional properties of airway secretions in cystic fibrosis--therapeutic approaches.
    Puchelle E; de Bentzmann S; Zahm JM
    Respiration; 1995; 62 Suppl 1():2-12. PubMed ID: 7792436
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rheological and transport properties of airway secretions in cystic fibrosis--relationships with the degree of infection and severity of the disease.
    Puchelle E; Jacquot J; Beck G; Zahm JM; Galabert C
    Eur J Clin Invest; 1985 Dec; 15(6):389-94. PubMed ID: 3938409
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Reduction in viscoelasticity in cystic fibrosis sputum in vitro using combined treatment with nacystelyn and rhDNase.
    Dasgupta B; King M
    Pediatr Pulmonol; 1996 Sep; 22(3):161-6. PubMed ID: 8893254
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sputum rheology changes in cystic fibrosis lung disease following two different types of physiotherapy: flutter vs autogenic drainage.
    App EM; Kieselmann R; Reinhardt D; Lindemann H; Dasgupta B; King M; Brand P
    Chest; 1998 Jul; 114(1):171-7. PubMed ID: 9674466
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The origin of DNA associated with mucus glycoproteins in cystic fibrosis sputum.
    Lethem MI; James SL; Marriott C; Burke JF
    Eur Respir J; 1990 Jan; 3(1):19-23. PubMed ID: 2107097
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mucus properties in children with primary ciliary dyskinesia: comparison with cystic fibrosis.
    Bush A; Payne D; Pike S; Jenkins G; Henke MO; Rubin BK
    Chest; 2006 Jan; 129(1):118-23. PubMed ID: 16424421
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rheology of cystic fibrosis sputum after in vitro treatment with hypertonic saline alone and in combination with recombinant human deoxyribonuclease I.
    King M; Dasgupta B; Tomkiewicz RP; Brown NE
    Am J Respir Crit Care Med; 1997 Jul; 156(1):173-7. PubMed ID: 9230743
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mucus structure and properties in cystic fibrosis.
    Rubin BK
    Paediatr Respir Rev; 2007 Mar; 8(1):4-7. PubMed ID: 17419972
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Elastic contributions dominate the viscoelastic properties of sputum from cystic fibrosis patients.
    Nielsen H; Hvidt S; Sheils CA; Janmey PA
    Biophys Chem; 2004 Dec; 112(2-3):193-200. PubMed ID: 15572248
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cystic fibrosis sputum: a barrier to the transport of nanospheres.
    Sanders NN; De Smedt SC; Van Rompaey E; Simoens P; De Baets F; Demeester J
    Am J Respir Crit Care Med; 2000 Nov; 162(5):1905-11. PubMed ID: 11069833
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.