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139 related items for PubMed ID: 7947982

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  • 4. Comparison of physicochemical properties of purified mucus glycoproteins isolated from respiratory secretions of cystic fibrosis and asthmatic patients.
    Chace KV, Flux M, Sachdev GP.
    Biochemistry; 1985 Dec 03; 24(25):7334-41. PubMed ID: 3002452
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  • 5. Peptide mapping reveals differences in the non-glycosylated domains of cystic fibrosis and normal tracheobronchial mucins.
    Desai VC, Shankar V, de la Rocha SR, Sachdev GP.
    Indian J Biochem Biophys; 1993 Dec 03; 30(6):382-8. PubMed ID: 8005622
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  • 13. 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 03; 31(1):86-91. PubMed ID: 14988081
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  • 16. Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airways.
    Abdullah LH, Evans JR, Wang TT, Ford AA, Makhov AM, Nguyen K, Coakley RD, Griffith JD, Davis CW, Ballard ST, Kesimer M.
    JCI Insight; 2017 Mar 23; 2(6):e89752. PubMed ID: 28352653
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  • 18. Respiratory mucous secretions in patients with cystic fibrosis: relationship between levels of highly sulfated mucin component and severity of the disease.
    Chace KV, Leahy DS, Martin R, Carubelli R, Flux M, Sachdev GP.
    Clin Chim Acta; 1983 Aug 15; 132(2):143-55. PubMed ID: 6616869
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  • 19. Heterogeneity of airways mucus: variations in the amounts and glycoforms of the major oligomeric mucins MUC5AC and MUC5B.
    Kirkham S, Sheehan JK, Knight D, Richardson PS, Thornton DJ.
    Biochem J; 2002 Feb 01; 361(Pt 3):537-46. PubMed ID: 11802783
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