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Journal Abstract Search

113 related items for PubMed ID: 2481421

  • 1. Characterization of the intracellular mechanism causing the alpha-1-antitrypsin Nullgranite falls deficiency state.
    Holmes M, Curiel D, Brantly M, Crystal RG.
    Am Rev Respir Dis; 1989 Dec; 140(6):1662-7. PubMed ID: 2481421
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  • 6. Ribonuclease A cleavage combined with the polymerase chain reaction for detection of the Z mutation of the alpha-1-antitrypsin gene.
    Abe T, Takahashi H, Holmes MD, Curiel DT, Crystal RG.
    Am J Respir Cell Mol Biol; 1989 Oct; 1(4):329-34. PubMed ID: 2624766
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  • 7. Molecular basis of the liver and lung disease associated with the alpha 1-antitrypsin deficiency allele Mmalton.
    Curiel DT, Holmes MD, Okayama H, Brantly ML, Vogelmeier C, Travis WD, Stier LE, Perks WH, Crystal RG.
    J Biol Chem; 1989 Aug 15; 264(23):13938-45. PubMed ID: 2788166
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  • 8. alpha 1-Antitrypsin nullGranite Falls, a nonexpressing alpha 1-antitrypsin gene associated with a frameshift to stop mutation in a coding exon.
    Nukiwa T, Takahashi H, Brantly M, Courtney M, Crystal RG.
    J Biol Chem; 1987 Sep 05; 262(25):11999-2004. PubMed ID: 3040726
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  • 11. Alpha 1-antitrypsin Wbethesda: molecular basis of an unusual alpha 1-antitrypsin deficiency variant.
    Holmes MD, Brantly ML, Fells GA, Crystal RG.
    Biochem Biophys Res Commun; 1990 Aug 16; 170(3):1013-20. PubMed ID: 2390072
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  • 12. Rapid, nonradioactive detection of mutations in the human genome by allele-specific amplification.
    Okayama H, Curiel DT, Brantly ML, Holmes MD, Crystal RG.
    J Lab Clin Med; 1989 Aug 16; 114(2):105-13. PubMed ID: 2787825
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  • 14. Characterization of the sequence of the normal alpha-1-antitrypsin M3 allele and function of the M3 protein.
    Curiel D, Laubach V, Vogelmeier C, Wurts L, Crystal RG.
    Am J Respir Cell Mol Biol; 1989 Dec 16; 1(6):471-7. PubMed ID: 2637759
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  • 17. Molecular characterisation of the defective alpha 1-antitrypsin alleles PI Mwurzburg (Pro369Ser), Mheerlen (Pro369Leu), and Q0lisbon (Thr68Ile).
    Poller W, Merklein F, Schneider-Rasp S, Haack A, Fechner H, Wang H, Anagnostopoulos I, Weidinger S.
    Eur J Hum Genet; 1999 Apr 16; 7(3):321-31. PubMed ID: 10234508
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