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Journal Abstract Search

148 related items for PubMed ID: 3262617

  • 1. Characterization of the gene and protein of the alpha 1-antitrypsin "deficiency" allele Mprocida.
    Takahashi H, Nukiwa T, Satoh K, Ogushi F, Brantly M, Fells G, Stier L, Courtney M, Crystal RG.
    J Biol Chem; 1988 Oct 25; 263(30):15528-34. PubMed ID: 3262617
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  • 2. Molecular basis of alpha 1-antitrypsin deficiency and emphysema associated with the alpha 1-antitrypsin Mmineral springs allele.
    Curiel DT, Vogelmeier C, Hubbard RC, Stier LE, Crystal RG.
    Mol Cell Biol; 1990 Jan 25; 10(1):47-56. PubMed ID: 1967187
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  • 3. 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 25; 1(6):471-7. PubMed ID: 2637759
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  • 6. Alpha 1-antitrypsin deficiency caused by the alpha 1-antitrypsin Nullmattawa gene. An insertion mutation rendering the alpha 1-antitrypsin gene incapable of producing alpha 1-antitrypsin.
    Curiel D, Brantly M, Curiel E, Stier L, Crystal RG.
    J Clin Invest; 1989 Apr 25; 83(4):1144-52. PubMed ID: 2539391
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  • 7. Molecular analysis of the heterogeneity among the P-family of alpha-1-antitrypsin alleles.
    Holmes MD, Brantly ML, Crystal RG.
    Am Rev Respir Dis; 1990 Nov 25; 142(5):1185-92. PubMed ID: 2240842
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  • 8. Characterization of the M1(Ala213) type of alpha 1-antitrypsin, a newly recognized, common "normal" alpha 1-antitrypsin haplotype.
    Nukiwa T, Brantly M, Ogushi F, Fells G, Satoh K, Stier L, Courtney M, Crystal RG.
    Biochemistry; 1987 Aug 25; 26(17):5259-67. PubMed ID: 2890373
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  • 9. Serum alpha 1-antitrypsin deficiency associated with the common S-type (Glu264----Val) mutation results from intracellular degradation of alpha 1-antitrypsin prior to secretion.
    Curiel DT, Chytil A, Courtney M, Crystal RG.
    J Biol Chem; 1989 Jun 25; 264(18):10477-86. PubMed ID: 2567291
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  • 10. Evaluation of the S-type of alpha-1-antitrypsin as an in vivo and in vitro inhibitor of neutrophil elastase.
    Ogushi F, Hubbard RC, Fells GA, Casolaro MA, Curiel DT, Brantly ML, Crystal RG.
    Am Rev Respir Dis; 1988 Feb 25; 137(2):364-70. PubMed ID: 3257660
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  • 11. Identification of a second mutation in the protein-coding sequence of the Z type alpha 1-antitrypsin gene.
    Nukiwa T, Satoh K, Brantly ML, Ogushi F, Fells GA, Courtney M, Crystal RG.
    J Biol Chem; 1986 Dec 05; 261(34):15989-94. PubMed ID: 3491072
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  • 12. Alpha 1-antitrypsin Null(isola di procida): an alpha 1-antitrypsin deficiency allele caused by deletion of all alpha 1-antitrypsin coding exons.
    Takahashi H, Crystal RG.
    Am J Hum Genet; 1990 Sep 05; 47(3):403-13. PubMed ID: 1975477
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  • 13. Characterization of the molecular basis of the alpha 1-antitrypsin F allele.
    Okayama H, Brantly M, Holmes M, Crystal RG.
    Am J Hum Genet; 1991 Jun 05; 48(6):1154-8. PubMed ID: 2035534
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  • 15. 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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  • 16. Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern.
    Holmes MD, Brantly ML, Curiel DT, Weidinger S, Crystal RG.
    Am J Hum Genet; 1990 Apr 15; 46(4):810-6. PubMed ID: 2316526
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  • 17. Alpha 1-antitrypsin nonsense mutation associated with a retained truncated protein and reduced mRNA.
    Lee J, Novoradovskaya N, Rundquist B, Redwine J, Saltini C, Brantly M.
    Mol Genet Metab; 1998 Apr 15; 63(4):270-80. PubMed ID: 9635295
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