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Journal Abstract Search

209 related items for PubMed ID: 2240842

  • 1. 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; 142(5):1185-92. PubMed ID: 2240842
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  • 2. Genetic diversity from a limited repertoire of mutations on different common allelic backgrounds: alpha 1-antitrypsin deficiency variant Pduarte.
    Hildesheim J, Kinsley G, Bissell M, Pierce J, Brantly M.
    Hum Mutat; 1993 Nov; 2(3):221-8. PubMed ID: 8364590
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  • 3. 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; 83(4):1144-52. PubMed ID: 2539391
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  • 4. 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; 1(6):471-7. PubMed ID: 2637759
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  • 5. 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; 10(1):47-56. PubMed ID: 1967187
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  • 6. 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; 46(4):810-6. PubMed ID: 2316526
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  • 7. 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. 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 25; 48(6):1154-8. PubMed ID: 2035534
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  • 11. 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 25; 140(6):1662-7. PubMed ID: 2481421
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  • 16. 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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  • 17. 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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  • 18. Alpha-1-antitrypsin deficiency associated with the Mattawa variant.
    Lara B, Martínez-Delgado B, Torres ML, Marín-Arguedas S, Bustamante A, Miravitlles M.
    Arch Bronconeumol; 2013 Dec 05; 49(12):548-50. PubMed ID: 24183282
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