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Journal Abstract Search

176 related items for PubMed ID: 2637759

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Characterization of the gene and protein of the common alpha 1-antitrypsin normal M2 allele.
    Nukiwa T, Brantly ML, Ogushi F, Fells GA, Crystal RG.
    Am J Hum Genet; 1988 Sep; 43(3):322-30. PubMed ID: 2901226
    [Abstract] [Full Text] [Related]

  • 3. Characterization of the coding sequence of the normal M4 alpha 1-antitrypsin gene.
    Okayama H, Holmes MD, Brantly ML, Crystal RG.
    Biochem Biophys Res Commun; 1989 Aug 15; 162(3):1560-70. PubMed ID: 2788414
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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 Oct 25; 2(3):221-8. PubMed ID: 8364590
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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 25; 46(4):810-6. PubMed ID: 2316526
    [Abstract] [Full Text] [Related]

  • 12. Z-type alpha 1-antitrypsin is less competent than M1-type alpha 1-antitrypsin as an inhibitor of neutrophil elastase.
    Ogushi F, Fells GA, Hubbard RC, Straus SD, Crystal RG.
    J Clin Invest; 1987 Nov 25; 80(5):1366-74. PubMed ID: 3500183
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. 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 05; 1(4):329-34. PubMed ID: 2624766
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Characterisation of the alpha-1-antitrypsin M3 gene, a normal variant.
    Graham A, Hayes K, Weidinger S, Newton CR, Markham AF, Kalsheker NA.
    Hum Genet; 1990 Aug 25; 85(3):381-2. PubMed ID: 2394452
    [Abstract] [Full Text] [Related]

  • 18. A null deficiency allele of alpha 1-antitrypsin, QOludwigshafen, with altered tertiary structure.
    Frazier GC, Siewertsen MA, Hofker MH, Brubacher MG, Cox DW.
    J Clin Invest; 1990 Dec 25; 86(6):1878-84. PubMed ID: 2254451
    [Abstract] [Full Text] [Related]

  • 19. 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 25; 63(4):270-80. PubMed ID: 9635295
    [Abstract] [Full Text] [Related]

  • 20. Rapid alpha-1-antitrypsin M-variant genotyping by primer-induced restriction analysis.
    Yajloo MM, Lotfi AS, Mesbah Namin SA, Hasannia S, Biglarzadeh M, Ardalan A.
    Diagn Mol Pathol; 2007 Mar 25; 16(1):54-6. PubMed ID: 17471159
    [Abstract] [Full Text] [Related]

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