180 related articles for article (PubMed ID: 2637759)
1. 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
[TBL] [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
[TBL] [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; 162(3):1560-70. PubMed ID: 2788414
[TBL] [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; 26(17):5259-67. PubMed ID: 2890373
[TBL] [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; 142(5):1185-92. PubMed ID: 2240842
[TBL] [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; 263(30):15528-34. PubMed ID: 3262617
[TBL] [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; 2(3):221-8. PubMed ID: 8364590
[TBL] [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; 10(1):47-56. PubMed ID: 1967187
[TBL] [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; 137(2):364-70. PubMed ID: 3257660
[TBL] [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; 83(4):1144-52. PubMed ID: 2539391
[TBL] [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; 46(4):810-6. PubMed ID: 2316526
[TBL] [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; 80(5):1366-74. PubMed ID: 3500183
[TBL] [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; 261(34):15989-94. PubMed ID: 3491072
[TBL] [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; 48(6):1154-8. PubMed ID: 2035534
[TBL] [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; 1(4):329-34. PubMed ID: 2624766
[TBL] [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; 264(18):10477-86. PubMed ID: 2567291
[TBL] [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; 85(3):381-2. PubMed ID: 2394452
[TBL] [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; 86(6):1878-84. PubMed ID: 2254451
[TBL] [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; 63(4):270-80. PubMed ID: 9635295
[TBL] [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; 16(1):54-6. PubMed ID: 17471159
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
