166 related articles for article (PubMed ID: 2901226)
1. 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]
2. 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]
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. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. Molecular analysis of the gene of the alpha 1-antitrypsin deficiency variant, Mnichinan.
Matsunaga E; Shiokawa S; Nakamura H; Maruyama T; Tsuda K; Fukumaki Y
Am J Hum Genet; 1990 Mar; 46(3):602-12. PubMed ID: 2309708
[TBL] [Abstract][Full Text] [Related]
13. 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; 47(3):403-13. PubMed ID: 1975477
[TBL] [Abstract][Full Text] [Related]
14. 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; 264(23):13938-45. PubMed ID: 2788166
[TBL] [Abstract][Full Text] [Related]
15. [Alpha 1-antitrypsin genes in patients with alpha 1AT deficiency in Japan: mutational analysis and allelic background].
Nukiwa T; Seyama K; Takahashi H; Kira S
Nihon Kyobu Shikkan Gakkai Zasshi; 1992 Aug; 30(8):1420-6. PubMed ID: 1434214
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Identification of DNA polymorphisms associated with the V type alpha1-antitrypsin gene.
Gaillard MC; Mahadeva R; Lomas DA
Biochim Biophys Acta; 1999 Feb; 1444(2):166-70. PubMed ID: 10023049
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]