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Volumn 45, Issue 5, 1999, Pages 688-690

Multiplex PCR assay for the detection of genetic variants of α1- antitrypsin

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA 1 ANTITRYPSIN;

EID: 0032920910     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (14)

References (21)
  • 1
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  • 2
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    • Alpha 1 antitrypsin deficiency: Biochemistry and clinical manifestations
    • 2. Perlmutter DH. Alpha 1 antitrypsin deficiency: biochemistry and clinical manifestations [Review]. Ann Med 1996;28:385-94.
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  • 3
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    • 1-Antitrypsin deficiency and asthma
    • 1-Antitrypsin deficiency and asthma [Review]. Postgrad Med 1997;101:153-68.
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  • 4
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    • Bronchial epithelial cell-cytokine interactions in airway inflammation
    • Shelhamer JH, moderator. Airway inflammation [NIH Conference]
    • 4. Shelhamer JH, Levine SJ, Wu T, Jacoby DB, Kaliner MA, Rennard SI. Bronchial epithelial cell-cytokine interactions in airway inflammation. In: Shelhamer JH, moderator. Airway inflammation [NIH Conference]. Ann Intern Med 1995;123:288-91.
    • (1995) Ann Intern Med , vol.123 , pp. 288-291
    • Shelhamer, J.H.1    Levine, S.J.2    Wu, T.3    Jacoby, D.B.4    Kaliner, M.A.5    Rennard, S.I.6
  • 9
    • 0030716755 scopus 로고    scopus 로고
    • Genetic epidemiology of asthma
    • 9. Duffy DL. Genetic epidemiology of asthma. Epidemiol Rev 1997;19:129-43.
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    • Duffy, D.L.1
  • 10
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    • Molecular basis of alpha 1-antitrypsin deficiency
    • 10. Brantly M, Nukiwa T, Crystal RG. Molecular basis of alpha 1-antitrypsin deficiency [Review]. Am J Med 1988;84:13-31.
    • (1988) Am J Med , vol.84 , pp. 13-31
    • Brantly, M.1    Nukiwa, T.2    Crystal, R.G.3
  • 12
    • 0022479394 scopus 로고
    • Prenatal diagnosis of alpha 1-antitrypsin deficiency by restriction fragment length polymorphisms, and comparison with oligonucleotide probe analysis
    • 12. Hejtmancik JF, Sifers RN, Ward PA, Harris S, Mansfield T, Cox DW. Prenatal diagnosis of alpha 1-antitrypsin deficiency by restriction fragment length polymorphisms, and comparison with oligonucleotide probe analysis. Lancet 1986;2:767-70.
    • (1986) Lancet , vol.2 , pp. 767-770
    • Hejtmancik, J.F.1    Sifers, R.N.2    Ward, P.A.3    Harris, S.4    Mansfield, T.5    Cox, D.W.6
  • 15
    • 0028297737 scopus 로고
    • Dual-color detection of DNA sequence variants by ligase-mediated analysis
    • 15. Samiotaki M, Kwiatkowski M, Parik J, Landegren U. Dual-color detection of DNA sequence variants by ligase-mediated analysis. Genomics 1994;20: 238-42.
    • (1994) Genomics , vol.20 , pp. 238-242
    • Samiotaki, M.1    Kwiatkowski, M.2    Parik, J.3    Landegren, U.4
  • 16
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    • Detection of the common alpha-1-antitrypsin variants by denaturing gradient gel electrophoresis
    • 16. Johnson PH, Cadiou H, Hopkinson DA. Detection of the common alpha-1-antitrypsin variants by denaturing gradient gel electrophoresis. Ann Hum Genet 1991;55:183-98.
    • (1991) Ann Hum Genet , vol.55 , pp. 183-198
    • Johnson, P.H.1    Cadiou, H.2    Hopkinson, D.A.3
  • 19
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    • Polymerase chain reaction-mediated site-directed mutagenesis detection of Z and S alpha 1-antitrypsin alleles in family members
    • 19. Hammerberg G, Keren DF. Polymerase chain reaction-mediated site-directed mutagenesis detection of Z and S alpha 1-antitrypsin alleles in family members. J Clin Lab Anal 1996;10:384-8.
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    • Hammerberg, G.1    Keren, D.F.2
  • 20
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    • Mutagenically separated PCR (MS-PCR): A highly specific one step procedure for easy mutation detection
    • 20. Rust S, Funke H, Assmann G. Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection. Nucleic Acids Res 1993;21:3623-9.
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    • Rust, S.1    Funke, H.2    Assmann, G.3
  • 21
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    • Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients
    • 21. Födinger M, Mannhalter C, Wölfl G, Pabinger I, Müller E, Schmid R, et al. Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients. Kidney Int 1997;52:517-23.
    • (1997) Kidney Int , vol.52 , pp. 517-523
    • Födinger, M.1    Mannhalter, C.2    Wölfl, G.3    Pabinger, I.4    Müller, E.5    Schmid, R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.