Kronik Obstrüktif Akciğer Hastalığında (KOAH) Genetik Risk Faktörleri
Öz
Anahtar Kelimeler
Kronik Obstrüktif Akciğer Hastalığı, KOAH, genetik, α-1-antitripsin
Kaynakça
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- Owen MC, Carrell RW, Brennan SO. The abnormality of the S variant of human alpha-1- antitrypsin. Biochim Biophys Acta. 1976;453:257–61.
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- Brantly ML, Paul LD, Miller BH, et al. Clinical features and history of the destructive lung disease associated with α1-antitrypsin deficiency of adults with pulmonary symptoms. Am Rev Respir Dis. 1988;138:327–36.
- Yoshida A, Lieberman J, Gaidulis L. Molecular abnormality of human alpha-1-antitrypsin variant (Pi-ZZ) associated with plasma activity deficiency. Proc Natl Acad Sci USA. 1976;73:1324-8.
- Bruce RM, Cohen BH, Diamond EL, et al. Collaborative study to assess risk of lung disease in PiMZ phenotype subjects. Am Rev Respir Dis. 1984;130:386–90.
- Nagase H, Woessner JF. Matrix metalloproteinases. J Biol Chem. 1999;274:21491–4.
- Pendas AM, Santamaria I, Alvarez MV, et al. Fine physical mapping of the human matrix metalloproteinase genes clustered on chromosome 11q22.3. Genomics, 1996;37:266–8.
- D’Armiento J, Dalal SS, Okada Y, et al. Collagenase expression in the lungs of transgenic mice causes pulmonary emphysema. Cell. 1992;71:955–61.
- Rutter JL, Mitchell TI, Buttice G, et al. A single nucleotide polymorphism in the matrix metalloproteinase-1 promoter creates an ETS binding site transcription. Cancer Res. 1998;58:5321–5.
