alpha 1-Antitrypsin: molecular pathology, leukocytes, and tissue damage.

Ítems similars

• Molecular basis of alpha 1-antitrypsin deficiency and emphysema associated with the alpha 1-antitrypsin Mmineral springs allele.
  per: Curiel, D T, et al.
  Publicat: (1990)
• Alpha-1-antitrypsin: molecular abnormality of S variant.
  Publicat: (1976)
• Expression of the alpha-1-antitrypsin gene in mononuclear phagocytes of normal and alpha-1-antitrypsin-deficient individuals.
  per: Mornex, J F, et al.
  Publicat: (1986)
• 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.
  per: Curiel, D, et al.
  Publicat: (1989)
• Alpha 1-antitrypsin is present within the primary granules of human polymorphonuclear leukocytes.
  per: Mason, D. Y., et al.
  Publicat: (1991)