Literature DB >> 4126636

Letter: Defect in alpha1-antitrypsin deficiency.

D W Cox.   

Abstract

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Year:  1973        PMID： 4126636     DOI： 10.1016/s0140-6736(73)90884-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  6 in total

1.  Molecular abnormality of human alpha1-antitrypsin variant (Pi-ZZ) associated with plasma activity deficiency.

Authors:  A Yoshida; J Lieberman; L Gaidulis; C Ewing
Journal:  Proc Natl Acad Sci U S A       Date:  1976-04       Impact factor: 11.205

2.  The effect of neuraminidase on genetic variants of alpha anitrypsin.

Authors:  D W Cox
Journal:  Am J Hum Genet       Date:  1975-03       Impact factor: 11.025

3.  Pathogenesis of deficient serum alpha1-antitrypsin in the type ZZ homozygote.

Authors:  P T Rowley; M L Sevilla; R H Schwartz
Journal:  Biochem Genet       Date:  1974-09       Impact factor: 1.890

4.  [Alpha-1-antitrypsin deficiency in children: liver ultrastructure and speculations (author's transl)].

Authors:  J M Scotto; H G Stralin; D Alagille
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1975-12-29

5.  Liver disease in infancy: histological features and relationship to alpha-antitrypsin phenotype.

Authors:  I C Talbot; A P Mowat
Journal:  J Clin Pathol       Date:  1975-07       Impact factor: 3.411

6.  A defect in the structure of type I procollagen in a patient who had osteogenesis imperfecta: excess mannose in the COOH-terminal propeptide.

Authors:  L Peltonen; A Palotie; D J Prockop
Journal:  Proc Natl Acad Sci U S A       Date:  1980-10       Impact factor: 11.205
  6 in total

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