Literature DB >> 4979093

Identification of ceruloplasmin in human liver cells by fluorescent antibodies and absence of this protein in Wilson disease.

A M Shaposhnikov, Y N Zubzitski, V S Shulman.   

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Year:  1969        PMID： 4979093     DOI： 10.1007/bf01899962

Source DB:  PubMed          Journal:  Experientia        ISSN： 0014-4754


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  5 in total

1.  On the defect of synthesis ceruloplasmin in the liver polyribosomes in Wilson's disease.

Authors:  V S Gaitskhoki; O I Kisselev; K A Moshkov; L V Puchkova; M M Shavlovski; V S Shulman; V G Vacharlovski; S A Neifakh
Journal:  Biochem Genet       Date:  1975-10       Impact factor: 1.890

2.  Isolation and partial purification of ceruloplasmin messenger RNA from rat liver.

Authors:  S A Neifakh; V S Gaitskhoki; N A Klimov; L V Puchkova; M M Shavlovski; A L Schwartzman
Journal:  Mol Biol Rep       Date:  1977-03       Impact factor: 2.316

3.  Molecular studies of ceruloplasmin deficiency in Wilson's disease.

Authors:  M J Czaja; F R Weiner; S J Schwarzenberg; I Sternlieb; I H Scheinberg; D H Van Thiel; N F LaRusso; M A Giambrone; R Kirschner; M L Koschinsky
Journal:  J Clin Invest       Date:  1987-10       Impact factor: 14.808

4.  Molecular pathology of ceruloplasmin.

Authors:  S A Neifakh; I M Vasiletz; M M Shavlovsky
Journal:  Biochem Genet       Date:  1972-04       Impact factor: 1.890

5.  Observations on copper associated protein in childhood liver disease.

Authors:  J Evans; S P Newman; S Sherlock
Journal:  Gut       Date:  1980-11       Impact factor: 23.059
  5 in total

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