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Two New Ceruloplasmin Variants in Negroes--data on Three Populations

Overview
Journal Biochem Genet
Specialty Molecular Biology
Date 1970 Aug 1
PMID 5456439
Citations 5
Authors
M H Shokeir
D C Shreffler
Affiliations
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Citing Articles

On the population genetics of the ceruloplasmin polymorphism.

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Molecular studies of ceruloplasmin deficiency in Wilson's disease.

Czaja M, Weiner F, Schwarzenberg S, Sternlieb I, Scheinberg I, Van Thiel D J Clin Invest. 1987; 80(4):1200-4.

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Characterization, mapping, and expression of the human ceruloplasmin gene.

Yang F, Naylor S, Lum J, Cutshaw S, McCombs J, Naberhaus K Proc Natl Acad Sci U S A. 1986; 83(10):3257-61.

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

GAITSKHOKI V, Kisselev O, Moshkov K, Puchkova L, Shavlovski M, Shulman V Biochem Genet. 1975; 13(9-10):533-50.

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Genetic studies of the Macushi and Wapishana Indians. I. Rare genetic variants and a "private polymorphism' of esterase A.

Neel J, Tanis R, Migliazza E, Spielman R, Salzano F, Oliver W Hum Genet. 1977; 36(1):81-107.

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References
1.
Stern C . Model estimates of the frequency of white and near-white segregants in the American Negro. Acta Genet Stat Med. 1953; 4(2-3):281-98. DOI: 10.1159/000150751. View
2.
Shreffler D, Brewer G, Gall J, Honeyman M . Electrophoretic variation in human serum ceruloplasmin: a new genetic polymorphism. Biochem Genet. 1967; 1(2):101-15. DOI: 10.1007/BF00486512. View
3.
Glass B, Li C . The dynamics of racial intermixture; an analysis based on the American Negro. Am J Hum Genet. 1953; 5(1):1-20. PMC: 1716445. View
4.
Shokeir M, Shreffler D . Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function. Proc Natl Acad Sci U S A. 1969; 62(3):867-72. PMC: 223678. DOI: 10.1073/pnas.62.3.867. View
5.
SMITHIES O . Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adults. Biochem J. 1955; 61(4):629-41. PMC: 1215845. DOI: 10.1042/bj0610629. View