1988
DOI: 10.1007/bf00201115
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Genetic polymorphism of desialyzed alpha2 HS-glycoprotein by ultrathin isoelectric focusing

Abstract: The genetically determined polymorphism of alpha 2 HS-glycoprotein was analyzed by immunoblotting ultrathin-layer polyacrylamide gel isoelectric focusing in the pH range 4-6.5 and neuraminidase pretreated sera. In a Libyan population sample from Tripoli (n = 110) three common phenotypes, alpha 2 HSG 1-1, 2-1, and 2-2, were observed. The allele frequencies were alpha 2 HSG1 = 0.8364 and alpha 2 HSG2 = 0.1636. The theoretical exclusion rate in cases of disputed paternity is 11.8%.

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Cited by 12 publications
(6 citation statements)
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“…In the Asian populations the frequencies of AHSG*I tends to decrease from Japan to Thai (Umetsu et al, 1984;Umetsu et al, 1988b). The frequencies of AHSG*I in Sri Lankans are sim- (1989) Paraguayan (200) 1.0000 0 0 0 The present study (1987) ilar to those in Libyan (Sebetan and Heshmat, 1988) and Indian-Pakistani (Westwood et al, 1987a). These populations show the highest frequency for AHSG*I in all the populations studied thus far.…”
Section: A Hsg Polymorphismsupporting
confidence: 43%
“…In the Asian populations the frequencies of AHSG*I tends to decrease from Japan to Thai (Umetsu et al, 1984;Umetsu et al, 1988b). The frequencies of AHSG*I in Sri Lankans are sim- (1989) Paraguayan (200) 1.0000 0 0 0 The present study (1987) ilar to those in Libyan (Sebetan and Heshmat, 1988) and Indian-Pakistani (Westwood et al, 1987a). These populations show the highest frequency for AHSG*I in all the populations studied thus far.…”
Section: A Hsg Polymorphismsupporting
confidence: 43%
“…Native plasma was used for typing F13A, C6, C7, and APOC2 according to the techniques of Sebetan (1988), Nakamura et al (1984), and Sepehrnia et al (1988a). Plasma desialylated overnight at 25°C with neuraminidase (1 U/ml in 0.005 M sodium acetate buffer, pH 5.5) was used for typing F13B, ORMl, and AHSG after Nakamura et al (1986) and Yuasa et al (1987).…”
Section: Methodsmentioning
confidence: 99%
“…Elevation of serum AHSG has been correlated with a common form of mild osteogenesis imperfecta where bone mass is lost (8). Homozygosity for AHSG*1, a polymorphism in the AHSG gene (9), is associated with shorter stature and reduced bone quality as measured by calcaneal broadband ultrasound (10). Fetuin does not appear to be required for embryogenesis, as mice lacking the protein are viable with no gross anatomical abnormality at birth (11).…”
mentioning
confidence: 99%