Literature DB >> 1693792

Platelet membrane glycoprotein Ib: genetic polymorphism detected in the intact molecule and in proteolytic fragments.

M Meyer1, I Schellenberg.   

Abstract

Genetic polymorphism of platelet membrane glycoprotein (GP) Ib was studied in 128 healthy German blood donors using immunoblotting with monospecific anti-glycocalicin antibodies. Only three GP Ib forms (B,C and D) were detected. In a smaller number of Vietnamese individuals analysed for comparison all four polymorphic GP Ib forms were found. The frequency distribution of GP Ib phenotypes in the German population was similar to that reported for U.S. Americans of Caucasian origin. GP Ib polymorphism was also observed in purified glycocalicin samples of single donors. Using trypsin-cleaved glycocalicin the polymorphic region could be located in the C-terminal carbohydrate-rich glycocalicin fragment (macroglycopeptide).

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Year:  1990        PMID: 1693792     DOI: 10.1016/0049-3848(90)90093-r

Source DB:  PubMed          Journal:  Thromb Res        ISSN: 0049-3848            Impact factor:   3.944


  3 in total

Review 1.  [Congenital thrombocytopathies].

Authors:  C M Kirchmaier; D Pillitteri
Journal:  Internist (Berl)       Date:  2010-09       Impact factor: 0.743

2.  Systematic screening for genetic polymorphism in human platelet glycoprotein Ibalpha.

Authors:  S Kaski; R Kekomäki; J Partanen
Journal:  Immunogenetics       Date:  1996       Impact factor: 2.846

3.  NH2-terminal globular domain of human platelet glycoprotein Ib alpha has a methionine 145/threonine145 amino acid polymorphism, which is associated with the HPA-2 (Ko) alloantigens.

Authors:  R W Kuijpers; N M Faber; H T Cuypers; W H Ouwehand; A E von dem Borne
Journal:  J Clin Invest       Date:  1992-02       Impact factor: 14.808

  3 in total

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