Literature DB >> 6072883

Red cell and saliva studies for the evaluation of ABH and Lewis factors among the Caucasian and Aboriginal populations of Western Australia.

G H Vos, P Comley.   

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Year:  1967        PMID： 6072883     DOI： 10.1159/000152103

Source DB:  PubMed          Journal:  Acta Genet Stat Med        ISSN： 0567-7440


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  3 in total

1.  Molecular basis for erythrocyte Le(a+ b+) and salivary ABH partial-secretor phenotypes: expression of a FUT2 secretor allele with an A-->T mutation at nucleotide 385 correlates with reduced alpha(1,2) fucosyltransferase activity.

Authors:  S Henry; R Mollicone; P Fernandez; B Samuelsson; R Oriol; G Larson
Journal:  Glycoconj J       Date:  1996-12       Impact factor: 2.916

2.  Correlation of a missense mutation in the human Secretor alpha 1,2-fucosyltransferase gene with the Lewis(a+b+) phenotype: a potential molecular basis for the weak Secretor allele (Sew).

Authors:  L C Yu; Y H Yang; R E Broadberry; Y H Chen; Y S Chan; M Lin
Journal:  Biochem J       Date:  1995-12-01       Impact factor: 3.857

3.  Expression of Lewis histo-blood group glycolipids in the plasma of individuals of Le(a+b+) and partial secretor phenotypes.

Authors:  S M Henry; R Oriol; B E Samuelsson
Journal:  Glycoconj J       Date:  1994-12       Impact factor: 2.916
  3 in total

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