The Molecular Basis for the B(A) Allele: An Amino Acid Alteration in the Human Histoblood Group B α-(1,3)-Galactosyltransferase Increases Its Intrinsic α-(1,3)-N-Acetylgalactosaminyltransferase Activity-Reference-Cited by-同舟云学术

The Molecular Basis for the B(A) Allele: An Amino Acid Alteration in the Human Histoblood Group B α-(1,3)-Galactosyltransferase Increases Its Intrinsic α-(1,3)-N-Acetylgalactosaminyltransferase Activity

Published:1999-08 Issue:2 Volume:262 Page:487-493
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Yu Lung-Chih,Lee Hui-Lin,Chan Yung-Syu,Lin Marie

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference25 articles.

1. Glycopreteins;Watkins,1995

2. Cloning and characterization of DNA complementary to human UDP-GalNAc: Fuc alpha 1----2Gal alpha 1----3GalNAc transferase (histo-blood group A transferase) mRNA.

3. Molecular genetic basis of the histo-blood group ABO system

4. Molecular genetic analysis of variant phenotypes of the ABO blood group system

5. Human histo-blood group A2 transferase coded by A2 allele, one of the a subtypes, is characterized by a single base deletion in the coding sequence, which results in an additional domain at the carboxyl terminal

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