Associated Papers
ABO gene editing for the conversion of blood type A to universal type O in Rhnull donor-derived human-induced pluripotent stem cells.
Petazzi P et al.
Clinical and Translational Medicine, 2022
First report of Rhnull individuals in the Indian population and characterization of the underlying molecular mechanisms.
Kulkarni SS et al.
Transfusion, 2017
A family study of the Chinese Rhnull individual of the regulator type: a novel single missense mutation identified in RHAG gene.
Tian L et al.
Transfusion, 2011
The Rh protein family: gene evolution, membrane biology, and disease association.
Huang CH et al.
Cellular and Molecular Life Sciences : Cmls, 2010
A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein.
Tilley L et al.
Vox Sanguinis, 2010
Molecular biology and genetics of the Rh blood group system.
Huang CH et al.
Seminars in Hematology, 2000
Molecular basis for Rh(null) syndrome: identification of three new missense mutations in the Rh50 glycoprotein gene.
Huang CH et al.
American Journal of Hematology, 1999
Blood group immunochemistry and genetics.
Unknown Author
Seminars in Hematology, 1981
Hydrophobic cluster analysis and modeling of the human Rh protein three-dimensional structures.
Callebaut I et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 0
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