Study of the D-- phenotype reveals erythrocyte membrane alterations in the absence of RHCE

Author:

Flatt Joanna F.1,Musa Rozi H.2,Ayob Yasmin2,Hassan Afifah2,Asidin Norhanim2,Yahya Nurul M.2,Mathlouthi Rosalind3,Thornton Nicole3,Anstee David J.1,Bruce Lesley J.1

Affiliation:

1. Bristol Institute for Transfusion Sciences; N.H.S. Blood and Transplant; Filton Bristol UK

2. Immunohaematology Division; National Blood Centre; Kuala Lumpur Malaysia

3. International Blood Group Reference Laboratory; N.H.S. Blood and Transplant; Filton Bristol UK

Publisher

Wiley

Subject

Hematology

Reference54 articles.

1. Investigating the key membrane protein changes during in vitro erythropoiesis of protein 4.2 (−) cells (mutations Chartres 1 and 2);den Akker;Haematologica,2010

2. New monoclonal antibodies in CD44 and CD58: their use to quantify CD44 and CD58 on normal human erythrocytes and to compare the distribution of CD44 and CD58 in human tissues;Anstee;Immunology,1991

3. Expression of intercellular adhesion molecule-1 (CD54) on hematopoietic progenitors;Arkin;Blood,1991

4. Rh(null) red blood cells with reduced CD47 do not show increased interactions with peripheral blood monocytes;Arndt;British Journal of Haematology,2004

5. The Rh blood group system: a review;Avent;Blood,2000

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1. Neonatal hemolytic anemia due to the mother's rare RhD–/– phenotype: A case report;Pediatric Blood & Cancer;2024-01-18

2. D−− phenotype caused by a novel RHCE null allele;Transfusion;2024-01-05

3. A comprehensive study of rare Rhesus phenotype case;Russian journal of hematology and transfusiology;2023-12-28

4. A Rare RhD-Phenotype Caused by Gene RHCE-D (1–9)-CE (10);Indian Journal of Hematology and Blood Transfusion;2023-12-07

5. A Study of the Molecular Characteristics of the Serologic D-- Blood Type in Korean Blood Donors;The Korean Journal of Blood Transfusion;2023-08-31

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