[HTML][HTML] Molecular basis of the Duffy blood group system
G Höher, M Fiegenbaum, S Almeida - Blood Transfusion, 2018 - ncbi.nlm.nih.gov
ACKR1, located on chromosome 1q23. 2, is the gene that encodes a glycoprotein
expressing the Duffy blood group antigens. This gene is transcribed in two mRNA variants …
expressing the Duffy blood group antigens. This gene is transcribed in two mRNA variants …
The biology of unconventional invasion of Duffy-negative reticulocytes by Plasmodium vivax and its implication in malaria epidemiology and public health
Plasmodium vivax has been largely neglected over the past century, despite a widespread
recognition of its burden across region where it is endemic. The parasite invades …
recognition of its burden across region where it is endemic. The parasite invades …
Atypical Chemokine Receptor 1 (DARC/ACKR1) in Breast Tumors Is Associated with Survival, Circulating Chemokines, Tumor-Infiltrating Immune Cells, and African …
Background: Tumor-specific immune response is an important aspect of disease prognosis
and ultimately impacts treatment decisions for innovative immunotherapies. The atypical …
and ultimately impacts treatment decisions for innovative immunotherapies. The atypical …
A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related …
SE Legge, AF Pardiñas, M Helthuis, JA Jansen… - Molecular …, 2019 - nature.com
Individuals of African ancestry in the United States and Europe are at increased risk of
developing schizophrenia and have poorer clinical outcomes. The antipsychotic clozapine …
developing schizophrenia and have poorer clinical outcomes. The antipsychotic clozapine …
The DARC side of inflamm-aging: Duffy antigen receptor for chemokines (DARC/ACKR1) as a potential biomarker of aging, immunosenescence, and breast …
The proclivity of certain pre-malignant and pre-invasive breast lesions to progress while
others do not continues to perplex clinicians. Clinicians remain at a crossroads with …
others do not continues to perplex clinicians. Clinicians remain at a crossroads with …
Frequency of Mia (MNS7) and Classification of Mia-Positive Hybrid Glycophorins in an Australian Blood Donor Population
GH Lopez, B Wilson, RM Turner, GM Millard… - Transfusion Medicine …, 2020 - karger.com
Background: MNS blood group system genes GYPA and GYPB share a high degree of
sequence homology and gene structure. Homologous exchanges between GYPA and …
sequence homology and gene structure. Homologous exchanges between GYPA and …
Genotyping analysis of MNS blood group GP (B‐A‐B) hybrid glycophorins in the Chinese Southern Han population using a high‐resolution melting assay
BACKGROUND MNS hybrid GP (B‐A‐B) glycophorins are more commonly found in
Southeast Asians and alloantibodies to antigens they carry are clinically significant …
Southeast Asians and alloantibodies to antigens they carry are clinically significant …
An open‐source python library for detection of known and novel Kell, Duffy and Kidd variants from exome sequencing
C Montemayor, A Simone, J Long… - Vox …, 2021 - Wiley Online Library
Background and objectives Next generation sequencing (NGS) has promising applications
in transfusion medicine. Exome sequencing (ES) is increasingly used in the clinical setting …
in transfusion medicine. Exome sequencing (ES) is increasingly used in the clinical setting …
[PDF][PDF] Identification of Anti-Gerbich Antibody in an Emirati Marrow Hematopoietic Progenitor Cell Donor with Fy (a− b−) Phenotype
SJ Choi, E Lee, S Kim, CJ Lyu… - Yonsei Medical …, 2018 - synapse.koreamed.org
In this study, we report a case of anti-Gerbich (Ge) alloantibody to a high-prevalence Ge
antigen in a donor with Fy (a− b−) phenotype. The alloantibody was detected in an Emirati …
antigen in a donor with Fy (a− b−) phenotype. The alloantibody was detected in an Emirati …
A D+ blood donor with a novel RHD*D‐CE(5‐6)‐D gene variant exhibits the low‐frequency antigen RH23 (DW) characteristic of the partial DVa phenotype
GH Lopez, EC McGowan, KA McGrath… - …, 2016 - Wiley Online Library
BACKGROUND Blood donors whose red blood cells (RBCs) exhibit a partial RhD
phenotype, lacking some D epitopes, present as D+ in routine screening. Such phenotypes …
phenotype, lacking some D epitopes, present as D+ in routine screening. Such phenotypes …