Associated Papers
Full-length haplotype reconstruction of CD36 by long-read sequencing: uncovers a novel structural variant.
Liang S et al.
Bmc Genomics, 2026
Comparative genetic analysis of blood and semen samples in sperm donors from Hunan, China.
Huang C et al.
Annals of Medicine, 2025
BGMP: a comprehensive database of human blood group gene mutations and phenotypes.
Gao C et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi, 2025
cfDNA Chimerism and Somatic Mutation Testing in Early Prediction of Relapse After Allogeneic Stem Cell Transplantation for Myeloid Malignancies.
Rowley SD et al.
Cancers, 2025
40002220 (PubMed )
Supplement: cancers-17-00625-s001.zip › cancers-3405985-supplementary.pdf
Haplotypes analysis reveals the genetic basis of type I CD36 deficiency.
Xia W et al.
Scientific Reports, 2024
The polymorphism analysis for CD36 among platelet donors.
Lyu Q et al.
Scientific Reports, 2024
Frequency and molecular basis of CD36 deficiency among platelet donors in Kunming, China.
Lyu Q et al.
Platelets, 2023
Genomic analysis of a Palestinian family with inherited cancer syndrome: a next-generation sequencing study.
Fares E et al.
Frontiers in Genetics, 2023
38028607 (PubMed )
Supplement: Table1.XLSX › Sheet1
[Molecular polymorphism Analysis on CD36 Deficiency among Platelet Blood Donors in Shenzhen].
Xu YP et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2022
Platelet CD36 deficiency is present in 2.6% of Arabian individuals and can cause NAIT and platelet refractoriness.
Flesch BK et al.
Transfusion, 2021
Mutation severity spectrum of rare alleles in the human genome is predictive of disease type.
Pei J et al.
Plos Computational Biology, 2020
Frequency of CD36 deficiency in Thais analyzed by quantification of CD36 on cell surfaces and in plasma.
Phuangtham R et al.
Transfusion, 2020
Whole-exome sequencing detects mutations in pediatric patients with atypical hemolytic uremic syndrome in Taiwan.
Tseng MH et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2019
Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.
Lu X et al.
Nature Genetics, 2017
Incidence and molecular basis of CD36 deficiency in Shanghai population.
Li R et al.
Transfusion, 2015
Variants of CD36 gene and their association with CD36 protein expression in platelets.
Xu X et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
Two sibling cases of hydrops fetalis due to alloimmune anti-CD36 (Nak a) antibody.
Okajima S et al.
Thrombosis and Haemostasis, 2006
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