Associated Papers
Development and clinical application of a low-cost high-resolution melting curve assay for CD36 gene variant screening in a chinese population.
Liu Z et al.
Molecular Biology Reports, 2025
Human CD36: Gene Regulation, Protein Function, and Its Role in Atherosclerosis Pathogenesis.
Rac M
Genes, 2025
Genetic variants identified in novel candidate genes for anorexia nervosa and analysis of molecular pathways for diagnostic applications.
Donato K et al.
European Review for Medical and Pharmacological Sciences, 2023
Mutation Analysis of Autosomal-Dominant Polycystic Kidney Disease Patients.
Suzuki Y et al.
Genes, 2023
36833371 (PubMed )
Supplement: genes-14-00443-s001.zip › genes-2152850-supplementary.xlsx › Table_S6
Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.
Wang T et al.
Ebiomedicine, 2022
35665681 (PubMed )
Supplement: mmc26.xlsx › Sheet1
New molecular basis associated with CD36-negative phenotype in the sub-Saharan African population.
Le Toriellec E et al.
Transfusion, 2020
Frequency of CD36 deficiency in Thais analyzed by quantification of CD36 on cell surfaces and in plasma.
Phuangtham R et al.
Transfusion, 2020
Optimizing clinical exome design and parallel gene-testing for recessive genetic conditions in preconception carrier screening: Translational research genomic data from 14,125 exomes.
Capalbo A et al.
Plos Genetics, 2019
31589614 (PubMed )
Supplement: pgen.1008409.s001.xlsx › P_LP_Variants
Diverse CD36 expression among Japanese population: defective CD36 mutations cause platelet and monocyte CD36 reductions in not only deficient but also normal phenotype subjects.
Masuda Y et al.
Thrombosis Research, 2015
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
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