Associated Papers
Distribution of Thrombophilia-Related Genetic Polymorphisms in Women with Reproductive Disorders.
Kurmanova A et al.
Biomedicines, 2026
The cytidine deaminase APOBEC3A regulates nucleolar function to promote cell growth and ribosome biogenesis.
McCool MA et al.
Plos Biology, 2024
38976757 (PubMed )
Supplement: pbio.3002718.s019.xlsx › Data_G_nuclear_variants
Simultaneous genotyping for human platelet antigen systems and HLA-A and HLA-B loci by targeted next-generation sequencing.
Wang J et al.
Frontiers in Immunology, 2022
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
36619910 (PubMed )
Supplement: Data_Sheet_6.ZIP › case2-C › 3.________ › CA2275B________.____Exonic_Variants.xlsx › sheet1
Mechanisms of thrombocytopenia in platelet-type von Willebrand disease.
Bury L et al.
Haematologica, 2019
30655369 (PubMed )
Supplement: 2018.200378.BURY_SUPPL.pdf
Variants in ABCB1, TGFB1, and XRCC1 genes and susceptibility to viral hepatitis A infection in Mexican Americans.
Zhang L et al.
Hepatology (baltimore, Md.), 2012
A new platelet alloantigen, Swi(a) , located on glycoprotein Ia identified in a family with fetal and neonatal alloimmune thrombocytopenia.
Kroll H et al.
Transfusion, 2011
The new platelet alloantigen Cab a: a single point mutation Gln 716 His on the alpha 2 integrin.
Bertrand G et al.
Transfusion, 2009
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