Associated Papers
Association between ANXA5 haplotypes and the risk of recurrent pregnancy loss.
Zheng M et al.
The Journal of International Medical Research, 2022
Genetic analysis of ANXA5 haplotype and its effect on recurrent pregnancy loss.
Cai Z et al.
Molecular Medicine Reports, 2022
Correlation of single nucleotide polymorphisms in the promoter region of the ANXA5 (annexin A5) gene with recurrent miscarriages in women of Greek origin.
Dryllis G et al.
The Journal of Maternal-fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2020
Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures.
Inagaki H et al.
Journal of Human Genetics, 2019
Assessment of M2/ANXA5 haplotype as a risk factor in couples with placenta-mediated pregnancy complications.
Rogenhofer N et al.
Journal of Assisted Reproduction and Genetics, 2018
Functional characterization of annexin A5 gene promoter allelic variants.
Tiscia GL et al.
Thrombosis Research, 2016
No association between Annexin A5 genetic variants and deep venous thrombosis.
de Jong PG et al.
British Journal of Haematology, 2015
Contribution of fetal ANXA5 gene promoter polymorphisms to the onset of pre-eclampsia.
Ota S et al.
Placenta, 2013
Genotyping analyses for polymorphisms of ANXA5 gene in patients with recurrent pregnancy loss.
Hayashi Y et al.
Fertility and Sterility, 2013
Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss.
Miyamura H et al.
Molecular Human Reproduction, 2011
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