Аndrey S. Glotov

ORCID: 0000-0002-7465-4504 · 3 papers in corpus
2023
Journal of personalized medicine ·doi:10.3390/jpm13081236

Today, whole-exome sequencing (WES) is used to conduct the massive screening of structural and regulatory genes in order to identify the allele frequencies of disease-associated polymorphisms in various populations and thus detect pathogeni…

article 2023
·doi:10.17816/jowd121803

BACKGROUND: Adenomyosis is a common gynecological disease with unknown pathogenesis. The HOXA10, HOXA11 and WNT4 genes may play an important role in the pathogenesis of adenomyosis both at the stage of embryonic development and in the postn…

article 2018
·doi:10.1134/s1022795418110133

Here, we determined basic differentially expressed genes in endometrial lesions compared to eutopic endometrium of the patients with endometriosis (EM). Endometrial biopsy and tissue sampling were performed in ten women with pelvic EM and n…