Search Results - "Belodedova, Alexandra V."

Rare single nucleotide variants in COL5A1 promoter do not play a major role in keratoconus susceptibility associated with rs1536482 by Skorodumova, Liubov O, Belodedova, Alexandra V, Sharova, Elena I, Zakharova, Elena S, Iulmetova, Liliia N, Bikbov, Mukharram M, Usubov, Emin L, Antonova, Olga P, Selezneva, Oksana V, Levchenko, Anastasia, Fedorenko, Olga Yu, Ivanova, Svetlana A, Gainetdinov, Raul R, Malyugin, Boris E

“…Keratoconus is a chronic degenerative disorder of the cornea characterized by thinning and cone-shaped protrusions. Although genetic factors play a key role in…”
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Dataset on transcriptome profiling of corneal endothelium from patients with Fuchs endothelial corneal dystrophy by Nikitina, Anastasia S., Belodedova, Alexandra V., Malyugin, Boris E., Sharova, Elena I., Kostryukova, Elena S., Larin, Andrey K., Veselovsky, Vladimir A., Antonova, Olga P., Skorodumova, Liubov O.

“…Fuchs endothelial corneal dystrophy (FECD) is a bilateral inherited eye disease with advanced forms only treatable by corneal transplantation. The pathogenesis…”
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Anterior vitreous detachment: risk factor for intraoperative complications during phacoemulsification by Anisimova, Natalia S, Arbisser, Lisa B, Shilova, Natalya F, Melnik, Maria A, Belodedova, Alexandra V, Knyazer, Boris, Malyugin, Boris E

“…To confirm the presence of incomplete vitreolenticular adhesion via microscope-integrated intraoperative optical coherence tomography (iOCT) during cataract…”
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CTG18.1 Expansion is the Best Classifier of Late-Onset Fuchs' Corneal Dystrophy Among 10 Biomarkers in a Cohort From the European Part of Russia by Skorodumova, Liubov O, Belodedova, Alexandra V, Antonova, Olga P, Sharova, Elena I, Akopian, Tatiana A, Selezneva, Oksana V, Kostryukova, Elena S, Malyugin, Boris E

“…To assess the occurrence and diagnostic performance of nine single-nucleotide variants (SNVs) in the TCF4, SLC4A11, LOXHD1, and AGBL1 genes and the CTG18.1…”
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