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International Journal of Molecular Sciences|April 17, 2025
From Genes to Disease: Reassessing LOXHD1 and AGBL1's Contribution to Fuchs' DystrophyTatiana Romanovna Tsedilina, Elena Ivanovna Sharova, Alexandra Vasilevna Kanygina, et al.
Frontiers in Medicine|November 7, 2022
Intermediate care in caring for dementia, the point of view of general practitioners: A key informant survey across EuropeClarisse Dibao-Dina, Caroline Oger, Tony Foley, et al.
International Journal of Molecular Sciences|December 30, 2025
Cross-Study Meta-Analysis of Blood Transcriptomes in Type 2 DiabetesAleksandr A Tkachenko, Ziravard N Tonyan, Yulia A Nasykhova, et al.
Cell Death & Disease|July 1, 2025
Current understanding of eryptosis: mechanisms, physiological functions, role in disease, pharmacological applications, and nomenclature recommendationsAnton Tkachenko, Mohammad A Alfhili, Jawaher Alsughayyir, et al.
Structural Dynamics (Melville, N.Y.)|October 30, 2023
Non-thermal structural transformation of diamond driven by x-raysPhilip Heimann, Nicholas J Hartley, Ichiro Inoue, et al.
F1000Research|February 10, 2021
The EU one-stop-shop collection of publicly available information on COVID-19 in vitro diagnostic medical devicesMauro Petrillo, Maddalena Querci, Olga Tkachenko, et al.
Clinical Mass Spectrometry (Del Mar, Calif.)|November 29, 2021
Unified representation of high- and low-resolution spectra to facilitate application of mass spectrometric techniques in clinical practiceE S Zhvansky, A A Sorokin, S I Pekov, et al.
Journal of the American Chemical Society|July 23, 2008
Near-edge X-ray absorption fine structure spectroscopy of diamondoid thiol monolayers on goldTrevor M Willey, Jason D Fabbri, Jonathan R I Lee, et al.
British Journal of Haematology|September 8, 2025
Circulating tumour DNA as a predictor of survival of patients with diffuse large B-cell lymphoma in a daily practiceProkop Vodicka, Iva Hamova, Adriana Velasova, et al.
Journal of Clinical Pathology|August 6, 2016
Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutationsLyailya Kh Dzhemlikhanova, Olga A Efimova, Natalia S Osinovskaya, et al.
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