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Iscience|May 8, 2023
Ultra-rare complement factor 8 coding variants in families with age-related macular degenerationLina Zelinger, Tammy M Martin, Jayshree Advani, et al.Cell Death & Disease|April 30, 2021
Glucocorticoid-induced leucine zipper regulates liver fibrosis by suppressing CCL2-mediated leukocyte recruitmentSara Flamini, Philipp Sergeev, Zenobio Viana de Barros, et al.Plos Genetics|March 12, 2010
Papillorenal syndrome-causing missense mutations in PAX2/Pax2 result in hypomorphic alleles in mouse and humanRamakrishna P Alur, Camasamudram Vijayasarathy, Jacob D Brown, et al.Journal of Medicinal Chemistry|March 7, 2020
Structure-Activity Relationship Studies of Tetrahydroquinolone Free Fatty Acid Receptor 3 ModulatorsElisabeth Rexen Ulven, Tezz Quon, Eugenia Sergeev, et al.Plos One|October 1, 2014
Whole exome analysis identifies frequent CNGA1 mutations in Japanese population with autosomal recessive retinitis pigmentosaSatoshi Katagiri, Masakazu Akahori, Yuri Sergeev, et al.Journal of Alzheimer'S Disease : JAD|August 2, 2017
Molecular Mechanisms Underlying Neuroprotective Effect of Intranasal Administration of Human Hsp70 in Mouse Model of Alzheimer's DiseaseMichail B Evgen'ev, George S Krasnov, Inna V Nesterova, et al.Physical Review Letters|September 24, 2016
Using Two-Dimensional Distributed Feedback for Synchronization of Radiation from Two Parallel-Sheet Electron Beams in a Free-Electron MaserA V Arzhannikov, N S Ginzburg, P V Kalinin, et al.American Journal of Human Genetics|May 20, 2005
Mutations in PIP5K3 are associated with François-Neetens mouchetée fleck corneal dystrophyShouling Li, Leila Tiab, Xiaodong Jiao, et al.Space Science Reviews|June 11, 2019
Explosive Magnetotail ActivityMikhail Sitnov, Joachim Birn, Banafsheh Ferdousi, et al.Biomaterials Science|January 13, 2025
Photocrosslinking of hyaluronic acid-based hydrogels through biotissue barriersAlexander G Savelyev, Anastasia V Sochilina, Gulalek Babayeva, et al.Pageof 157