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Journal of Aging Research|September 22, 2025
Variation in the Content of Three Tandem Repeats of the Human Genome (Ribosomal, Satellite III, and Telomere) in Peripheral Blood Leukocyte DNA of People of Different Ages (5-101 Years)E S Ershova, P E Umriukhin, R A Zinchenko, et al.Journal of Clinical Laboratory Analysis|July 12, 2025
Harmonizing TREC Thresholds in Newborn Screening for SCID: Insights From Russian Validation CohortAndrey Marakhonov, Ekaterina Kalinina, Sergey Larin, et al.Clinical Genetics|January 19, 2021
Mutation in PHACTR1 associated with multifocal epilepsy with infantile spasms and hypsarrhythmiaAndrey V Marakhonov, Magdalena Přechová, Fedor A Konovalov, et al.Bioorganicheskaia Khimiia|January 25, 2000
[Point amino acid substitutions in the Ca2+-binding centers of recoverin. I. Mechanism of successive filling of Ca2+-binding centers]S E Permiakov, I I Senin, V N Uverskiĭ, et al.Bioorganicheskaia Khimiia|July 22, 2009
[Nanocomplexes of recombinant proteins and polysialic acid: preparation, characteristics, and biological activity]V V Bezuglov, N M Gretskaya, D V Klinov, et al.Biomedical Optics Express|October 28, 2015
Optical monitoring of stress-related changes in the brain tissues and vessels associated with hemorrhagic stroke in newborn ratsOxana Semyachkina-Glushkovskaya, Alexey Pavlov, Jürgen Kurths, et al.CNS & Neurological Disorders Drug Targets|February 26, 2015
Ca2+ -myristoyl switch in neuronal calcium sensor-1: a role of C-terminal segmentViktoriia E Baksheeva, Aliya A Nazipova, Dmitry V Zinchenko, et al.Genes|September 28, 2023
Clinical and Genetic Characteristics of a Patient with Cystic Fibrosis with a Complex Allele [E217G;G509D] and Functional Evaluation of the CFTR ChannelElena Kondratyeva, Yuliya Melyanovskaya, Anna Efremova, et al.International Journal of Molecular Sciences|July 27, 2022
Complex Diagnostics of Non-Specific Intellectual Developmental DisorderOlga Levchenko, Elena Dadali, Ludmila Bessonova, et al.Clinical Genetics|March 22, 2017
Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutationsT A Vasilyeva, A A Voskresenskaya, B Käsmann-Kellner, et al.Pageof 84