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Наследственные заболевания человека со скелетной патологией – молекулярный патогенез и клиническая характеристикаHereditary human diseases with skeletal pathology – molecular pathogenesis and clinical

that is unfortunately poor. Despite considerable progress in the field, the intricate molecular basis of this cancer

respiratory disease. The molecular pathogenesis of COPD may include dysregulation of the stress responses

research to uncover the underlying molecular mechanisms of CC and to discover novel diagnostic

, Ltd. 2024. ISSN 0026-8933, Molecular Biology, 2024, Vol. 58, No. 2, pp. 246–254. Pleiades Publishing

Эпидемиологические и клинические аспекты геморрагической лихорадки с почечным синдромом на современном этапеmolecular genetic studies

attractive for use as prognostic molecular genetic biomarkers. We evaluated exosomal miRNAs (miRNA-424, -146a

of molecular genetic methods, a large number of studies have been accumulated on the role of epigenetic

(GWAS), many molecular genetic processes that increase susceptibility to schizophrenia have been

Molecular genetic studies make it possible to determine associations of multifactorial diseases

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