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Анализ профиля экспрессии длинных некодирующих РНК у больных с идиопатическим и COVID-19-индуцированным легочным фиброзом методы. Учитывая роль днРНК TP53TG1, LINC00342, H19, MALAT1, DNM3OS и MEG3 как регуляторов сигнальных

), and HRH3 (rs3787429) genes was performed by real-time polymerase chain reaction. Using regression analysis

of alleles and genotypes of 15 polymorphic genes variants, those involved in the regulation of memory span

and SLC6A20 gene variants (OR = 2.36, 95% CI 1.31–4.24) and OR = 1.94, 95% CI 1.08–3.49, respectively

Клинико-генетическая характеристика муковисцидоза в Республике Башкортостанgene CFTR


with osteogenesis imperfecta. The disease is caused by pathogenic variants in the SGMS2 gene, the protein product

and frequencies of mutations in the responsible genes, and examine clinical and genetic correlations. Based

the association of cytokines and inflammatory genes polymorphisms and their combinations with COPD. SNPs

transcription polymerase chain reaction (qRT-PCR). 2−ΔΔCT method was used for quantitative gene expression

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