ОЦЕНКА ЗНАЧИМОСТИ ВЗАИМОСВЯЗИ МЕЖДУ ПОКАЗАТЕЛЯМИ РЕМОДЕЛИРОВАНИЯ СОСУДОВ, ВОСПАЛИТЕЛЬНОГО ОТВЕТА И ПОЛИМОРФИЗМА ГЕНОВ ДИСФУНКЦИИ ЭНДОТЕЛИЯ У ПАЦИЕНТОВ МУЖСКОГО ПОЛА С ИНФАРКТОМ МИОКАРДА В ЗАВИСИМОСТИ ОТ НАЛИЧИЯ ИЛИ ОТСУТСТВИЯ ГИПЕРТОНИЧЕСКОГО АНАМНЕЗА AND POLYMORPHISM OF ENDOTHELIAL DYSFUNCTION GENES IN MALE PATIENTS WITH MYOCARDIAL INFARCTION DUE TO HYPERTENTION

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

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

Методы экстракорпоральной детоксикации и система гемостаза пациентов с раком яичников. Клинический случайExtracorporeal Detoxification Methods and Hemostasis System for Ovarian Cancer Patients. Clinical

of possible new candidate genes, associated with the increased risk of gastric cancer development. Whole exome

IA) from the DRD2 gene as well as the TT genotype rs13212041 (77461407 C>T) from the HTR1B gene were found