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in Europeans is HSP associated with mutations in the spastin gene (SPG4). Analysis of the gene SPG4 was carried

МАЖОРНАЯ МУТАЦИЯ В ГЕНЕ SPAST У ПАЦИЕНТОВ С АУТОСОМНО-ДОМИНАНТНОЙ СПАСТИЧЕСКОЙ ПАРАПЛЕГИЕЙ ИЗ РЕСПУБЛИКИ БАШКОРТОСТАН of the disease in most of these families corresponded to the uncomplicated phenotype, typical of the SPG4 form

predominant lesion of the pyramidal tract. The autosomal dominant form of SPG3A, associated with mutations

obtained ten hub genes, such as IL6, TLR2, CXCL1, TIMP1, PLAUR, SERPINE1, SELE, CCL4, CCL20, and CD163

revealed that some SNPs in chemokine genes are associated with obesity, insulin resistance, type 2 diabetes

РОЛЬ МЕЖГЕННЫХ ВЗАИМОДЕЙСТВИЙ ГЕНОВ НЕЙРОТРОФИЧЕСКОЙ И НЕЙРОМЕДИАТОРНОЙ СИСТЕМЫ В РАЗВИТИИ ПРЕДРАСПОЛОЖЕННОСТИ К ПАРАНОИДНОЙ ШИЗОФРЕНИИ genes of the neurotransmitter system (DRD2, DRD3, DRD4, COMT, GRM3, GRIK2, GRIA2, GRIN2B, RGS2

in blood serum for the remaining 4 SNP in folate cycle genes (р> 0.1). Examined SNP in MTHFR and MTR genes

the polymorphic loci of immune response mediator genes (TNFA rs1800629, LTA rs909253, IL1B rs16944, IL2-IL21 rs

of neurotransmitter genes can impact eating behavior. The aim of this study was to detect the associations between

of interleukins genes IL4 (rs2243250), IL4R (rs1805010), IL10 (rs1800872), IL13 (rs20541) and tumor necrosis

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