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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

An attempt is made to create transgenic plants using rol genes from A4, 15834, and K599 strains

with psychological well-being has been shown for the APOE, OXTR, OXT, NMUR2, CNR1, CRHR1, and CYP19A1 genes

Asthma is a common chronic multifactorial respiratory disease. Genes involved in the metabolism

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

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