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in the ATL1 gene, is one of the most common forms of HSP in European populations. Analysis of the ATL1 gene

The high risk of ovarian cancer is primarily associated with mutations in BRCA1 and BRCA2 genes

patients, to clarify the common genes of both, and to identify common pathways and potential drugs

expression level in ccRCC patients with CTCAE grade 3–4 (M±SEM 1.71 ± 0.13) compared to CTCAE grade 0–2 group

ASSOCIATIONS OF THE NRF2/KEAP1 PATHWAY AND ANTIOXIDANT DEFENSE GENE POLYMORPHISMS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE parenchyma. This work was designed as a case-control study aimed at investigating the association of the NRF2

3129934 (C6orf10), rs1109670 (DDEF2/MBOAT2 gene), rs9523762 (GPC5 gene), rs28362491 (NFKB1 gene), rs

significantly over-represented in active gene regulatory regions and transcription factor binding sites. We

ВЛИЯНИЕ ПОЛИМОРФИЗМА ГЕНА G1082AIL-10 НА ТЕЧЕНИЕ ОСТРЫХ КИШЕЧНЫХ ИНФЕКЦИЙ is played by the polymorphism of genes responsible for the induction of the synthesis of inflammatory

Ассоциация Gasdermin B Gene GSDMB полиморфизма с риском аллергических заболеваний семейства IKAROS), ZPBP2 (подобный белку , связывающий пеллюцидную зону ), GSDMB (газдермин B), ORMDL3

dynamic, cumulative gene-environment interactions that cause lung tissue injury, alteration of its normal

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