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Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia
Khidiyatova, I.M., Saifullina, E.V., Karunas, A.S., Akhmetgaleyeva, A.F., Kutlubaeva, R.F., Smakova, L.A., Lobov, S.L., Polyakov, A.V., Shchagina, O.A., Kadnikova, V.A., Ryzhkova, O.P., Magzhanov, R.V. (2022)
predominant lesion of the pyramidal tract. The autosomal dominant form of SPG3A, associated with mutations
Interaction of immune response mediator genes in a predisposition to juvenile idiopathic arthritis
Nazarova, Liliia Sh., Danilko, Ksenia V., Malievsky, Viktor A., Karimov, Denis O., Bakirov, Akhat B., Viktorova, Tatyana V. (2022)
the polymorphic loci of immune response mediator genes (TNFA rs1800629, LTA rs909253, IL1B rs16944, IL2-IL21 rs
ГЕНЫ-МАРКЕРЫ ЯЗВЕННОЙ БОЛЕЗНИ
Genes-markers of peptic ulcer disease
Сагадатова, Ю.Р., Хасанов, А.Г., Гилязова, И.Р., Бадретдинов, А.Ф., Фаязов, Р.Р., Суфияров, И.Ф., Sagadatova, Yu.R., Khasanov, A.G., Gilyazova, I.R., Badretdinov, A.F., Fayazov, R.R., Sufiyarov, I.F. (2022)
Genes-markers of peptic ulcer disease
ASSOCIATION OF 22 POTENTIAL PATHOGENIC VARIANTS OF NEW CANDIDATE GENES AND THE RISK OF OVARIAN CANCER
Mingazheva, E.T., Prokofyeva, D.S., Valova, Ya.V., Andreeva, E.A., Nurgalieva, A.Kh., Valiev, R.R., Ekomasova, N.V., Faishanova, R.R., Romanova, A.R., Khusnutdinova, E.K. (2022)
The high risk of ovarian cancer is primarily associated with mutations in BRCA1 and BRCA2 genes
Exosomal miRNA-146a is downregulated in clear cell renal cell carcinoma patients with severe immune-related adverse events
Ivanova, E., Asadullina, D., Rakhimov, R., Izmailov, A., Izmailov, Al., Gilyazova, G., Galimov, Sh., Pavlov, V., Khusnutdinova, E., Gilyazova, I. (2022)
expression level in ccRCC patients with CTCAE grade 3–4 (M±SEM 1.71 ± 0.13) compared to CTCAE grade 0–2 group
Bioinformatics analysis of potential therapeutic targets for COVID-19 infection in patients with carotid atherosclerosis
Yanchao, L., Sibin, Z., Gareev, I., Huan, X., Junfei, Z., Chunyang, L., Beylerli, O., Sufianov, A., Chao, Y., Yuyan, G., Xun, X., Ahmad, A. (2022)
patients, to clarify the common genes of both, and to identify common pathways and potential drugs
ASSESSING RISKS OF FUNCTIONAL DISORDERS OF HEPATOBILIARY SYSTEM IN WORKERS EMPLOYED AT BUTYL RUBBER PRODUCTION ALLOWING FOR ANALYSIS OF THE OGG1 GENE POLYMORPHIC VARIANT rs1052133
Kudoyarov, E.R., Karimov, D.O., Bakirov, A.B., Mukhammadieva, G.F., Karimova, L.K., Galimova, R.R. (2022)
of the OGG1 gene and the severity of DNA breaks. The study revealed adverse effects produced by the chemical
Immunogenetic aspects of osteoarthritis (literature review)
Kazanсev, Yu.A., Urazaeva, A.T., Mustafin, R.N., Deryabina, S.S. (2022)
genes, HLA genes and in the anti-inflammatory cytokine (IL-4) gene, polymorphisms in phospholipase
ATYPICAL CLINICAL MANIFESTATIONS AND GENOTYPE-PHENOTYPE CORRELATIONS OF NEUROFIBROMATOSIS TYPE 1
Мустафин, Р.Н., Mustafin, R.N. (2022)
by specific mutations in the NF1 gene (causing substitutions of amino acids in neurofibromin: p.Arg1038, p
Association of a Single-Nucleotide Variant rs11100494 of the NPY5R Gene with Antipsychotic-Induced Metabolic Disorders
Dobrodeeva, V.S., Shnayder, N.A., Novitsky, M.A., Asadullin, A.R., Vaiman, E.E., Petrova, M.M., Limankin, O.V., Neznanov, N.G., Garganeeva, N.P., Nasyrova, R.F. (2022)
6837793 of the NPY5R gene, and rs16147, rs5573, rs5574 of the NPY gene, with metabolic disorders

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