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Evaluation of VDR and PAI allelic genes in patients with avascular necrosis of the femoral head
Volkov, E.E., Goloshchapov, A.P., Mustafin, R.N. (2021)
out. A comparative analysis of the alleles and genotypes frequency distribution of polymorphisms rs
ANALYSIS OF CLINICAL MANIFESTATIONS OF NEUROFIBROMATOSIS TYPE 1 IN PATIENTS WITH NONSENSE PATHOGENIC VARIANTS IN THE NF1 GENE FROM THE REPUBLIC OF BASHKORTOSTAN
Mustafin, R.N., Bermisheva, M.A., Karunas, A.S., Akhmetshin, A.A., Monakhova, A.S., Khusnutdinova, E.K. (2025)
Relevance: neurofibromatosis type 1 (NF1) is a hereditary tumor syndrome occurring with a frequency
Interrelation of Telomeres with Transposable Elements in Aging
Mustafin, R. N. (2020)
Abstract: The nature of telomere functioning, which affects the aging of the body, reflects global
A Replication Study of GWAS-Associated Variants in the TUFM, SH2B1, ZNF638, NEGR1, ATP2A1, EXOC4, and CSE1L Genes and Cognitive Abilities
Kazantseva, A.V., Davydova, Yu. D., Enikeeva, R.F., Takhirova, Z.R., Mustafin, R.N., Lobaskova, M.M., Malykh, S.B., Khusnutdinova, E.K. (2023)
< 0.05) in the genotype frequency distribution of ATP2A1 rs8055138, NEGR1 rs12128707, and ZNF638 rs
ГИПОТЕЗА ПРОИСХОЖДЕНИЯ ВИРУСОВ ОТ ТРАНСПОЗОНОВ
HYPOTHESIS ON THE ORIGIN OF VIRUSES FROM TRANSPOSONS
MUSTAFIN, R.N., Мустафин, Р.Н. (2018)
of viruses from transposons in evolution are discussed. The genomic elements exhibiting a dual nature
ANALYSIS OF ASSOCIATIONS OF ALLELES AND GENOTYPES OF POLYMORPHIC LOCI OF A RANGE OF CANDIDATE GENES WITH PHENOTYPIC VARIATIONS AT THE LEVEL OF INTELLIGENCE
Nurgalieva, A.Kh., Bashkatov, S.A., Volkova, E.V., Petrova, S.G., Takhirova, Z.R., Mustafin, R.N., Fedorova, Y.Y., Prokofyeva, D.S., Khusnutdinova, E.K. (2023)
of future endeavors. There has been conducted a molecular genetic study of the frequency distribution
THE ROLE OF REVERSE TRANSCRIPTASE IN THE ORIGIN OF LIFE
MUSTAFIN, R.N., KHUSNUTDINOVA, E.K. (2019)
properties. We hypothesize that natural selection of mechanisms for the defense against insertions based
THE ROLE OF OXYTOCIN RECEPTOR (OXTR) GENE POLYMORPHISMS IN THE DEVELOPMENT OF AGGRESSIVE BEHAVIOR IN HEALTHY INDIVIDUALS
DAVYDOVA, YU. D., KAZANTSEVA, A. V., ENIKEEVA, R. F., MUSTAFIN, R.N., ENIKEEVA, R. F., LOBASKOVA, M. M., MALYKH, S. B., GILYAZOVA, I.R., KHUSNUTDINOVA, E.K. (2020)
its binding to oxytocin receptor (OXTR). Considering the multifactorial nature of developing
Изменения иммунной системы в патогенезе нейрофиброматоза 1-го типа
Immune system changes in the pathogenesis of neurofibromatosis type 1
Mustafin, R.N., Мустафин, Р.Н. (2022)
Neurofibromatosis type 1 (NF1) is a hereditary tumor syndrome occurring with a frequency of 1: 3000
Skeletal anomalies in patients with neurofibromatosis type 1
Mustafin, R.N. (2022)
», «treatment», «frequency», «prevalence», «genotype-phenotype correlation», « modifier genes». Results

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