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A RANDOMIZED PHASE 2 STUDY OF LONG-ACTING TRANSCON GH VS DAILY GH IN CHILDHOOD GH DEFICIENCY
Chatelain, Pierre, Malievskiy, Oleg, Radziuk, Klaudziya, Senatorova, Ganna, Abdou, Magdy O., Vlachopapadopoulou, Elpis, Skorodok, Yulia, Peterkova, Valentina, Leff, Jonathan A., Beckert, Michael (2017)
received one of three TransCon GH doses (0.14, 0.21, or 0.30 mg GH/kg/wk) or Genotropin 0.03 mg GH
РОЛЬ МЕТИЛИРОВАНИЯ ДНК В НАРУШЕНИИ КОСТНОГО МЕТАБОЛИЗМА
THE ROLE OF DNA METHYLATION IN THE DISORDERS OF BONE METABOLISM
Yalaev, B.I., Tyurin, A.V., Mirgalieva, R.Y., Khusainova, R.I., ЯЛАЕВ Б.И., ТЮРИН А.В., МИРГАЛИЕВА Р.Я., ХУСАИНОВА Р.И. (2019)
Osteoporosis is one of multifactorial diseases, it develops from interactions between the genetic
SYNTHESIS OF BIS(ISOXAZOL-4-YLMETHYLSULFANYL)ALKANES AND SOME METAL COMPLEXES AS A HEPATOPROTECTIVE AGENTS
AKHMETOVA, V.R., AKHMADIEV, N.S., NURTDINOVA, G.M., GALIMOVA, R.A., GALIMOVA, A.M., AGLETDINOV, E.F., KATAEV, V.A., KHISAMUTDINOV, R.A. (2018)
: Bis(isoxazol-4-ylmethylsulfanyl)alkanes were synthesized using the one-pot method. The structures
LYNCH SYNDROME GERMLINE MUTATIONS IN BREAST CANCER: NEXT GENERATION SEQUENCING CASE-CONTROL STUDY OF 1,263 PARTICIPANTS
NIKITIN, A.G., CHUDAKOVA, D.A., ENIKEEV, R.F., GORDIEV, M.G., SAKAEVA, D., DRUZHKOV, M., SHIGAPOVA, L.H., BROVKINA, O.I., SHAGIMARDANOVA, E.I., GUSEV, O.A. (2020)
cell to tolerate high mutation burden—is one of the drivers of cancer. Genome instability results from
TREATMENT EFFICACY OF DRUG-RESISTANT TUBERCULOSIS IN BASHKORTOSTAN, RUSSIA: A RETROSPECTIVE COHORT STUDY
Yunusbaeva, M., Borodina, L., Alekseev, P., Davydov, R., Sharipov, R., Bilalov, F., Yunusbayev, B. (2019)
Background: Russia, together with other former Soviet Union countries, is characterized by one
EFFECTS OF NOVEL HEXAHYDROPYRIMIDINE DERIVATIVES AS POTENTIAL LIGANDS OF M1 MUSCARINIC ACETYLCHOLINE RECEPTOR ON COGNITIVE FUNCTION, HYPOXIA-INDUCED LETHALITY, AND OXIDATIVE STRESS IN RODENTS
SAPOZHNIKOVA, T.A., BORISEVICH, S.S., KIREEVA, D.R., GABDRAKHMANOVA, S.F., KHISAMUTDINOVA, R.Y., MAKARA, N.S., GIBADULLINA, N.N., KHURSAN, S.L., ZARUDII, F.S. (2019)
/kg dose (p.o.)one hour before the tests increased the latency time to enter the dark compartment
DOES ESCHERICHIA COLI HAVE PATHOGENIC POTENTIAL AT A LOW LEVEL OF BACTERIURIA IN RECURRENT, UNCOMPLICATED URINARY TRACT INFECTION?
NABOKA, Y.L., MAVZYUTOV, A.R., KOGAN, M.I., GUDIMA, I.A., IVANOV, S.N., NABER, K.G. (2020)
.7%). VFGs were verified in all 15 strains at a low level of bacteriuria (102 CFU/mL): one VFG (pap
PADI4 GENE POLYMORPHISM AS A PREDICTOR OF RESPONSE TO METHOTREXATE IN PATIENTS WITH JUVENILE IDIOPATHIC ARTHRITIS
Nazarova, L.S., Danilko, K.V., Malievsky, V.A., Viktorova, T.V. (2016)
of the response to MTX. No unequivocal predictive SNP has been found yet, because many were assessed in only one
Origin and diffusion of human Y chromosome haplogroup J1-M267
Sahakyan, H., Margaryan, A., Saag, L., Karmin, M., Flores, R., Haber, M., Kushniarevich, A., Khachatryan, Z., Bahmanimehr, A., Parik, J., Karafet, T., Yunusbayev, B., Reisberg, T., Solnik, A., Metspalu, E., Hovhannisyan, A., Khusnutdinova, E.K., Behar, D.M., Metspalu, M., Yepiskoposyan, L., Rootsi, S., Villems, R. (2021)
Human Y chromosome haplogroup J1-M267 is a common male lineage in West Asia. One high
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene
Barashkov, N.A., Konovalov, F.A., Borisova, T.V., Teryutin, F.M., Solovyev, A.V., Pshennikova, V.G., Sapojnikova, N.V., Vychuzhina, L.S., Romanov, G.P., Gotovtsev, N.N., Morozov, I.V., Bondar, A.A., Platonov, F.A., Burtseva, T.E., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A. (2021)
Congenital autosomal recessive cataract with unknown genetic etiology is one of the most common

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