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Page 1
Identification of Novel Candidate Markers of Type 2 Diabetes and Obesity in Russia by Exome Sequencing with a Limited Sample Size.
Barbitoff YA, Serebryakova EA, Nasykhova YA, Predeus AV, Polev DE, Shuvalova AR, Vasiliev EV, Urazov SP, Sarana AM, Scherbak SG, Gladyshev DV, Pokrovskaya MS, Sivakova OV, Meshkov AN, Drapkina OM, Glotov OS, Glotov AS. Barbitoff YA, et al. Among authors: glotov os, glotov as. Genes (Basel). 2018 Aug 17;9(8):415. doi: 10.3390/genes9080415. Genes (Basel). 2018. PMID: 30126146 Free PMC article.
Targeted next-generation sequencing (NGS) of nine candidate genes with custom AmpliSeq in patients and a cardiomyopathy risk group.
Glotov AS, Kazakov SV, Zhukova EA, Alexandrov AV, Glotov OS, Pakin VS, Danilova MM, Poliakova IV, Niyazova SS, Chakova NN, Komissarova SM, Kurnikova EA, Sarana AM, Sherbak SG, Sergushichev AA, Shalyto AA, Baranov VS. Glotov AS, et al. Among authors: glotov os. Clin Chim Acta. 2015 Jun 15;446:132-40. doi: 10.1016/j.cca.2015.04.014. Epub 2015 Apr 17. Clin Chim Acta. 2015. PMID: 25892673
Genetic determination of the vascular reactions in humans in response to the diving reflex.
Baranova TI, Berlov DN, Glotov OS, Korf EA, Minigalin AD, Mitrofanova AV, Ahmetov II, Glotov AS. Baranova TI, et al. Among authors: glotov os, glotov as. Am J Physiol Heart Circ Physiol. 2017 Mar 1;312(3):H622-H631. doi: 10.1152/ajpheart.00080.2016. Epub 2016 Dec 6. Am J Physiol Heart Circ Physiol. 2017. PMID: 27923785 Free article.
Whole-exome sequencing provides insights into monogenic disease prevalence in Northwest Russia.
Barbitoff YA, Skitchenko RK, Poleshchuk OI, Shikov AE, Serebryakova EA, Nasykhova YA, Polev DE, Shuvalova AR, Shcherbakova IV, Fedyakov MA, Glotov OS, Glotov AS, Predeus AV. Barbitoff YA, et al. Among authors: glotov os, glotov as. Mol Genet Genomic Med. 2019 Nov;7(11):e964. doi: 10.1002/mgg3.964. Epub 2019 Sep 3. Mol Genet Genomic Med. 2019. PMID: 31482689 Free PMC article.
Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes.
Glotov OS, Serebryakova EA, Turkunova ME, Efimova OA, Glotov AS, Barbitoff YA, Nasykhova YA, Predeus AV, Polev DE, Fedyakov MA, Polyakova IV, Ivashchenko TE, Shved NY, Shabanova ES, Tiselko AV, Romanova OV, Sarana AM, Pendina AA, Scherbak SG, Musina EV, Petrovskaia-Kaminskaia AV, Lonishin LR, Ditkovskaya LV, Zhelenina LА, Tyrtova LV, Berseneva OS, Skitchenko RK, Suspitsin EN, Bashnina EB, Baranov VS. Glotov OS, et al. Among authors: glotov as. Mol Med Rep. 2019 Dec;20(6):4905-4914. doi: 10.3892/mmr.2019.10751. Epub 2019 Oct 16. Mol Med Rep. 2019. PMID: 31638168 Free PMC article.
The spectrum of pathogenic variants of the ATP7B gene in Wilson disease in the Russian Federation.
Balashova MS, Tuluzanovskaya IG, Glotov OS, Glotov AS, Barbitoff YA, Fedyakov MA, Alaverdian DA, Ivashchenko TE, Romanova OV, Sarana AM, Scherbak SG, Baranov VS, Filimonov MI, Skalny AV, Zhuchenko NA, Ignatova TM, Asanov AY. Balashova MS, et al. Among authors: glotov os, glotov as. J Trace Elem Med Biol. 2020 May;59:126420. doi: 10.1016/j.jtemb.2019.126420. Epub 2019 Oct 25. J Trace Elem Med Biol. 2020. PMID: 31708252
Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities.
Pendina AA, Shilenkova YV, Talantova OE, Efimova OA, Chiryaeva OG, Malysheva OV, Dudkina VS, Petrova LI, Serebryakova EA, Shabanova ES, Mekina ID, Komarova EM, Koltsova AS, Tikhonov AV, Tral TG, Tolibova GK, Osinovskaya NS, Krapivin MI, Petrovskaia-Kaminskaia AV, Korchak TS, Ivashchenko TE, Glotov OS, Romanova OV, Shikov AE, Urazov SP, Tsay VV, Eismont YA, Scherbak SG, Sagurova YM, Vashukova ES, Kozyulina PY, Dvoynova NM, Glotov AS, Baranov VS, Gzgzyan AM, Kogan IY. Pendina AA, et al. Among authors: glotov os, glotov as. Front Genet. 2019 Nov 20;10:1164. doi: 10.3389/fgene.2019.01164. eCollection 2019. Front Genet. 2019. PMID: 31824569 Free PMC article.
41 results