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Items: 26

1.

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.

J Trace Elem Med Biol. 2019 Oct 25:126420. doi: 10.1016/j.jtemb.2019.126420. [Epub ahead of print]

PMID:
31708252
2.

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.

Mol Med Rep. 2019 Dec;20(6):4905-4914. doi: 10.3892/mmr.2019.10751. Epub 2019 Oct 16.

PMID:
31638168
3.

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.

Mol Genet Genomic Med. 2019 Nov;7(11):e964. doi: 10.1002/mgg3.964. Epub 2019 Sep 3.

4.

Recent advances and perspectives in next generation sequencing application to the genetic research of type 2 diabetes.

Nasykhova YA, Barbitoff YA, Serebryakova EA, Katserov DS, Glotov AS.

World J Diabetes. 2019 Jul 15;10(7):376-395. doi: 10.4239/wjd.v10.i7.376. Review.

5.

Genome-wide sequence analyses of ethnic populations across Russia.

Zhernakova DV, Brukhin V, Malov S, Oleksyk TK, Koepfli KP, Zhuk A, Dobrynin P, Kliver S, Cherkasov N, Tamazian G, Rotkevich M, Krasheninnikova K, Evsyukov I, Sidorov S, Gorbunova A, Chernyaeva E, Shevchenko A, Kolchanova S, Komissarov A, Simonov S, Antonik A, Logachev A, Polev DE, Pavlova OA, Glotov AS, Ulantsev V, Noskova E, Davydova TK, Sivtseva TM, Limborska S, Balanovsky O, Osakovsky V, Novozhilov A, Puzyrev V, O'Brien SJ.

Genomics. 2019 Mar 19. pii: S0888-7543(18)30741-9. doi: 10.1016/j.ygeno.2019.03.007. [Epub ahead of print]

PMID:
30902755
6.

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.

Genes (Basel). 2018 Aug 17;9(8). pii: E415. doi: 10.3390/genes9080415.

7.

Analytical "bake-off" of whole genome sequencing quality for the Genome Russia project using a small cohort for autoimmune hepatitis.

Zhernakova DV, Kliver S, Cherkasov N, Tamazian G, Rotkevich M, Krasheninnikova K, Evsyukov I, Sidorov S, Dobrynin P, Yurchenko AA, Shimansky V, Shcherbakova IV, Glotov AS, Valle DL, Tang M, Shin E, Schwarz KB, O'Brien SJ.

PLoS One. 2018 Jul 11;13(7):e0200423. doi: 10.1371/journal.pone.0200423. eCollection 2018.

8.

Targeted sequencing analysis of ACVR2A gene identifies novel risk variants associated with preeclampsia.

Glotov AS, Kazakov SV, Vashukova ES, Pakin VS, Danilova MM, Nasykhova YA, Masharsky AE, Mozgovaya EV, Eremeeva DR, Zainullina MS, Baranov VS.

J Matern Fetal Neonatal Med. 2019 Sep;32(17):2790-2796. doi: 10.1080/14767058.2018.1449204. Epub 2018 Mar 21.

PMID:
29506428
9.

Catching hidden variation: systematic correction of reference minor allele annotation in clinical variant calling.

Barbitoff YA, Bezdvornykh IV, Polev DE, Serebryakova EA, Glotov AS, Glotov OS, Predeus AV.

Genet Med. 2018 Mar;20(3):360-364. doi: 10.1038/gim.2017.168. Epub 2017 Oct 26.

PMID:
29155419
10.

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.

Am J Physiol Heart Circ Physiol. 2017 Mar 1;312(3):H622-H631. doi: 10.1152/ajpheart.00080.2016. Epub 2016 Dec 6.

11.

Placental microRNA expression in pregnancies complicated by superimposed pre‑eclampsia on chronic hypertension.

Vashukova ES, Glotov AS, Fedotov PV, Efimova OA, Pakin VS, Mozgovaya EV, Pendina AA, Tikhonov AV, Koltsova AS, Baranov VS.

Mol Med Rep. 2016 Jul;14(1):22-32. doi: 10.3892/mmr.2016.5268. Epub 2016 May 13.

12.

Detection of human genome mutations associated with pregnancy complications using 3-D microarray based on macroporous polymer monoliths.

Glotov AS, Sinitsyna ES, Danilova MM, Vashukova ES, Walter JG, Stahl F, Baranov VS, Vlakh EG, Tennikova TB.

Talanta. 2016 Jan 15;147:537-46. doi: 10.1016/j.talanta.2015.09.066. Epub 2015 Oct 21.

PMID:
26592644
13.

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.

Clin Chim Acta. 2015 Jun 15;446:132-40. doi: 10.1016/j.cca.2015.04.014. Epub 2015 Apr 17.

PMID:
25892673
14.

Molecular association of pathogenetic contributors to pre-eclampsia (pre-eclampsia associome).

Glotov AS, Tiys ES, Vashukova ES, Pakin VS, Demenkov PS, Saik OV, Ivanisenko TV, Arzhanova ON, Mozgovaya EV, Zainulina MS, Kolchanov NA, Baranov VS, Ivanisenko VA.

BMC Syst Biol. 2015;9 Suppl 2:S4. doi: 10.1186/1752-0509-9-S2-S4. Epub 2015 Apr 15.

15.

AGTR2 gene polymorphism is associated with muscle fibre composition, athletic status and aerobic performance.

Mustafina LJ, Naumov VA, Cieszczyk P, Popov DV, Lyubaeva EV, Kostryukova ES, Fedotovskaya ON, Druzhevskaya AM, Astratenkova IV, Glotov AS, Alexeev DG, Mustafina MM, Egorova ES, Maciejewska-Karłowska A, Larin AK, Generozov EV, Nurullin RE, Jastrzębski Z, Kulemin NA, Ospanova EA, Pavlenko AV, Sawczuk M, Akimov EB, Danilushkina AA, Zmijewski P, Vinogradova OL, Govorun VM, Ahmetov II.

Exp Physiol. 2014 Aug;99(8):1042-52. doi: 10.1113/expphysiol.2014.079335. Epub 2014 May 30.

16.

[Molecular genetic basis of proximal spinal muscular atrophy and experience in its pharmaceutical treatment].

Baranov VS, Kiselev AV, Vakharlovskiĭ VG, Zhelezniakova GIu, Komantsev VN, Malysheva OV, Glotov AS, Ivashchenko TE, Baranov AN.

Genetika. 2008 Oct;44(10):1325-37. Review. Russian.

PMID:
19062530
17.

TPMT genetic variations in populations of the Russian Federation.

Samochatova EV, Chupova NV, Rudneva A, Makarova O, Nasedkina TV, Fedorova OE, Glotov AS, Kozhekbaeva Zh, Maiorova OA, Roumyantsev AG, Krynetski EY, Krynetskaia NF, Evans WE, Ribeiro RC.

Pediatr Blood Cancer. 2009 Feb;52(2):203-8. doi: 10.1002/pbc.21837.

18.

[Genetic polymorphism in GST, NAT2, and MTRR and susceptibility to childhood acute leukemia].

Gra OA, Glotov AS, Kozhekbaeva Zhm, Makarova OV, Nasedkina TV.

Mol Biol (Mosk). 2008 Mar-Apr;42(2):214-25. Russian.

PMID:
18610829
19.

[Correlation between the bone mass of athletes and biochemical and genetic markers of bone tissue remodeling].

Oganov VS, Vinogradova OL, Dudov NS, Baranov VS, Minenkov AS, Bakulin AV, Novikov VE, Kabitskaia OE, Moskalenko MV, Glotov AS, Glotov OS, Popov DV.

Fiziol Cheloveka. 2008 Mar-Apr;34(2):56-65. Russian. No abstract available.

PMID:
18472573
20.

Polymorphisms in xenobiotic-metabolizing genes and the risk of chronic lymphocytic leukemia and non-Hodgkin's lymphoma in adult Russian patients.

Gra OA, Glotov AS, Nikitin EA, Glotov OS, Kuznetsova VE, Chudinov AV, Sudarikov AB, Nasedkina TV.

Am J Hematol. 2008 Apr;83(4):279-87.

21.

[Identification of functionally significant mutations in NAT2 gene using biological microchips].

Kozhekbaeva ZhM, Glotov AS, Gra OA, Goldenkova-Pavlova IV, Bruskin SA, Agafonova EE, Markarova EV, Abdeev RM, Korsunskaia IM, Piruzian AL, Barskiĭ VE, Zasedatelev AS, Nasedkin TV.

Mol Biol (Mosk). 2007 Jul-Aug;41(4):725-33. Russian.

PMID:
17936995
22.

[Renin-angiotensin and kinin-bradykinin genes polymorphism effects on permanent arterial hypertension in children].

Glotov AS, Ivashchenko TE, Obraztsova GI, Nasedkina TV, Baranov VS.

Mol Biol (Mosk). 2007 Jan-Feb;41(1):18-25. Russian.

PMID:
17380887
23.

[Comparative analysis of N-acetylation polymorphism in humans as determined by phenotyping and genotyping].

Goldenkova-Pavlova IV, Bruskin SA, Abdeev RM, Markarova EV, Bigvava SG, Radkevich LA, Kozhekbaeva ZhM, Glotov AS, Gra OA, Zasedatelev AS, Nasedkina TV, Kurdanov KhA, Piruzian ES.

Genetika. 2006 Aug;42(8):1143-50. Russian.

PMID:
17025166
24.

Rapid genotyping of common deficient thiopurine S-methyltransferase alleles using the DNA-microchip technique.

Nasedkina TV, Fedorova OE, Glotov AS, Chupova NV, Samochatova EV, Maiorova OA, Zemlyakova VV, Roudneva AE, Chudinov AV, Yurasov RA, Kozhekbaeva JM, Barsky VE, Krynetskiy EY, Krynetskaia NF, Cheng C, Ribeiro RC, Evans WE, Roumyantsev AG, Zasedatelev AS.

Eur J Hum Genet. 2006 Sep;14(9):991-8. Epub 2006 May 17.

25.

[Biochip development for polymorphism analysis in biotransformation system genes].

Glotov aS, Nasedkina TV, Ivashchenko TE, Iurasov RA, Surzhikov SA, Pan'kov SV, Chudinov AV, Baranov VS, Zasedatelev AS.

Mol Biol (Mosk). 2005 May-Jun;39(3):403-12. Russian.

PMID:
15981570
26.

[Analysis of deletional damage in SMN1, SMN2, and NAIP genes in patients with spinal muscular atrophy in the northwestern region of Russia].

Glotov AS, Kiselev AV, Ivashchenko TE, Baranov VS.

Genetika. 2001 Aug;37(8):1156-9. Russian.

PMID:
11642117

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