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Items: 31

1.

A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259*) in the MITF gene in Yakut patient from the Eastern Siberia (Sakha Republic, Russia).

Barashkov NA, Romanov GP, Borisova UP, Solovyev AV, Pshennikova VG, Teryutin FM, Bondar AA, Morozov IV, Khusnutdinova EK, Posukh OL, Burtseva TE, Odland JØ, Fedorova SA.

Int J Circumpolar Health. 2019 Dec;78(1):1630219. doi: 10.1080/22423982.2019.1630219.

PMID:
31213145
2.

Unique Mutational Spectrum of the GJB2 Gene and its Pathogenic Contribution to Deafness in Tuvinians (Southern Siberia, Russia): A High Prevalence of Rare Variant c.516G>C (p.Trp172Cys).

Posukh OL, Zytsar MV, Bady-Khoo MS, Danilchenko VY, Maslova EA, Barashkov NA, Bondar AA, Morozov IV, Maximov VN, Voevoda MI.

Genes (Basel). 2019 Jun 5;10(6). pii: E429. doi: 10.3390/genes10060429.

3.

A serological survey of echinococcosis, toxocariasis and trichinellosis among rural inhabitants of Central Yakutia.

Nakhodkin SS, Pshennikova VG, Dyachkovskaya PS, Barashkov NA, Nikanorova AA, Teryutin FM, Melnichuk OA, Crubézy E, Fedorova SA, Magnaval JF.

Int J Circumpolar Health. 2019 Dec;78(1):1603550. doi: 10.1080/22423982.2019.1603550.

4.

Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A).

Pshennikova VG, Barashkov NA, Romanov GP, Teryutin FM, Solov'ev AV, Gotovtsev NN, Nikanorova AA, Nakhodkin SS, Sazonov NN, Morozov IV, Bondar AA, Dzhemileva LU, Khusnutdinova EK, Posukh OL, Fedorova SA.

ScientificWorldJournal. 2019 Mar 20;2019:5198931. doi: 10.1155/2019/5198931. eCollection 2019.

5.

Evaluation of the Use of Microtracers™ in a Proficiency Testing Program.

Thiex N, Carlson M, Kieffer R, Kieffer A, Eisenberg D, Barashkov N, Ramsey C.

J AOAC Int. 2019 May 1;102(3):767-775. doi: 10.5740/jaoacint.18-0354. Epub 2019 Jan 16.

PMID:
30651161
6.

Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia.

Zytsar MV, Barashkov NA, Bady-Khoo MS, Shubina-Olejnik OA, Danilenko NG, Bondar AA, Morozov IV, Solovyev AV, Danilchenko VY, Maximov VN, Posukh OL.

BMC Med Genet. 2018 Aug 7;19(1):138. doi: 10.1186/s12881-018-0650-5.

7.

A novel pathogenic variant c.975G>A (p.Trp325*) in the POU3F4 gene in Yakut family (Eastern Siberia, Russia) with the X-linked deafness-2 (DFNX2).

Barashkov NA, Klarov LA, Teryutin FM, Solovyev AV, Pshennikova VG, Konnikova EE, Romanov GP, Tobokhov AV, Morozov IV, Bondar AA, Posukh OL, Dzhemileva LU, Tomsky MI, Khusnutdinova EK, Fedorova SA.

Int J Pediatr Otorhinolaryngol. 2018 Jan;104:94-97. doi: 10.1016/j.ijporl.2017.11.001. Epub 2017 Nov 6.

PMID:
29287890
8.

Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations.

Solovyev AV, Dzhemileva LU, Posukh OL, Barashkov NA, Bady-Khoo MS, Lobov SL, Popova NY, Romanov GP, Sazonov NN, Bondar AA, Morozov IV, Tomsky MI, Fedorova SA, Khusnutdinova EK.

J Community Genet. 2017 Jul;8(3):167-171. doi: 10.1007/s12687-017-0299-3. Epub 2017 Mar 21.

9.

Perylene Derivative Dyes Luminescence in Polysiloxane Matrix in Presence of Gold Nanoparticles.

Mantel A, Shautenbaeva N, Irgibaeva I, Aldongarov A, Lang A, Barashkov N, Mukatayev I.

J Fluoresc. 2016 Nov;26(6):2213-2223. Epub 2016 Sep 3.

PMID:
27592354
10.

Genomic analyses inform on migration events during the peopling of Eurasia.

Pagani L, Lawson DJ, Jagoda E, Mörseburg A, Eriksson A, Mitt M, Clemente F, Hudjashov G, DeGiorgio M, Saag L, Wall JD, Cardona A, Mägi R, Wilson Sayres MA, Kaewert S, Inchley C, Scheib CL, Järve M, Karmin M, Jacobs GS, Antao T, Iliescu FM, Kushniarevich A, Ayub Q, Tyler-Smith C, Xue Y, Yunusbayev B, Tambets K, Mallick CB, Saag L, Pocheshkhova E, Andriadze G, Muller C, Westaway MC, Lambert DM, Zoraqi G, Turdikulova S, Dalimova D, Sabitov Z, Sultana GNN, Lachance J, Tishkoff S, Momynaliev K, Isakova J, Damba LD, Gubina M, Nymadawa P, Evseeva I, Atramentova L, Utevska O, Ricaut FX, Brucato N, Sudoyo H, Letellier T, Cox MP, Barashkov NA, Skaro V, Mulahasanovic L, Primorac D, Sahakyan H, Mormina M, Eichstaedt CA, Lichman DV, Abdullah S, Chaubey G, Wee JTS, Mihailov E, Karunas A, Litvinov S, Khusainova R, Ekomasova N, Akhmetova V, Khidiyatova I, Marjanović D, Yepiskoposyan L, Behar DM, Balanovska E, Metspalu A, Derenko M, Malyarchuk B, Voevoda M, Fedorova SA, Osipova LP, Lahr MM, Gerbault P, Leavesley M, Migliano AB, Petraglia M, Balanovsky O, Khusnutdinova EK, Metspalu E, Thomas MG, Manica A, Nielsen R, Villems R, Willerslev E, Kivisild T, Metspalu M.

Nature. 2016 Oct 13;538(7624):238-242. doi: 10.1038/nature19792. Epub 2016 Sep 21.

11.

Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic).

Barashkov NA, Pshennikova VG, Posukh OL, Teryutin FM, Solovyev AV, Klarov LA, Romanov GP, Gotovtsev NN, Kozhevnikov AA, Kirillina EV, Sidorova OG, Vasilyevа LM, Fedotova EE, Morozov IV, Bondar AA, Solovyevа NA, Kononova SK, Rafailov AM, Sazonov NN, Alekseev AN, Tomsky MI, Dzhemileva LU, Khusnutdinova EK, Fedorova SA.

PLoS One. 2016 May 25;11(5):e0156300. doi: 10.1371/journal.pone.0156300. eCollection 2016.

12.

[The audiological analysis in the patients homozygous for the c.-23+1G>A mutation in the GJB2 gene presenting with the loss of hearing in Yakutiya].

Teryutin FM, Barashkov NA, Kunel'skaya NL, Pshennikova VG, Solov'ev AV.

Vestn Otorinolaringol. 2016;81(1):19-24. doi: 10.17116/otorino201681119-24. Russian.

PMID:
26977562
13.

The genetic legacy of the expansion of Turkic-speaking nomads across Eurasia.

Yunusbayev B, Metspalu M, Metspalu E, Valeev A, Litvinov S, Valiev R, Akhmetova V, Balanovska E, Balanovsky O, Turdikulova S, Dalimova D, Nymadawa P, Bahmanimehr A, Sahakyan H, Tambets K, Fedorova S, Barashkov N, Khidiyatova I, Mihailov E, Khusainova R, Damba L, Derenko M, Malyarchuk B, Osipova L, Voevoda M, Yepiskoposyan L, Kivisild T, Khusnutdinova E, Villems R.

PLoS Genet. 2015 Apr 21;11(4):e1005068. doi: 10.1371/journal.pgen.1005068. eCollection 2015 Apr.

14.

A recent bottleneck of Y chromosome diversity coincides with a global change in culture.

Karmin M, Saag L, Vicente M, Wilson Sayres MA, Järve M, Talas UG, Rootsi S, Ilumäe AM, Mägi R, Mitt M, Pagani L, Puurand T, Faltyskova Z, Clemente F, Cardona A, Metspalu E, Sahakyan H, Yunusbayev B, Hudjashov G, DeGiorgio M, Loogväli EL, Eichstaedt C, Eelmets M, Chaubey G, Tambets K, Litvinov S, Mormina M, Xue Y, Ayub Q, Zoraqi G, Korneliussen TS, Akhatova F, Lachance J, Tishkoff S, Momynaliev K, Ricaut FX, Kusuma P, Razafindrazaka H, Pierron D, Cox MP, Sultana GN, Willerslev R, Muller C, Westaway M, Lambert D, Skaro V, Kovačevic L, Turdikulova S, Dalimova D, Khusainova R, Trofimova N, Akhmetova V, Khidiyatova I, Lichman DV, Isakova J, Pocheshkhova E, Sabitov Z, Barashkov NA, Nymadawa P, Mihailov E, Seng JW, Evseeva I, Migliano AB, Abdullah S, Andriadze G, Primorac D, Atramentova L, Utevska O, Yepiskoposyan L, Marjanovic D, Kushniarevich A, Behar DM, Gilissen C, Vissers L, Veltman JA, Balanovska E, Derenko M, Malyarchuk B, Metspalu A, Fedorova S, Eriksson A, Manica A, Mendez FL, Karafet TM, Veeramah KR, Bradman N, Hammer MF, Osipova LP, Balanovsky O, Khusnutdinova EK, Johnsen K, Remm M, Thomas MG, Tyler-Smith C, Underhill PA, Willerslev E, Nielsen R, Metspalu M, Villems R, Kivisild T.

Genome Res. 2015 Apr;25(4):459-66. doi: 10.1101/gr.186684.114. Epub 2015 Mar 13.

15.

Age-Related Hearing Impairment (ARHI) associated with GJB2 single mutation IVS1+1G>A in the Yakut population isolate in Eastern Siberia.

Barashkov NA, Teryutin FM, Pshennikova VG, Solovyev AV, Klarov LA, Solovyeva NA, Kozhevnikov AA, Vasilyeva LM, Fedotova EE, Pak MV, Lekhanova SN, Zakharova EV, Savvinova KE, Gotovtsev NN, Rafailo AM, Luginov NV, Alexeev AN, Posukh OL, Dzhemileva LU, Khusnutdinova EK, Fedorova SA.

PLoS One. 2014 Jun 24;9(6):e100848. doi: 10.1371/journal.pone.0100848. eCollection 2014.

16.

Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia.

Dzhemileva LU, Posukh OL, Barashkov NA, Fedorova SA, Teryutin FM, Akhmetova VL, Khidiyatova IM, Khusainova RI, Lobov SL, Khusnutdinova EK.

Acta Naturae. 2011 Jul;3(3):52-63.

17.

Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia: extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect.

Barashkov NA, Dzhemileva LU, Fedorova SA, Teryutin FM, Posukh OL, Fedotova EE, Lobov SL, Khusnutdinova EK.

J Hum Genet. 2011 Sep;56(9):631-9. doi: 10.1038/jhg.2011.72. Epub 2011 Jul 21.

PMID:
21776002
18.

Fluorescent chemosensor for detection and quantitation of carbon dioxide gas.

Liu Y, Tang Y, Barashkov NN, Irgibaeva IS, Lam JW, Hu R, Birimzhanova D, Yu Y, Tang BZ.

J Am Chem Soc. 2010 Oct 13;132(40):13951-3. doi: 10.1021/ja103947j.

PMID:
20853831
19.

Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia.

Dzhemileva LU, Barashkov NA, Posukh OL, Khusainova RI, Akhmetova VL, Kutuev IA, Gilyazova IR, Tadinova VN, Fedorova SA, Khidiyatova IM, Lobov SL, Khusnutdinova EK.

J Hum Genet. 2010 Nov;55(11):749-54. doi: 10.1038/jhg.2010.101. Epub 2010 Aug 26.

PMID:
20739944
20.

[Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia].

Dzhemileva LU, Posukh OL, Tazetdinov AM, Barashkov NA, Zhuravskiĭ SG, Ponidelko SN, Markova TG, Tadinova VN, Fedorova SA, Maksimova NR, Khusnutdinova EK.

Genetika. 2009 Jul;45(7):982-91. Russian.

PMID:
19705751
21.

[Cochlear implantation in a child with congenital sensorineural deafness due to 35 DELG mutation in GJB2 (connexin 26) gene].

Teriutin FM, Barashkov NA, Dzhemileva LU, Posukh OL, Fedotova EE, Gurinova EE, Fedorova SA, Tavartkiladze GA, Khusnutdinova EK.

Vestn Otorinolaringol. 2009;(2):17-9. Russian.

PMID:
19491791
22.

[Connexin gene 26 (GJB2) mutations in patients with hereditary non-syndromic sensorineural loss of hearing in the Republic of Sakha (Yakutia)].

Barashkov NA, Dzhemileva LU, Fedorova SA, Maksimova NR, Khusnutdinova EK.

Vestn Otorinolaringol. 2008;(5):23-8. Russian.

PMID:
19008837
23.

Photodegradation of polymer-dispersed perylene di-imide dyes.

Tanaka N, Barashkov N, Heath J, Sisk WN.

Appl Opt. 2006 Jun 1;45(16):3846-51.

PMID:
16724148
24.

Controlling Schottky energy barriers in organic electronic devices using self-assembled monolayers.

Campbell IH, Rubin S, Zawodzinski TA, Kress JD, Martin RL, Smith DL, Barashkov NN, Ferraris JP.

Phys Rev B Condens Matter. 1996 Nov 15;54(20):R14321-R14324. No abstract available.

PMID:
9985517
25.

[Optimizing the teaching of therapy in a military medicine department].

Barashkov NA, Kliachkin LM.

Voen Med Zh. 1981 Sep;(9):17-9. Russian. No abstract available.

PMID:
7303524
26.

[Visual aids utilization in teaching military field therapy].

Barashkov NA, Kliachkin LM.

Voen Med Zh. 1980 Dec;(12):19-22. Russian. No abstract available.

PMID:
6162274
27.

[Training of students for the performance of the duties of the troop physician].

Barashkov NA.

Voen Med Zh. 1980 Feb;(2):19-22. Russian. No abstract available.

PMID:
7376505
28.

[Several ways to optimize the learning process in the military medicine faculty].

Barashkov NA, Ovchenkov DN, Shtannikov EV, Garber EI, Shindriaev AA.

Voen Med Zh. 1970 Aug;8:14-7. Russian. No abstract available.

PMID:
5515336
29.

[On the preliminary training of the military surgeon in the department of military medicine].

Barashkov NA.

Voen Med Zh. 1969 Apr;4:20-3. Russian. No abstract available.

PMID:
5822256
30.

[Programmed instruction in the system of military medical training of students].

Barashkov NA, Ovchenkov DN, Shtannikov EV, Garber EI, Shindriaev AA.

Voen Med Zh. 1968 Jun;6:14-8. Russian. No abstract available.

PMID:
5706299
31.

[On the method of teaching the subject "Organization of the work of the medico-sanitary battalion"].

Barashkov NA.

Voen Med Zh. 1965 Jun;6:10-3. Russian. No abstract available.

PMID:
5870815

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