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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 2
1990 5
1991 2
1992 1
1993 2
1994 1
1997 2
1998 3
1999 2
2000 3
2001 3
2002 2
2003 2
2004 1
2005 1
2006 1
2007 2
2008 1
2013 1
2014 2
2016 2
2017 1
2019 3
2020 1
2024 1

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45 results

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Page 1
Case report: Preimplantation genetic testing for infantile GM1 gangliosidosis.
Zagaynova VA, Nasykhova YA, Tonyan ZN, Danilova MM, Dvoynova NM, Lazareva TE, Ivashchenko TE, Shabanova ES, Krikheli IO, Lesik EA, Bespalova ON, Kogan IY, Glotov AS. Zagaynova VA, et al. Among authors: ivashchenko te. Front Genet. 2024 Feb 9;15:1344051. doi: 10.3389/fgene.2024.1344051. eCollection 2024. Front Genet. 2024. PMID: 38404665 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: ivashchenko te. 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: ivashchenko te. Front Genet. 2019 Nov 20;10:1164. doi: 10.3389/fgene.2019.01164. eCollection 2019. Front Genet. 2019. PMID: 31824569 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: ivashchenko te. 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.
Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutations.
Dzhemlikhanova LK, Efimova OA, Osinovskaya NS, Parfenyev SE, Niauri DA, Sultanov IY, Malysheva OV, Pendina AA, Shved NY, Ivashchenko TE, Yarmolinskaya MI, Kakhiani MI, Gorovaya EA, Tkachenko AN, Baranov VS. Dzhemlikhanova LK, et al. Among authors: ivashchenko te. J Clin Pathol. 2017 Mar;70(3):233-236. doi: 10.1136/jclinpath-2016-203976. Epub 2016 Aug 4. J Clin Pathol. 2017. PMID: 27491313
[Suppression of nonsense mutations in the Dystrophin gene by a suppressor tRNA gene].
Kiselev AV, Ostapenko OV, Rogozhkina EV, Kholod NS, Seit Nebi AS, Baranov AN, Lesina EA, Ivashchenko TE, Sabetskiĭ VA, Shavlovskiĭ MM, Rechinskiĭ VO, Kiselev LL, Baranov VC. Kiselev AV, et al. Among authors: ivashchenko te. Mol Biol (Mosk). 2002 Jan-Feb;36(1):43-7. Mol Biol (Mosk). 2002. PMID: 11862712 Russian.
45 results