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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.
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.
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: skitchenko rk.
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.
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Phenome-wide functional dissection of pleiotropic effects highlights key molecular pathways for human complex traits.
Shikov AE, Skitchenko RK, Predeus AV, Barbitoff YA.
Shikov AE, et al. Among authors: skitchenko rk.
Sci Rep. 2020 Jan 23;10(1):1037. doi: 10.1038/s41598-020-58040-4.
Sci Rep. 2020.
PMID: 31974475
Free PMC article.
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Estimation of amyloid aggregate sizes with semi-denaturing detergent agarose gel electrophoresis and its limitations.
Drozdova PB, Barbitoff YA, Belousov MV, Skitchenko RK, Rogoza TM, Leclercq JY, Kajava AV, Matveenko AG, Zhouravleva GA, Bondarev SA.
Drozdova PB, et al. Among authors: skitchenko rk.
Prion. 2020 Dec;14(1):118-128. doi: 10.1080/19336896.2020.1751574.
Prion. 2020.
PMID: 32306832
Free PMC article.
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No More Tears: Mining Sequencing Data for Novel Bt Cry Toxins with CryProcessor.
Shikov AE, Malovichko YV, Skitchenko RK, Nizhnikov AA, Antonets KS.
Shikov AE, et al. Among authors: skitchenko rk.
Toxins (Basel). 2020 Mar 23;12(3):204. doi: 10.3390/toxins12030204.
Toxins (Basel). 2020.
PMID: 32210056
Free PMC article.
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Census of halide-binding sites in protein structures.
Skitchenko RK, Usoltsev D, Uspenskaya M, Kajava AV, Guskov A.
Skitchenko RK, et al.
Bioinformatics. 2020 May 1;36(10):3064-3071. doi: 10.1093/bioinformatics/btaa079.
Bioinformatics. 2020.
PMID: 32022861
Free PMC article.
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A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.
Zlotina A, Melnik O, Fomicheva Y, Skitchenko R, Sergushichev A, Shagimardanova E, Gusev O, Gazizova G, Loevets T, Vershinina T, Kozyrev I, Gordeev M, Vasichkina E, Pervunina T, Kostareva A.
Zlotina A, et al.
BMC Med Genomics. 2020 Nov 20;13(1):175. doi: 10.1186/s12920-020-00821-x.
BMC Med Genomics. 2020.
PMID: 33218365
Free PMC article.
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