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Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report.
BMC Nephrol. 2019 Oct 26;20(1):389. doi: 10.1186/s12882-019-1579-4.
BMC Nephrol. 2019.
PMID: 31655555
Free PMC article.
A novel MFSD8 mutation in a Russian patient with neuronal ceroid lipofuscinosis type 7: a case report.
Kozina AA, Okuneva EG, Baryshnikova NV, Krasnenko AY, Tsukanov KY, Klimchuk OI, Kondakova OB, Larionova AN, Batysheva TT, Surkova EI, Shatalov PA, Ilinsky VV.
Kozina AA, et al. Among authors: klimchuk oi.
BMC Med Genet. 2018 Aug 25;19(1):151. doi: 10.1186/s12881-018-0669-7.
BMC Med Genet. 2018.
PMID: 30144815
Free PMC article.
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Phylogenomic Analysis Identifies a Sodium-Translocating Decarboxylating Oxidoreductase in Thermotogae.
Klimchuk OI, Dibrova DV, Mulkidjanian AY.
Klimchuk OI, et al.
Biochemistry (Mosc). 2016 May;81(5):481-90. doi: 10.1134/S0006297916050059.
Biochemistry (Mosc). 2016.
PMID: 27297898
Free article.
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COGNAT: a web server for comparative analysis of genomic neighborhoods.
Klimchuk OI, Konovalov KA, Perekhvatov VV, Skulachev KV, Dibrova DV, Mulkidjanian AY.
Klimchuk OI, et al.
Biol Direct. 2017 Nov 22;12(1):26. doi: 10.1186/s13062-017-0196-z.
Biol Direct. 2017.
PMID: 29166914
Free PMC article.
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Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report.
Kozina AA, Okuneva EG, Baryshnikova NV, Fedonyuk ID, Kholin AA, Il'ina ES, Krasnenko AY, Stetsenko IF, Plotnikov NA, Klimchuk OI, Surkova EI, Ilinsky VV.
Kozina AA, et al. Among authors: klimchuk oi.
BMC Med Genet. 2020 Oct 21;21(1):209. doi: 10.1186/s12881-020-01119-6.
BMC Med Genet. 2020.
PMID: 33087045
Free PMC article.
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Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers.
Kozina AA, Okuneva EG, Baryshnikova NV, Kondakova OB, Nikolaeva EA, Fedoniuk ID, Mikhailova SV, Krasnenko AY, Stetsenko IF, Plotnikov NA, Klimchuk OI, Popov YV, Surkova EI, Shatalov PA, Rakitko AS, Ilinsky VV.
Kozina AA, et al. Among authors: klimchuk oi.
Mol Genet Genomic Med. 2020 Jul;8(7):e1228. doi: 10.1002/mgg3.1228. Epub 2020 May 15.
Mol Genet Genomic Med. 2020.
PMID: 32412666
Free PMC article.
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A novel elastin gene frameshift mutation in a Russian family with cutis laxa: a case report.
Okuneva EG, Kozina AA, Baryshnikova NV, Krasnenko AY, Tsukanov KY, Klimchuk OI, Surkova EI, Ilinsky VV.
Okuneva EG, et al. Among authors: klimchuk oi.
BMC Dermatol. 2019 Jan 31;19(1):4. doi: 10.1186/s12895-019-0084-6.
BMC Dermatol. 2019.
PMID: 30704477
Free PMC article.
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