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Case Report: Compound Heterozygous Variants of the MAN1B1 Gene in a Russian Patient with Rafiq Syndrome.
Int J Mol Sci. 2022 Sep 13;23(18):10606. doi: 10.3390/ijms231810606.
Int J Mol Sci. 2022.
PMID: 36142510
Free PMC article.
Analysis of mutations spectrum in the ATP7B gene in patients with Wilson disease using massively parallel sequencing.
Sivtsev AA, Zhalsanova IZ, Postrigan AE, Fonova EA, Vasilyeva OY, Zarubin AA, Minaicheva LI, Agafonova AA, Petrova VV, Ravzhaeva EG, Salyukova OA, Skryabin NA.
Sivtsev AA, et al. Among authors: zhalsanova iz.
Klin Lab Diagn. 2022 Apr 17;67(4):250-256. doi: 10.51620/0869-2084-2022-67-4-250-256.
Klin Lab Diagn. 2022.
PMID: 35575400
English.
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Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B gene.
Zhigalina DI, Malakhova AA, Vasilyeva OY, Grigor'eva EV, Sivtsev AA, Kolesnikov NA, Lopatkina ME, Savchenko RR, Zhalsanova IZ, Postrigan' AE, Zarubin AA, Nikitina TV, Bueverov AO, Bogomolov PO, Zakian SM, Skryabin NA.
Zhigalina DI, et al. Among authors: zhalsanova iz.
Stem Cell Res. 2021 Dec;57:102556. doi: 10.1016/j.scr.2021.102556. Epub 2021 Sep 30.
Stem Cell Res. 2021.
PMID: 34736038
Free article.
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Putative regulatory functions of SNPs associated with bronchial asthma, arterial hypertension and their comorbid phenotype.
Goncharova IA, Bragina EY, Zhalsanova IZ, Freidin MB, Nazarenko MS.
Goncharova IA, et al. Among authors: zhalsanova iz.
Vavilovskii Zhurnal Genet Selektsii. 2021 Dec;25(8):855-863. doi: 10.18699/VJ21.099.
Vavilovskii Zhurnal Genet Selektsii. 2021.
PMID: 35088020
Free PMC article.
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Molecular Relationships between Bronchial Asthma and Hypertension as Comorbid Diseases.
Bragina EY, Goncharova IA, Garaeva AF, Nemerov EV, Babovskaya AA, Karpov AB, Semenova YV, Zhalsanova IZ, Gomboeva DE, Saik OV, Zolotareva OI, Ivanisenko VA, Dosenko VE, Hofestaedt R, Freidin MB.
Bragina EY, et al. Among authors: zhalsanova iz.
J Integr Bioinform. 2018 Dec 10;15(4):20180052. doi: 10.1515/jib-2018-0052.
J Integr Bioinform. 2018.
PMID: 30530896
Free PMC article.
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Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI.
Zhalsanova IZ, Postrigan AE, Valiakhmetov NR, Kolesnikov NA, Zhigalina DI, Zarubin AA, Petrova VV, Minaycheva LI, Seitova GN, Skryabin NA, Stepanov VA.
Zhalsanova IZ, et al.
Int J Mol Sci. 2023 Apr 3;24(7):6672. doi: 10.3390/ijms24076672.
Int J Mol Sci. 2023.
PMID: 37047644
Free PMC article.
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