Anna Zlotina
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Explore the profile of Anna Zlotina including associated specialties, affiliations and a list of published articles.
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26
Citations
244
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Recent Articles
1.
Zlotina A, Barashkova S, Zhuk S, Skitchenko R, Usoltsev D, Sokolnikova P, et al.
Orphanet J Rare Dis
. 2024 Aug;
19(1):310.
PMID: 39180133
Background: Primary ciliary dyskinesia (PCD) is a group of rare genetically heterogeneous disorders caused by defective cilia and flagella motility. The clinical phenotype of PCD patients commonly includes chronic oto-sino-pulmonary...
2.
Rodina N, Khudiakov A, Perepelina K, Muravyev A, Boytsov A, Zlotina A, et al.
Stem Cell Res
. 2021 Dec;
59:102640.
PMID: 34971933
Human iPSC cell line FAMRCi009-A was generated from a patient with restrictive cardiomyopathy and congenital myopathy carrying FLNC p.Val2264Met genetic variant. Patient-specific peripheral blood mononuclear cells were reprogrammed using non-integrative...
3.
Perepelina K, Khudiakov A, Rodina N, Boytsov A, Vavilova T, Zlotina A, et al.
Stem Cell Res
. 2021 Dec;
59:102639.
PMID: 34971931
Human iPSC cell line FAMRCi010-A was generated from a patient with restrictive cardiomyopathy carrying FLNC p.Gly2011Arg genetic variant. Patient-specific peripheral blood mononuclear cells were reprogrammed using non-integrative Sendai viruses containing...
4.
Kovalchuk T, Yakovleva E, Fetisova S, Vershinina T, Lebedeva V, Lyubimtseva T, et al.
Front Cardiovasc Med
. 2021 May;
8:668231.
PMID: 34026875
Emery-Dreifuss muscular dystrophy (EDMD) is inherited muscle dystrophy often accompanied by cardiac abnormalities in the form of supraventricular arrhythmias, conduction defects and sinus node dysfunction. Cardiac phenotype typically arises years...
5.
Zlotina A, Melnik O, Fomicheva Y, Skitchenko R, Sergushichev A, Shagimardanova E, et al.
BMC Med Genomics
. 2020 Nov;
13(1):175.
PMID: 33218365
Background: Triphalangeal thumb-polysyndactyly syndrome (TPT-PS) is a rare well-defined autosomal dominant disorder characterized by long thumbs with three phalanges combined with pre- and postaxial polydactyly/syndactyly of limbs. By now, the...
6.
Jorholt J, Formicheva Y, Vershinina T, Kiselev A, Muravyev A, Demchenko E, et al.
Genes (Basel)
. 2020 Oct;
11(10).
PMID: 33076350
Hypertrophic cardiomyopathy associated with damaging variants in the gene is a fairly recent discovery, and only a small number of patients have been described thus far. Here we present two...
7.
Kulikova T, Surkova A, Zlotina A, Krasikova A
Mol Cytogenet
. 2020 Aug;
13:32.
PMID: 32774459
Background: The epigenetic regulation of genome is crucial for implementation of the genetic program of ontogenesis through establishing and maintaining differential gene expression. Thus mapping of various epigenetic modifications to...
8.
Perepelina K, Kostina A, Klauzen P, Khudiakov A, Rabino M, Crasto S, et al.
Stem Cell Res
. 2020 Jul;
47:101895.
PMID: 32659731
Human iPSC lines were generated from peripheral blood mononuclear cells of patient carrying LMNA mutation associated with Emery-Dreifuss muscular dystrophy accompanied by atrioventricular block and paroxysmal atrial fibrillation. Reprogramming factors...
9.
Zlotina A, Maslova A, Pavlova O, Kosyakova N, Al-Rikabi A, Liehr T, et al.
Front Genet
. 2020 Mar;
11:57.
PMID: 32127797
Giant lampbrush chromosomes (LBCs) typical for growing oocytes of various animal species are characterized by a specific chromomere-loop appearance and massive transcription. Chromomeres represent universal units of chromatin packaging at...
10.
Smolina N, Khudiakov A, Knyazeva A, Zlotina A, Sukhareva K, Kondratov K, et al.
Biochim Biophys Acta Mol Basis Dis
. 2020 Feb;
1866(6):165745.
PMID: 32105824
Desmin, being a major intermediate filament of muscle cells, contributes to stabilization and positioning of mitochondria. Desmin mutations have been reported in conjunction with skeletal myopathies accompanied by mitochondrial dysfunction....