Works matching AU Zharikova, Anastasia A.


Results: 30
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    A Novel Bradycardia-Associated Variant in HCN4 as a Candidate Modifier in Type 3 Long QT Syndrome: Case Report and Deep In Silico Analysis.

    Published in:
    Biomedicines, 2025, v. 13, n. 4, p. 1008, doi. 10.3390/biomedicines13041008
    By:
    • Bukaeva, Anna A.;
    • Blokhina, Anastasia V.;
    • Kharlap, Maria S.;
    • Zaicenoka, Marija;
    • Zotova, Evgenia D.;
    • Petukhova, Anna V.;
    • Garbuzova, Elizaveta V.;
    • Zharikova, Anastasia A.;
    • Divashuk, Mikhail G.;
    • Kiseleva, Anna V.;
    • Ershova, Alexandra I.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
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    Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases.

    Published in:
    Journal of Personalized Medicine, 2022, v. 12, n. 7, p. 1132, doi. 10.3390/jpm12071132
    By:
    • Sotnikova, Evgeniia A.;
    • Kiseleva, Anna V.;
    • Kutsenko, Vladimir A.;
    • Zharikova, Anastasia A.;
    • Ramensky, Vasily E.;
    • Divashuk, Mikhail G.;
    • Vyatkin, Yuri V.;
    • Klimushina, Marina V.;
    • Ershova, Alexandra I.;
    • Revazyan, Karina Z.;
    • Skirko, Olga P.;
    • Zaicenoka, Marija;
    • Efimova, Irina A.;
    • Pokrovskaya, Maria S.;
    • Kopylova, Oksana V.;
    • Glechan, Anush M.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
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    A Data-Driven Approach to Carrier Screening for Common Recessive Diseases.

    Published in:
    Journal of Personalized Medicine, 2020, v. 10, n. 3, p. 140, doi. 10.3390/jpm10030140
    By:
    • Kiseleva, Anna V.;
    • Klimushina, Marina V.;
    • Sotnikova, Evgeniia A.;
    • Divashuk, Mikhail G.;
    • Ershova, Alexandra I.;
    • Skirko, Olga P.;
    • Kurilova, Olga V.;
    • Zharikova, Anastasia A.;
    • Khlebus, Eleonora Yu.;
    • Efimova, Irina A.;
    • Pokrovskaya, Maria S.;
    • Slominsky, Petr A.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
    9

    Cystic Fibrosis Polymorphic Variants in a Russian Population.

    Published in:
    Pharmacogenomics & Personalized Medicine, 2020, v. 13, p. 679, doi. 10.2147/PGPM.S278806
    By:
    • Kiseleva, Anna;
    • Klimushina, Marina;
    • Sotnikova, Evgeniia;
    • Skirko, Olga;
    • Divashuk, Mikhail;
    • Kurilova, Olga;
    • Ershova, Alexandra;
    • Khlebus, Eleonora;
    • Zharikova, Anastasia;
    • Efimova, Irina;
    • Pokrovskaya, Maria;
    • Slominsky, Petr A;
    • Shalnova, Svetlana;
    • Meshkov, Alexey;
    • Drapkina, Oxana
    Publication type:
    Article
    10

    Mesenchymal stromal cell-derived extracellular vesicles afford neuroprotection by modulating PI3K/AKT pathway and calcium oscillations.

    Published in:
    International Journal of Biological Sciences, 2022, v. 18, n. 14, p. 5345, doi. 10.7150/ijbs.73747
    By:
    • Turovsky, Egor A.;
    • Golovicheva, Victoria V.;
    • Varlamova, Elena G.;
    • Danilina, Tatyana I.;
    • Goryunov, Kirill V.;
    • Shevtsova, Yulia A.;
    • Pevzner, Irina B.;
    • Zorova, Ljubava D.;
    • Babenko, Valentina A.;
    • Evtushenko, Ekaterina A.;
    • Zharikova, Anastasia A.;
    • Khutornenko, Anastasia A.;
    • Kovalchuk, Sergey I.;
    • Plotnikov, Egor Y.;
    • Zorov, Dmitry B.;
    • Sukhikh, Gennady T.;
    • Silachev, Denis N.
    Publication type:
    Article
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    Back Cover, Volume 40, Issue 6.

    Published in:
    Human Mutation, 2019, v. 40, n. 6, p. ii, doi. 10.1002/humu.23796
    By:
    • Marakhonov, Andrey V.;
    • Brodehl, Andreas;
    • Myasnikov, Roman P.;
    • Sparber, Peter A.;
    • Kiseleva, Anna V.;
    • Kulikova, Olga V.;
    • Meshkov, Alexey N.;
    • Zharikova, Anastasia A.;
    • Koretsky, Serguey N.;
    • Kharlap, Maria S.;
    • Stanasiuk, Caroline;
    • Mershina, Elena A.;
    • Sinitsyn, Valentin E.;
    • Shevchenko, Alexey O.;
    • Mozheyko, Natalia P.;
    • Drapkina, Oksana M.;
    • Boytsov, Sergey A.;
    • Milting, Hendrik;
    • Skoblov, Mikhail Yu.
    Publication type:
    Article
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    Noncompaction cardiomyopathy is caused by a novel in‐frame desmin (DES) deletion mutation within the 1A coiled‐coil rod segment leading to a severe filament assembly defect.

    Published in:
    Human Mutation, 2019, v. 40, n. 6, p. 734, doi. 10.1002/humu.23747
    By:
    • Marakhonov, Andrey V.;
    • Brodehl, Andreas;
    • Myasnikov, Roman P.;
    • Sparber, Peter A.;
    • Kiseleva, Anna V.;
    • Kulikova, Olga V.;
    • Meshkov, Alexey N.;
    • Zharikova, Anastasia A.;
    • Koretsky, Serguey N.;
    • Kharlap, Maria S.;
    • Stanasiuk, Caroline;
    • Mershina, Elena A.;
    • Sinitsyn, Valentin E.;
    • Shevchenko, Alexey O.;
    • Mozheyko, Natalia P.;
    • Drapkina, Oksana M.;
    • Boytsov, Sergey A.;
    • Milting, Hendrik;
    • Skoblov, Mikhail Yu.
    Publication type:
    Article
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    Spectrum and Prevalence of Rare APOE Variants and Their Association with Familial Dysbetalipoproteinemia.

    Published in:
    International Journal of Molecular Sciences, 2024, v. 25, n. 23, p. 12651, doi. 10.3390/ijms252312651
    By:
    • Blokhina, Anastasia V.;
    • Ershova, Alexandra I.;
    • Kiseleva, Anna V.;
    • Sotnikova, Evgeniia A.;
    • Zharikova, Anastasia A.;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri V.;
    • Ramensky, Vasily E.;
    • Kutsenko, Vladimir A.;
    • Garbuzova, Elizaveta V.;
    • Divashuk, Mikhail G.;
    • Litinskaya, Olga A.;
    • Pokrovskaya, Maria S.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
    16

    The Yield of Genetic Testing and Putative Genetic Factors of Disease Heterogeneity in Long QT Syndrome Patients.

    Published in:
    International Journal of Molecular Sciences, 2024, v. 25, n. 22, p. 11976, doi. 10.3390/ijms252211976
    By:
    • Bukaeva, Anna;
    • Ershova, Alexandra;
    • Kharlap, Maria;
    • Kiseleva, Anna;
    • Kutsenko, Vladimir;
    • Sotnikova, Evgeniia;
    • Divashuk, Mikhail;
    • Pokrovskaya, Maria;
    • Garbuzova, Elizaveta;
    • Blokhina, Anastasia;
    • Kopylova, Oksana;
    • Zotova, Evgenia;
    • Petukhova, Anna;
    • Zharikova, Anastasia;
    • Ramensky, Vasily;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri;
    • Meshkov, Alexey;
    • Drapkina, Oxana
    Publication type:
    Article
    17

    A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.

    Published in:
    International Journal of Molecular Sciences, 2024, v. 25, n. 14, p. 7556, doi. 10.3390/ijms25147556
    By:
    • Bukaeva, Anna;
    • Myasnikov, Roman;
    • Kulikova, Olga;
    • Meshkov, Alexey;
    • Kiseleva, Anna;
    • Petukhova, Anna;
    • Zotova, Evgenia;
    • Sparber, Peter;
    • Ershova, Alexandra;
    • Sotnikova, Evgeniia;
    • Kudryavtseva, Maria;
    • Zharikova, Anastasia;
    • Koretskiy, Sergey;
    • Mershina, Elena;
    • Ramensky, Vasily;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri;
    • Muraveva, Alisa;
    • Abisheva, Alexandra;
    • Nikityuk, Tatiana
    Publication type:
    Article
    18

    Applicability of Diagnostic Criteria and High Prevalence of Familial Dysbetalipoproteinemia in Russia: A Pilot Study.

    Published in:
    International Journal of Molecular Sciences, 2023, v. 24, n. 17, p. 13159, doi. 10.3390/ijms241713159
    By:
    • Blokhina, Anastasia V.;
    • Ershova, Alexandra I.;
    • Kiseleva, Anna V.;
    • Sotnikova, Evgeniia A.;
    • Zharikova, Anastasia A.;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri V.;
    • Ramensky, Vasily E.;
    • Kutsenko, Vladimir A.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
    19

    Do Extracellular Vesicles Derived from Mesenchymal Stem Cells Contain Functional Mitochondria?

    Published in:
    International Journal of Molecular Sciences, 2022, v. 23, n. 13, p. 7408, doi. 10.3390/ijms23137408
    By:
    • Zorova, Ljubava D.;
    • Kovalchuk, Sergei I.;
    • Popkov, Vasily A.;
    • Chernikov, Valery P.;
    • Zharikova, Anastasia A.;
    • Khutornenko, Anastasia A.;
    • Zorov, Savva D.;
    • Plokhikh, Konstantin S.;
    • Zinovkin, Roman A.;
    • Evtushenko, Ekaterina A.;
    • Babenko, Valentina A.;
    • Pevzner, Irina B.;
    • Shevtsova, Yulia A.;
    • Goryunov, Kirill V.;
    • Plotnikov, Egor Y.;
    • Silachev, Denis N.;
    • Sukhikh, Gennady T.;
    • Zorov, Dmitry B.
    Publication type:
    Article
    20

    Gut Microbiota as a Source of Uremic Toxins.

    Published in:
    International Journal of Molecular Sciences, 2022, v. 23, n. 1, p. 483, doi. 10.3390/ijms23010483
    By:
    • Popkov, Vasily A.;
    • Zharikova, Anastasia A.;
    • Demchenko, Evgenia A.;
    • Andrianova, Nadezda V.;
    • Zorov, Dmitry B.;
    • Plotnikov, Egor Y.
    Publication type:
    Article
    21

    The Double Mutation DSG2 -p.S363X and TBX20 -p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 6775, doi. 10.3390/ijms22136775
    By:
    • Myasnikov, Roman;
    • Brodehl, Andreas;
    • Meshkov, Alexey;
    • Kulikova, Olga;
    • Kiseleva, Anna;
    • Pohl, Greta Marie;
    • Sotnikova, Evgeniia;
    • Divashuk, Mikhail;
    • Klimushina, Marina;
    • Zharikova, Anastasia;
    • Pokrovskaya, Maria;
    • Koretskiy, Sergey;
    • Kharlap, Maria;
    • Mershina, Elena;
    • Sinitsyn, Valentin;
    • Basargina, Elena;
    • Gandaeva, Leila;
    • Barskiy, Vladimir;
    • Boytsov, Sergey;
    • Milting, Hendrik
    Publication type:
    Article
    22

    Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3786, doi. 10.3390/ijms22073786
    By:
    • Brodehl, Andreas;
    • Meshkov, Alexey;
    • Myasnikov, Roman;
    • Kiseleva, Anna;
    • Kulikova, Olga;
    • Klauke, Bärbel;
    • Sotnikova, Evgeniia;
    • Stanasiuk, Caroline;
    • Divashuk, Mikhail;
    • Pohl, Greta Marie;
    • Kudryavtseva, Maria;
    • Klingel, Karin;
    • Gerull, Brenda;
    • Zharikova, Anastasia;
    • Gummert, Jan;
    • Koretskiy, Sergey;
    • Schubert, Stephan;
    • Mershina, Elena;
    • Gärtner, Anna;
    • Pilus, Polina
    Publication type:
    Article
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    Ectopic expression of HIV-1 Tat modifies gene expression in cultured B cells: implications for the development of B-cell lymphomas in HIV-1-infected patients.

    Published in:
    PeerJ, 2022, p. 1, doi. 10.7717/peerj.13986
    By:
    • Valyaeva, Anna A.;
    • Tikhomirova, Maria A.;
    • Potashnikova, Daria M.;
    • Bogomazova, Alexandra N.;
    • Snigiryova, Galina P.;
    • Penin, Aleksey A.;
    • Logacheva, Maria D.;
    • Arifulin, Eugene A.;
    • Shmakova, Anna A.;
    • Germini, Diego;
    • Kachalova, Anastasia I.;
    • Saidova, Aleena A.;
    • Zharikova, Anastasia A.;
    • Musinova, Yana R.;
    • Mironov, Andrey A.;
    • Vassetzky, Yegor S.;
    • Sheval, Eugene V.
    Publication type:
    Article
    26

    Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region.

    Published in:
    Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.709419
    By:
    • Ramensky, Vasily E.;
    • Ershova, Alexandra I.;
    • Zaicenoka, Marija;
    • Kiseleva, Anna V.;
    • Zharikova, Anastasia A.;
    • Vyatkin, Yuri V.;
    • Sotnikova, Evgeniia A.;
    • Efimova, Irina A.;
    • Divashuk, Mikhail G.;
    • Kurilova, Olga V.;
    • Skirko, Olga P.;
    • Muromtseva, Galina A.;
    • Belova, Olga A.;
    • Rachkova, Svetlana A.;
    • Pokrovskaya, Maria S.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
    27

    A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.

    Published in:
    Genes, 2022, v. 13, n. 2, p. 309, doi. 10.3390/genes13020309
    By:
    • Myasnikov, Roman;
    • Bukaeva, Anna;
    • Kulikova, Olga;
    • Meshkov, Alexey;
    • Kiseleva, Anna;
    • Ershova, Alexandra;
    • Petukhova, Anna;
    • Divashuk, Mikhail;
    • Zotova, Evgenia;
    • Sotnikova, Evgeniia;
    • Kharlap, Maria;
    • Zharikova, Anastasia;
    • Vyatkin, Yuri;
    • Ramensky, Vasily;
    • Abisheva, Alexandra;
    • Muraveva, Alisa;
    • Koretskiy, Sergey;
    • Kudryavtseva, Maria;
    • Popov, Sergey;
    • Utkina, Marina
    Publication type:
    Article
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    The LDLR , APOB , and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.

    Published in:
    Genes, 2021, v. 12, n. 1, p. 66, doi. 10.3390/genes12010066
    By:
    • Meshkov, Alexey;
    • Ershova, Alexandra;
    • Kiseleva, Anna;
    • Zotova, Evgenia;
    • Sotnikova, Evgeniia;
    • Petukhova, Anna;
    • Zharikova, Anastasia;
    • Malyshev, Pavel;
    • Rozhkova, Tatyana;
    • Blokhina, Anastasia;
    • Limonova, Alena;
    • Ramensky, Vasily;
    • Divashuk, Mikhail;
    • Khasanova, Zukhra;
    • Bukaeva, Anna;
    • Kurilova, Olga;
    • Skirko, Olga;
    • Pokrovskaya, Maria;
    • Mikova, Valeriya;
    • Snigir, Ekaterina
    Publication type:
    Article
    30

    Clinical and biochemical features of atherogenic hyperlipidemias with different genetic basis: A comprehensive comparative study.

    Published in:
    PLoS ONE, 2024, v. 19, n. 12, p. 1, doi. 10.1371/journal.pone.0315693
    By:
    • Blokhina, Anastasia V.;
    • Ershova, Alexandra I.;
    • Kiseleva, Anna V.;
    • Sotnikova, Evgeniia A.;
    • Zharikova, Anastasia A.;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri V.;
    • Ramensky, Vasily E.;
    • Kutsenko, Vladimir A.;
    • Litinskaya, Olga A.;
    • Pokrovskaya, Maria S.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article