Hasil Pencarian - Maria S Nazarenko

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  1. 1
    Human exome sequence data in support of somatic mosaicism in carotid atherosclerosis

    Human exome sequence data in support of somatic mosaicism in carotid atherosclerosis oleh Alexei A. Sleptcov, Alexei A. Zarubin, Polina M. Bogaychuk, Mikhail S. Kuznetsov, Boris N. Kozlov, Maria S. Nazarenko

    Diterbitkan 2021-12-01
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  2. 2
    Meier–Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of <i>ORC6</i> Mutations and the Development of a Prenatal Test

    Meier–Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of <i>ORC6</i> Mutations and the Development of a Prenatal Test oleh Maria S. Nazarenko, Iuliia V. Viakhireva, Mikhail Y. Skoblov, Elena V. Soloveva, Aleksei A. Sleptcov, Ludmila P. Nazarenko

    Diterbitkan 2022-08-01
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  3. 3
    Apoptosis Genes as a Key to Identification of Inverse Comorbidity of Huntington’s Disease and Cancer

    Apoptosis Genes as a Key to Identification of Inverse Comorbidity of Huntington’s Disease and Cancer oleh Elena Yu. Bragina, Densema E. Gomboeva, Olga V. Saik, Vladimir A. Ivanisenko, Maxim B. Freidin, Maria S. Nazarenko, Valery P. Puzyrev

    Diterbitkan 2023-05-01
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  4. 4
    A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy

    A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy oleh Maria V. Golubenko, Elena N. Pavlyukova, Ramil R. Salakhov, Oksana A. Makeeva, Konstantin V. Puzyrev, Oleg S. Glotov, Valery P. Puzyrev, Maria S. Nazarenko

    Diterbitkan 2024-02-01
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  5. 5
    Application of Long-Read Nanopore Sequencing to the Search for Mutations in Hypertrophic Cardiomyopathy

    Application of Long-Read Nanopore Sequencing to the Search for Mutations in Hypertrophic Cardiomyopathy oleh Ramil R. Salakhov, Maria V. Golubenko, Nail R. Valiakhmetov, Elena N. Pavlyukova, Aleksei A. Zarubin, Nadezhda P. Babushkina, Aksana N. Kucher, Aleksei A. Sleptcov, Maria S. Nazarenko

    Diterbitkan 2022-12-01
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  6. 6
    A comparison of genome-wide DNA methylation patterns between different vascular tissues from patients with coronary heart disease.

    A comparison of genome-wide DNA methylation patterns between different vascular tissues from patients with coronary heart disease. oleh Maria S Nazarenko, Anton V Markov, Igor N Lebedev, Maxim B Freidin, Aleksei A Sleptcov, Iuliya A Koroleva, Aleksei V Frolov, Vadim A Popov, Olga L Barbarash, Valery P Puzyrev

    Diterbitkan 2015-01-01
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  7. 7
    Induced pluripotent stem cell line ICGi038-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to compound heterozygous c.1246C > T/c.940 + 3_940 + 6del mutations in LDLR

    Induced pluripotent stem cell line ICGi038-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to compound heteroz... oleh Irina S. Zakharova, Alexander I. Shevchenko, Narek A. Tmoyan, Eugeny A. Elisaphenko, Ekaterina S. Zubkova, Aleksei A. Sleptcov, Maria S. Nazarenko, Marat V. Ezhov, Valery V. Kukharchuk, Yelena V. Parfyonova, Suren M. Zakian

    Diterbitkan 2022-04-01
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  8. 8
    Induced pluripotent stem cell line ICGi036-A generated by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia caused due to compound heterozygous p.Ser177Leu/p.Cys352Arg mutations in LDLR

    Induced pluripotent stem cell line ICGi036-A generated by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia caused due to compound... oleh Irina S. Zakharova, Alexander I. Shevchenko, Narek A. Tmoyan, Eugeny A. Elisaphenko, Ekaterina S. Zubkova, Aleksei A. Sleptcov, Maria S. Nazarenko, Marat V. Ezhov, Valery V. Kukharchuk, Yelena V. Parfyonova, Suren M. Zakian

    Diterbitkan 2022-03-01
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  9. 9
    Identification of Variants of Uncertain Significance in the Genes Associated with Thoracic Aortic Disease in Russian Patients with Nonsyndromic Sporadic Subtypes of the Disorder

    Identification of Variants of Uncertain Significance in the Genes Associated with Thoracic Aortic Disease in Russian Patients with Nonsyndromic Sporadic Subtypes of the Disorder oleh Irina A. Goncharova, Sofia A. Shipulina, Aleksei A. Sleptcov, Aleksei A. Zarubin, Nail R. Valiakhmetov, Dmitry S. Panfilov, Evgeniya V. Lelik, Viktor V. Saushkin, Boris N. Kozlov, Ludmila P. Nazarenko, Maria S. Nazarenko

    Diterbitkan 2024-07-01
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  10. 10
    Induced pluripotent stem cell line ICGi037-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to heterozygous p.Trp443Arg mutations in LDLR

    Induced pluripotent stem cell line ICGi037-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to heterozygous p.T... oleh Irina S. Zakharova, Alexander I. Shevchenko, Narek A. Tmoyan, Eugeny A. Elisaphenko, Alexander P. Kalinin, Aleksei A. Sleptcov, Maria S. Nazarenko, Marat V. Ezhov, Valery V. Kukharchuk, Yelena V. Parfyonova, Suren M. Zakian

    Diterbitkan 2022-04-01
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  11. 11
    ABCA1 and ABCG1 DNA methylation in epicardial adipose tissue of patients with coronary artery disease

    ABCA1 and ABCG1 DNA methylation in epicardial adipose tissue of patients with coronary artery disease oleh Valentina V. Miroshnikova, Alexandra A. Panteleeva, Irina A. Pobozheva, Natalia D. Razgildina, Ekaterina A. Polyakova, Anton V. Markov, Olga D. Belyaeva, Olga A. Berkovich, Elena I. Baranova, Maria S. Nazarenko, Valery P. Puzyrev, Sofya N. Pchelina

    Diterbitkan 2021-11-01
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  12. 12
    Calling and Phasing of Single-Nucleotide and Structural Variants of the <i>LDLR</i> Gene Using Oxford Nanopore MinION

    Calling and Phasing of Single-Nucleotide and Structural Variants of the <i>LDLR</i> Gene Using Oxford Nanopore MinION oleh Maria S. Nazarenko, Aleksei A. Sleptcov, Aleksei A. Zarubin, Ramil R. Salakhov, Alexander I. Shevchenko, Narek A. Tmoyan, Eugeny A. Elisaphenko, Ekaterina S. Zubkova, Nina V. Zheltysheva, Marat V. Ezhov, Valery V. Kukharchuk, Yelena V. Parfyonova, Suren M. Zakian, Irina S. Zakharova

    Diterbitkan 2023-02-01
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  13. 13
    iPSC-Derived Endothelial Cells Reveal LDLR Dysfunction and Dysregulated Gene Expression Profiles in Familial Hypercholesterolemia

    iPSC-Derived Endothelial Cells Reveal LDLR Dysfunction and Dysregulated Gene Expression Profiles in Familial Hypercholesterolemia oleh Irina S. Zakharova, Alexander I. Shevchenko, Mhd Amin Arssan, Aleksei A. Sleptcov, Maria S. Nazarenko, Aleksei A. Zarubin, Nina V. Zheltysheva, Vlada A. Shevchenko, Narek A. Tmoyan, Shoraan B. Saaya, Marat V. Ezhov, Valery V. Kukharchuk, Yelena V. Parfyonova, Suren M. Zakian

    Diterbitkan 2024-01-01
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