Hasil Pencarian - Stanislav A. Vasilyev

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  1. 1
    Abnormal methylation of PRDM16 and PTPRN2 genes in chorionic villi in miscarriage

    Abnormal methylation of PRDM16 and PTPRN2 genes in chorionic villi in miscarriage oleh Stanislav A. Vasilyev, Oksana Yu. Vasilyeva, Bismark Oppong-Peprah, Victoria V. Demeneva, Andrey S. Zuev, Elena A. Sazhenova, Tatiana V. Nikitina, Ekaterina N. Tolmacheva

    Diterbitkan 2023-12-01
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  2. 2
    Method of targeted bisulfite massive parallel sequencing of the human LINE-1 retrotransposon promoter

    Method of targeted bisulfite massive parallel sequencing of the human LINE-1 retrotransposon promoter oleh Stanislav A. Vasilyev, Anton V. Markov, Oksana Yu. Vasilyeva, Ekaterina N. Tolmacheva, Lada A. Zatula, Diana V. Sharysh, Daria I. Zhigalina, Victoria V. Demeneva, Igor N. Lebedev

    Diterbitkan 2021-01-01
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  3. 3
    Identification of differentially methylated genes in first-trimester placentas with trisomy 16

    Identification of differentially methylated genes in first-trimester placentas with trisomy 16 oleh Ekaterina N. Tolmacheva, Stanislav A. Vasilyev, Tatiana V. Nikitina, Ekaterina S. Lytkina, Elena A. Sazhenova, Daria I. Zhigalina, Oksana Yu. Vasilyeva, Anton V. Markov, Victoria V. Demeneva, Liubov A. Tashireva, Anna A. Kashevarova, Igor N. Lebedev

    Diterbitkan 2022-01-01
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  4. 4
    Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22

    Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22 oleh Anna A. Kashevarova, Elena O. Belyaeva, Aleksandr M. Nikonov, Olga V. Plotnikova, Nikolay A. Skryabin, Tatyana V. Nikitina, Stanislav A. Vasilyev, Yulia S. Yakovleva, Nadezda P. Babushkina, Ekaterina N. Tolmacheva, Mariya E. Lopatkina, Renata R. Savchenko, Lyudmila P. Nazarenko, Igor N. Lebedev

    Diterbitkan 2018-04-01
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  5. 5
    Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing

    Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing oleh Igor N. Lebedev, Tatyana V. Karamysheva, Eugeny A. Elisaphenko, Alexey I. Makunin, Daria I. Zhigalina, Maria E. Lopatkina, Gleb V. Drozdov, Aleksander D. Cheremnykh, Natalia B. Torkhova, Gulnara N. Seitova, Stanislav A. Vasilyev, Anna A. Kashevarova, Ludmila P. Nazarenko, Nikolay B. Rubtsov

    Diterbitkan 2021-08-01
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