Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Tatyana V. Kuznetzova"'
Autor:
Alla S. Koltsova, Anna A. Pendina, Olga A. Efimova, Olga G. Chiryaeva, Tatyana V. Kuznetzova, Vladislav S. Baranov
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
In the present review, we focus on the phenomenon of chromothripsis, a new type of complex chromosomal rearrangements. We discuss the challenges of chromothripsis detection and its distinction from other chromoanagenesis events. Along with already kn
Externí odkaz:
https://doaj.org/article/c5c92e643dbf4fee95f40ee11471aa24
Autor:
Elizaveta E. Nevskaia, S. G. Scherbak, Rena A. Kuznetsova, Oleg S. Glotov, Alsu Saifitdinova, Natalia K. Bichevaya, Anton E. Shikov, Irina L. Puppo, Stanislav P. Urazov, Andrei M. Sarana, Tatyana V. Kuznetzova, Olga A. Leonteva, Irina V. Poliakova, Vladislav S Baranov, Julia A. Loginova, Olga A. Pavlova
Publikováno v:
Интегративная физиология, Vol 1, Iss 3 (2020)
Since the very first publications on preimplantation genetic testing, researchers have faced a serious problem — a high mosaicism level in the preimplantation human embryos obtained by means of in vitro fertilization cycles. The nature of this mosa
Publikováno v:
Russian Journal of Genetics. 55:1171-1182
Experimental embryology achievements in the century resulted in the birth of the first child conceived artificially. Besides its obvious social significance, the successful solution of the “test-tube babies” provided also the unique chance for di
Autor:
Elena L. Grigorenko, Sergey A. Kornilov, Veronika V. Odintsova, Tatyana V. Kuznetzova, Oxana Yu. Naumova, Sergey Rychkov
Publikováno v:
Clinical Case Reports
Key Clinical Message This manuscript reports on genomewide epigenetic alterations in cri‐du‐chat syndrome related to a partial aneusomy of chromosome 5. A systematic analysis of these alterations will open up new possibilities for the prognostic
Autor:
Olga A. Efimova, Ilona A. Galembo, Olga G. Chiryaeva, Igor Yu. Kogan, V. S. Baranov, Irina S. Stepanova, Oleg S. Glotov, Svetlana A. Shlykova, Evgeniia M. Komarova, Mariia A. Mazilina, Andrei V. Tikhonov, Sergey E. Parfenyev, Irina D. Mekina, Alexander M. Gzgzyan, Eugene V. Daev, Anna A. Pendina, Mikhail I. Krapivin, Tatyana V. Kuznetzova
Publikováno v:
Oncotarget
// Olga A. Efimova 1,2,* , Anna A. Pendina 1,2,3,* , Andrei V. Tikhonov 1,2,3,* , Sergey E. Parfenyev 2 , Irina D. Mekina 1 , Evgeniia M. Komarova 1 , Mariia A. Mazilina 1,2 , Eugene V. Daev 2 , Olga G. Chiryaeva 1,4,5 , Ilona A. Galembo 3 , Mikhail
Publikováno v:
Journal of obstetrics and women's diseases. 66:33-39
Advantages and drawbacks of noninvasive prenatal testing (NIPT) of chromosomal anomalies are briefly reviewed. Material supply, employment issues, financial and management problems in European countries and in Russia are discussed. Many problems are
Publikováno v:
Journal of obstetrics and women's diseases. 65:70-80
Some novel molecular and cell methods implicated into assistant reproductive technology and prenatal diagnostics are reviewed. Special attention is paid to new generation sequencing (NGS) technique, arrayCGH, genome editing (CRISPR/Cas9 method), cell
Publikováno v:
Journal of obstetrics and women's diseases. 64:4-12
Modern molecular approaches to prenatal diagnostic of inherited diseases are briefly reviewed. Advantages and limitations of molecular methods for analysis of chromosomal anomalies (QF-PCR, aCGH, NGS) are considered in line with conventional prenatal
Publikováno v:
Экологическая генетика, Vol 12, Iss 1, Pp 3-13 (2014)
The present review summarizes data on 5-hydroxymethylcytosine - a modification of cytosine with a recently discovered epigenetic effect. The biochemical mechanisms of 5-hydroxymethylcytosine formation and further modification in the mammalian genome
Autor:
Vera S. Dudkina, Olga A. Efimova, Lubov’ I. Petrova, Irina Dmitrievna Fedorova, Tatyana V. Kuznetzova, Anna A. Pendina, Ilona A. Galembo, Andrei V. Tikhonov, Natalia Aleksandrovna Sadik, Alexander M. Gzgzyan, Olga G. Chiryaeva, V. S. Baranov
Publikováno v:
Journal of Assisted Reproduction and Genetics. 31:149-155
To compare the frequency and the spectrum of karyotype abnormality in the first trimester miscarriages in women aged under and over 35 years, who conceived naturally (NC) and who conceived through in vitro fertilization (IVF). Comparative analysis of