Zobrazeno 1 - 8
of 8
pro vyhledávání: '"T O, Kochetkova"'
Autor:
Ilya Yu. Barkov, Olga K. Stupko, I. S. Mukosey, T. O. Kochetkova, A.Y. Goltsov, Dmitry Yu. Trofimov, J. Shubina, Denis V. Rebrikov, Maria Kuznetsova
Publikováno v:
Bulletin of Russian State Medical University. :15-18
Timely detection of fetal aneuploidy is an important aspect of clinical practice. At present, analytical techniques involving high-throughput sequencing are on the rise. Noninvasive prenatal testing (NIPT) ensures reliable results as early as week 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21add37504f17d2ce8e38d73c528a686
https://doi.org/10.24075/brsmu.2019.040
https://doi.org/10.24075/brsmu.2019.040
Autor:
Maria Kuznetsova, Olga K. Stupko, J. Shubina, Gennady T. Sukhikh, T. O. Kochetkova, A.Y. Goltsov, Dmitry Yu. Trofimov, Ilya Yu. Barkov
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Background PWS is challenging to diagnose prenatally due to a lack of precise and well‐characterized fetal phenotypes and noninvasive markers. Here we present the case of prenatal diagnosis of Prader‐Willi syndrome, which was suspected with whole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fabbc4500ea2534a2778fb1359b8c5b7
https://pubmed.ncbi.nlm.nih.gov/32857485
https://pubmed.ncbi.nlm.nih.gov/32857485
Autor:
L. V. Kim, J. Shubina, DNA-Technology Llc, Moscow, Russia, I. Yu. Barkov, A. A. Bystritsky, T Jankevic, N. K. Tetruashvili, Moscow Perinatology, T. O. Kochetkova, I. S. Mukosey, A. Yu. Goltsov, D. Yu. Trofimov
Publikováno v:
Bulletin of Russian State Medical University. :29-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da31c7fbe806921515aaa957dab2801d
https://doi.org/10.24075/brsmu.2018.031
https://doi.org/10.24075/brsmu.2018.031
Autor:
J. Shubina, Gennady T. Sukhikh, Ilya Yu. Barkov, T. O. Kochetkova, Regina V. Krasheninnikova, Lyudmila V. Kim, Natalia A. Karetnikova, Olga K. Stupko, Irina S. Mukosey, Andrey A. Bystritskiy, N. K. Tetruashvili, A.Y. Goltsov, Dmitry Yu. Trofimov, Vladimir A. Bakharev
Publikováno v:
Prenatal Diagnosis. 37:1305-1310
Objectives The aim of this study was to establish maternal contribution to false positive noninvasive prenatal DNA screening (NIPS) results and develop the method to distinguish maternal and fetal origin of high-risk monosomy X NIPS calls including m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94dc1914c56398297c65aa6c4c44cb10
https://doi.org/10.1002/pd.5178
https://doi.org/10.1002/pd.5178
Autor:
I. S. Mukosey, O. V. Ionov, A B Gordeev, L A Lyubasovskaya, V V Zubkov, D V Dubodelov, Dmitry Yu. Trofimov, T. V. Priputnevich, T. O. Kochetkova, J V Rodchenko, I.V. Nikitina
Publikováno v:
Вестник Российского государственного медицинского университета.
Staphylococcus epidermidis is a member of the normal bacterial flora of humans capable of causing potentially dangerous diseases in neonates with very or extremely low birth weight. The number of genes responsible for virulence and antibiotic resista
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0183faceb3c12898b021304a1ba853a
http://cyberleninka.ru/article/n/genetic-polymorphism-of-staphylococcus-epidermidis-strains-in-patients-of-the-neonatal-intensive-care-unit
http://cyberleninka.ru/article/n/genetic-polymorphism-of-staphylococcus-epidermidis-strains-in-patients-of-the-neonatal-intensive-care-unit
Autor:
E A Kalinina, I. Sadelov, J. Shubina, Andrey Donnikov, A. Ekimov, T. O. Kochetkova, A.Y. Goltsov, Dmitry Yu. Trofimov, I. S. Mukosey, M. Veyukova, Aydar Abubakirov, N. P. Makarova
Publikováno v:
Reproductive BioMedicine Online. 39:e58
Introduction Up to 2% of newborn children have untreatable monogenic disorder. Preconception carrier screening is performed rarely. If a sperm donor is a carrier of mutation causing of frequent monogenic disorder probability of having a child with mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6356e733222d565ac3ecc5cd352fa53
https://doi.org/10.1016/j.rbmo.2019.04.104
https://doi.org/10.1016/j.rbmo.2019.04.104
Autor:
D V, Dubodelov, L A, Lubasovskaya, E S, Shubina, I S, Mukosey, D O, Korostin, T O, Kochetkova, N A, Bogacheva, A A, Bistritskiy, A B, Gordeev, D Y, Trofimov, T V, Priputnevich, V V, Zubkov
Publikováno v:
Genetika. 52(9)
According to the results of analysis of whole genome sequencing, the presence of genes having resistance to β-lactam antibiotics in hospital-associated strains of Klebsiella pneumoniae was studied. The strains were isolated from neonatal intensive c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d85105e1138272eb0b2f80d506372b93
https://pubmed.ncbi.nlm.nih.gov/29369564
https://pubmed.ncbi.nlm.nih.gov/29369564
Autor:
E. A. Shestopalova, A. I. Nikifirova, G. U. Zobkova, N. O. Brjuhanova, T. O. Kochetkova, V. V. Kadochnikova, K. A. Ogurtsova, Ekaterina Shubina, A E Donnikov, D. Yu. Trofimov, D. D. Abramov
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a8a1378ff7e749834c15001ed9512b9
http://www.scopus.com/inward/record.url?eid=2-s2.0-85032796991&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-85032796991&partnerID=MN8TOARS
