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Natalia Shved
Natalia Shved
D.O.Ott Research Institute of Obstetrics, Gynecology and Reproductology
在 post.su 的电子邮件经过验证
标题
引用次数
引用次数
年份
Frequency and spectrum of MED12 exon 2 mutations in multiple versus solitary uterine leiomyomas from Russian patients
NS Osinovskaya, OV Malysheva, NY Shved, TE Ivashchenko, IY Sultanov, ...
International journal of gynecological pathology 35 (6), 509-515, 2016
512016
Анализ полиморфных аллелей генов, кодирующих ферменты 1-й и 2-й фазы детоксикации, у больных эндометриозом
ТЭ Иващенко, НЮ Швед, НА Крамарова, ЭК Айламазян, ВС Баранов
Генетика 39 (4), 525-525, 2003
372003
Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes
OS Glotov, EA Serebryakova, ME Turkunova, OA Efimova, AS Glotov, ...
Molecular medicine reports 20 (6), 4905-4914, 2019
332019
Oestrogen and insulin-like growth factors during the reproduction and growth of the tilapia Oreochromis niloticus and their interactions
JF Baroiller, H D’Cotta, N Shved, G Berishvili, A Toguyeni, A Fostier, ...
General and comparative endocrinology 205, 142-150, 2014
322014
Analysis of the polymorphic alleles of genes encoding phase 1 and phase 2 detoxication enzymes in patients with endometriosis
TE Ivashchenko, NI Shved, NA Kramareva, EK Aĭlamazian, VS Baranov
Genetika 39 (4), 525-529, 2003
322003
Генетические факторы предрасположенности и терапии эндометриоза
ВС Баранов, ТЭ Иващенко, НЮ Швед, МИ Ярмолинская, СА Сельков, ...
Генетика 35 (2), 243, 1999
321999
Генетические основы предрасположенности к акушерской и гинекологической патологии
ТЭ Иващенко, НЮ Швед, ОH Беспалова, ОА Тарасенко, ...
Молекулярная медицина, 19-26, 2007
242007
Дефицит овариальной ароматазы как причина нормогонадотропной ановуляции
ЯА Самойлович, ВВ Потин, МА Тарасова, МИ Ярмолинская, НЮ Швед, ...
Российский вестник акушера-гинеколога 15 (2), 25-30, 2015
212015
Genetic factors of predisposition to endometriosis and response to its treatment
VS Baranov, TE Ivashchenko, S NIu, MI Iarmolinskata, SA Sel'kov, ...
Genetika 35 (2), 243-248, 1999
211999
Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutations
LK Dzhemlikhanova, OA Efimova, NS Osinovskaya, SE Parfenyev, ...
Journal of Clinical Pathology 70 (3), 233-236, 2017
182017
Five years' experience of prenatal diagnosis of cystic fibrosis in the former USSR
VS Baranov, VN Gorbunova, TE Ivaschenko, NY Shwed, NS Osinovskaya, ...
Prenatal diagnosis 12 (7), 575-586, 1992
181992
Frequency of the F508 deletion in cystic fibrosis patients from the European part of the USSR
VS Baranov, TE Ivaschenko, VN Gorbunova, LA Livshitz, MT Venozinskis, ...
Human genetics 87, 61-64, 1991
151991
Association of matrix metalloproteinases' polymorphisms of MMP3 and MMP9 with development of genital endometriosis
MI Iarmolinskaia, AS Molotkov, VF Bezhenar, S NIu, TE Ivashchenko, ...
Genetika 50 (2), 230-235, 2014
142014
Polycondensed peptide carriers modified with cyclic RGD ligand for targeted suicide gene delivery to uterine fibroid cells
A Egorova, S Shtykalova, M Maretina, A Selutin, N Shved, D Deviatkin, ...
International Journal of Molecular Sciences 23 (3), 1164, 2022
132022
Development of irgd-modified peptide carriers for suicide gene therapy of uterine leiomyoma
A Egorova, S Shtykalova, A Selutin, N Shved, M Maretina, S Selkov, ...
Pharmaceutics 13 (2), 202, 2021
122021
Case of chromothripsis in a large solitary non-recurrent uterine leiomyoma
AA Pendina, AS Koltsova, OA Efimova, OV Malysheva, NS Osinovskaya, ...
European journal of obstetrics, gynecology, and reproductive biology 219 …, 2017
122017
Аллельные варианты гена CYP 19 (ароматазы р450) и активность ароматазы р450 у больных с синдромом поликистозных яичников
ВА Савина, НЮ Швед, ВВ Потин, МА Тарасова, МИ Ярмолинская, ...
Медицинская генетика 11 (4), 36-41, 2012
122012
Пренатальная диагностика хромосомных болезней у плода: метод. реком
ВС Баранов, ТВ Кузнецова, НЮ Швед, АН Баранов
Баранов ВС, Кузнецова ТВ, Швед НЮ, Баранов АН—СПб, 1995
111995
Next-generation sequencing of matched ectopic and eutopic endometrium identifies novel endometriosis-related genes
AV Predeus, ES Vashukova, AS Glotov, MM Danilova, NS Osinovskaya, ...
Russian Journal of Genetics 54, 1358-1365, 2018
102018
Differential DNA Hydroxymethylation in Human Uterine Leiomyoma Cells Depending on the Phase of Menstrual Cycle and Presence of MED12 Gene Mutations
AS Kol’Tsova, AA Pendina, OA Efimova, AN Kaminskaya, AV Tikhonov, ...
Bulletin of Experimental Biology and Medicine 163, 646-649, 2017
102017
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