Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Andrei Sõritsa"'
Autor:
Merli Saare, Kadri Rekker, Triin Laisk-Podar, Deniss Sõritsa, Anne Mari Roost, Jaak Simm, Agne Velthut-Meikas, Külli Samuel, Tauno Metsalu, Helle Karro, Andrei Sõritsa, Andres Salumets, Maire Peters
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e112630 (2014)
Accumulating data have shown the involvement of microRNAs (miRNAs) in endometriosis pathogenesis. In this study, we used a novel approach to determine the endometriotic lesion-specific miRNAs by high-throughput small RNA sequencing of paired samples
Externí odkaz:
https://doaj.org/article/494b0674edc84e3dbc1e10e6a82a276d
Autor:
Andres Salumets, Margit Nuut, Siret Läänelaid, Signe Altmäe, Andrei Sõritsa, Deniss Sõritsa, Jarek Mäestu, Francisco B. Ortega, Aire Sekavin, Jairo H. Migueles, Aivar Ehrenberg, Evelin Mäestu
Publikováno v:
J Assist Reprod Genet
PURPOSE: To evaluate the association of objectively measured physical activity (PA) and sedentary behaviour before and during in vitro fertilization (IVF) with controlled ovarian stimulation (COS) and pregnancy outcomes. METHODS: This longitudinal st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68bff177895163dfce6c0c06171b4be9
https://hdl.handle.net/10668/15810
https://hdl.handle.net/10668/15810
Autor:
Andres Salumets, Maire Peters, Alexander W. Drong, Balaji Rajashekar, Nilufer Rahmioglu, Deniss Sõritsa, Christian M. Becker, Andrei Sõritsa, Cecilia M. Lindgren, Vijayachitra Modhukur, Marina Suhorutshenko, Pille Soplepmann, Merli Saare, Krina T. Zondervan, Kadri Rekker, Helle Karro
Publikováno v:
Clinical Epigenetics
Background Alterations in endometrial DNA methylation profile have been proposed as one potential mechanism initiating the development of endometriosis. However, the normal endometrial methylome is influenced by the cyclic hormonal changes, and the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ec87ac01d6fcae7267e75d2549c92f3
https://doi.org/10.1186/s13148-015-0168-z
https://doi.org/10.1186/s13148-015-0168-z
Autor:
Merli Saare, Carlos Simón, Helle Karro, Tanel Kaart, Andrei Sõritsa, Andres Salumets, Deniss Sõritsa, Kadri Rekker, Maire Peters, Anne Mari Roost
Publikováno v:
Fertility and Sterility
Objective To determine whether circulating micro-RNA (miR) 200a, miR-200b, and miR-141 have altered levels in patients with endometriosis compared with control individuals. Design Experimental laboratory study. Setting University. Patient(s) Patients
Autor:
Andres Salumets, Maire Peters, Deniss Sõritsa, Merli Saare, Helle Karro, Triin Laisk-Podar, Kadri Matt, Andrei Sõritsa
Publikováno v:
Gynecologic and Obstetric Investigation
Aim: To evaluate the effects of combined treatment approaches on endometriosis-associated infertility in different stages of endometriosis using laparoscopy, gonadotropin-releasing hormone (GnRH) agonist (GnRHa) therapy and in vitro fertilization (IV
Autor:
Triin Laisk-Podar, Deniss Sõritsa, Kadri Rekker, Helle Karro, Agne Velthut-Meikas, Tauno Metsalu, Anne Mari Roost, Jaak Simm, Maire Peters, Merli Saare, Kuelli Samuel, Andres Salumets, Andrei Sõritsa
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e112630 (2014)
PLoS ONE
PLoS ONE
Accumulating data have shown the involvement of microRNAs (miRNAs) in endometriosis pathogenesis. In this study, we used a novel approach to determine the endometriotic lesion-specific miRNAs by high-throughput small RNA sequencing of paired samples
Autor:
Deniss Sõritsa, Andres Salumets, Helle Karro, K Vaidla, Martti Laan, Priit Palta, Andrei Sõritsa, Thomas D'Hooghe, Maido Remm, Marleen Peters, Merly Saare
Publikováno v:
Human reproduction (Oxford, England). 27(6)
background: De novo somatic copy number aberrations (SCNAs) in eutopic and ectopic endometria are thought to be involved in the pathogenesis of endometriosis. In this study we used, for the first time, high-density single nucleotide polymorphism-arra
Autor:
Andres Salumets, Kadri Haller-Kikkatalo, Maire Peters, Tiia Reimand, Andrei Sõritsa, Kai Kisand
Publikováno v:
American journal of medical genetics. Part A. (23)
To the Editor:Incontinentia pigmenti (IP) also known as Bloch-Sulzberger syndrome is an X-chromosome-linkedgenodermatosis caused by mutations of nuclearfactor (NF)-kB essential modulator (NEMO) gene atXq28. The vast majority of NEMO mutations involve