Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Mahdiyeh Harati-Sadegh"'
Publikováno v:
Journal of Biomedical Science, Vol 26, Iss 1, Pp 1-10 (2019)
Abstract Background Preeclampsia (PE), as a multisystem disorder, is associated with maternal hypertension and proteinuria. Apoptosis seems to be involved in the pathophysiology of PE, although its precise pathogenic mechanisms are not well establish
Externí odkaz:
https://doaj.org/article/01788d46d20849d3bad3865ad1a9882c
Autor:
Mahnaz Rezaei, Fatemeh Eskandari, Abbas Mohammadpour-Gharehbagh, Mahdiyeh Harati-Sadegh, Batool Teimoori, Saeedeh Salimi
Publikováno v:
Clinical and Experimental Hypertension, Vol 41, Iss 2, Pp 118-122 (2019)
Purpose: PE is a pregnancy-specific complication, which genetic and epigenetic factors play key roles in its pathogenesis. DNA methylation is a main epigenetic alteration with important roles in gene regulation. Micro RNAs (miRNAs) as another member
Externí odkaz:
https://doaj.org/article/8ded68cf53454ceba2aa1a2b1595c985
Autor:
Mahdiyeh HARATI-SADEGH, Saman SARGAZI, Roghayeh SHEERVALILOU, Saeed HOSSEINI TESHNIZI, Ramin SARAVANI, Shekoufeh MIRINEJAD
Publikováno v:
Iranian Journal of Public Health, Vol 49, Iss 12 (2020)
Background: The rs315952 (Ser133Ser) has been reported to influence the risk for immune-mediated as well as inflammatory diseases in many studies; however, the results remain inconsistent. The current meta-analysis was performed to give a more precis
Externí odkaz:
https://doaj.org/article/5c21e8058a214fa9b48aaa17c153348b
Autor:
Mahdiyeh Harati-Sadegh, Roghayeh Sheervalilou, Ramin Saravani, Alireza Ansari-Moghaddam, Saman Sargazi, Shekoufeh Mirinejad, Milad Khorasani
Publikováno v:
Ophthalmic Genetics. 42:503-513
Background: Several single-nucleotide polymorphisms (SNPs) in IL1B genes have been associated with KTCN. However, the results of these studies were not conclusive. This meta-analysis association st...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cbf2b8113f80f13c936801fc7363a4a
https://doi.org/10.1080/13816810.2021.1925926
https://doi.org/10.1080/13816810.2021.1925926
Autor:
Shekoufeh Mirinejad, Roghayeh Sheervalilou, Ramin Saravani, Mohsen Saravani, Saman Sargazi, Mahdiyeh Harati-Sadegh
Publikováno v:
Nucleosides, Nucleotides & Nucleic Acids. 40:578-591
Recent studies have suggested that single-nucleotide polymorphisms (SNPs) located in the miR-143/145 cluster might be linked to cancer risk. In this meta-analysis association study, we sought to qu...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33c66d91eefb6503b13d9eef48334e6f
https://doi.org/10.1080/15257770.2021.1916030
https://doi.org/10.1080/15257770.2021.1916030
Autor:
Mahdiyeh Harati-Sadegh, Sheida Shahraki, Ramin Saravani, Saman Sargazi, Milad Mohammadoo-Khorasani, Ebrahim Eskandari
Publikováno v:
Laboratory Medicine. 52:36-46
ObjectiveGrowing evidence suggests that IL-1β -511C>T, as a functional variant, affects the risk of developing breast cancer (BC); however, the results have not been conclusive. This meta-analysis was conducted to estimate the link between this vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71274012ea91753e735367a7cf5efea2
https://doi.org/10.1093/labmed/lmaa055
https://doi.org/10.1093/labmed/lmaa055
Autor:
Mahdiyeh, Harati-Sadegh, Saman, Sargazi, Roghayeh, Sheervalilou, Saeed, Hosseini Teshnizi, Ramin, Saravani, Shekoufeh, Mirinejad
Publikováno v:
Iranian Journal of Public Health
Background: The rs315952 (Ser133Ser) has been reported to influence the risk for immune-mediated as well as inflammatory diseases in many studies; however, the results remain inconsistent. The current meta-analysis was performed to give a more precis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b24c26c5bcef64498d09d397a306af42
https://pubmed.ncbi.nlm.nih.gov/34178738
https://pubmed.ncbi.nlm.nih.gov/34178738
Publikováno v:
IUBMB Life. 72:413-425
The effect of DNA methylation on gene expression triggered it as a susceptibility factor in various diseases including preeclampsia (PE). The pathogenesis of PE is closely associated with the methylation status and genetic variants of relevant genes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd26a57bc261bcb88e8f0b93a47a7490
https://doi.org/10.1002/iub.2199
https://doi.org/10.1002/iub.2199
Publikováno v:
Journal of Biomedical Science, Vol 26, Iss 1, Pp 1-10 (2019)
Journal of Biomedical Science
Journal of Biomedical Science
Background Preeclampsia (PE), as a multisystem disorder, is associated with maternal hypertension and proteinuria. Apoptosis seems to be involved in the pathophysiology of PE, although its precise pathogenic mechanisms are not well established. In th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e64656ad85d5398924026d8e70aa4c27
http://link.springer.com/article/10.1186/s12929-019-0586-x
http://link.springer.com/article/10.1186/s12929-019-0586-x
Autor:
Saeedeh Salimi, Mahnaz Rezaei, Maryam Moradi-shahrebabak, Maryam Razavi, Batool Teimoori, Mahdiyeh Harati-Sadegh
Publikováno v:
Molecular Biology Reports. 46:6099-6104
Preeclampsia (PE) is a serious pregnancy complication whose etiology is not fully understood. However, previous reports have suggested that oxidative stress and genetic variants may contribute to the development of PE. This study aimed to examine the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56c8c3a00af181a39a114bb23be47009
https://doi.org/10.1007/s11033-019-05045-6
https://doi.org/10.1007/s11033-019-05045-6