Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Mahdiyeh MOUDI"'
Publikováno v:
Obstetrics & Gynecology Science, Vol 67, Iss 5, Pp 506-510 (2024)
Trisomy 9 is a rare chromosomal abnormality that occurs in both mosaic and non-mosaic states. The present study reports a case of mosaic trisomy 9 detected during pregnancy in a 41-year-old woman in the second trimester screening. Maternal serum scre
Externí odkaz:
https://doaj.org/article/ea7b6be77f534e3190d4822be4391284
Autor:
Mahdiyeh Moudi, Mohammad Yahya Vahidi Mehrjardi, Seyed Mehdi Kalantar, Mohsen Taheri, Zahra Metanat, Nasrin Ghasemi, Mohammadreza Dehghani
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-11 (2022)
Abstract Background Intellectual disability is characterized by impairments in adaptive behavior and cognitive functioning manifested during the developmental period. Since disabilities are heterogeneous, variant analysis can help us confirm and accu
Externí odkaz:
https://doaj.org/article/aaaf3bc712984e0f865a23fa4db68948
Publikováno v:
Iranian Journal of Medical Sciences, Vol 45, Iss 5, Pp 359-367 (2020)
Background: Achillea wilhelmsii C. Koch hydroalcoholic extract (AWHE) is proven to induce cell death. Previous studies suggested that AWHE is an effective inhibitor against the proliferation of prostate cancer cells. The present study aimed to evalua
Externí odkaz:
https://doaj.org/article/4b342245e59e4f1289eae0252d6a3655
Autor:
Milad Heidari Nia, Mahdieh Jafari Shahroudi, Ramin Saravani, Saman Sargazi, Mahdiyeh Moudi, Azizollah Mojahed
Publikováno v:
Iranian Journal of Public Health, Vol 50, Iss 5 (2021)
Background: Schizophrenia (SZN) is a heterogeneous disorder. Recently, the role of purinergic receptor’s signaling in mental disorders has implicated. There is no evidence regarding the association of P2XR4 single nucleotide polymorphisms (SNPs) an
Externí odkaz:
https://doaj.org/article/613f75112f1e47f181c23ea1dd5a2bbf
Autor:
Saman SARGAZI, Milad HEIDARI NIA, Shekoufeh MIRINEJAD, Mahdiyeh MOUDI, Mahdiyeh Jafari JAFARI SHAHROUDI, Ramin SARAVANI, Sadegh VALIAN-BOROJENI
Publikováno v:
Iranian Journal of Public Health, Vol 50, Iss 2 (2021)
Background: KIF26B gene is found to play essential roles in regulating different aspects of cell proliferation and development of the nervous system. We aimed to determine if rs12407427 T/C polymorphism could affect susceptibility to schizophrenia (S
Externí odkaz:
https://doaj.org/article/325d20e233314fa2a196ea56995157b8
Autor:
Saman Sargazi, Fariba Mirani Sargazi, Mahdiyeh Moudi, Milad Heidari Nia, Ramin Saravani, Shekoufeh Mirinejad, Sheida Shahraki, Mansoor Shakiba
Publikováno v:
Iranian Journal of Psychiatry, Vol 15, Iss 4 (2020)
Objective: Schizophrenia (SCZ) is a common psychiatric disorder characterized by a complex mode of inheritance. Peroxisome proliferator-activated receptor-γ (PPARG) mainly regulates lipid and glucose metabolisms while it is constitutively expressed
Externí odkaz:
https://doaj.org/article/8d729166bc1b490fb2f48440828b0c07
Publikováno v:
Current Medical Mycology, Vol 4, Iss 1, Pp 1-5 (2018)
Background and Purpose: Vulvovaginal candidiasis is one of the most common infections in female genital organs, which is caused by Candida species. Candida albicans is the causative agent of more than 80% of infections, and the role of non-Candida st
Externí odkaz:
https://doaj.org/article/c07703e6d94145e7b4556feea92ecec8
Publikováno v:
Nanomedicine Research Journal, Vol 2, Iss 2, Pp 78-86 (2017)
Objective(s): In this work, CuO- NiO nano-composites were synthesized via free-surfactant co-precipitation method and then their physiochemical properties, as well as cytotoxicity and antifungal effects, were studied. Methods: The structural and opti
Externí odkaz:
https://doaj.org/article/d2770efa1ca344a59816ef0e3770ac2a
Publikováno v:
Iranian Journal of Public Health, Vol 47, Iss 11 (2018)
Background: Nitric oxide (NO) has been associated with insulin resistance and type 2 diabetes (T2D). NO is synthesized enzymatically from l-arginine (l-Arg) by three NO synthase (NOS) isoforms, Neuronal NOS (nNOS or NOS1), Inducible NOS (iNOS or NOS2
Externí odkaz:
https://doaj.org/article/4acc6c28c5004e4f95904fc499d70587
Autor:
Milad Shirvaliloo, Milad Heidari Nia, Mansoor Shakiba, Saman Sargazi, Ramin Saravani, Mahdiyeh Moudi
Publikováno v:
Journal of Molecular Neuroscience. 70:2093-2101
Schizophrenia (SCZ) is a multifactorial disorder caused by environmental and genetic factors. Studies have shown that various single-nucleotide polymorphisms (SNPs) in the binding sites of microRNAs contribute to the risk of developing SCZ. We aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d4b96a5b130c114d6d8d1cdd249a20e
https://doi.org/10.1007/s12031-020-01616-6
https://doi.org/10.1007/s12031-020-01616-6