Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Aida Vahidi"'
Autor:
Morteza Gholami, Zeynab Nickhah Klashami, Pirooz Ebrahimi, Amir Ali Mahboobipour, Amir Salehi Farid, Aida Vahidi, Marziyeh Zoughi, Mojgan Asadi, Mahsa M. Amoli
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-20 (2023)
Abstract Breast cancer (BC) is the second most common cancer and cause of death in women. In recent years many studies investigated the association of long non-coding RNAs (lncRNAs), as novel genetic factors, on BC risk, survival, clinical and pathol
Externí odkaz:
https://doaj.org/article/9a05d094bbf943cf806420d040da48b0
Publikováno v:
Journal of Tehran University Heart Center, Vol 17, Iss 3 (2022)
Background: In-stent restenosis (ISR) is an inevitable complication of percutaneous coronary intervention, with genetic factors thought to play a role in its pathogenesis. The VEGF gene can have an inhibitory effect on ISR development. Accordingly, i
Externí odkaz:
https://doaj.org/article/d5164e9b200b4bde8c7166f6b32422dd
Autor:
Morteza Gholami, Saeedeh Asgarbeik, Farideh Razi, Ensieh Nasli Esfahani, Marzieh Zoughi, Aida Vahidi, Bagher Larijani, Mahsa Mohammad Amoli
Publikováno v:
Journal of Research in Medical Sciences, Vol 25, Iss 1, Pp 56-56 (2020)
Background: Type 2 diabetes mellitus (T2DM) is a metabolic disorder with growing prevalence and increasing economic burden. Based on the role of genetics and epigenetic factors on T2DM, we aimed to carry a systematic review and meta-analysis for all
Externí odkaz:
https://doaj.org/article/a34c1fbaa6c64db3866ccfff323d31c9
Publikováno v:
Journal of Diabetes & Metabolic Disorders.
Due to the high prevalence of metabolic diseases and the role of genetic factors in their susceptibility, the use of basic research in this field can be useful for screening, prevention, and treatment of metabolic disorders. Therefore, in the Immunog
Autor:
Neda Jalili, Armita Kakavand Hamidi, Aida Vahidi, Mahsa M. Amoli, Nasrin Yazdani, Nakisa Zarabi Ahrabi, Negin Soroush, Ardavan Tajdini
Publikováno v:
Acta Oto-Laryngologica. 138:904-908
Sudden sensorineural hearing loss (SSNHL) causes the loss of hearing of 30 dB or greater on at least three contiguous frequencies. It is known to be a multifactorial disease which the exact cause is unknown, rendering it as an idiopathic disorder of
Evaluation of ERRFI1 +808 T/G variant and its mRNA expression in coronary artery in-stent restenosis
Publikováno v:
Gene Reports. 24:101248
Background One of the common treatments in cardiovascular disease as the first cause of death in the world is stent implantation. In-Stent Restenosis (ISR) is the major drawback of stent implantation. As there are several lines of evidence suggesting
Publikováno v:
Gene Reports. 24:101244
Background Meniere's disease is an idiopathic disorder of the inner ear that causes hearing loss, episodic vertigo, and tinnitus. In this study, the role of rs2010963, and rs35569394 polymorphisms of the VEGFA gene in Meniere's disease was evaluated.
Autor:
Saleh Mohebbi, Aida Vahidi, Mohammad Mohseni, Saeedeh Asgarbeik, Ahmad Daneshi, Mohammad Farhadi, Nasrin Yazdani, Alimohamad Asghari, Mahsa M. Amoli
Publikováno v:
Meta Gene. 24:100659
Background Meniere's disease is an inner ear disorder presenting with recurrent episodic vertigo, fluctuating sensorineural hearing loss, tinnitus, and aural fullness as its main symptoms. Previous studies have demonstrated the role of blood pressure