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Akademický článek
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Autor:
Heris, Helaleh Vaezi, Zahraei, Zohreh
Publikováno v:
In Mutation Research-Reviews in Mutation Research July-December 2022 790
Autor:
Zahra Hassanpour Aydinlou, Helaleh Vaezi, Mortaza Bonyadi, Abbas Rafat, Mohammad Hossein Jabbarpoor Bonyadi, Masoud Soheilian
Publikováno v:
Ophthalmic Genetics. 43:446-449
Rhegmatogenous retinal detachment (RRD) is the most common type of retinal detachment. Purpose of this study is to evaluate the possible association of ARMS2 (age-related macular susceptibility 2) A69S and CFH (complement factor H) Y402H polymorphism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee5381bbf01dabbe9ee918eea471a88c
https://doi.org/10.1080/13816810.2022.2045510
https://doi.org/10.1080/13816810.2022.2045510
Autor:
Leila Hosseinzadeh Anvar, Asghar Alejafar, Seyyed Ebrahim Moosavi, Saeid Charsouei, Narges Zeynalzadeh, Leila Mehdizadeh Fanid, Babak Emamalizadeh, Zahra Hassanpour Aydinlou, Helaleh Vaezi, Adel Kashefi, Carlos Tomaz, Masoud Nikanfar, Ali Ahmadalipour
Publikováno v:
Epilepsy Research. 192:107100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e38e19a586872cfd3a0d466c4c14e21
https://doi.org/10.1016/j.eplepsyres.2023.107100
https://doi.org/10.1016/j.eplepsyres.2023.107100
Autor:
Helaleh Vaezi, Maedeh Alizadeh, Narges Zeinalzadeh, Zahra Hassanpour Aydinlou, Leila Mehdizadeh Fanid, Ali Ahmadalipour, Seyed Gholamreza Noorazar
Publikováno v:
Genomics. 112:1330-1334
Several single nucleotide polymorphisms (SNPs) of the fatty acid amide hydrolase (FAAH), the degrading enzyme of the endocannabinoids, have been shown to be associated with many neuropsychiatric disorders. Here, FAAH rs2295633 was studied in ADHD and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32f343ec8dd8b9650b4cd9dc135e29a9
https://doi.org/10.1016/j.ygeno.2019.07.024
https://doi.org/10.1016/j.ygeno.2019.07.024
Autor:
Helaleh Vaezi Heris, Zohreh Zahraei
Publikováno v:
Mutation research. Reviews in mutation research. 790
Diabetes, one of the most common multifactorial metabolic disorders, is a jeopardizing cause of human health worldwide. MicroRNAs (miRNAs) are a group of small non-coding RNAs that have been contributed to the regulation of gene expression through po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac7d4dd85b49dccb6c4044356561c23c
https://pubmed.ncbi.nlm.nih.gov/36089265
https://pubmed.ncbi.nlm.nih.gov/36089265
Autor:
Mohammad hossein Jabbrpoor bonyadi, Zahra Hassanpour Aydinlou, Helaleh Vaezi, Masoud Soheilian, Mortaza Bonyadi, Abbas Rafat
Background: Rhegmatogenous retinal detachment (RRD) is the most common type of retinal detachment. Purpose of this study is to evaluate the possible association of ARMS2 A69S and CFH Y402H polymorphisms with RRD and its postoperative complications. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e9d036f9fa998a0d7421a6110b3b554
https://doi.org/10.21203/rs.3.rs-294151/v1
https://doi.org/10.21203/rs.3.rs-294151/v1
