Výsledky vyhledávání - "Siavash Shakerian"

Copy number analysis in a large-scale study of spinal muscular atrophy patients between two continuous generations in Iran

Autor: Siavash Shakerian, Gholamreza Shariati, Marzieh Mohammadi anaie, Nehzat Abdorasouli, Fatemeh Nanvazadeh, Hamid Galehdari, Mohammad Hamid, Alireza Sedaghat, Alihossein Saberi

Background:Spinal muscular atrophy (SMA) is a rare autosomal recessive inherited neuromuscular disease with about 1:6000 to 1:10,000 in newborns. Objectives:To evaluate the copy number variation of SMN1 and SMN2 genes between two generations, we expe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6b72afee84bfe1c8478bd7774b2d2eee
https://doi.org/10.21203/rs.3.rs-2029090/v1

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KCNQ1 rs2237895 polymorphism is associated with the therapeutic response to sulfonylureas in Iranian type 2 diabetes mellitus patients

Autor: Siavash Shakerian, Homeira Rashidi, Maryam Tahmasebi Birgani, Alihossein Saberi

Publikováno v: J Diabetes Metab Disord

BACKGROUND AND AIMS: Sulfonylureas are the most secondary prescribed oral anti-diabetic drug. Understanding its genetic role in pharmacodynamics can elucidate a considerable knowledge about personalized treatment in type 2 diabetes patients. This stu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71909c721a2d9822b9330e6fbd101a44
https://europepmc.org/articles/PMC9167421/

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Crosstalk between ferroptosis and the epithelial-mesenchymal transition: Implications for inflammation and cancer therapy

Autor: Nasim Ebrahimi, Samaneh Adelian, Siavash Shakerian, Maral Afshinpour, Siavash Rahimian Chaleshtori, Nadi Rostami, Fatemeh Rezaei-Tazangi, Sheida Beiranvand, Michael R. Hamblin, Amir Reza Aref

Publikováno v: Cytokinegrowth factor reviews. 64

Both genomic instability and the presence of chronic inflammation are involved in carcinogenesis and tumor progression. These alterations predispose the cancer cells to undergo metabolic reprogramming as well as the epithelial-mesenchymal transition

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04938852642703a20decb7b920f18e75
https://pubmed.ncbi.nlm.nih.gov/35219587

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Deletion and duplication mutations spectrum in Duchenne muscular dystrophy in the southwest of Iran

Autor: Alireza Sedaghat, Alihossein Saberi, Siavash Shakerian, Marzieh Mohammadi Anaie, Mostafa Sedighi, Fateme Nanvazadeh, Nehzat Abdorasouli, Gholamreza Shariati

Publikováno v: Meta Gene. 23:100641

Background Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked disorders caused by the mutation within the dystrophin gene. Objectives the primary objective of this study was to evaluate the deletion and duplication mut

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f1e8dfc3fd6fb489c4ec4ba6db79dcc4
https://doi.org/10.1016/j.mgene.2019.100641

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