Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Isa Abdi Rad"'
Autor:
Morteza Bagheri, Kamal Khadem-Vatani, Isa Abdi Rad, MirHossein Seyed-Mohammadzad, Alireza Rostamzadeh, Behzad Rahimi, Negin Kavosi
Publikováno v:
Health Science Monitor, Vol 3, Iss 2, Pp 84-89 (2024)
Background & Aims: Premature coronary artery disease (CAD) is common in men and women under 45 and 55 years, respectively. It has been demonstrated that R202Q mutation of MEFV gene may increase the risk of cardiovascular disease in individuals with m
Externí odkaz:
https://doaj.org/article/7c92eedfb1f04f1990329e2790c55716
Publikováno v:
Clinical Case Reports, Vol 9, Iss 2, Pp 732-736 (2021)
Abstract A novel splice site mutation in the GTPBP2 gene was identified by whole‐exome sequencing in two siblings with microcephaly and progressive generalized muscular atrophy associated with hypotrichosis.
Externí odkaz:
https://doaj.org/article/ae66994a6a8e4a64b84881c2541f24b0
Publikováno v:
International Journal of Fertility and Sterility, Vol 14, Iss 3, Pp 223-227 (2020)
Background: 3,4-Methylenedioxymethamphetamine (MDMA) disrupts function of the endocrine system and differentorgans such as heart, blood vessels, kidney, liver and nervous systems. This study was conducted to evaluateimpact of MDMA on apoptosis and Zi
Externí odkaz:
https://doaj.org/article/27a5f2026059412181bd38ee3c7dd029
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 18, Pp 777-784 (2020)
Background: 3, 4-Methylenedioxymethamphetamine (MDMA) is commonly known as the most famous amphetamine derivative. Objective: To evaluate the influence of zinc on MDMA-induced apoptosis and caspase- 3 gene expression in Leydig cell line (TM3). Materi
Externí odkaz:
https://doaj.org/article/57dd23c7c6514bcaa3e99c9646d4a684
Publikováno v:
Artificial Cells, Nanomedicine, and Biotechnology, Vol 47, Iss 1, Pp 882-890 (2019)
Osteoarthritis (OA) is a major cause of disability across the world, which its prevalence is relatively high in elder population. Current accepted therapies such as exercise, anti-inflammatory drugs and intra-articular inoculation of corticosteroids
Externí odkaz:
https://doaj.org/article/120b31da29e0466b92e9fb53f889f0d7
Autor:
Saeed Farajzadeh Valilou, Javad Karimzad Hagh, Mohammad Salimi Asl, Isa Abdi Rad, Masoud Edizadeh, Arash Pooladi
Publikováno v:
Clinical Case Reports, Vol 9, Iss 8, Pp n/a-n/a (2021)
Abstract The report of LMNB2‐related progressive myoclonus epilepsy and ataxia due to missense homozygous c.473G>T variant.
Externí odkaz:
https://doaj.org/article/551eceae835f4494abe7a33e1e50a671
Autor:
Morteza Bagheri, Kamal Khadem-Vatani, Mir Hossein Seyed Mohammad Zad, Isa Abdi Rad, Behzad Rahimi, Alireza Rostamzadeh, Mojtaba Godarzi, Shabnam Ashena
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 10, Iss 1, Pp 20-23 (2018)
Introduction: Premature coronary heart disease (PCHD) affects public health and leads to death. PCHD has several genetic and environmental risk factors. The aim of this study was to analysis of the mutations in exon 10 of MEFV gene in patients with P
Externí odkaz:
https://doaj.org/article/6e7d79609867430584be0360d55a5f22
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 12 (2019)
Introduction: Autosomal recessive non-syndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder with an approximate incidence of 1.4:1000 in neonates. Mutations in more than 60 genes including the MYO15A gene has been repo
Externí odkaz:
https://doaj.org/article/3c42886854094f9a929ba69efd7c8688
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 18, Iss 7, Pp 649-653 (2015)
Objective(s):Phenylketonuria (PKU) is a genetic inborn error of phenylalanine (Phe) metabolism resulting from insufficiency in the hepatic enzyme, phenylalanine hydroxylase (PAH), which leads to elevated levels of Phe in the blood. The present study
Externí odkaz:
https://doaj.org/article/6d2acc29960346b4b2edb1c8741ae69e
Publikováno v:
International Journal of Fertility and Sterility, Vol 7, Iss 2, Pp 116-121 (2013)
Background: Polycystic ovary syndrome (PCOS) is known as a metabolic disorder. The results of recent studies implied that vitamin D receptor (VDR) genetic variants may impact PCOS and insulin resistance in women with PCOS. The aim of the present stud
Externí odkaz:
https://doaj.org/article/b317617efffe4aa4b9aad2e8ff3a8db0