Search Results - "Azizi, Reza"

Inhibition of didscoidin domain receptor 1 reduces epithelial–mesenchymal transition and induce cell‐cycle arrest and apoptosis in prostate cancer cell lines by Azizi, Reza, Salemi, Zahra, Fallahian, Faranak, Aghaei, Mahmoud

“…Didscoidin domain receptor 1 (DDR1) is involved in the progression of prostate cancer metastasis through stimulation of epithelial–mesenchymal transition…”
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Developing a specific model to exploring the determinant of individuals’ attitude toward forest conservation by Maleknia, Rahim, Azizi, Reza, Hălălișan, Aureliu Florin

“…Introduction In the context of forest conservation, individuals’ attitude can significantly influence their intentions and subsequent behaviors towards…”
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The characteristics of a novel environmentally friendly countermeasure against bridge abutments scour depth by Shafai Bejestan, Mahmood, Raee, Narges, Azizi, Reza

“…Destruction of many bridges around the world has been found to be due to the collapse of its abutments owing to the formation of scour. Various methods have…”
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Innovative human resource management strategies during the COVID-19 pandemic: A systematic narrative review approach by Azizi, Mohammad Reza, Atlasi, Rasha, Ziapour, Arash, Abbas, Jaffar, Naemi, Roya

“…The spread of COVID-19 creates disruption, uncertainty, complexity, and ambiguity in all organizations. People are the primary asset of any organization and…”
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Evaluation of MYC Oncogene Expression in Human Breast Cancer and Its Relationship with ACSL4 and Lipin-1 Expression by Dinarvand, Negar, Azizi, Reza, Rastaghi, Sedighe, Karimi, Farzaneh, Sheikhi, Abdolkarim, Pourfarzam, Morteza

“…Background: Disturbances in lipid metabolism are one of the hallmarks of cancer cells. Fatty acid synthesis and oxidation play a crucial role in the…”
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Identification of a Novel Stop Loss Mutation in P2RX2 Gene in an Iranian Family with Autosomal Nonsyndromic Hearing Loss by Azizi Malamiri, Reza, Mohammadi Asl, Javad, Ghanbari, Farideh

“…Hearing loss, a congenital genetic disorder in human, is difficult to diagnose. Whole exome sequencing is a powerful approach for ethiological disgnosis of…”
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Modeling the Price of Emergency Power Transmission Lines in the Reserve Market Due to the Influence of Renewable Energies by Iranmehr, Hamid, Aazami, Rahmat, Tavoosi, Jafar, Shirkhani, Mohammadamin, Azizi, Amir-Reza, Mohammadzadeh, Ardashir, Mosavi, Amir H., Guo, Wei

“…The law of free access to the transmission network obliges the transmission network to be in orbit, and on the other hand, the high loads in the transmission…”
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Early Detection of Diabetic Nephropathy Based on Urinary and Serum Biomarkers: An Updated Systematic Review by Karimi, Farzaneh, Moazamfard, Mostafa, Taghvaeefar, Rasul, Sohrabipour, Shahla, Dehghani, Aghdas, Azizi, Reza, Dinarvand, Negar

“…Diabetic nephropathy (DN) is a leading cause of chronic kidney disease (CKD) and end-stage renal disease worldwide, particularly among individuals with type 2…”
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Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy by Osborn, Daniel P.S., Pond, Heather L., Mazaheri, Neda, Dejardin, Jeremy, Munn, Christopher J., Mushref, Khaloob, Cauley, Edmund S., Moroni, Isabella, Pasanisi, Maria Barbara, Sellars, Elizabeth A., Hill, R. Sean, Partlow, Jennifer N., Willaert, Rebecca K., Bharj, Jaipreet, Malamiri, Reza Azizi, Galehdari, Hamid, Shariati, Gholamreza, Maroofian, Reza, Mora, Marina, Swan, Laura E., Voit, Thomas, Conti, Francesco J., Jamshidi, Yalda, Manzini, M. Chiara

“…Congenital muscular dystrophies display a wide phenotypic and genetic heterogeneity. The combination of clinical, biochemical, and molecular genetic findings…”
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The First Comprehensive Cohort of the Duchenne Muscular Dystrophy in Iranian Population: Mutation Spectrum of 314 Patients and Identifying Two Novel Nonsense Mutations by Zamani, Gholamreza, Hosseini Bereshneh, Ali, Azizi Malamiri, Reza, Bagheri, Sayna, Moradi, Kamyar, Ashrafi, Mahmoud Reza, Tavasoli, Ali Reza, Mohammadi, Mahmoud, Badv, Reza Shervin, Ghahvechi Akbari, Masood, Heidari, Morteza

“…Mutations in the dystrophin gene could cause Duchenne muscular dystrophy (DMD), which is the most common muscular disorder in pediatrics. Considering the…”
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Genetic features of patients with MPS type IIIB: Description of five pathogenic gene variations by Nasir Shalal, Mahzad, Aminzadeh, Majid, Saberi, Alihossein, Azizi Malmiri, Reza, Aminzadeh, Reza, Ghandil, Pegah

“…•Identified five pathogenic variations in NAGLU gene in 14 independent families.•Two novel variants found in two families, three previously reported.•In silico…”
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A decreased level of high‐density lipoprotein is a possible risk factor for type 2 diabetes mellitus: A review by Bodaghi, Ali Bayat, Ebadi, Erfan, Gholami, Mohammad Javad, Azizi, Reza, Shariati, Aref

“…Introduction Type 2 diabetes mellitus (T2DM) is characterized primarily by dyslipidemia and hyperglycemia due to insulin resistance. High‐density lipoprotein…”
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Kinetic Study and Optimization of Dehydration of Dimethyl Amino Ethyl Azide (DMAZ) Using Response Surface Methodology by Pakdehi, Shahram Ghanbari, Babaee, Saeed, Azizi, Hamid Reza

“…This research highlights the dehydration of dimethyl amino ethyl azide (DMAZ), parametric optimization, and describes equilibrium and kinetics of water…”
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Synthesis and investigation of nano-biologic structures’ effect on soil pathogenic fungi in maize by Almasian, Nafiseh, Ebrahimi, Asa, Diyanat, Marjan, Azizi Nezhad, Reza, Khosrowshahli, Mahmood

“…Maize soil pathogenic fungi, Fusarium moniliforme, Macrophomina phaseolina, and Rhizoctonia zeae are important causes of annual economic losses worldwide…”
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LHRH Targeted Chonderosomes of Mitomycin C in Breast Cancer: An In Vitro/ In Vivo Study by Varshosaz, Jaleh, Sarrami, Nasim, Aghaei, Mahmoud, Aliomrani, Mehdi, Azizi, Reza

“…Mitomycin C (MMC) is an anti-cancer drug used for the treatment of breast cancer with limited therapeutic index, extreme gastric adverse effects and bone…”
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Use of Nuclear Factor Erythroid 2-Eelated Factor Activators as A Strategy to Improve the Side Effects of COVID-19 by Samimi, Fatemeh, Azizi, Reza, Jalali Mashayekhi, Farideh

“…Coronavirus disease-19 (COVID-19) is a new member of the coronavirus family causing acute respiratory infection. Patients with COVID-19 have a higher risk of…”
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Development of an integrated multi-objective approach to formulate optimal harvesting policies with the aim of sustainable management of groundwater resources: study area: Varamin Plain by Azizi, Hamid reza, Azizi, Hamed

“…Abstract In the present study, an integrated multi-objective simulation -optimization model was developed using a NSGA-II optimization algorithm and GMS…”
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Curcumin and saroglitazar attenuate diet-induced nonalcoholic steatohepatitis by activating the Nrf2 pathway and suppressing ERK1/2 signaling by Afarin, Reza, Dinarvand, Negar, Azizi Dariuni, Hossein, Orak, Ghazal, Jaberian Asl, Bahar, Azizi, Reza, Khedri, Azam

“…Non-alcoholic fatty liver disease (NAFLD) is a chronic steatohepatitis disorder. If left untreated, it can progress to hepatocellular carcinoma. Several…”
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Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy by Zamani, Gholamreza, Hosseinpour, Sareh, Ashrafi, Mahmoud Reza, Mohammadi, Mahmoud, Badv, Reza Shervin, Tavasoli, Ali Reza, Akbari, Masood Ghahvechi, Bereshneh, Ali Hosseini, Malamiri, Reza Azizi, Heidari, Morteza

“…Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy in the pediatric population. The manifestations of this disease include progressive…”
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Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant by Helal, Mayada, Mazaheri, Neda, Shalbafan, Bita, Malamiri, Reza Azizi, Dilaver, Nafi, Buchert, Rebecca, Mohammadiasl, Javad, Golchin, Neda, Sedaghat, Alireza, Mehrjardi, Mohammad Yahya Vahidi, Haack, Tobias B., Riess, Olaf, Chung, Wendy K., Galehdari, Hamid, Shariati, Gholamreza, Maroofian, Reza

“…Biallelic mutations of the alsin Rho guanine nucleotide exchange factor ( ALS2 ) gene cause a group of overlapping autosomal recessive neurodegenerative…”
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