Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Mohammad Soleiman Soltanpour"'
Autor:
Ehsan Aali, Habib Ghaznavi, Mohammad Soleiman Soltanpour, Massoud Mahmoudian, Massoumeh Shafiei
Publikováno v:
Iranian Journal of Medical Sciences, Vol 46, Iss 2, Pp 136-143 (2021)
Background: Mebudipine, a dihydropyridine calcium-channel blocker (CCB), shows greater time- and voltage-dependent inhibitory effects than nifedipine. Its significant negative chronotropic effects without having considerable negative inotropic proper
Externí odkaz:
https://doaj.org/article/e64b846dc1c348aea76114e248296c2f
Autor:
Parisa Farhoumand, Hassan Hassanzadazar, Mohammad Soleiman Soltanpour, Majid Aminzare, Zahra Abbasi
Publikováno v:
Iranian Journal of Microbiology, Vol 12, Iss 6 (2020)
Background and Objectives: The aim of present study was to evaluate the prevalence of Listeria monocytogenes and Escherichia coli, characterization and antimicrobial resistance of their serotypes and genotyping profiles in fresh beef and poultry meat
Externí odkaz:
https://doaj.org/article/3e7048b23d884ac99639dc8ac624ce7e
Publikováno v:
Oman Medical Journal, Vol 35, Iss 4, Pp e151-e151 (2020)
Objectives: Chronic lymphocytic leukemia (CLL) is characterized by the accumulation of apparently mature B-type lymphocytes in the lymphohematopoietic organs. Methylation in promoters of tumor suppressor genes is one of the mechanisms that causes blo
Externí odkaz:
https://doaj.org/article/a1ae6498dadd44be80a43e626b8f392d
Publikováno v:
Oman Medical Journal, Vol 35, Iss 3, Pp e131-e131 (2020)
Objectives: Colorectal cancer (CRC) is a common malignancy with a high rate of mortality. The dysregulation of genes involved in the Wnt/β-catenin signaling pathway is a common finding in cancers. Wnt-inhibitory factor-1 (WIF-1) suppresses the Wnt/
Externí odkaz:
https://doaj.org/article/8704cde76ea84fb5ae4441b7204cdfdf
Publikováno v:
Oman Medical Journal, Vol 33, Iss 4, Pp 309-315 (2018)
Objectives: ATP-binding cassette transporter A1 (ABCA1) plays a pivotal role in reverse cholesterol transport from peripheral tissues back to the liver. Abnormalities in ABCA1 function may lead to dyslipidemia and coronary artery disease (CAD). We in
Externí odkaz:
https://doaj.org/article/ed58e6de6f9a43eb860433d02911b4d4
Autor:
Fatemeh Hoseini, Sanaz Mahmazi, Khalil Mahmoodi, Gholam Ali Jafari, Mohammad Soleiman Soltanpour
Publikováno v:
Oman Medical Journal, Vol 33, Iss 2, Pp 118-125 (2018)
Objectives: Interleukin-18 (IL-18) is a proinflammatory and proatherogenic cytokine, and its genetic variations may contribute to the development of coronary artery disease (CAD). We sought to investigate the role of -137G/C polymorphism and gene exp
Externí odkaz:
https://doaj.org/article/00bc42a2717141a69329adc21a4b0241
Publikováno v:
Oman Medical Journal, Vol 33, Iss 1, Pp 48-54 (2018)
Objectives: Organ-specific hemosiderosis and iron overload complications are more serious and more frequent in some patients with beta thalassemia major (BTM) compared with others. We investigated whether coinheritance of HFE H63D or C282Y gene mutat
Externí odkaz:
https://doaj.org/article/83a1f5e2e9a44b0c9848a417651f1e17
Publikováno v:
Asian Journal of Transfusion Science, Vol 10, Iss 1, Pp 88-92 (2016)
Background: Thalassemia is one of the most common monogenic disorders characterized by reduced production of globin chains. Although regular red blood cell (RBC) transfusion support is the main treatment for these patients, it may be associated with
Externí odkaz:
https://doaj.org/article/874a5d9ee59a49cd81be4f017d065acc
Autor:
Mohammad Soleiman Soltanpour, Zahra Soheili, Ali Shakerizadeh, Ali Akbar Pourfathollah, Shahram Samiei, Reza Meshkani, Mohammad Shahjahani, Abbas Karimi
Publikováno v:
Journal of Research in Medical Sciences, Vol 18, Iss 6, Pp 487-491 (2013)
Background: Elevated plasma homocysteine (Hcy) level has been established as a significant risk factor for venous thrombosis and cardiovascular disease. Homozygosity for the methylenetetrahydrofolate reductase (MTHFR) C677T mutation has been associat
Externí odkaz:
https://doaj.org/article/403cd1cb133f42e9871c571a418d626c
Publikováno v:
Journal of Research in Medical Sciences, Vol 22, Iss 1, Pp 8-8 (2017)
Background: Matrix metalloproteinase 9 (MMP9) -1562C>T (rs3918242) polymorphism has been proposed as a risk factor for coronary artery disease (CAD) with conflicting results. The aim of the present study was to investigate the association of -1562C>T
Externí odkaz:
https://doaj.org/article/7d96fc1e2efc4a748cd7a3a84bb31d9a