Zobrazeno 1 - 10
of 58
pro vyhledávání: '"hossein fahimi"'
Autor:
Elaheh Mohandesi Khosroshahi, Mazaher Maghsoudloo, Hossein Fahimi, Khatere Mokhtari, Maliheh Entezari, Maryam Peymani, Mehrdad Hashemi, Runlan Wan
Publikováno v:
Heliyon, Vol 10, Iss 14, Pp e34464- (2024)
Membrane transporters are proteins responsible for facilitating the movement of molecules within biological membranes. They play a vital role in maintaining cellular homeostasis by regulating the transport of nutrients, ions, and other molecules into
Externí odkaz:
https://doaj.org/article/9eb69c856d5d441e82c5b6107b566b36
Publikováno v:
PLoS ONE, Vol 19, Iss 11, p e0310368 (2024)
The clustered regularly interspaced short palindromic repeats (CRISPR) system offers cost-effectiveness, high efficiency, precision, and ease of use compared to traditional gene editing techniques. In this study, we employed findings from prestigious
Externí odkaz:
https://doaj.org/article/c459947d72174911b36347b8690d32ef
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 13 (2024)
Small regulatory RNAs (sRNAs) encapsulated in outer membrane vesicles (OMVs) are critical post-transcriptional regulators of gene expression in prokaryotic and eukaryotic organisms. OMVs are small spherical structures released by Gram-negative bacter
Externí odkaz:
https://doaj.org/article/f6a3444cf21f43adb0fd560dccb0f23a
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 19, Iss 7, Pp 607-618 (2021)
Background: Coenzyme Q10 (CoQ10) and Lepidium sativum (LS) have therapeutic effects on infertility. Objective: To evaluate the combined effects of LS and CoQ10 on reproductive function in adult male NMRI mice. Materials and Methods: Eighty three-mont
Externí odkaz:
https://doaj.org/article/9889f530399742b89083629bcfc6cf05
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background Autosomal recessive non-syndromic hearing loss (ARNSHL) is genetically and phenotypically heterogeneous with over 110 genes causally implicated in syndromic and non-syndromic hearing loss. Here, we investigate the genetic etiology
Externí odkaz:
https://doaj.org/article/826d40a9695f4866847f7028041f60c4
Publikováno v:
مجله انفورماتیک سلامت و زیست پزشکی, Vol 7, Iss 3, Pp 326-336 (2020)
Introduction: FAD is the cofactor of FAD-FR protein family. Sulfite reductase flavoprotein alpha-component is one of the main enzymes of this family. Based on applications of this enzyme in biotechnology and industry, it was chosen as the subject of
Externí odkaz:
https://doaj.org/article/3fcefbcea0f24f6c8fef9976a0884c94
Autor:
Suliman Khan, Arif Hussain, Hossein Fahimi, Fakhteh Aliakbari, Samir Haj Bloukh, Zehra Edis, Mohammad Mahdi Nejadi Babadaei, Zhila Izadi, Behrang Shiri Varnamkhasti, Fatemeh Jahanshahi, Yueting Lin, Xiao Hao, Rizwan Hasan Khan, Behnam Rasti, Gholamreza Vaghar-Lahijani, Linlin Hua, Hossein Derakhshankhah, Majid Sharifi, Mojtaba Falahati
Publikováno v:
Arabian Journal of Chemistry, Vol 15, Iss 2, Pp 103626- (2022)
The advancement in early diagnosis and precise treatments options result in more predictable and powerful health care modalities. Aptamers are known as nucleic acid structures with three-dimensional conformation to selectively bind a target site. Phy
Externí odkaz:
https://doaj.org/article/bf4fb4a7fcf545ada29e6afbfaa3d79c
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 22, Iss 9, Pp 1004-1009 (2019)
Objective(s): Prevalence of high-fat food consumption, such as fast foods is one of the major causes of hypercholesterolemia, which can lead to cardiovascular diseases. 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) and cytochrome P450 7A1 (
Externí odkaz:
https://doaj.org/article/3603d636f824482692871dceceebbd43
Autor:
Sadaf Noavar, Samira Behroozi, Taraneh Tatarcheh, Farshid Parvini, Majid Foroutan, Hossein Fahimi
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background The SLC29A3 gene, encoding a nucleoside transporter protein, is found in intracellular membranes. Based on the literatures, mutations in this gene cause a wide range of clinical manifestations including H syndrome, pigmented hyper
Externí odkaz:
https://doaj.org/article/d91c0495f34f4b1a948aa093a236fffd
Publikováno v:
Iranian Journal of Medical Microbiology, Vol 13, Iss 1, Pp 32-43 (2019)
Background and Aims: The rate of variation in various genes of a bacterial species is different during evolution. Therefore, in systematic bacterial studies many researchers compare the phylogenetic tree of a particular gene to the standard tree of a
Externí odkaz:
https://doaj.org/article/4f8384648fb144bda30b1fb781cfa5a2