M
Mohammad Karimian
Researcher at University of Mazandaran
Publications - 80
Citations - 1218
Mohammad Karimian is an academic researcher from University of Mazandaran. The author has contributed to research in topics: Male infertility & Genotype. The author has an hindex of 18, co-authored 65 publications receiving 715 citations. Previous affiliations of Mohammad Karimian include Islamic Azad University & Kashan University of Medical Sciences.
Papers
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Oxidative stress and male infertility: current knowledge of pathophysiology and role of antioxidant therapy in disease management
TL;DR: Physiological ROS production, roles of genetic and epigenetic factors on the OS and male infertility with various mechanisms such as lipid peroxidation, DNA damage, and disorder of male hormone profile, inflammation, and varicocele are described.
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Association of C677T transition of the human methylenetetrahydrofolate reductase (MTHFR) gene with male infertility.
TL;DR: It is suggested that C677T transition in MTHFR may increase the risk of male infertility, and detection of the C677 T polymorphism biomarker may be helpful in the screening of idiopathic male infertility.
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The regulatory role of Toll-like receptors after ischemic stroke: neurosteroids as TLR modulators with the focus on TLR2/4
Saeedeh Tajalli-Nezhad,Mohammad Karimian,Cordian Beyer,Mohammad Ali Atlasi,Abolfazl Azami Tameh +4 more
TL;DR: The relationship between neurosteroids and TLRs as neuroprotective mechanism is highlighted in the context of brain ischemia and the gene and protein structures, common genetic polymorphisms of TLR2 and TLR4, TLR-related molecular pathways and their putative role after ischemic stroke are delineated.
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MTHFR-Ala222Val and male infertility: a study in Iranian men, an updated meta-analysis and an in silico-analysis
Hossein Nikzad,Mohammad Karimian,Mohammad Karimian,Kobra Sareban,Maryam Khoshsokhan,Abasalt Hosseinzadeh Colagar +5 more
TL;DR: A meta-analysis and in-silico analysis suggested significant association of MTHFR-Ala222Val with risk of male infertility, especially in Asian populations.
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Association of sperm mitochondrial DNA deletions with male infertility in an Iranian population.
TL;DR: It is suggested that 4977 and 7599 bp deletions of mtDNA may be genetic risk factors for male infertility, however, it is a preliminary study and is presenting data for future comprehensive study for making a clinical conclusion that these deletions are biomarkers for susceptibility to male infertility.