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S.M. Khaledur Rahman

Researcher at Kagawa University

Publications -  7
Citations -  94

S.M. Khaledur Rahman is an academic researcher from Kagawa University. The author has contributed to research in topics: Medicine & Disease. The author has an hindex of 2, co-authored 4 publications receiving 26 citations. Previous affiliations of S.M. Khaledur Rahman include Jessore University of Science & Technology.

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Programmable Molecular Scissors: Applications of a New Tool for Genome Editing in Biotech

TL;DR: The progress toward editable nuclease-based therapies and the minimization of off-target mutagenesis are described and the future prospects of this challenging scientific field are discussed.
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Roles of Endocannabinoids and Endocannabinoid-Like Molecules in Energy Homeostasis and Metabolic Regulation: A Nutritional Perspective.

TL;DR: In this article, the authors outline the structure, metabolism, and biological activities of endocannabinoids and related molecules, and focus on their involvement in energy homeostasis and metabolic regulation.
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Emerging SARS-CoV-2 Variants and Subvariants: Challenges and Opportunities in the Context of COVID-19 Pandemic

TL;DR: It is suggested that the global healthcare organizations can decide on the declaration of the end of the pandemic phase of COVID-19 soon and the covid-19 will continue, and the currently dominant Omicron subvariants and the effectiveness of antiviral agents and vaccines are discussed.
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Increased serum resistin but not G-CSF levels are associated in the pathophysiology of major depressive disorder: Findings from a case-control study

TL;DR: Higher serum resistin levels are suggested to be associated with the pathophysiology of major depressive disorder, and this elevated serum Resistin level may serve as an early risk assessment indicator for MDD.
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Involvement of the γ Isoform of cPLA2 in the Biosynthesis of Bioactive N-Acylethanolamines.

TL;DR: In this article, the authors investigated a possible involvement of isoforms other than ǫ in the NAE biosynthesis, and they showed that when the cells overexpressing one of the cPLA2 isoforms were labeled with [14C]ethanolamine, the increase in the production of [ 14C]NAPE was observed only with the Ãǫ-expressing cells.