F
Farhana Yasmin
Researcher at University of Chittagong
Publications - 6
Citations - 92
Farhana Yasmin is an academic researcher from University of Chittagong. The author has contributed to research in topics: Epitope & Minimum bactericidal concentration. The author has an hindex of 2, co-authored 6 publications receiving 41 citations.
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Journal Article
Outcome of neonatal hyperbilirubinemia in a tertiary care hospital in bangladesh.
TL;DR: ABO incompatibility is twice as common as Rh incompatibility and the majority of kernicterus patients died in the acute phase, according to this study.
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Epitope-based universal vaccine for Human T-lymphotropic virus-1 (HTLV-1).
TL;DR: In this article, the conformational linear B-cell and T-cell epitopes for HTLV-1 TAX viral protein have been predicted for their possible collective use as vaccine candidates.
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Immunoinformatics approach to designing a multi-epitope vaccine against Saint Louis Encephalitis Virus
Md. Shakhawat Hossain,Mohammad Imran Hossan,Shagufta Mizan,Abu Tayab Moin,Farhana Yasmin,Al-Shahriar Akash,Shams Nur Powshi,A.K Rafeul Hasan,Afrin Sultana Chowdhury +8 more
TL;DR: Although the computational assays used in this study returned defensible results, further validation of the proposed vaccine candidate is required through in vitro and in vivo experiments to comment on its circumstantial efficacy.
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Monosaccharide derivatives: synthesis, antimicrobial, pass, antiviral and molecular docking studies against sars-cov-2 m-pro inhibitors
Farhana Yasmin,Mohammed R. Amin,Mohammed Anowar Hosen,Mohammed Z. H. Bulbul,Sujan Dey,Sarkar M. A. Kawsar +5 more
TL;DR: In this paper, a series of methyl alpha-D-mannopyranoside derivatives (2-6) were synthesized through facile regioselective acylation, using the direct method affording 6-O-(3-chlorobenzoyl) derivatives.
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Synthesis, Antimicrobial, Anticancer, PASS, Molecular Docking, Molecular Dynamic Simulations & Pharmacokinetic Predictions of Some Methyl β-D-Galactopyranoside Analogs.
Md. Ruhul Amin,Farhana Yasmin,Mohammed Anowar Hosen,Sujan Dey,Shafi Mahmud,Md. Abu Saleh,Talha Bin Emran,Imtiaj Hasan,Yuki Fujii,Masao Yamada,Yasuhiro Ozeki,Sarkar M. A. Kawsar +11 more
TL;DR: A series of methyl β-D-galactopyranoside (MGP, 1) analogs were selectively acylated with cinnamoyl chloride in anhydrous N,N-dimethylformamide/triethylamine to yield 6-O-substitution products, which were subsequently converted into 2,3,4-tri-Oacyl analogs with different acyl halides as mentioned in this paper.