P
Pranjal Biswas
Researcher at University of Calcutta
Publications - 17
Citations - 178
Pranjal Biswas is an academic researcher from University of Calcutta. The author has contributed to research in topics: Schizosaccharomyces pombe & Heme. The author has an hindex of 6, co-authored 13 publications receiving 120 citations. Previous affiliations of Pranjal Biswas include University of Nebraska Medical Center & Cleveland Clinic Lerner Research Institute.
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Journal ArticleDOI
Nitric oxide production by necrotrophic pathogen Macrophomina phaseolina and the host plant in charcoal rot disease of jute: complexity of the interplay between necrotroph-host plant interactions.
TL;DR: Interestingly, M. phaseolina was found to produce nitric oxide which was detected in vitro inside the mycelium and in the surrounding medium and may have important physiological significance in necrotrophic host pathogen interaction.
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The extracellular role of DNA damage repair protein APE1 in regulation of IL-6 expression
Somsubhra Nath,Shrabasti Roychoudhury,Matthew J. Kling,Heyu Song,Pranjal Biswas,Ashima Shukla,Hamid Band,Shantaram S. Joshi,Kishor K. Bhakat +8 more
TL;DR: It is found that monocytes secrete APE1 upon inflammatory challenges and it is shown that APE 1 is secreted through extracellular vesicles formation via endosomal sorting complex required for transport (ESCRT)-dependent pathway.
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Regulation of cell cycle and stress responses under nitrosative stress in Schizosaccharomyces pombe.
TL;DR: A novel molecular mechanism of cell cycle control under nitrosative stress is proposed based on the experimental results and bioinformatics analysis of the fission yeast Schizosaccharomyces pombe.
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Targeting Histone Chaperone FACT Complex Overcomes 5-Fluorouracil Resistance in Colon Cancer
Heyu Song,Jiping Zeng,Shrabasti Roychoudhury,Pranjal Biswas,Bhopal Mohapatra,Sutapa Ray,Kayvon Dowlatshahi,Jing Wang,Vimla Band,Geoffrey A. Talmon,Kishor K. Bhakat +10 more
TL;DR: Targeting the FACT complex with curaxins significantly improves the 5-FU efficacy in dMMR colorectal cancer in vitro (∼50-fold decrease in IC50) and in vivo xenograft models.
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Myoglobin maturation is driven by the hsp90 chaperone machinery and by soluble guanylyl cyclase.
TL;DR: It is suggested that hsp90 works in concert with cochaperons and an active sGC‐cGMP signaling pathway to promote heme insertion into immature apo‐Mb, and thus generate functional Mb during muscle myotube formation.