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Meenu Kesarwani

Researcher at Cincinnati Children's Hospital Medical Center

Publications -  12
Citations -  367

Meenu Kesarwani is an academic researcher from Cincinnati Children's Hospital Medical Center. The author has contributed to research in topics: Leukemia & Oxalate decarboxylase. The author has an hindex of 8, co-authored 12 publications receiving 296 citations. Previous affiliations of Meenu Kesarwani include Jawaharlal Nehru University.

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Journal ArticleDOI

Oxalate decarboxylase from Collybia velutipes. Molecular cloning and its overexpression to confer resistance to fungal infection in transgenic tobacco and tomato.

TL;DR: Transgenic tobacco and tomato plants expressing oxalate decarboxylase show remarkable resistance to phytopathogenic fungus Sclerotinia sclerotiorum that utilizes oxalic acid during infestation.
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Targeting c-FOS and DUSP1 abrogates intrinsic resistance to tyrosine-kinase inhibitor therapy in BCR-ABL-induced leukemia

TL;DR: It is shown that oncogenic kinase and growth-factor signaling converge to induce the expression of the signaling proteins FBJ osteosarcoma oncogene (c-FOS, encoded by Fos) and dual-specificity phosphatase 1 (DUSP1), which might represent a unifying Achilles' heel of kinase-driven cancers.
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Targeting substrate-site in Jak2 kinase prevents emergence of genetic resistance.

TL;DR: This work reports a novel mechanism of JAK2 kinase inhibition by fedratinib that prevents emergence of genetic resistance and suggests that in order to develop resistance-free kinase inhibitors, the next-generation drug design should target the substrate-binding site.
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Cloning and characterization of the 5'-flanking region of the oxalate decarboxylase gene from Flammulina velutipes.

TL;DR: Results suggest that in F. velutipes cells, activation of OXDC transcription in response to low pH is mediated by the binding of a novel transcription factor through the LPRE site in the OxDC promoter.
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The high NRF2 expression confers chemotherapy resistance partly through up-regulated DUSP1 in myelodysplastic syndromes

TL;DR: This study found that NRF2 expression levels in bone marrow from high-risk patients exceeded that of low-risk MDS patients, and suggested that targetingNRF2 in combination with conventional chemotherapy could pave the way for future therapy for high- risk MDS.