Manisha Das

ORCID: 0000-0002-0067-9186
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About
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Research Areas
  • Magnetism in coordination complexes
  • Metal complexes synthesis and properties
  • Metal-Organic Frameworks: Synthesis and Applications
  • Metal-Catalyzed Oxygenation Mechanisms
  • Cancer Cells and Metastasis
  • Cancer Treatment and Pharmacology
  • Fuel Cells and Related Materials
  • Hemoglobinopathies and Related Disorders
  • Adenosine and Purinergic Signaling
  • Iron Metabolism and Disorders
  • Biochemical and Molecular Research
  • Electron Spin Resonance Studies
  • Signaling Pathways in Disease
  • COVID-19 Clinical Research Studies
  • Computational Drug Discovery Methods
  • Fluorine in Organic Chemistry
  • SARS-CoV-2 and COVID-19 Research
  • Endoplasmic Reticulum Stress and Disease
  • Synthesis and Reactions of Organic Compounds
  • Global Maternal and Child Health
  • COVID-19 Impact on Reproduction
  • HER2/EGFR in Cancer Research
  • Parasitic Infections and Diagnostics
  • Click Chemistry and Applications
  • Lanthanide and Transition Metal Complexes

Dhaka Medical College and Hospital
2024-2025

University of Cincinnati
2022-2023

University of Cincinnati Medical Center
2023

Biomedical Research Foundation
2022

Indian Institute of Technology Kharagpur
2018-2019

Johns Hopkins University
2014-2018

Johns Hopkins Medicine
2014-2018

State University of New York
2009-2012

Stony Brook University
2009-2012

Growing evidence suggests that the majority of tumors are organized hierarchically, comprising a population tumor-initiating, or cancer stem cells (CSCs) responsible for tumor development, maintenance and resistance to drugs. Previously we have shown CD133high/CD44high fraction colon is different from their bulk counterparts at functional, morphological genomic levels. In contrast expressing moderate levels CD133, CD44 CD166, with high combined expression CD133 possessed several...

10.1186/1476-4598-9-192 article EN cc-by Molecular Cancer 2010-01-01

Background and Purpose Finding new indications for existing drugs, also known as drug repositioning or repurposing, is a powerful approach to accelerate discovery development. The unfolded protein response pathways have been proposed be viable target developing anticancer drugs. Experimental Approach We screened the J ohns H opkins D rug L ibrary inhibitors of prostate cancer cell proliferation identify antiprostate treatments among systematically investigated mechanism underlying activity...

10.1111/bph.12800 article EN British Journal of Pharmacology 2014-06-06

e16475 Background: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal of gastrointestinal tract, primarily driven by KIT or PDGFRA mutations. Imatinib has transformed GIST treatment; however, resistance typically emerges within 20–24 months, necessitating effective second-line therapies such as sunitinib, regorafenib, ripretinib, and masitinib. Methods: A Bayesian network meta-analysis 17 studies including 2,422 patients evaluated efficacy tyrosine kinase inhibitors...

10.1200/jco.2025.43.16_suppl.e16475 article EN Journal of Clinical Oncology 2025-05-28

Ligand backbone alteration leads to different mechanisms for catecholase activity and order of interaction with DNA molecules.

10.1039/c8dt04183k article EN Dalton Transactions 2018-12-13

Competitive bridging modes of HO<sup>−</sup> and NCS<sup>−</sup> were explored for four Ni<sup>II</sup>-based coordination aggregates in cubane dicubane topology.

10.1039/c8nj03269f article EN New Journal of Chemistry 2018-01-01

Enforced coordination by NO<sub>3</sub><sup>−</sup>, ClO<sub>4</sub><sup>−</sup> and CF<sub>3</sub>COO<sup>−</sup> groups resulted in the formation of [Cu<sub>2</sub>] (<bold>1</bold>), [Cu<sub>4</sub>] (<bold>2</bold>) [Cu<sub>5</sub>] (<bold>3</bold>) complexes using H<sub>5</sub>L1.

10.1039/c8nj02131g article EN New Journal of Chemistry 2018-01-01

Abstract Simultaneous incorporation of both Co II and III ions within a new thioether S‐bearing phenol‐based ligand system, H 3 L (2,6‐bis‐[{2‐(2‐hydroxyethylthio)ethylimino}methyl]‐4‐methylphenol) formed [Co 5 ] aggregates 4 2 ( μ ‐OH) 1,3 ‐O CCH ) ](ClO ⋅H O 1 CC ). The magnetic studies revealed axial zero‐field splitting (ZFS) parameter, D / hc =−23.6 −24.3 cm −1 , E =0.03 0.00, respectively for . Dynamic data confirmed the complexes as SIMs with U eff /k B =30 K 33 ), τ 0 =9.1×10 −8 s...

10.1002/asia.201901109 article EN Chemistry - An Asian Journal 2019-09-23

The Schiff base ligand HL1 ({2,6-bis(allylimino)methyl}-4-methylphenol) having no coordinating donor arm has been examined for its reaction medium and ancillary bridge dependent reactivity a hierarchical family of CuII complexes. showed unique pattern toward in solution. bridging nature situ generated HO- ions the absence presence externally added carboxylates (RCOO-; R = CF3, C6H5 CH3) utilized to produce complexes {[Cu2(μ-L2)2(H2O)]2[Cu2(μ-L2)2(H2O)2](ClO4)6} (1) (HL2...

10.1039/c8dt03390k article EN Dalton Transactions 2018-01-01

Abstract This study aimed to investigate thalassemia awareness and prevention among university students in Bangladesh, with a focus on demographic factors, attitudes, opinions regarding safe marriage influencing their knowledge behavior. Key findings showed that 54% of the participants were female, emphasizing need for targeted educational efforts address gender disparity. Furthermore, 92% unmarried, highlighting importance preventive measures this group. Science exhibited higher levels...

10.21203/rs.3.rs-3801245/v1 preprint EN cc-by Research Square (Research Square) 2023-12-29

Abstract In vast majority of human cancers, malignant stem cells (CSCs) are responsible for tumor development, maintenance and resistance to drugs. Previously we have shown that colon prostate CSCs not only functionally morphologically different from their bulk counterparts, but themselves may represent heterogeneous phenotypic populations. contrast the major (bulk) cancer expressing low levels CD133 CD44, with a high combined expression these markers, as well lacking CD133, possessed...

10.1158/1538-7445.am10-3331 article EN Cancer Research 2010-04-01

&lt;p&gt;Rapamycin and FK506 are macrocyclic natural products with an extraordinary mode of action, in which they form binary complexes FK506-binding protein (FKBP) through a shared FKBP-binding domain before forming ternary their respective targets, mechanistic target rapamycin (mTOR) calcineurin, respectively. Inspired by this, we sought to build rapamycin-like macromolecule library new cellular proteins replacing the effector combinatorial oligopeptides. We developed robust...

10.32920/21979724.v1 preprint EN 2023-01-30

&lt;p&gt;Rapamycin and FK506 are macrocyclic natural products with an extraordinary mode of action, in which they form binary complexes FK506-binding protein (FKBP) through a shared FKBP-binding domain before forming ternary their respective targets, mechanistic target rapamycin (mTOR) calcineurin, respectively. Inspired by this, we sought to build rapamycin-like macromolecule library new cellular proteins replacing the effector combinatorial oligopeptides. We developed robust...

10.32920/21979724 preprint EN 2023-01-30

10.1016/s0735-1097(23)04176-1 article EN publisher-specific-oa Journal of the American College of Cardiology 2023-03-01
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