Debosreeta Bose

发表

Interaction of NPC2 protein with Lysobisphosphatidic Acid is required for normal endolysosomal cholesterol trafficking

P. Kahn, J. Storch, O. Ilnytska, 2019, bioRxiv.

Photophysics and rotational dynamics of a beta-carboline analogue in nonionic micelles: effect of variation of length of the headgroup and the tail of the surfactant.

A. Girigoswami, N. Chattopadhyay, D. Sarkar, 2009, The journal of physical chemistry. B.

Excited state intramolecular proton transfer of 2-hydroxy-1-naphthaldehyde semicarbazone: A combined fluorometric and quantum chemical study

N. Chattopadhyay, Sayanti Datta, Debosreeta Bose, 2011 .

Differential interaction of beta-cyclodextrin with lipids of varying surface charges: a spectral deciphering using a cationic phenazinium dye.

N. Chattopadhyay, D. Sarkar, Debanjana Ghosh, 2010, The journal of physical chemistry. B.

Spectroscopic exploration of mode of binding of ctDNA with 3-hydroxyflavone: a contrast to the mode of binding with flavonoids having additional hydroxyl groups.

S. Senapati, N. Chattopadhyay, Debanjana Ghosh, 2012, The journal of physical chemistry. B.

Photophysics and rotational relaxation dynamics of a beta-carboline based fluorophore in cationic alkyltrimethylammonium bromide micelles.

N. Chattopadhyay, D. Sarkar, Paramita Das, 2009, Journal of colloid and interface science.

Studies of Triton X-165-beta-cyclodextrin interactions using both extrinsic and intrinsic fluorescence.

N. Chattopadhyay, B. Bhattacharya, D. Sarkar, 2010, Journal of colloid and interface science.

Binding of a cationic phenazinium dye in anionic liposomal membrane: a spectacular modification in the photophysics.

A. Girigoswami, N. Chattopadhyay, D. Sarkar, 2010, Chemistry and physics of lipids.

Probing the binding interaction of zinc (II) Schiff bases with bovine serum albumin: A spectroscopic and molecular docking study

J. Mukhopadhyay, D. Das, Madhumita Mukhopadhyay, 2021 .

Photophysics and rotational relaxation dynamics of cationic phenazinium dyes in anionic reverse micelles: Effect of methyl substitution.

A. Girigoswami, N. Chattopadhyay, D. Sarkar, 2009, The Journal of chemical physics.

Photometric Study of the Interaction of Zinc (II) Complexes of Schiff Bases with Cetyltrimethyl Ammonium Bromide

A. Pandey, Madhumita Mukhopadhyay, Sanchari Dasgupta, 2019, Macromolecular Symposia.

Supramolecular Arrangement and DFT analysis of Zinc(II) Schiff Bases: An Insight towards the Influence of Compartmental Ligands on Binding Interaction with Protein

J. Mukhopadhyay, Y. Akinay, Saumya Dasgupta, 2022, ChemistryOpen.

Structure-function relationships of cholesterol mobilization from the endo-lysosome compartment of NPC1-deficient human cells by β-CD polyrotaxanes

J. Storch, Bradley P. Loren, David H. Thompson, 2022, PloS one.

Intracellular cholesterol trafficking is dependent upon NPC2 interaction with lysobisphosphatidic acid

P. Kahn, J. Storch, O. Ilnytska, 2019, eLife.

Multiple emissions of benzil at room temperature and 77 K and their assignments from ab initio quantum chemical calculations.

N. Chattopadhyay, B. Bhattacharya, Debosreeta Bose, 2011, The Journal of chemical physics.

Functionalization of Doped ZnO through Solution Route Synthesis: A study Using Spectroscopy & Density of States

Poulami Roy, Madhumita Mukhopadhyay, S. Sutradhar, 2021, Biointerface Research in Applied Chemistry.

Probing the Binding Interaction of a Phenazinium Dye with Serum Transport Proteins: A Combined Fluorometric and Circular Dichroism Study

N. Chattopadhyay, D. Sarkar, Debosreeta Bose, 2010, Photochemistry and photobiology.

Understanding the Excited State Intramolecular Proton Transfer Phenomena of 2‐Hydroxy‐3‐Naphthaldehyde Thiosemicarbazone

Madhumita Mukhopadhyay, Debosreeta Bose, Akash Sil, 2023, Macromolecular Symposia.

DFT Analyses of arsylsemicarbazone group as functional compound for application as excellent fluorescent probes and medicament: study on virtual screening through molecular docking

Madhumita Mukhopadhyay, Debosreeta Bose, Akash Sil, 2024, Chemical Papers.