D. Chakrabarti

发表

Gene sequence tags from Plasmodium falciparum genomic DNA fragments prepared by the "genease" activity of mung bean nuclease.

G. Reddy, D. Chakrabarti, S. Schuster, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Cloning and characterization of subunit genes of ribonucleotide reductase, a cell-cycle-regulated enzyme, from Plasmodium falciparum.

D. Chakrabarti, S. Schuster, R. Chakrabarti, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Protein Farnesyltransferase and Protein Prenylation inPlasmodium falciparum *

D. Chakrabarti, T. D. da Silva, J. Barger, 2002, The Journal of Biological Chemistry.

Evidence for the shikimate pathway in apicomplexan parasites

D. Chakrabarti, F. Roberts, C. Roberts, 1998, Nature.

PfPK6, a novel cyclin-dependent kinase/mitogen-activated protein kinase-related protein kinase from Plasmodium falciparum.

D. Chakrabarti, R. Chakrabarti, S. Barik, 2000, The Biochemical journal.

Plasmodium falciparum NIMA-related kinase Pfnek-1: sex specificity and assessment of essentiality for the erythrocytic asexual cycle

Laurent Meijer, Jean-Philippe Semblat, L. Meijer, 2011, Microbiology.

Structurally simple farnesyltransferase inhibitors arrest the growth of malaria parasites.

D. Chakrabarti, F. Buckner, C. Verlinde, 2005, Angewandte Chemie.

Co‐ordinated programme of gene expression during asexual intraerythrocytic development of the human malaria parasite Plasmodium falciparum revealed by microarray analysis

Christian Hott, D. Chakrabarti, J. Dame, 2001, Molecular microbiology.

Chapter 11 – Intracellular signaling

D. Chakrabarti, J. Kelly, L. Ruben, 2003 .

Analysis of Efficiency of Different Distribution Channels for Select Vegetables â€“ An Analytical Study of Telangana Region

D. Chakrabarti, Kavitha Desai, 2020 .

Structurally simple, potent, Plasmodium selective farnesyltransferase inhibitors that arrest the growth of malaria parasites.

D. Chakrabarti, F. Buckner, S. Fletcher, 2006, Journal of medicinal chemistry.

Discovery of fast-acting dual-stage antimalarial agents by profiling pyridylvinylquinoline chemical space via copper catalyzed azide-alkyne cycloadditions.

D. Chakrabarti, Yu Yuan, J. Miao, 2020, European journal of medicinal chemistry.

4-Nitro styrylquinoline is an antimalarial inhibiting multiple stages of Plasmodium falciparum asexual life cycle

D. Chakrabarti, L. Ayong, Yongsheng Zheng, 2017, International journal for parasitology. Drugs and drug resistance.

2-Oxo-tetrahydro-1,8-naphthyridines as selective inhibitors of malarial protein farnesyltransferase and as anti-malarials.

D. Chakrabarti, M. Gelb, C. Verlinde, 2008, Bioorganic & medicinal chemistry letters.

Cyclin-dependent kinase homologues of Plasmodium falciparum.

J. Endicott, D. Chakrabarti, C. Doerig, 2002, International journal for parasitology.

Evidence for prenylation-dependent targeting of a Ykt6 SNARE in Plasmodium falciparum.

D. Chakrabarti, C. M. Allen, J. Mauser, 2011, Molecular and biochemical parasitology.

Structure-activity and structure-property relationship studies of spirocyclic chromanes with antimalarial activity.

D. Chakrabarti, D. Kyle, L. Wojtas, 2022, Bioorganic & medicinal chemistry.

Cloning and characterization of complementary DNA encoding the eukaryotic initiation factor 2-associated 67-kDa protein (p67).

D. Chakrabarti, N. Gupta, T. Kinzy, 1993, The Journal of biological chemistry.

Synthesis, structure-activity relationship and antimalarial efficacy of 6-chloro-2-arylvinylquinolines.

D. Chakrabarti, Yu Yuan, J. Miao, 2020, Journal of medicinal chemistry.

Characterization of a novel serine/threonine protein phosphatase (PfPPJ) from the malaria parasite, Plasmodium falciparum.

D. Chakrabarti, S. Barik, S. Dobson, 2001, Molecular and biochemical parasitology.

Mechanism of protein synthesis inhibition by vaccinia viral core and reversal of this inhibition by reticulocyte peptide chain initiation factors

D. Chakrabarti, N. Gupta, A. Roy, 1987, Journal of Biosciences.

Mechanism of peptide chain initiation in animal cells: A reevaluation

D. Chakrabarti, N. Gupta, 1986, Molecular and Cellular Biochemistry.

Natural mRNA is required for directing Met-tRNA(f) binding to 40S ribosomal subunits in animal cells: involvement of Co-eIF-2A in natural mRNA-directed initiation complex formation.

D. Chakrabarti, N. Gupta, A. Roy, 1988, Biochemistry.

Identification of Bis-Cyclic Guanidines as Antiplasmodial Compounds from Positional Scanning Mixture-Based Libraries

D. Chakrabarti, A. Nefzi, Ginamarie Debevec, 2019, Molecules.

Antiplasmodial Compounds from Deep-Water Marine Invertebrates

S. Pomponi, D. Chakrabarti, M. Diaz, 2021, Marine drugs.

Protein farnesyltransferase inhibitors exhibit potent antimalarial activity.

David K Williams, Patricia C Weber, D. Chakrabarti, 2005, Journal of medicinal chemistry.

Spirocyclic chromanes exhibit antiplasmodial activities and inhibit all intraerythrocytic life cycle stages

D. Chakrabarti, D. Kyle, L. Ayong, 2016, International journal for parasitology. Drugs and drug resistance.

Efficacy, Pharmacokinetics, and Metabolism of Tetrahydroquinoline Inhibitors of Plasmodium falciparum Protein Farnesyltransferase

D. Chakrabarti, M. Gelb, F. Buckner, 2007, Antimicrobial Agents and Chemotherapy.

Microwave-assisted, rapid synthesis of 2-vinylquinolines and evaluation of their antimalarial activity.

D. Chakrabarti, Yuxin Su, Liuyu Huang, 2019, Tetrahedron letters.

Antimalarial Activities of Polyhydroxyphenyl and Hydroxamic Acid Derivatives

D. Chakrabarti, S. Schuster, H. Elford, 1998, Antimicrobial Agents and Chemotherapy.

Potent, Plasmodium-selective farnesyltransferase inhibitors that arrest the growth of malaria parasites: structure-activity relationships of ethylenediamine-analogue scaffolds and homology model validation.

William P. Katt, D. Chakrabarti, M. Gelb, 2008, Journal of medicinal chemistry.

Chemotherapeutics of neglected waterborne parasites: current status and future perspectives.

D. Chakrabarti, R. Chakrabarti, 2009 .

Characterization of a PRL protein tyrosine phosphatase from Plasmodium falciparum.

D. Chakrabarti, R. Chakrabarti, C. M. Allen, 2008, Molecular and biochemical parasitology.

The cell cycle in protozoan parasites.

D. Chakrabarti, K. Matthews, B. Kappes, 2000, Progress in cell cycle research.

Second generation tetrahydroquinoline-based protein farnesyltransferase inhibitors as antimalarials.

D. Chakrabarti, M. Gelb, F. Buckner, 2007, Journal of medicinal chemistry.

Resistance to a Protein Farnesyltransferase Inhibitor in Plasmodium falciparum*

P. Rathod, D. Chakrabarti, M. Gelb, 2005, Journal of Biological Chemistry.

Re-engineering of Yohimbine's Biological Activity through Ring Distortion: Identification and Structure-Activity Relationships of a New Class of Antiplasmodial Agents.

D. Chakrabarti, Srinivasarao Tenneti, R. W. Huigens, 2020, ACS infectious diseases.

Current status of the Plasmodium falciparum genome project.

X. Su, N. Goodman, A. Craig, 1996, Molecular and biochemical parasitology.

Chloroplast-derived vaccine antigens confer dual immunity against cholera and malaria by oral or injectable delivery.

D. Chakrabarti, A. Davoodi-Semiromi, H. Daniell, 2010, Plant biotechnology journal.

Detection of a functional promoter/enhancer in an intron-less human gene encoding a glutamine synthetase-like enzyme.

D. Chakrabarti, R. Chakrabarti, W. Souba, 1995, Gene.

Characterization of a unique aspartate-rich protein of the SET/TAF-family in the human malaria parasite, Plasmodium falciparum, which inhibits protein phosphatase 2A.

D. Chakrabarti, S. Barik, V. Bracchi-Ricard, 2003, Molecular and biochemical parasitology.

A methods‐based biotechnology course for undergraduates

Debopam Chakrabarti, D. Chakrabarti, 2009, Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology.

Identification, Cloning, and Mutational Analysis of the Casein Kinase 1 cDNA of the Malaria Parasite, Plasmodium falciparum

D. Chakrabarti, S. Barik, Russell E. Taylor, 1997, The Journal of Biological Chemistry.

Sequence microheterogeneity of the three small subunit ribosomal RNA genes of Babesia bigemina: expression in erythrocyte culture

G. Roman Reddy, Debopam Chakrabarti, Charles A. Yowell, 1991, Nucleic Acids Res..

Protein prenyl transferase activities of Plasmodium falciparum.

D. Chakrabarti, C. M. Allen, Y. Park, 1998, Molecular and biochemical parasitology.

Identification and Initial Characterization of Three Novel Cyclin-related Proteins of the Human Malaria Parasite Plasmodium falciparum*

D. Chakrabarti, K. L. Le Roch, Shelley Patterson, 2003, Journal of Biological Chemistry.

Global analysis of protein expression and phosphorylation of three stages of Plasmodium falciparum intraerythrocytic development.

Edward L Huttlin, Steven P Gygi, Edward L. Huttlin, 2013, Journal of proteome research.

An atypical cyclin-dependent kinase controls Plasmodium falciparum proliferation rate

D. Chakrabarti, D. Goldberg, L. Tilley, 2013 .

Two Plasmodium falciparum ribonucleotide reductase small subunits, PfR2 and PfR4, interact with each other and are components of the in vivo enzyme complex.

D. Chakrabarti, V. Bracchi-Ricard, David Moe, 2005, Journal of molecular biology.

Cyclic Tetrapeptide HDAC Inhibitors with Improved Plasmodium falciparum Selectivity and Killing Profile.

D. Chakrabarti, R. Cichewicz, L. Du, 2021, ACS infectious diseases.

Roles of Eukaryotic Initiation Factor 2 and Eukaryotic Initiation Factor 2 Ancillary Protein Factors in Eukaryotic Protein Synthesis Initiation

D. Chakrabarti, N. Gupta, N. Nasrin, 1987 .

Pre-replication complex organization in the atypical DNA replication cycle of Plasmodium falciparum: characterization of the mini-chromosome maintenance (MCM) complex formation.

D. Chakrabarti, R. Chakrabarti, Shelley Patterson, 2006, Molecular and biochemical parasitology.

Human Polo-like Kinase Inhibitors as Antiplasmodials.

Edward L. Huttlin, E. Winzeler, S. Gygi, 2023, ACS infectious diseases.

Identification of a family of Rab G-proteins in Plasmodium falciparum and a detailed characterisation of pfrab6.

D. Chakrabarti, G. Langsley, G. Ward, 1996, Molecular and biochemical parasitology.

Molecular machinery of signal transduction and cell cycle regulation in Plasmodium.

D. Chakrabarti, Celia R. S. Garcia, F. Koyama, 2009, Molecular and biochemical parasitology.

Analysis of expressed sequence tags from Plasmodium falciparum.

G. Reddy, D. Chakrabarti, S. Schuster, 1994, Molecular and biochemical parasitology.

Dragmacidin G, a Bioactive Bis-Indole Alkaloid from a Deep-Water Sponge of the Genus Spongosorites

S. Pomponi, D. Chakrabarti, A. Wright, 2017, Marine drugs.

In vitro and in vivo antimalarial activity of peptidomimetic protein farnesyltransferase inhibitors with improved membrane permeability.

D. Chakrabarti, S. Croft, M. Gelb, 2004, Bioorganic & medicinal chemistry.

The Bis(Indolyl)Imidazole Alkaloid Nortopsentin A Exhibits Antiplasmodial Activity

D. Chakrabarti, A. Wright, Stephenie Alvarado, 2013, Antimicrobial Agents and Chemotherapy.

Characterization of protein Ser/Thr phosphatases of the malaria parasite, Plasmodium falciparum: inhibition of the parasitic calcineurin by cyclophilin-cyclosporin complex.

D. Chakrabarti, A. Fairlamb, S. Barik, 1999, Molecular and biochemical parasitology.

A Plasmodium falciparum Transcriptional Cyclin-Dependent Kinase-Related Kinase with a Crucial Role in Parasite Proliferation Associates with Histone Deacetylase Activity

D. Chakrabarti, N. Waters, K. L. Le Roch, 2010, Eukaryotic Cell.

Melatonin-Induced Temporal Up-Regulation of Gene Expression Related to Ubiquitin/Proteasome System (UPS) in the Human Malaria Parasite Plasmodium falciparum

D. Chakrabarti, Célia R. S. Garcia, A. Budu, 2014, International journal of molecular sciences.

DeepMalaria: Artificial Intelligence Driven Discovery of Potent Antiplasmodials

Debopam Chakrabarti, Arash Keshavarzi Arshadi, Milad Salem, 2020, Frontiers in Pharmacology.

Glycosylation of eukaryotic peptide chain initiation factor 2 (eIF-2)-associated 67-kDa polypeptide (p67) and its possible role in the inhibition of eIF-2 kinase-catalyzed phosphorylation of the eIF-2 alpha-subunit.

D. Chakrabarti, N. Gupta, B. Datta, 1989, The Journal of biological chemistry.

Cloning and characterization of Plasmodium falciparum ADP-ribosylation factor and factor-like genes.

D. Chakrabarti, D. Goldberg, S. Francis, 1997, Molecular and biochemical parasitology.

Functional characterisation of the regulatory subunit of cyclic AMP-dependent protein kinase A homologue of Giardia lamblia: Differential expression of the regulatory and catalytic subunits during encystation.

D. Chakrabarti, R. Chakrabarti, Brian C. Schanen, 2006, International journal for parasitology.

Characterization of the rDNA unit and sequence analysis of the small subunit rRNA and 5.8S rRNA genes from Tritrichomonas foetus.

R. Gutell, D. Chakrabarti, J. Dame, 1992, Molecular and biochemical parasitology.

Activation of a Plasmodium falciparum cdc2-related Kinase by Heterologous p25 and Cyclin H

Barbara Kappes, Laurent Meijer, L. Meijer, 2000, The Journal of Biological Chemistry.

Molecular characterization and expression of an alternate proliferating cell nuclear antigen homologue, PfPCNA2, in Plasmodium falciparum.

D. Chakrabarti, Shelley Patterson, Christina M. Whittle, 2002, Biochemical and biophysical research communications.

Avelumab (anti–PD-L1) in combination with crizotinib or lorlatinib in patients with previously treated advanced NSCLC: Phase 1b results from JAVELIN Lung 101.

D. Chakrabarti, A. Shaw, E. Felip, 2018 .

Ubiquitin proteasome system and the atypical kinase PfPK7 are involved in melatonin signaling in Plasmodium falciparum

D. Chakrabarti, Celia R. S. Garcia, R. Y. Ribeiro, 2012, Journal of pineal research.

Protein synthesis in rabbit reticulocytes: Mg2+-inhibition of ternary complex (Met-tRNA(f).eIF-2.GTP) formation by reticulocyte eIF-2.

D. Chakrabarti, N. Gupta, A. Roy, 1987, Biochemical and biophysical research communications.

Protein synthesis in rabbit reticulocytes. A study of the mechanism of Co-eIF-2 action.

D. Chakrabarti, N. Gupta, B. Datta, 1985, The Journal of biological chemistry.

The Longin Domain Regulates the Steady-State Dynamics of Sec22 in Plasmodium falciparum

D. Chakrabarti, D. Fidock, A. Raghavan, 2009, Eukaryotic Cell.

Characterization of Plasmodium falciparum Atypical Kinase PfPK7- Dependent Phosphoproteome.

Edward L Huttlin, Steven P Gygi, Ratna Chakrabarti, 2018, Journal of proteome research.

Plasmodium falciparum: the small GTPase rab11.

D. Chakrabarti, G. Langsley, 1996, Experimental parasitology.

Spatially resolved micro-absorption spectroscopy with a broadband source and confocal detection

D. Chakrabarti, A. Schulte, J. Mauser, 2015 .

Characterization of an eukaryotic peptide deformylase from Plasmodium falciparum.

D. Chakrabarti, P. Rajagopalan, D. Pei, 2001, Archives of biochemistry and biophysics.

Marine Microbiome as a Source of Antimalarials

D. Chakrabarti, A. Carbonell, A. Wright, 2019, Tropical medicine and infectious disease.

Identification of Plasmodium falciparum family of SNAREs.

D. Chakrabarti, G. Pagnotti, Lawrence Ayong, 2007, Molecular and biochemical parasitology.

A multicentre, international, randomised, open-label phase 3 trial of avelumab + best supportive care (BSC) vs BSC alone as maintenance therapy after first-line platinum-based chemotherapy in patients with advanced urothelial cancer (JAVELIN bladder 100)

D. Chakrabarti, T. Powles, D. Petrylak, 2016 .

Reply: Shikimate pathway in apicomplexan parasites

J. Finnerty, D. Chakrabarti, F. Roberts, 1999, Nature.

PfPK7, an atypical MEK‐related protein kinase, reflects the absence of classical three‐component MAPK pathways in the human malaria parasite Plasmodium falciparum

D. Chakrabarti, Shelley Patterson, Christina M. Whittle, 2004, Molecular microbiology.

An RCC1-type guanidine exchange factor for the Ran G protein is found in the Plasmodium falciparum nucleus.

D. Chakrabarti, A. Sultan, D. Arnot, 1998, Molecular and biochemical parasitology.

LBA17RANDOMISED STUDY OF AXITINIB (AXI) PLUS BEST SUPPORTIVE CARE (BSC) VERSUS PLACEBO (PBO) PLUS BSC IN PATIENTS WITH ADVANCED HEPATOCELLULAR CARCINOMA (HCC) FOLLOWING PRIOR ANTIANGIOGENIC THERAPY

D. Chakrabarti, M. Kudo, T. Yau, 2014 .

Second generation tetrahydroquinoline-based protein farnesyltransferase inhibitors as antimalarials.

D. Chakrabarti, F. Buckner, C. Verlinde, 2007, Journal of medicinal chemistry.

Randomized phase II study of axitinib versus placebo plus best supportive care in second-line treatment of advanced hepatocellular carcinoma.

D. Chakrabarti, M. Casey, M. Kudo, 2015, Annals of oncology : official journal of the European Society for Medical Oncology.