BAMA CHARAN MONDAL
@bhu.ac.in
Scopus Publications
- Red-Emitting Glutathione-Templated Copper Nanoclusters for Fluorescence Enhancement–Based Detection of Arsenic(III) Contamination in Water
Vaibhav Arya, Sova Yadav, Deepak Maurya, Bama Charan Mondal, Samantapudi Venkata Satyanarayana Raju, Chandra Shekhar Pati Tripathi, Debanjan Guin
ACS Applied Nano Materials, 2026
Arsenic contamination in drinking water continues to pose serious risks to public health, particularly because detection of its most toxic trivalent form remains a challenge. In this work, glutathione-templated copper nanoclusters (Cu NCs) were prepared via a chemical reduction approach, yielding red-emissive, water-dispersible, and stable nanoprobes. These Cu NCs show weak photoluminescence at 644 nm when excited at 370 nm, and their fluorescence is notably enhanced in the presence of As 3+ due to aggregation-induced emission. The sensing approach allows reliable quantification of As 3+ down to 1.27 μM with excellent linearity ( R 2 = 0.9995), high reproducibility across multiple measurements, and high selectivity against common metal ions, nonmetallic interferents, and complex biological matrices. The method was successfully validated using MCF-7 cell lysates and Drosophila melanogaster gut tissues, where significant fluorescence enhancement ( p < 0.01) confirmed As 3+ detection. The Cu NCs also enable clear fluorescence imaging of intracellular As 3+ in Drosophila melanogaster tissues and MCF-7 human cell lines, demonstrating increased fluorescence both within the tissue and at the cellular level, which confirms their biocompatibility and suitability for biological studies. Structural and surface analyses (TEM, AFM, FTIR, XPS) show that the nanoclusters are consistently templated and well-formed. Overall, this study demonstrates that GSH-templated Cu NCs are scalable and cost-effective as practical probes for both As 3+ detection and bioimaging, making routine monitoring of environmental and biological arsenic exposure possible. - Protocol to study DNA strand breaks during development and apoptosis using in situ nick translation in Drosophila
Deepak Maurya, Bama Charan Mondal
STAR Protocols, 2025
Cellular stress causes DNA strand breaks that are typically repaired to maintain homeostasis and regulate cell fate. However, unrepaired DNA breaks can be lethal, leading to cell death. Here, we present a protocol to study DNA strand breaks in Drosophila during development and apoptosis using in situ nick translation. We describe the steps for labeling DNA strand breaks using digoxigenin (DIG)-labeled nucleotide (DIG-11-dUTP) and visualizing them with anti-DIG immunostaining. We then detail procedures for mounting, imaging, and analysis. For complete details on the use and execution of this protocol, please refer to Maurya et al. 1 and Rigby et al. 2 - One-Step Room Temperature Synthesis of Printable Carbon Quantum Dots Ink for Visual Encryption and High-Performance Photodetector
Baishali Thakurta, Sobhan Hazra, Alapan Samanta, Adnan Nasir, Amresh Kumar Singh, Deepak Maurya, Bama Charan Mondal, Anupam Giri, Bhola Nath Pal, Monalisa Pal
Advanced Optical Materials, 2024
Carbon quantum dots (CQDs) have emerged as promising materials for optoelectronic applications and have garnered much interest as potential competitors to conventional inorganic or hybrid semiconductor quantum dots because of carbon's intrinsic merits of high stability, low cost, and environment‐friendliness. The ability of easy formulation of functional ink of CQDs is necessary for the development of industrial‐scale, reliable, inexpensive printing/coating processes, for its full exploitation in the ever‐growing class of applications in sensors, optoelectronics, and energy storage and conversion. Here a facile one‐step room‐temperature synthesis of printable, fluorescent CQD ink is demonstrated. The as‐synthesized fluorescent CQD ink is used for invisible fingerprint stamps, printing of micro‐patterns, and soft lithographic patterning with a resolution down to 1.5 µm. This functional CQD ink is also used to fabricate a high‐performance CQD‐ZnO heterojunction ultraviolet (UV) photodetector with a photo‐responsivity of 3.85 A W−1, detectivity of 6.78 × 1010 Jones, and an external quantum efficiency (EQE) of 15.3%. The enhanced device performance can be attributed to CQD's high photocurrent generation efficiency and rational combination of the asymmetric electrode materials. This work enables a high‐temperature stable CQD fluorescent ink synthesis method to fulfill the processing requirements of printing and soft lithographic patterning for visual encryption and optoelectronics. - Wnt signaling couples G2 phase control with differentiation during hematopoiesis in Drosophila
Lauren M. Goins, Juliet R. Girard, Bama Charan Mondal, Sausan Buran, Chloe C. Su, Ruby Tang, Titash Biswas, Jessica A. Kissi, Utpal Banerjee
Developmental Cell, 2024 - Transient caspase-mediated activation of caspase-activated DNase causes DNA damage required for phagocytic macrophage differentiation
Deepak Maurya, Gayatri Rai, Debleena Mandal, Bama Charan Mondal
Cell Reports, 2024
Phagocytic macrophages are crucial for innate immunity and tissue homeostasis. Most tissue-resident macrophages develop from embryonic precursors that populate every organ before birth to lifelong self-renew. However, the mechanisms for versatile macrophage differentiation remain unknown. Here, we use in vivo genetic and cell biological analysis of the Drosophila larval hematopoietic organ, the lymph gland that produces macrophages. We show that the developmentally regulated transient activation of caspase-activated DNase (CAD)-mediated DNA strand breaks in intermediate progenitors is essential for macrophage differentiation. Insulin receptor-mediated PI3K/Akt signaling regulates the apoptosis signal-regulating kinase 1 (Ask1)/c-Jun kinase (JNK) axis to control sublethal levels of caspase activation, causing DNA strand breaks during macrophage development. Furthermore, caspase activity is also required for embryonic-origin macrophage development and efficient phagocytosis. Our study provides insights into developmental signaling and CAD-mediated DNA strand breaks associated with multifunctional and heterogeneous macrophage differentiation. - A functional genomics screen identifying blood cell development genes in Drosophila by undergraduates participating in a course-based research experience
Cory J Evans, John M Olson, Bama Charan Mondal, Pratyush Kandimalla, Ariano Abbasi, Mai M Abdusamad, Osvaldo Acosta, Julia A Ainsworth, Haris M Akram, Ralph B Albert, Elitzander Alegria-Leal, Kai Y Alexander, Angelica C Ayala, Nataliya S Balashova, Rebecca M Barber, Harmanjit Bassi, Sean P Bennion, Miriam Beyder, Kush V Bhatt, Chinmay Bhoot, Aaron W Bradshaw, Tierney G Brannigan, Boyu Cao, Yancey Y Cashell, Timothy Chai, Alex W Chan, Carissa Chan, Inho Chang, Jonathan Chang, Michael T Chang, Patrick W Chang, Stephen Chang, Neel Chari, Alexander J Chassiakos, Iris E Chen, Vivian K Chen, Zheying Chen, Marsha R Cheng, Mimi Chiang, Vivian Chiu, Sharon Choi, Jun Ho Chung, Liset Contreras, Edgar Corona, Courtney J Cruz, Renae L Cruz, Jefferson M Dang, Suhas P Dasari, Justin R O De La Fuente, Oscar M A Del Rio, Emily R Dennis, Petros S Dertsakyan, Ipsita Dey, Rachel S Distler, Zhiqiao Dong, Leah C Dorman, Mark A Douglass, Allysen B Ehresman, Ivy H Fu, Andrea Fua, Sean M Full, Arash Ghaffari-Rafi, Asmar Abdul Ghani, Bosco Giap, Sonia Gill, Zafar S Gill, Nicholas J Gills, Sindhuja Godavarthi, Talin Golnazarian, Raghav Goyal, Ricardo Gray, Alexander M Grunfeld, Kelly M Gu, Natalia C Gutierrez, An N Ha, Iman Hamid, Ashley Hanson, Celesti Hao, Chongbin He, Mengshi He, Joshua P Hedtke, Ysrael K Hernandez, Hnin Hlaing, Faith A Hobby, Karen Hoi, Ashley C Hope, Sahra M Hosseinian, Alice Hsu, Jennifer Hsueh, Eileen Hu, Spencer S Hu, Stephanie Huang, Wilson Huang, Melanie Huynh, Carmen Javier, Na Eun Jeon, Sunjong Ji, Jasmin Johal, Amala John, Lauren Johnson, Saurin Kadakia, Namrata Kakade, Sarah Kamel, Ravinder Kaur, Jagteshwar S Khatra, Jeffrey A Kho, Caleb Kim, Emily Jin-Kyung Kim, Hee Jong Kim, Hyun Wook Kim, Jin Hee Kim, Seong Ah Kim, Woo Kyeom Kim, Brian Kit, Cindy La, Jonathan Lai, Vivian Lam, Nguyen Khoi Le, Chi Ju Lee, Dana Lee, Dong Yeon Lee, James Lee, Jason Lee, Jessica Lee, Ju-Yeon Lee, Sharon Lee, Terrence C Lee, Victoria Lee, Amber J Li, Jialing Li, Alexandra M Libro, Irvin C Lien, Mia Lim, Jeffrey M Lin, Connie Y Liu, Steven C Liu, Irene Louie, Shijia W Lu, William Y Luo, Tiffany Luu, Josef T Madrigal, Yishan Mai, Darron I Miya, Mina Mohammadi, Sayonika Mohanta, Tebogo Mokwena, Tonatiuh Montoya, Dallas L Mould, Mark R Murata, Janani Muthaiya, Seethim Naicker, Mallory R Neebe, Amy Ngo, Duy Q Ngo, Jamie A Ngo, Anh T Nguyen, Huy C X Nguyen, Rina H Nguyen, Thao T T Nguyen, Vincent T Nguyen, Kevin Nishida, Seo-Kyung Oh, Kristen M Omi, Mary C Onglatco, Guadalupe Ortega Almazan, Jahzeel Paguntalan, Maharshi Panchal, Stephanie Pang, Harin B Parikh, Purvi D Patel, Trisha H Patel, Julia E Petersen, Steven Pham, Tien M Phan-Everson, Megha Pokhriyal, Davis W Popovich, Adam T Quaal, Karl Querubin, Anabel Resendiz, Nadezhda Riabkova, Fred Rong, Sarah Salarkia, Nateli Sama, Elaine Sang, David A Sanville, Emily R Schoen, Zhouyang Shen, Ken Siangchin, Gabrielle Sibal, Garuem Sin, Jasmine Sjarif, Christopher J Smith, Annisa N Soeboer, Cristian Sosa, Derek Spitters, Bryan Stender, Chloe C Su, Jenny Summapund, Beatrice J Sun, Christine Sutanto, Jaime S Tan, Nguon L Tan, Parich Tangmatitam, Cindy K Trac, Conny Tran, Daniel Tran, Duy Tran, Vina Tran, Patrick A Truong, Brandon L Tsai, Pei-Hua Tsai, C Kimberly Tsui, Jackson K Uriu, Sanan Venkatesh, Maique Vo, Nhat-Thi Vo, Phuong Vo, Timothy C Voros, Yuan Wan, Eric Wang, Jeffrey Wang, Michael K Wang, Yuxuan Wang, Siman Wei, Matthew N Wilson, Daniel Wong, Elliott Wu, Hanning Xing, Jason P Xu, Sahar Yaftaly, Kimberly Yan, Evan Yang, Rebecca Yang, Tony Yao, Patricia Yeo, Vivian Yip, Puja Yogi, Gloria Chin Young, Maggie M Yung, Alexander Zai, Christine Zhang, Xiao X Zhang, Zijun Zhao, Raymond Zhou, Ziqi Zhou, Mona Abutouk, Brian Aguirre, Chon Ao, Alexis Baranoff, Angad Beniwal, Zijie Cai, Ryan Chan, Kenneth Chang Chien, Umar Chaudhary, Patrick Chin, Praptee Chowdhury, Jamlah Dalie, Eric Y Du, Alec Estrada, Erwin Feng, Monica Ghaly, Rose Graf, Eduardo Hernandez, Kevin Herrera, Vivien W Ho, Kaitlyn Honeychurch, Yurianna Hou, Jo M Huang, Momoko Ishii, Nicholas James, Gah-Eun Jang, Daphne Jin, Jesse Juarez, Ayse Elif Kesaf, Sat Kartar Khalsa, Hannah Kim, Jenna Kovsky, Chak Lon Kuang, Shraddha Kumar, Gloria Lam, Ceejay Lee, Grace Lee, Li Li, Joshua Lin, Josephine Liu, Janice Ly, Austin Ma, Hannah Markovic, Cristian Medina, Jonelle Mungcal, Bilguudei Naranbaatar, Kayla Patel, Lauren Petersen, Amanda Phan, Malcolm Phung, Nadiyah Priasti, Nancy Ruano, Tanveer Salim, Kristen Schnell, Paras Shah, Jinhua Shen, Nathan Stutzman, Alisa Sukhina, Rayna Tian, Andrea Vega-Loza, Joyce Wang, Jun Wang, Rina Watanabe, Brandon Wei, Lillian Xie, Jessica Ye, Jeffrey Zhao, Jill Zimmerman, Colton Bracken, Jason Capili, Andrew Char, Michel Chen, Pingdi Huang, Sena Ji, Emily Kim, Kenneth Kim, Julie Ko, Sean Louise G Laput, Sam Law, Sang Kuk Lee, Olivia Lee, David Lim, Eric Lin, Kyle Marik, Josh Mytych, Andie O'Laughlin, Jensen Pak, Claire Park, Ruth Ryu, Ashwin Shinde, Manny Sosa, Nick Waite, Mane Williams, Richard Wong, Jocelyn Woo, Jonathan Woo, Vishaal Yepuri, Dorothy Yim, Dan Huynh, Dinali Wijiewarnasurya, Casey Shapiro, Marc Levis-Fitzgerald, Leslie Jaworski, David Lopatto, Ira E Clark, Tracy Johnson, Utpal Banerjee
G3 Genes Genomes Genetics, 2021
Undergraduate students participating in the UCLA Undergraduate Research Consortium for Functional Genomics (URCFG) have conducted a two-phased screen using RNA interference (RNAi) in combination with fluorescent reporter proteins to identify genes important for hematopoiesis in Drosophila. This screen disrupted the function of approximately 3500 genes and identified 137 candidate genes for which loss of function leads to observable changes in the hematopoietic development. Targeting RNAi to maturing, progenitor, and regulatory cell types identified key subsets that either limit or promote blood cell maturation. Bioinformatic analysis reveals gene enrichment in several previously uncharacterized areas, including RNA processing and export and vesicular trafficking. Lastly, the participation of students in this course-based undergraduate research experience (CURE) correlated with increased learning gains across several areas, as well as increased STEM retention, indicating that authentic, student-driven research in the form of a CURE represents an impactful and enriching pedagogical approach. - Pvr expression regulators in equilibrium signal control and maintenance of Drosophila blood progenitors
Bama Charan Mondal, Jiwon Shim, Cory J Evans, Utpal Banerjee
Elife, 2014
Blood progenitors within the lymph gland, a larval organ that supports hematopoiesis in Drosophila melanogaster, are maintained by integrating signals emanating from niche-like cells and those from differentiating blood cells. We term the signal from differentiating cells the ‘equilibrium signal’ in order to distinguish it from the ‘niche signal’. Earlier we showed that equilibrium signaling utilizes Pvr (the Drosophila PDGF/VEGF receptor), STAT92E, and adenosine deaminase-related growth factor A (ADGF-A) (<xref ref-type="bibr" rid="bib43">Mondal et al., 2011</xref>). Little is known about how this signal initiates during hematopoietic development. To identify new genes involved in lymph gland blood progenitor maintenance, particularly those involved in equilibrium signaling, we performed a genetic screen that identified bip1 (bric à brac interacting protein 1) and Nucleoporin 98 (Nup98) as additional regulators of the equilibrium signal. We show that the products of these genes along with the Bip1-interacting protein RpS8 (Ribosomal protein S8) are required for the proper expression of Pvr. - XOlfactory control of blood progenitor maintenance
Jiwon Shim, Tina Mukherjee, Bama Charan Mondal, Ting Liu, Gloria Chin Young, Dinali Priasha Wijewarnasuriya, Utpal Banerjee
Cell, 2013 - Interaction between differentiating cell- and niche-derived signals in hematopoietic progenitor maintenance
Bama Charan Mondal, Tina Mukherjee, Lolitika Mandal, Cory J. Evans, Sergey A. Sinenko, Julian A. Martinez-Agosto, Utpal Banerjee
Cell, 2011 - Methylation status of promoter-associated CpG islands in primary acute myeloid leukemia
Bama Charan Mondal, Ashis Mukhopadhyay, Utpal Chaudhuri, Bhaswati Ganguli, Uma B. Dasgupta
Acta Haematologica, 2009
tion of CpG islands may exert the same effects as a mutation or deletion in a coding region in one copy of the gene and thus represent an alternative mechanism to contribute to the loss of function of one or both alleles. Several genes of basic cellular pathways are affected by aberrant CpG island methylation in human cancers [6] . The profile of promoter hypermethylation is tumor type and gene specific. However, despite a broad tumor-specific pattern of global methylation, there is significant interindividual variability. These differences may indicate differences in the subtypes included in the studies, etiology of the disease, or differences in the cohort of patients. In the present work, we have examined the methylation status of 9 cancer-related genes CDKN2A (P16), ARF (P14), CDKN2B (P15) , TP73 and CDKN1A (P21, Cip1) , the CDH1 (E-cadherin, tumor cell invasion or tumor architecture), hMLH1 (repair of DNA damage), retinoic acid receptor2 (RAR 2) , and the cytokine regulator suppressor of cytokine signaling-1 (SOCS1) in de novo AML patient samples at diagnosis and explored possible correlations between methylation patterns and clinical parameters. Sixty-three de novo AML patients diagnosed at the Department of Hematology, Park Point Nursing Home and Institute of Haematology and Transfusion Medicine, Kolkata, India, during November 2002 to March 2006 were the subjects of this study. All M3 subtypes were treated by Acute myeloid leukemia (AML), a clonal hematological malignancy of the myeloid line of cells is a heterogeneous disease characterized by many different genetic defects. The disease can be classified into different categories and according to the French-American-British (FAB) system, AML is divided into subtypes, M0–M7, based on the type of cell from which the leukemia developed and how mature the cells are. This is defined largely using cytochemical staining. Some subtypes of AML are linked with certain symptoms and respond to specific treatments. Specific cytogenetic lesions are also powerful determinants of therapeutic response [1] . Chromosomal translocations involving oncogenes and transcription factors, activation of signal transduction pathways, and alterations of growth factor receptors have been documented in AML [1, 2] . Disruption of tumor suppressor networks is also associated with most types of tumorigenesis. This might be achieved through deletions, mutations or epigenetic processes and the latter play a major role in human carcinogenesis [3] . Hypermethylation of the CpG islands near the promoter regions is followed by binding of complexes of methyl-CpG-binding proteins, transcriptional corepressors, chromatin-remodeling proteins and histone deacetylases to the hypermethylated DNA regions, resulting in a transcriptionally repressive chromatin state [4, 5] . In this context, abnormal methylaReceived: July 30, 2008 Accepted after revision: November 3, 2008 Published online: January 20, 2009 - Haplotype analysis at the FRAXA locus in an Indian population
S. Saha Chakraborty, Bama Charan Mondal, S. Das, K. Das, U.B. Dasgupta
American Journal of Medical Genetics Part A, 2008 - Association of cytochrome P450, glutathione S-transferase and N-acetyl transferase 2 gene polymorphisms with incidence of acute myeloid leukemia
Sunipa Majumdar, Bama Charan Mondal, Moloy Ghosh, Sarmistha Dey, Ashis Mukhopadhyay, Sarmila Chandra, Uma B. Dasgupta
European Journal of Cancer Prevention, 2008 - Molecular profiling of chronic myeloid leukemia in Eastern India
Bama C. Mondal, Aditi Bandyopadhyay, Sunipa Majumdar, Ashis Mukhopadhyay, Sarmila Chandra, Utpal Chaudhuri, Prantar Chakrabarti, Shibashish Bhattacharyya, Uma B. Dasgupta
American Journal of Hematology, 2006 - e19a2 BCR-ABL fusion transcript in typical chronic myeloid leukaemia: A report of two cases
B C Mondal, S Majumdar, U B Dasgupta, U Chaudhuri, P Chakrabarti, S Bhattacharyya
Journal of Clinical Pathology, 2006 - Two β-globin cluster-linked polymorphic loci in thalassemia patients of variable levels of fetal hemoglobin
Sanmay Bandyopadhyay, Bama Charan Mondal, Pabak Sarkar, Sarmila Chandra, M. K. Das, Uma B. Dasgupta
European Journal of Haematology, 2005 - Glutathione S-transferase M1 and T1 null genotype frequency in chronic myeloid leukaemia
B C Mondal, N Paria, S Majumdar, Sarmila Chandra, A Mukhopadhyay, U Chaudhuri, U B Dasgupta
European Journal of Cancer Prevention, 2005 - Profile of β-thalassemia in eastern India and its prenatal diagnosis
Aditi Bandyopadhyay, Sanmay Bandyopadhyay, Jayasri Basak, Bama Charan Mondal, Anjali Angelika Sarkar, Sunipa Majumdar, Mani Kanchan Das, Sharmila Chandra, Ashis Mukhopadhyay, Mamtaj Sanghamita, Kusagradhi Ghosh, Uma B. Dasgupta
Prenatal Diagnosis, 2004
RECENT SCHOLAR PUBLICATIONS
- Red-Emitting Glutathione-Templated Copper Nanoclusters for Fluorescence Enhancement–Based Detection of Arsenic (III) Contamination in Water
V Arya, S Yadav, D Maurya, BC Mondal, SVS Raju, CSP Tripathi, D Guin
ACS Applied Nano Materials 9 (8), 3889-3900 , 2026
2026 - Gadd45 regulates fate decisions of myeloid-type blood progenitor cells in Drosophila
P Jaiswal, BC Mondal
bioRxiv, 2025.12. 16.694615 , 2025
2025 - Protocol to study DNA strand breaks during development and apoptosis using in situ nick translation in Drosophila
D Maurya, BC Mondal
STAR protocols 6 (3) , 2025
2025 - Larval hematopoietic organs of multiple Drosophila species show effector caspase activity and DNA damage response
D Maurya, BC Mondal
microPublication Biology 2024, 10.17912/micropub. biology. 001392 , 2024
2024
Citations: 1 - One‐Step Room Temperature Synthesis of Printable Carbon Quantum Dots Ink for Visual Encryption and High‐Performance Photodetector
B Thakurta, S Hazra, A Samanta, A Nasir, AK Singh, D Maurya, ...
Advanced Optical Materials 12 (36), 2401886 , 2024
2024
Citations: 5 - Wnt signaling couples G2 phase control with differentiation during hematopoiesis in Drosophila
LM Goins, JR Girard, BC Mondal, S Buran, CC Su, R Tang, T Biswas, ...
Developmental cell 59 (18), 2477-2496. e5 , 2024
2024
Citations: 12 - Transient caspase-mediated activation of caspase-activated DNase causes DNA damage required for phagocytic macrophage differentiation
D Maurya, G Rai, D Mandal, BC Mondal
Cell reports 43 (5) , 2024
2024
Citations: 13 - Macrophage differentiation requires DNA damage caused by Caspase-Activated DNase
D Maurya, G Rai, D Mandal, BC Mondal
bioRxiv, 2023.10. 16.562503 , 2023
2023
Citations: 1 - Wnt signaling couples G2 phase control with differentiation during hematopoiesis
LM Goins, JR Girard, BC Mondal, S Buran, CC Su, R Tang, T Biswas, ...
bioRxiv, 2023.06. 29.547151 , 2023
2023
Citations: 2 - A functional genomics screen identifying blood cell development genes in Drosophila by undergraduates participating in a course-based research experience
CJ Evans, JM Olson, BC Mondal, P Kandimalla, A Abbasi, ...
G3 11 (1), jkaa028 , 2021
2021
Citations: 17 - Pvr expression regulators in equilibrium signal control and maintenance of Drosophila blood progenitors
BC Mondal, J Shim, CJ Evans, U Banerjee
eLife, e03626 , 2014
2014
Citations: 70 - Olfactory control of blood progenitor maintenance
J Shim, T Mukherjee, BC Mondal, T Liu, GC Young, DP Wijewarnasuriya, ...
Cell 155 (5), 1141-1153 , 2013
2013
Citations: 143 - Interaction between differentiating cell-and niche-derived signals in hematopoietic progenitor maintenance
BC Mondal, T Mukherjee, L Mandal, CJ Evans, SA Sinenko, ...
Cell 147 (7), 1589-1600 , 2011
2011
Citations: 227 - Methylation status of promoter-associated CPG islands in primary acute myeloid leukemia
BC Mondal, A Mukhopadhyay, U Chaudhuri, B Ganguli, UB Dasgupta
Acta Haematologica 120 (4), 207-210 , 2009
2009
Citations: 2 - Haplotype analysis at the FRAXA locus in an Indian population
SS Chakraborty, BC Mondal, S Das, K Das, UB Dasgupta
American Journal of Medical Genetics Part A 146 (15), 1980-1985 , 2008
2008
Citations: 7 - Association of cytochrome P450, glutathione S-transferase and N-acetyl transferase 2 gene polymorphisms with incidence of acute myeloid leukemia
S Majumdar, BC Mondal, M Ghosh, S Dey, A Mukhopadhyay, S Chandra, ...
European Journal of Cancer Prevention 17 (2), 125-132 , 2008
2008
Citations: 50 - Molecular profiling of chronic myeloid leukemia in eastern India
BC Mondal, A Bandyopadhyay, S Majumdar, A Mukhopadhyay, ...
American journal of hematology 81 (11), 845-849 , 2006
2006
Citations: 41 - e19a2 BCR–ABL fusion transcript in typical chronic myeloid leukaemia: a report of two cases
BC Mondal, S Majumdar, UB Dasgupta, U Chaudhuri, P Chakrabarti, ...
Journal of clinical pathology 59 (10), 1102-1103 , 2006
2006
Citations: 34 - IMATINIB MESYLATE AS FIRST LINE THERAPY IN PATIENTS WITH PAEDIATRIC CHRONIC MYELOID LEUKEMIA (CML)-AN EXPERIENCE FROM EASTERN INDIA: PJ 008
A Mukhopadhyay, S Mukhopadhyay, B Barman, K Saha, A Dhara, ...
Pediatric Blood & Cancer 45 (4), 526 , 2005
2005 - Two β ‐globin cluster‐linked polymorphic loci in thalassemia patients of variable levels of fetal hemoglobin
S Bandyopadhyay, BC Mondal, P Sarkar, S Chandra, MK Das, ...
European journal of haematology 75 (1), 47-53 , 2005
2005
Citations: 21
MOST CITED SCHOLAR PUBLICATIONS
- Interaction between differentiating cell-and niche-derived signals in hematopoietic progenitor maintenance
BC Mondal, T Mukherjee, L Mandal, CJ Evans, SA Sinenko, ...
Cell 147 (7), 1589-1600 , 2011
2011
Citations: 227 - Olfactory control of blood progenitor maintenance
J Shim, T Mukherjee, BC Mondal, T Liu, GC Young, DP Wijewarnasuriya, ...
Cell 155 (5), 1141-1153 , 2013
2013
Citations: 143 - Pvr expression regulators in equilibrium signal control and maintenance of Drosophila blood progenitors
BC Mondal, J Shim, CJ Evans, U Banerjee
eLife, e03626 , 2014
2014
Citations: 70 - Association of cytochrome P450, glutathione S-transferase and N-acetyl transferase 2 gene polymorphisms with incidence of acute myeloid leukemia
S Majumdar, BC Mondal, M Ghosh, S Dey, A Mukhopadhyay, S Chandra, ...
European Journal of Cancer Prevention 17 (2), 125-132 , 2008
2008
Citations: 50 - Glutathione S-transferase M1 and T1 null genotype frequency in chronic myeloid leukaemia
BC Mondal, N Paria, S Majumdar, S Chandra, A Mukhopadhyay, ...
European journal of cancer prevention 14 (3), 281-284 , 2005
2005
Citations: 45 - Molecular profiling of chronic myeloid leukemia in eastern India
BC Mondal, A Bandyopadhyay, S Majumdar, A Mukhopadhyay, ...
American journal of hematology 81 (11), 845-849 , 2006
2006
Citations: 41 - e19a2 BCR–ABL fusion transcript in typical chronic myeloid leukaemia: a report of two cases
BC Mondal, S Majumdar, UB Dasgupta, U Chaudhuri, P Chakrabarti, ...
Journal of clinical pathology 59 (10), 1102-1103 , 2006
2006
Citations: 34 - Profile of β‐thalassemia in eastern India and its prenatal diagnosis
A Bandyopadhyay, S Bandyopadhyay, J Basak, BC Mondal, AA Sarkar, ...
Prenatal Diagnosis: Published in Affiliation With the International Society … , 2004
2004
Citations: 23 - Two β ‐globin cluster‐linked polymorphic loci in thalassemia patients of variable levels of fetal hemoglobin
S Bandyopadhyay, BC Mondal, P Sarkar, S Chandra, MK Das, ...
European journal of haematology 75 (1), 47-53 , 2005
2005
Citations: 21 - A functional genomics screen identifying blood cell development genes in Drosophila by undergraduates participating in a course-based research experience
CJ Evans, JM Olson, BC Mondal, P Kandimalla, A Abbasi, ...
G3 11 (1), jkaa028 , 2021
2021
Citations: 17 - Transient caspase-mediated activation of caspase-activated DNase causes DNA damage required for phagocytic macrophage differentiation
D Maurya, G Rai, D Mandal, BC Mondal
Cell reports 43 (5) , 2024
2024
Citations: 13 - Wnt signaling couples G2 phase control with differentiation during hematopoiesis in Drosophila
LM Goins, JR Girard, BC Mondal, S Buran, CC Su, R Tang, T Biswas, ...
Developmental cell 59 (18), 2477-2496. e5 , 2024
2024
Citations: 12 - Haplotype analysis at the FRAXA locus in an Indian population
SS Chakraborty, BC Mondal, S Das, K Das, UB Dasgupta
American Journal of Medical Genetics Part A 146 (15), 1980-1985 , 2008
2008
Citations: 7 - One‐Step Room Temperature Synthesis of Printable Carbon Quantum Dots Ink for Visual Encryption and High‐Performance Photodetector
B Thakurta, S Hazra, A Samanta, A Nasir, AK Singh, D Maurya, ...
Advanced Optical Materials 12 (36), 2401886 , 2024
2024
Citations: 5 - Wnt signaling couples G2 phase control with differentiation during hematopoiesis
LM Goins, JR Girard, BC Mondal, S Buran, CC Su, R Tang, T Biswas, ...
bioRxiv, 2023.06. 29.547151 , 2023
2023
Citations: 2 - Methylation status of promoter-associated CPG islands in primary acute myeloid leukemia
BC Mondal, A Mukhopadhyay, U Chaudhuri, B Ganguli, UB Dasgupta
Acta Haematologica 120 (4), 207-210 , 2009
2009
Citations: 2 - Larval hematopoietic organs of multiple Drosophila species show effector caspase activity and DNA damage response
D Maurya, BC Mondal
microPublication Biology 2024, 10.17912/micropub. biology. 001392 , 2024
2024
Citations: 1 - Macrophage differentiation requires DNA damage caused by Caspase-Activated DNase
D Maurya, G Rai, D Mandal, BC Mondal
bioRxiv, 2023.10. 16.562503 , 2023
2023
Citations: 1 - Red-Emitting Glutathione-Templated Copper Nanoclusters for Fluorescence Enhancement–Based Detection of Arsenic (III) Contamination in Water
V Arya, S Yadav, D Maurya, BC Mondal, SVS Raju, CSP Tripathi, D Guin
ACS Applied Nano Materials 9 (8), 3889-3900 , 2026
2026 - Gadd45 regulates fate decisions of myeloid-type blood progenitor cells in Drosophila
P Jaiswal, BC Mondal
bioRxiv, 2025.12. 16.694615 , 2025
2025