PUBLICATIONS

Citations 9478, H-index 44

For complete list of publications see the link below.

https://scholar.google.com/citations?user=AEqA61gAAAAJ&hl=en

Selected Publications

  1. Chini A., Guha P., A. Rishi, Bhat N., Covarrubias A., Martinez V., Devejian L., Nguyen B., and Mandal, S.S.* HDLR-SR-BI expression and cholesterol uptake is regulated via Indoleamine-2,3-dioxygenase 1 in macrophages under inflammation, manuscript submitted, 2024.
  2. Guha P, Chini A., Rishi A., and Mandal, S.S.* Long noncoding RNAs in ubiquitination, protein degradation, and human diseases, Biochimica Biophysica Acta-Gene Regulatory Mechanism, 2024, In press.
  3. Chini A., Guha P., A. Rishi, Obaid M., Udden N. and Mandal, S.S.* Discovery and functional characterization of LncRNAs associated with inflammation and macrophage activation, Methods, 2024, 1-16.
  4. Deb, P., Chini A., Guha P., Rishi A., Bhan, A., Brady B., Perrotti, L., and Manal S.S. *. Dynamic regulation of BDNF expression via ovarian hormone and lncRNA HOTAIR, Gene 2024, 897, 148055.
  5. Price R. Chini A., Bhan A., and Manal S.S. * Long noncoding RNAs: in inflammation, cancer and in cancer therapy, RNA -Based Mechanism in Cancer, 2023, 373-402.
  6. Chini A., Guha P., Malladi V. Zhang G. and Mandal S.S. *, Novel long-noncoding RNAs associated with inflammation and macrophage activation in Human, Scientific Reports 2023,13 (1), 4036.
  7. Aziz MN., Patel A., Iskander A., Chini A., Gout D., Mandal S.S., and CJ Lovely, One-pot synthesis of novel 2-imino-5-arylidine-thiazolidine analogues and evaluation of their anti-proliferative activity against MCF7 breast cancer cell line, Molecules 2022, 27 (3), 841.
  8. Price RL., Bhan A. and Mandal S.S. *, LncRNA HOTAIR- Beyond repression: In protein degradation, inflammation and repair, DNA Repair, 2021, 105, 103141.
  9. Obaid M., Udden S.M.N., Alluri P. and Mandal S.S.*, LncRNA HOTAIR regulates glucose transporter Glut1 expression and glucose uptake in macrophages during inflammation, Scientific Reports 2021, 11: 232.
  10. Hussain I., Deb P., Chini A., Obaid M., Bhan A., Ansari KI., Mishra BP., Bobzean, S. A.M., Udden S.M.N., Alluri P., Das H.K.,Brothers M., Perrotti, L., and Mandal SS*, HOXA5 expression is elevated in breast cancer and is transcriptionally regulated by estradiol, Frontiers in Genetics 2020, 11:592436.
  11. Obaid M., Udden S.M.N., Deb P., Shihabeddin N., Zaki M.H., and Mandal S.S.*, LncRNA HOTAIR regulates lipopolysaccharide-induced cytokine expression and inflammatory response in macrophages, Scientific Reports  2018, 8(1):15670.
  12. Bhan, A., Deb, P., Shihabeddin, N., Ansari, K. I., Brotto, M., Mandal, S. S*. Histone methylase MLL1 coordinates with HIF and regulate lncRNA HOTAIR expression under hypoxia. Gene 2017, 629, 16-28.
  13. Bhan, A., Soleimani, M., Mandal, S. S*. Long Noncoding RNA and Cancer: A New Paradigm. Cancer Research 2017, 77(15), 3965-3981.
  14. Deb, P., Bhan, A., Hussain, I., Ansari, K. I., Bobzean, S. A., Pandita, T. K., Perrotti, L., Mandal, S. S*. . Endocrine disrupting chemical, bisphenol-A, induces breast cancer associated gene HOXB9 expression in vitro and in vivo. Gene 2016, 590(2), 234-243.
  15. Hussain, I., Bhan, A., Ansari, K. I., Deb, P., Bobzean, S. A.M., Perrotti, L., Mandal, S. S*. Bisphenol-A induces expression of HOXC6, an estrogen-regulated homeobox-containing gene associated with breast cancer. BBA – Gene Regulatory Mechanisms 2015, 1849(6), 697-708.
  16. Bhan, A., Hussain, I., Ansari, K. I., Bobzean, S. A.M., Perrotti, L., Mandal, S. S*. Histone Methyltransferase EZH2 Is Transcriptionally Induced by Estradiol as Well as Estrogenic Endocrine Disruptors Bisphenol-A and Diethylstilbestrol. Journal of Molecular Biology 2014, 426(20), 3426-3441. http://dx.doi.org/10.1016/j.jmb.2014.07.025.
  17. Bhan, A., Hussain, I., Ansari, K. I., Bobzean, Samara A. M., Perrotti, L., Mandal, S. S*. Bisphenol-A and diethylstilbestrol exposure induces the expression of breast cancer associated long noncoding RNA HOTAIR in vitro and in vivo. Journal of Steroid biochemistry and Molecular Biology 2014, 141, 160-170.
  18. Bhan, A., Hussain, I., Ansari, K. I., Kasiri, S., Bashyal, A., Mandal, S. S*. Antisense Transcript Long Noncoding RNA (lncRNA) HOTAIR is Transcriptionally Induced by Estradiol. Journal of Molecular Biology, 2013, 425(19), 3707-3722.
  19. Kasiri, S., Ansari, K. I., Hussain, I., Bhan, A., Mandal, S. S*. Antisense oligonucleotide mediated knockdown of HOXC13 affects cell growth and induces apoptosis in tumor cells and over expression of HOXC13 induces 3D-colony formation. RSC Advances, 2013, 3(10), 3260-3269.
  20. Ansari, K. I., Kasiri, S., Mandal, S. S*. Histone methylase MLL1 has critical roles in tumor growth and angiogenesis and its knockdown suppresses tumor growth in vivo. Oncogene, 2013, 32(28), 3359-3370.
  21. Ansari, K. I., Kasiri, S., Hussain, I., Bobzean, S. A., Perrotti, L., Mandal, S. S*. MLL Histone Methylases Regulate Expression of HDLR-SR-B1 in Presence of Estrogen and Control Plasma Cholesterol in Vivo. Molecular Endocrinology, 2013, 27(1), 92-105.
  22. Ansari, K., Kasiri, S., Mishra, B., Mandal, S. S*. (2012). Mixed lineage leukemia-4 regulates cell cycle progression, cell viability and its depletion suppresses growth of xenografted tumor in vivo. British Journal of Cancer, 2012, 107, 315-324.
  23. Ansari, K. I., Hussain, I., Kasiri, S., Mandal, S. S*. HOXC10 is overexpressed in breast cancer and transcriptionally regulated by estrogen via involvement of histone methylases MLL3 and MLL4. Journal of Molecular Endocrinology, 2012, 48(1), 61-75.
  24. Ansari, K. I., Hussain, I., Shrestha, B., Kasiri, S., Mandal, S. S*. HOXC6 Is Transcriptionally Regulated via Coordination of MLL Histone Methylase and Estrogen Receptor in an Estrogen Environment. Journal of Molecular Biology, 2011, 411(2), 334-349.
  25. Ansari, K. I., Shrestha, B., Hussain, I., Kasiri, S., Mandal, S. S*. Histone Methylases MLL1 and MLL3 Coordinate with Estrogen Receptors in Estrogen-Mediated HOXB9 Expression. Biochemistry, 2011, 50(17), 3517-3527.
  26. Ansari, K. I., Kasiri, S., Grant, J. D., Mandal, S. S* Apoptosis and anti-tumour activities of manganese(iii)-salen and -salphen complexes. Dalton Transactions, 2009, (40), 8525.
  27. Ansari, K. I., Grant, J. D., Woldemariam, G. A., Kasiri, S., Mandal, S. S*. Iron(III)-salen complexes with less DNA cleavage activity exhibit more efficient apoptosis in MCF7 cells. Organic & Biomolecular Chemistry, 2009, 7(5), 926.
  28. Pavri R., Zhu B., Li G., Trojer P., Mandal SS., Shilatifard A., and Reinberg D. Histone H2B monoubiquitination functions cooperatively with FACT to regulate elongation by RNA polymerase II. Cell 2006, 125(4):703-17
  29. Zhu B., Zheng Y., Pham AD., Mandal SS., Erdjument-Bromade H., Tempst P., and Reinberg D. Mono-Ubiquitination of Human Histone H2B: The Factors Involved and their Roles in HOX Gene Regulation. Molecular Cell 2005, 20, 601-11.
  30. Zhu B, Mandal SS, Pham AD, Zheng Y, Erdjument-Bromage H, Batra SK, Tempst P, Reinberg D. The human PAF complex coordinates transcription with events downstream of RNA synthesis. Genes and Development 2005, 19, 1668-73.
  31. Mandal SS., Chun C. Wada T., Handa H., Shatkin A. and Reinberg D. Functional interactions between mRNA capping enzyme and factors that positively and negatively regulate promoter escape by RNA polymerase II. Proceedings of National Academy of Sciences (USA) 2004, 101, 7275-7280.
  32. Mandal SS., Cho H., Kim S., Cabane K. and Reinberg D., FCP1 a phosphatase specific for the heptapeptide repeat of the largest subunit of RNA polymerase II stimulates transcription elongation. Molecular and Cellular Biology 2002, 22, 7543-7552.
  33. Mandal SS. Fidalgo Da Silva E. and Reha-Krantz LJ., Using 2-aminopurine fluorescence to detect base unstacking in the template strand during nucleotide incorporation by the bacteriophage T4 DNA polymerase. Biochemistry 2002, 41(13), 4399-4406.
  34. Bhattacharya S. and Mandal SS. Evidence of interlipidic ion pairing in anion induced DNA release from the cationic amphiphile-DNA complexes. Mechanistic implication in transfection. Biochemistry 1998, 37, 7764-7777.
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