Articles

  1. Gohain D, Tamuli R (2019) Calcineurin responsive zinc-finger-1 binds to a unique promoter sequence to upregulate neuronal calcium sensor-1, whose interaction with MID-1 increases tolerance to calcium stress in Neurospora crassa. Molecular Microbiology. https://doi.org/10.1111/mmi.14234 [Epub ahead of print]

  2. Tiwari A, Ngiilmei SD, Tamuli R (2018). The NcZrg-17 gene of Neurospora crassa encodes a cation diffusion facilitator transporter required for vegetative development, tolerance to endoplasmic reticulum stress and cellulose degradation under low zinc conditions. Current Genetics 64(4) 811-819. https://doi.org/10.1007/s00294-017-0794-4

  3. Barman A, Gohain D, Bora U, Tamuli R (2018) Phospholipases play multiple cellular roles including growth, stress tolerance, sexual development, and virulence in fungi. Microbiological Research 209: 55-69. https://doi.org/10.1016/j.micres.2017.12.012

  4. Gohain D, Roy A, Tamuli R (2017). Calcium signaling proteins in human diseases and their potential as drug targets. Annals of Pharmacology and Pharmaceutics 2(22): 1117

  5. Laxmi V, Tamuli R (2017). Calmodulin is necessary for vegetative growth, ultraviolet survival, and sexual development in the model filamentous fungus Neurospora crassa. Arch Microbiol. 2017 May. http://atlasofscience.org/

  6. Barman A, Tamuli R (2017) The pleiotropic vegetative and sexual development phenotypes of Neurospora crassa arise from double mutants of the calcium signaling genes plc-1, splA2, and cpe-1. Current Genetics 63(5):861-875. doi:10.1007/s00294-017-0682-y

  7. Laxmi V, Tamuli R (2017) The calmodulin gene in Neurospora crassa is required for normal vegetative growth, ultraviolet survival, and sexual development. Archives of Microbiology 199(4):531-542. doi:10.1007/s00203-016-1319-0

  8. Gohain D, Deka R, Tamuli R (2016) Identification of critical amino acid residues and functional conservation of the Neurospora crassa and Rattus norvegicus orthologues of neuronal calcium sensor-1. Genetica 144(6):665-674. doi:10.1007/s10709-016-9933-y

  9. Tamuli R, Deka R, Borkovich KA (2016) Calcineurin subunits A and B interact to regulate growth and asexual and sexual development in Neurospora crassa. PLoS One 11(3): e0151867. https://doi.org/10.1371/journal.pone.0151867

  10. Tamuli R (2016) Neurospora: A scientific journey by the orange mold since 1843. North East Bioline 1: 8-9.

  11. Deka R, Ghosh A, Tamuli R, Borkovich KA (2016) Heterotrimeric G Proteins. In H. Drik (ed.), pp 119-144, The mycota III. Springer-Verlag, Berlin, Germany.https://link.springer.com/chapter/10.1007%2F978-3-319-27790-5_7 DOI 10.1007/978-3-319-27790-5_77: 2.

  12. Laxmi.V and Tamuli.R (2015). The Neurospora crassa cmd, trm-9, and nca-2 genes play a role in growth, development, and survival in stress conditions. Genomics and Applied Biology. 6:1-8

  13. Barman A. and Tamuli R. (2015). Multiple cellular roles of Neurospora crassa plc-1, splA2 and cpe-1 in regulation of cytosolic free calcium, carotenoid accumulation, stress responses, and acquisition of thermotolerance. Journal of Microbiology doi: 10.1007/s12275-015-4465-1

  14. Kumar R. and Tamuli R. (2014). Calcium/calmodulin-dependent kinases are involved in growth, thermotolerance, oxidative stress survival, and fertility in Neurospora crassa. Archives of Microbiology 196: 295-305. doi: 10.1007/s00203-014-0966-2

  15. Deka R. and Tamuli R. (2013). Neurospora crassa ncs-1, mid-1 and nca-2 double mutant phenotypes suggest diverse interaction among three Ca2+ regulating gene products. Journal of Genetics. 92: 559-563

  16. Tamuli R., Kumar R., Srivastava D. A. and Deka R. (2013). Calcium signaling. In Neurospora: Genomics and Molecular Biology (ed. D. P. Kasbekar and K. McCluskey), pp. 35-57. Caister Academic Press, Norfolk, UK

  17. Deka, R., Kumar, R. and Tamuli, R. (2011). Neurospora crassa homologue of Neuronal Calcium Sensor-1 has a role in growth, calcium stress tolerance, and ultraviolet survival. Genetica 139: 885-894. doi:10.1007/s10709-011-9592-y

  18. Tamuli, R., Kumar R. and Deka, R. (2011). Cellular roles of neuronal calcium sensor-1 and calcium/calmodulin-dependent kinases in fungi. J. Basic Microbio. 51: 120-128. https://doi.org/10.1002/jobm.201000184

  19. Goel M, Tamuli R. (2011). RPL10 (ribosomal protein L10). Atlas Genet Cytogenet Oncol Haematol. 15: 425-427

  20. Mandrawalia R, Tamuli R. (2010). AMOT (angiomotin). Atlas Genet Cytogenet Oncol Haematol.14:1121-1123

  21. Deka R, Tamuli R. (2010). CDT1 (chromatin licensing and DNA replication factor 1). Atlas Genet Cytogenet Oncol Haematol.14:812-814.

  22. Singh PK, Tamuli R. (2010). CAPG (capping protein (actin filament), gelsolin-like). Atlas Genet Cytogenet Oncol Haematol. 14:809-811.

  23. Bhattacharyya, M., Tamuli, R. (2010). SEMA3B (sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B). Atlas Genet Cytogenet Oncol Haematol. 14:662-664.

  24. Sinha, N., Tamuli, R. (2010). RBBP7 (retinoblastoma binding protein 7). Atlas Genet Cytogenet Oncol Haematol. 14:578-580..

  25. Mandrawalia, R., Tamuli, R. (2010). KCMF1 (potassium channel modulatory factor 1). Atlas Genet Cytogenet Oncol Haematol.14:560-561.

  26. Tamuli, R. (2010). Genome Defense Mechanisms in Neurospora and Associated Specialized Proteins. Journal of Proteins and Proteomics 1: 15-23.

  27. Roy, D., Tamuli, R. (2009). NRF1 (nuclear respiratory factor 1). Atlas Genet Cytogenet Oncol Haematol.13:861-863.

  28. Tamuli, R. and Kasbekar, D. P. (2008). Dominant suppression of repeat-induced point mutation (RIP) in Neurospora crassa by a variant catalytic subunit of DNA polymerase zeta (Pol z). Genetics 178: 1169-1176.

  29. Tamuli, R., Ravindran, C. and Kasbekar, D. P. (2006). Translesion DNA polymerases Pol z, Pol h, Pol i , Pol k and Rev1 are not essential for repeat-induced point mutation (RIP) in Neurospora crassa. J. Biosci. 31: 557-564.

  30. Bhat, A., Tamuli, R., and Kasbekar, D. P. (2004). Genetic transformation of Neurospora tetrasperma, demonstration of repeat-induced point mutation (RIP) in self-crosses and a screen for recessive RIP-defective mutants. Genetics 167: 1155-1164.

 

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