Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Eshan Khan"'
Autor:
Neeraj Kumar Chauhan, Anjali Anand, Arun Sharma, Kanika Dhiman, Tannu Priya Gosain, Prashant Singh, Padam Singh, Eshan Khan, Gopinath Chattopadhyay, Amit Kumar, Deepak Sharma, Ashish, Tarun Kumar Sharma, Ramandeep Singh
Publikováno v:
Microbiology Spectrum, Vol 11, Iss 1 (2023)
ABSTRACT In order to adapt in host tissues, microbial pathogens regulate their gene expression through a variety of transcription factors. Here, we have functionally characterized Rv0792c, a HutC homolog from Mycobacterium tuberculosis. In comparison
Externí odkaz:
https://doaj.org/article/4a30e7c26e8640c5afada19b8127efd4
Autor:
Swetha Rajasekaran, Jalal Siddiqui, Jessica Rakijas, Brandon Nicolay, Chenyu Lin, Eshan Khan, Rahi Patel, Robert Morris, Emanuel Wyler, Myriam Boukhali, Jayashree Balasubramanyam, R. Ranjith Kumar, Capucine Van Rechem, Christine Vogel, Sailaja V. Elchuri, Markus Landthaler, Benedikt Obermayer, Wilhelm Haas, Nicholas Dyson, Wayne Miles
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-13 (2021)
Swetha Rajasekaran et al. integrate transcriptional, proteomic, and metabolomic data to explore how cells adapt to inactivation of RB1, a hallmark of cancer. Combined with their genetic analyses in a Drosophila model, the authors identify key metabol
Externí odkaz:
https://doaj.org/article/c522d3a225e8419ab1ce5e0411f3ed84
Autor:
Mukhtar Ahmad Dar, Pawan Kumar, Prakash Kumar, Ashish Shrivastava, Muneer Ahmad Dar, Richa Chauhan, Vinita Trivedi, Ashutosh Singh, Eshan Khan, Ravichandiran Velayutham, Sameer Dhingra
Publikováno v:
Vaccines, Vol 10, Iss 11, p 1850 (2022)
Gallbladder cancer (GBC) is an aggressive and difficult to treat biliary tract carcinoma with a poor survival rate. The aim of this study was to design a peptide-based multi-epitope vaccine construct against GBC using immunoinformatics approaches. Th
Externí odkaz:
https://doaj.org/article/d6e125a4150d44f1b630eaa2a206fc29
Autor:
Arun Kumar Verma, Eshan Khan, Subodh Kumar Mishra, Amit Mishra, Nicolas Charlet-Berguerand, Amit Kumar
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
Fragile X-associated tremor ataxia syndrome is an untreatable neurological and neuromuscular disorder caused by unstable expansion of 55–200 CGG nucleotide repeats in 5′ UTR of Fragile X intellectual disability 1 (FMR1) gene. The expansion of CGG
Externí odkaz:
https://doaj.org/article/8e13f031b8a34d21b52f676c7532bf3a
Autor:
Swetha Rajasekaran, Jalal Siddiqui, Jessica Rakijas, Brandon Nicolay, Chenyu Lin, Eshan Khan, Rahi Patel, Robert Morris, Emanuel Wyler, Myriam Boukhali, Jayashree Balasubramanyam, R. Ranjith Kumar, Capucine Van Rechem, Christine Vogel, Sailaja V. Elchuri, Markus Landthaler, Benedikt Obermayer, Wilhelm Haas, Nicholas Dyson, Wayne Miles
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-1 (2021)
Externí odkaz:
https://doaj.org/article/35e9a7db329246f0b30b2c0bbe0dc5d6
Autor:
Neeraj Kumar Chauhan, Anjali Anand, Arun Sharma, Kanika Dhiman, Tannu Priya Gosain, Prashant Singh, Padam Singh, Eshan Khan, Gopinath Chattopadhyay, Amit Kumar, Deepak Sharma, null Ashish, Tarun Kumar Sharma, Ramandeep Singh
Publikováno v:
Microbiology spectrum.
In order to adapt in host tissues, microbial pathogens regulate their gene expression through a variety of transcription factors. Here, we have functionally characterized Rv0792c, a HutC homolog from Mycobacterium tuberculosis. In comparison to the p
Publikováno v:
ACS Applied Nano Materials. 4:14197-14207
Factors like oxidative stress, environmental risk factors, genetics, chemical treatments, and resistance to treatment strategies all have serious impediments in scientific progress for treating dis...
Autor:
Bhavana Joshi, Jaspreet Kaur, Eshan Khan, Supriya Vishwakarma, Amit Kumar, Deepti Joshi, Ashok Kumar, Abhijeet Joshi
Publikováno v:
Journal of Drug Delivery Science and Technology. 84:104532
Autor:
Swetha Rajasekaran, Eshan Khan, Samuel R Ching, Misbah Khan, Jalal K Siddiqui, Daniela F Gradia, Chenyu Lin, Stephanie J Bouley, Dayna L Mercadante, Amity L Manning, André P Gerber, James A Walker, Wayne O Miles
Publikováno v:
Nucleic acids research. 50(12)
DICER1 syndrome is a cancer pre-disposition disorder caused by mutations that disrupt the function of DICER1 in miRNA processing. Studying the molecular, cellular and oncogenic effects of these mutations can reveal novel mechanisms that control cell
Autor:
Eshan Khan, Amit Kumar, Ramandeep Singh, Tarun Kumar Sharma, Arun Sharma, Tannu Priya Gosain, Ashish Ganguly, Prashant Singh, Kanika Dhiman, Anjali Anand, Deepak Sharma, Neeraj Chauhan
In order to adapt in host tissues, microbial pathogens regulate their gene expression through an array of transcription factors. Here, we have functionally characterized Rv0792c, a GntR homolog from M. tuberculosis. In comparison to the parental stra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cec57e0f2d9bef38b759a95f83f805d2
https://doi.org/10.1101/2021.09.17.460839
https://doi.org/10.1101/2021.09.17.460839