Scientist Profile

Nishant Singhal, Ph.D.

Stem Cell and Neurobiology lab
Email

nsinghal@nccs.res.in

Research Areas

Neuroscience, Stem Cells and Regeneration

Education and Experience

 

Education

 

Ph.D.:  Adolf Butenandt Institute, Ludwig Maximilian University, Munich, Germany, 2005

 

 

Experience

 

Scientist D: National Centre for Cell Science, 2017- present

Assistant Project Scientist: University of California, San Diego, California, USA, 2012 -2017

Postdoctoral fellow: Max Planck Institute for Molecular Biomedicine, Muenster, Germany, 2005- 2012

Research

 

Finding treatments for more than 700 neurological disorders, including neurodevelopmental disorders like Down Syndrome, Autism, Neurodegenerative disorders like Alzheimer’s, Huntington and Neuropsychiatric disorders like Schizophrenia, bipolar disorder is the most significant challenge for the current scientific community.

 

Over decades exciting research has been carried out in these areas using various model systems. However, these models have posed several limitations in finding treatments for these neurological disorders due to differences with humans at the cellular and molecular level.

The invention of induced pluripotent stem cells (iPSCs) has provided an opportunity to model neurological disorders in a dish. It allows us to understand the cellular and molecular mechanism and develop drug screening strategies to identify treatments for these neurological disorders.

 

Currently, our lab focuses on Down syndrome caused by the trisomy of chromosome 21. Individuals with Down syndrome suffer from more than 80 health-related conditions, including intellectual disability. By the 4th decade of age, almost 100% of individuals with Down syndrome develop Alzheimer’s pathology. We are using human iPSCs technology to understand cellular and molecular mechanisms of Down Syndrome related neurological disorders and find treatment for improving the quality of life of individuals with Down syndrome.

 

We encourage enthusiastic researchers at postdoctoral, doctoral, JRF, SRF, and project assistant levels to contact us to identify opportunities to work in this area.

Publications and Patents

 

Nehra, S., Sharma, V., Singh, M., Singhal, P. & Singhal, N. Generation of integration free hiPSCs clones, NSi001-A, NSi001-B, and NSi001-C from peripheral blood mononuclear cells of an individual with down syndrome having Robertsonian translocation. Stem cell research 61, 102771, doi:10.1016/j.scr.2022.102771 (2022).

Wagner, G* and Singhal, N*. et al. Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition. PLoS genetics 13, e1006757, doi:10.1371/journal.pgen.1006757 (2017).

* Equal First author

Singhal, N.*, Bravo, MJA., Sinn M., Zaehres, H. (2016) BAF complex enhances reprogramming of adult human fibroblasts. Journal of Stem Cell Research and Therapy 6: 336. doi:10.4172/2157-7633.1000336

* Corresponding author

Belichenko, PV.,*# Madani, R.,# Rey-Bellet, L., Pihlgren,M.,  Becker, A., Plassard, A., Vuillermot, S., Giriens, V., Nosheny, RL., Kleschevnikov, AM.,  Valletta, JS., Bengtsson, S., Linke, GR., Maloney, MT., Hickman, DT., Reis, P., Granet, A., Mlaki, D., Lopez-Deber, MP., Do, L.,  Singhal, N., Masliah, E  Pearn, ML., Pfeifer, A., Muhs, A., * Mobley, WC., (2016) An anti-β-Amyloid Vaccine for Treating Cognitive Deficits in Down Syndrome. PLOS ONE 11 (3) e0152471

Do, L., Mobley, WC., Singhal, N*. (2015) Questioned validity of GEDDs in Down Syndrome. F1000Research 2015, 4:269 (doi: 10.12688/f1000research.6735.1)

* Corresponding author

Singhal, N.*, Esch, D., Stehling, M., Schöler, HR. (2014) BRG1 is required to maintain pluripotency of murine embryonic stem cells. Bioresearch Open Access, 3, 1-8.                  

* Corresponding author

Wu, W., Han, D., Gong, Y., Sebastiano, V., Gentile, L., Singhal, N., Adachi, K., Fischedick, G., Ortmeier, C., Sinn, M., Radstaak, M., Tomilin, A., Schöler, HR* (2013) Establishment of Totipotency does not depend on Oct4. Nature Cell Biology. 15, 1089-1097.

  • Highlighted by http://www.sciguru.com/newsitem/1644

Sharma, A.D*., Narain, N., Handel, E.M., Iken, M., Singhal, N., Cathomen, T., Manns, M.P., Schöler, HR., Ott, M., and Cantz, T. (2011). MicroRNA-221 regulates FAS-induced fulminant liver failure. Hepatology 53, 1651-1661.

Singhal, N., Graumann, J, Wu, G., Bravo, MJA., Han, DW., Greber, B., Gentile, L., Mann, M., and Schöler, HR*. (2010). Chromatin Remodeling Components of the BAF Complex Facilitate Reprogramming. Cell 141, 943-955

  • Highlighter in Nature Reviews Molecular Cell Biology doi:10.1038/nrm2942

Zaehres, H*., Do, J.T., Singhal, N., Tapia, N., Han, D.W., and Schöler, H. (2008). Genetic modulation of self-renewal factors for induced reprogramming of somatic cells. Cell Res 18.

Rupp, R. A. W*., Singhal, N., and Veenstra, G. J. C. (2002). When the embryonic genome flexes its muscles – chromatin and myogenic specification. European Journal of Biochemistry 269, 2294-2299. (Citations:22)

 

 

 

 

 

 

 

 

 

 

 

Current/Past Lab Members

 

 

Ph.D. Student

  1. Sunita Nehra (Since November 2018)

  2. Vishi Sharma (Since November 2018)

 

Project Assistant

  1. Princy Kakani

 

Project/Summer trainee

 

  1. Princy Kakani

  2. Abhishek Soni

  3. Navia John

  4. Palak Sangal


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