Search Results - "Pandey, Nishtha"

Network-based metabolic characterization of renal cell carcinoma by Pandey, Nishtha, Lanke, Vinay, Vinod, P. K.

“…An emerging hallmark of cancer is metabolic reprogramming, which presents opportunities for cancer diagnosis and treatment based on metabolism. We performed a…”
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Modeling the Control of Meiotic Cell Divisions: Entry, Progression, and Exit by Dangarh, Prakrati, Pandey, Nishtha, Vinod, Palakkad Krishnanunni

“…Upon nitrogen starvation, Schizosaccharomyces pombe exit the mitotic cell cycle and become irreversibly committed to the completion of meiosis program. Meiotic…”
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Mathematical modelling of reversible transition between quiescence and proliferation by Pandey, Nishtha, Vinod, P K

“…Cells switch between quiescence and proliferation states for maintaining tissue homeostasis and regeneration. At the restriction point (R-point), cells become…”
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Model scenarios for cell cycle re-entry in Alzheimer's disease by Pandey, Nishtha, Vinod, P.K.

“…Alzheimer's disease (AD) is the most prevalent neurodegenerative disease. Aberrant production and aggregation of amyloid beta (Aβ) peptide into plaques is a…”
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Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE by Ganapathy, Aparna, Pandey, Nishtha, Srisailapathy, C R Srikumari, Jalvi, Rajeev, Malhotra, Vikas, Venkatappa, Mohan, Chatterjee, Arunima, Sharma, Meenakshi, Santhanam, Rekha, Chadha, Shelly, Ramesh, Arabandi, Agarwal, Arun K, Rangasayee, Raghunath R, Anand, Anuranjan

“…Mutations in the autosomal genes TMPRSS3, TMC1, USHIC, CDH23 and TMIE are known to cause hereditary hearing loss. To study the contribution of these genes to…”
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Cosmopolitan Identity Formation and Consumer Culture: A Study of Ndibe’s Foreign Gods, Inc by Pandey, Nishtha

“…The dream of a cosmopolitan utopia and the idea of being locally situated yet globally connected has never seemed more plausible than today. Globality has made…”
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"Do not shoot, I'm a B-b-British object!": Reading David Malouf in Indian universities by Pandey, Nishtha, Parui, Avishek

“…Since 2009, Australian author David Malouf's texts have been included and then excluded from key courses in Indian universities. Malouf's place in the…”
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Mutations in OTOF, CLDN14 & SLC26A4 genes as major causes of hearing impairment in Dhadkai village, Jammu & Kashmir, India by Pandey, Nishtha, Rashid, Tabassum, Jalvi, Rajeev, Sharma, Meenakshi, Rangasayee, Raghunath, Andrabi, Khurshid, Anand, Anuranjan

“…Background & objectives: A high incidence of hearing impairment is reported from the village of Dhadkai in the State of Jammu and Kashmir, India. Prevalence of…”
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Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma: Cx30 Mutation for Syndromic Hearing Loss by Pandey, Nishtha, Xavier, Dennis F., Chatterjee, Arunima, Mani, Ram-Shankar, Hiremagalore, Ravi, Tharakan, Ajith, Rajashekhar, B., Anand, Anuranjan

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Adsorption of Cr(VI) from aqueous solutions on tea waste and coconut husk by Dave, Pragnesh N, Pandey, Nishtha, Thomas, Hannah

“…Adsorption of Cr (VI) from aqueous solutions on tea wastes and coconut husk has been studied. The effect of experimental parameters like contact time,…”
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Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma by Pandey, Nishtha, Xavier, Dennis F., Chatterjee, Arunima, Mani, Ram‐Shankar, Hiremagalore, Ravi, Tharakan, Ajith, Rajashekhar, B., Anand, Anuranjan

“…Summary Mutations in the gap‐junction gene Cx30 (Connexin30, GJB6) are a known cause of hearing loss. Here, we report our findings on a large multigeneration…”
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novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3 by Chatterjee, Arunima, Jalvi, Rajeev, Pandey, Nishtha, Rangasayee, R, Anand, Anuranjan

“…Autosomal dominant nonsyndromic hearing loss (ADNSHL) accounts for about one-fifth of hereditary hearing loss in humans. In the present study, we have analyzed…”
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Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE: e84773 by Ganapathy, Aparna, Pandey, Nishtha, Srisailapathy, C RSrikumari, Jalvi, Rajeev, Malhotra, Vikas, Venkatappa, Mohan, Chatterjee, Arunima, Sharma, Meenakshi, Santhanam, Rekha, Chadha, Shelly

“…Mutations in the autosomal genes TMPRSS3, TMC1, USHIC, CDH23 and TMIE are known to cause hereditary hearing loss. To study the contribution of these genes to…”
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Mobility in the structure of E.coli recQ helicase upon substrate binding as seen from molecular dynamics simulations by Pandey, Nishtha, Govardhan, Savitha, Pathak, Ravi Kant

“…RecQ helicases feature multiple domains in their structure, of which the helicase domain, the RecQ-Ct domain and the HRDC domains are well conserved among the…”
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