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Journal of Cellular Biochemistry|November 24, 2021
Understanding the impact of missense mutations on the structure and function of the EDA gene in X-linked hypohidrotic ectodermal dysplasia: A bioinformatics approachPrashant Ranjan, Parimal Das
Journal of Biotechnology|May 13, 2024
Exploring G-quadruplex structure in PRCC-TFE3 fusion oncogene: Plausible use as anti cancer therapy for translocation Renal cell carcinoma (tRCC)Neha Neha, Parimal Das
International Journal of Biological Macromolecules|January 26, 2023
An inclusive study of deleterious missense PAX9 variants using user-friendly tools reveals structural, functional alterations, as well as potential therapeutic targetsPrashant Ranjan, Parimal Das
Plos One|October 19, 2018
Novel splicing in IGFN1 intron 15 and role of stable G-quadruplex in the regulation of splicing in renal cell carcinomaShiv Prakash Verma, Parimal Das
In Vitro Cellular & Developmental Biology. Animal|October 17, 2018
Monensin induces cell death by autophagy and inhibits matrix metalloproteinase 7 (MMP7) in UOK146 renal cell carcinoma cell lineShiv Prakash Verma, Parimal Das
Biochimica Et Biophysica Acta. General Subjects|December 16, 2023
Calcimycin mediates apoptosis in breast and cervical cancer cell lines by inducing intracellular calcium levels in a P2RX4-dependent mannerNeha, Prashant Ranjan, Parimal Das
Biochimica Et Biophysica Acta. General Subjects|November 16, 2017
G-quadruplex structure at intron 2 of TFE3 and its role in Xp11.2 translocation and splicingShiv Prakash Verma, Parimal Das
Biochimica Et Biophysica Acta. General Subjects|September 4, 2020
Dual role of G-quadruplex in translocation renal cell carcinoma: Exploring plausible Cancer therapeutic innovationNeha, Parimal Das, Shiv Prakash Verma
Gene|August 30, 2017
A novel G to A transition at initiation codon and exon-intron boundary of PAX9 identified in association with familial isolated oligodontiaTanmoy Sarkar, Rajesh Bansal, Parimal Das
Plos One|September 10, 2014
Whole genome sequencing reveals novel non-synonymous mutation in ectodysplasin A (EDA) associated with non-syndromic X-linked dominant congenital tooth agenesisTanmoy Sarkar, Rajesh Bansal, Parimal Das
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