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Advances in Protein Chemistry and Structural Biology|February 23, 2020
Computational model to analyze and characterize the functional mutations of NOD2 protein causing inflammatory disorder - Blau syndromeD Thirumal Kumar, S Udhaya Kumar, Ahmed Shaikh Nishaat Laeeque, et al.Genes|October 29, 2020
Involvement of Essential Signaling Cascades and Analysis of Gene Networks in DiabesityUdhaya Kumar S, Bithia Rajan, Thirumal Kumar D, et al.Journal of Cellular Biochemistry|July 21, 2021
Comparison of potential inhibitors and targeting fat mass and obesity-associated protein causing diabesity through docking and molecular dynamics strategiesS Udhaya Kumar, Bithia Rajan, D Thirumal Kumar, et al.Molecules (Basel, Switzerland)|August 24, 2018
Protective Effect of Cyclically Pressurized Solid⁻Liquid Extraction Polyphenols from <i>Cagnulari</i> Grape Pomace on Oxidative Endothelial Cell DeathAnna Maria Posadino, Grazia Biosa, Hatem Zayed, et al.Metabolic Brain Disease|December 28, 2023
Genomic insights and advanced machine learning: characterizing autism spectrum disorder biomarkers and genetic interactionsLaila Dabab Nahas, Ankur Datta, Alsamman M Alsamman, et al.3 Biotech|April 5, 2021
A review of novel coronavirus disease (COVID-19): based on genomic structure, phylogeny, current shreds of evidence, candidate vaccines, and drug repurposingS Udhaya Kumar, N Madhana Priya, S R Nithya, et al.Advances in Protein Chemistry and Structural Biology|August 3, 2021
An integrative analysis to distinguish between emphysema (EML) and alpha-1 antitrypsin deficiency-related emphysema (ADL)-A systems biology approachS Udhaya Kumar, N Madhana Priya, D Thirumal Kumar, et al.Journal of Tissue Engineering and Regenerative Medicine|October 13, 2017
Differences in the neovascular potential of thymus versus subcutaneous adipose-derived stem cells from patients with myocardial ischaemiaWilfredo Oliva-Olivera, Leticia Coín-Aragüez, Said Lhamyani, et al.Advances in Protein Chemistry and Structural Biology|February 23, 2020
Comprehensive in silico screening and molecular dynamics studies of missense mutations in Sjogren-Larsson syndrome associated with the ALDH3A2 geneS Udhaya Kumar, D Thirumal Kumar, Pinky D Mandal, et al.Metabolic Brain Disease|August 2, 2016
Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase geneAhmed Moseilhy, Magdy M Hassan, Heba S A El Abd, et al.Pageof 18