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Diabetes Research and Clinical Practice|April 7, 2017
Neuropathy of type 1 diabetes in the Arab world: A systematic review and meta-analysisUssama M Abdel-Motal, Essam M Abdelalim, Haissam Abou-Saleh, et al.International Journal of Biological Sciences|November 17, 2018
Novel CD44-downstream signaling pathways mediating breast tumor invasionAllal Ouhtit, Balsam Rizeq, Haissam Abou Saleh, et al.Clinical Proteomics|February 12, 2025
Identification of novel proteomic biomarkers for hypertension: a targeted approach for precision medicineRana S Aldisi, Alsamman M Alsamman, Peter Krawitz, et al.Metabolic Brain Disease|May 28, 2018
Computational insights of K1444N substitution in GAP-related domain of NF1 gene associated with neurofibromatosis type 1 disease: a molecular modeling and dynamics approachAshish Kumar Agrahari, Meghana Muskan, C George Priya Doss, et al.Journal of Theoretical Biology|November 8, 2017
Substitution impact of highly conserved arginine residue at position 75 in GJB1 gene in association with X-linked Charcot-Marie-tooth disease: A computational studyAshish Kumar Agrahari, Amit Kumar, Siva R, et al.Plos One|April 15, 2017
Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approachSneha P, Thirumal Kumar D, George Priya Doss C, et al.Nutrients|March 11, 2020
Association between Soft Drink Consumption and Aggressive Behaviour among a Quarter Million Adolescents from 64 Countries Based on the Global School-Based Student Health Survey (GSHS)Zumin Shi, Ahmed Malki, Abdel-Salam G Abdel-Salam, et al.Expert Review of Hematology|December 15, 2020
The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic reviewAisha Moeen Khan, Asma Mohammed Al-Sulaiti, Salma Younes, et al.Current Issues in Molecular Biology|November 25, 2003
The Sleeping Beauty transposable element: evolution, regulation and genetic applicationsZoltán Ivics, Christopher D Kaufman, Hatem Zayed, et al.Metabolic Brain Disease|October 20, 2017
A profound computational study to prioritize the disease-causing mutations in PRPS1 geneAshish Kumar Agrahari, P Sneha, C George Priya Doss, et al.Pageof 18