Showing results (21-30 of 43) with videos related to
Sort By:
Pageof 5
Genomics|May 22, 2021
Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type AMuhammad Umair, Oliva Palander, Muhammad Bilal, et al.Bioinformation|March 22, 2023
Effect of rifampicin combination-regimens against multi-drug resistant strains in North IndiaMisbahuddin M Rafeeq, Alaa Hamed Habib, Ahmad Alzamami, et al.European Journal of Medical Genetics|July 8, 2021
Targeted exome sequencing identified a novel frameshift variant in the PGAM2 gene causing glycogen storage disease type XAnam Nayab, Qamre Alam, Othman R Alzahrani, et al.Frontiers in Neuroscience|June 13, 2022
Brain-Derived Neurotrophic Factor: A Connecting Link Between Nutrition, Lifestyle, and Alzheimer's DiseaseBin Xue, Shah Mohammad Abbas Waseem, Zhixin Zhu, et al.Journal of Biomolecular Structure & Dynamics|November 1, 2022
PheroxyPyrabenz and Carbopyrropyridin against major proteins of SARS CoV-2: a comprehensive in-silico molecular docking and dynamics simulation studiesMisbahuddin M Rafeeq, Alaa F Nahhas, Najat Binothman, et al.Journal of Biomolecular Structure & Dynamics|August 21, 2023
Unveiling the multitargeted potency of Sodium Danshensu against cervical cancer: a multitargeted docking-based, structural fingerprinting and molecular dynamics simulation studySaad Alghamdi, Hanadi M Baeissa, Mohammad Azhar Kamal, et al.Medical Oncology (Northwood, London, England)|October 20, 2023
Multitargeted inhibitory effect of Mitoxantrone 2HCl on cervical cancer cell cycle regulatory proteins: a multitargeted docking-based MM\GBSA and MD simulation studyMohammed Ali Alshehri, Saeed Ahmed Asiri, Abdulrahman Alzahrani, et al.Plos One|June 16, 2022
Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairmentMohib Ullah Kakar, Muhammad Akram, Muhammad Zubair Mehboob, et al.Frontiers in Genetics|February 3, 2023
Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasiaMisbahuddin M Rafeeq, Hussam Aly Sayed Murad, Najumuddin, et al.Plos One|June 21, 2024
Unrevealing the multitargeted potency of 3-1-BCMIYPPA against lung cancer structural maintenance and suppression proteins through pharmacokinetics, QM-DFT, and multiscale MD simulation studiesMohammed Ali Alshehri, Saeed A Asiri, Nawal Helmi, et al.Pageof 5