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Neurogenetics|December 26, 2025
Mutation screening of the ASPM gene in multiple Pashtun origin MCPH families revealed the recurrent nonsense mutation p.Trp1326*: A step towards the development of a genetic diagnostic testHamna Batool Hashmi, Muhammad Muzammal, Aiman Saleem, et al.Genes|April 23, 2022
In Silico Analysis of the L-2-Hydroxyglutarate Dehydrogenase Gene Mutations and Their Biological Impact on Disease EtiologyMuhammad Muzammal, Alessandro Di Cerbo, Eman M Almusalami, et al.Pharmaceuticals (Basel, Switzerland)|June 24, 2022
Structural Elucidation of Rift Valley Fever Virus L Protein towards the Discovery of Its Potential InhibitorsMubarak A Alamri, Muhammad Usman Mirza, Muhammad Muzammal Adeel, et al.Molecules (Basel, Switzerland)|April 23, 2022
A Novel Distachionate from Breynia distachia Treats Inflammations by Modulating COX-2 and Inflammatory Cytokines in Rat Liver TissueMalik Saadullah, Muhammad Asif, Arshad Farid, et al.Genes|April 23, 2022
In Silico Analysis Identified Putative Pathogenic Missense nsSNPs in Human SLITRK1 GeneMuhammad Zeeshan Ali, Arshad Farid, Safeer Ahmad, et al.Molecules (Basel, Switzerland)|July 9, 2022
Pharmacological Properties of 4', 5, 7-Trihydroxyflavone (Apigenin) and Its Impact on Cell Signaling PathwaysRameesha Abid, Shakira Ghazanfar, Arshad Farid, et al.Molecules (Basel, Switzerland)|September 23, 2022
Synthesis of Starch-Grafted Polymethyl Methacrylate via Free Radical Polymerization Reaction and Its Application for the Uptake of Methylene BlueUzma Yasmeen, Fazal Haq, Mehwish Kiran, et al.Microorganisms|May 28, 2022
Identification, Biochemical Characterization, and Safety Attributes of Locally Isolated Lactobacillus fermentum from Bubalus bubalis (buffalo) Milk as a ProbioticSana Abid, Arshad Farid, Rameesha Abid, et al.Frontiers in Neurology|June 12, 2023
Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanismsNazif Muhammad, Syeda Iqra Hussain, Zia Ur Rehman, et al.Frontiers in Genetics|January 20, 2026
Expanding the mutational spectrum of congenital microcephaly in Pakistani familiesSundas Farooq, Maria Asif, Ansar A Abbasi, et al.Pageof 7