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Molecular Biology Reports|November 5, 2022
Characterization and expression analysis of basic leucine zipper (bZIP) transcription factors responsive to chilling injury in peach fruitMuhammad Muzammal Aslam, Li Deng, Junren Meng, et al.Insect Science|December 30, 2018
The role of chemosensory protein 10 in the detection of behaviorally active compounds in brown planthopper, Nilaparvata lugensMuhammad Irfan Waris, Aneela Younas, Muhammad Muzammal Adeel, et al.International Journal of Molecular Sciences|November 11, 2020
An Odorant Binding Protein (SaveOBP9) Involved in Chemoreception of the Wheat Aphid <i>Sitobion avenae</i>Rana Muhammad Kaleem Ullah, Sundas Rana Quershi, Muhammad Muzammal Adeel, et al.Neurogenetics|October 1, 2025
Expanding the ethnic and clinical spectrum of the IDS c.1122C>T mutation: first report from PakistanSana Fatima, Hunza Malik, Aftab Ali, et al.European Journal of Public Health|July 6, 2010
Prevalence of hepatitis B and C in internally displaced persons of war against terrorism in Swat, PakistanAbdul Rauf, Muhammad Shahid Nadeem, Akbar Ali, et al.Journal of Translational Medicine|October 29, 2018
Peptide vaccine against chikungunya virus: immuno-informatics combined with molecular docking approachMuhammad Tahir Ul Qamar, Amna Bari, Muhammad Muzammal Adeel, et al.Molecules (Basel, Switzerland)|July 2, 2021
Therapeutic Attributes of Endocannabinoid System against Neuro-Inflammatory Autoimmune DisordersIshtiaq Ahmed, Saif Ur Rehman, Shiva Shahmohamadnejad, et al.Expert Review of Hematology|July 26, 2023
Genetic basis of ß-thalassemia in families of pashtun ethnicity in Dera Ismail Khan district of Khyber Pakhtun-Khwa province, PakistanMuhammad Ayaz, Muhammad Muzammal, Sami Siraj, et al.Genes|April 28, 2023
Identification of <i>GLI1</i> and <i>KIAA0825</i> Variants in Two Families with Postaxial PolydactylySafeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal, et al.Molecular Genetics & Genomic Medicine|July 12, 2019
Exome sequence analysis in consanguineous Pakistani families inheriting Bardet-Biedle syndrome determined founder effect of mutation c.299delC (p.Ser100Leufs*24) in BBS9 geneMuhammad Muzammal, Muhammad Zubair, Sophie Bierbaumer, et al.Pageof 7