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Molecules (Basel, Switzerland)|December 23, 2022
The Detailed Pharmacodynamics of the Gut Relaxant Effect and GC-MS Analysis of the <i>Grewia tenax</i> Fruit Extract: In Vivo and Ex Vivo ApproachNajeeb Ur Rehman, Mohd Nazam Ansari, Wasim Ahmad, et al.Human Genome Variation|December 22, 2017
A novel homozygous missense mutation in <i>BHLHA9</i> causes mesoaxial synostotic syndactyly with phalangeal reduction in a Pakistani familyAmjad Khan, Rongrong Wang, Shirui Han, et al.Frontiers in Bioscience (Landmark Edition)|January 30, 2024
Pharmacological Basis for the Antidiarrheal and Antispasmodic Effects of Cuminaldehyde in Experimental Animals: <i>In Silico</i>, <i>Ex Vivo</i> and <i>In Vivo</i> StudiesMohd Nazam Ansari, Najeeb Ur Rehman, Abdul Samad, et al.Toxicology Research|November 2, 2023
Hexaconazole exposure disrupt acetylcholinesterase, leading to mental illnessAbuzer Ali, Sayed Aliul Hasan Abdi, Amena Ali, et al.Journal of Pharmacy & Bioallied Sciences|December 19, 2015
Bergenin determination in different extracts by high-performance thin-layer chromatographic densitometryMasood Shah Khan, Washim Khan, Wasim Ahmad, et al.Reviews on Environmental Health|May 13, 2021
Understanding Holism in the light of principle underlying practice of Unani MedicineWasim Ahmad, Ghulamuddin Sofi, Md Anzar Alam, et al.Archives of Dermatological Research|February 9, 2010
A novel splice-acceptor site mutation in CDH3 gene in a consanguineous family exhibiting hypotrichosis with juvenile macular dystrophySyed Kamran-ul-Hassan Naqvi, Zahid Azeem, Ghazanfar Ali, et al.Scientific Reports|February 4, 2026
Enhancing fruit supply chain traceability through blockchain and cryptographic protocols for achieving UN sustainable development goalsAqsa Rashid, Raja Wasim Ahmad, Mirna Nachouki, et al.European Journal of Medical Genetics|March 2, 2016
Genetics of human isolated acromesomelic dysplasiaSaadullah Khan, Sulman Basit, Muzammil Ahmad Khan, et al.Gene|October 4, 2011
A novel splice site mutation in gene C2orf37 underlying Woodhouse-Sakati syndrome (WSS) in a consanguineous family of Pakistani originRabia Habib, Sulman Basit, Saadullah Khan, et al.Pageof 34