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Scientific Reports|July 23, 2021
Phylogenetic analysis of the 5' untranslated region of HCV from cirrhotic patients in Khyber Pakhtunkhwa, PakistanAmin Ullah, Irshad Ur Rehman, Jamshaid Ahmad, et al.Current Drug Targets|October 14, 2020
Physcion and Physcion 8-O-β-D-glucopyranoside: Natural Anthraquinones with Potential Anticancer ActivitiesMuhammad Adnan, Azhar Rasul, Ghulam Hussain, et al.Nanomaterials (Basel, Switzerland)|July 9, 2022
Applications of Various Types of Nanomaterials for the Treatment of Neurological DisordersAbdul Waris, Asmat Ali, Atta Ullah Khan, et al.Human Mutation|January 4, 2017
In Silico Functional Meta-Analysis of 5,962 ABCA4 Variants in 3,928 Retinal Dystrophy CasesStéphanie S Cornelis, Nathalie M Bax, Jana Zernant, et al.Canadian Journal of Anaesthesia = Journal Canadien D'Anesthesie|December 2, 2020
Effects of an anesthesia perioperative surgical home for total knee and hip arthroplasty at a Veterans Affairs Hospital: a quality improvement before-and-after cohort studyBret D Alvis, Roland G Amsler, Philip J Leisy, et al.Molecular Biology Reports|February 8, 2012
Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patientsWaqas Ahmed, Muhammad Ajmal, Ahmed Sadeque, et al.Neurochemical Research|September 17, 2020
Exploring the Therapeutic Potentials of Highly Selective Oxygenated Chalcone Based MAO-B Inhibitors in a Haloperidol-Induced Murine Model of Parkinson's DiseaseDella Grace Thomas Parambi, Uzma Saleem, Muhammad Ajmal Shah, et al.Plants (Basel, Switzerland)|March 6, 2021
Response of Olive Shoots to Salinity Stress Suggests the Involvement of Sulfur MetabolismMuhammad Ajmal Bashir, Cristian Silvestri, Eleonora Coppa, et al.Journal of the American College of Cardiology|March 16, 2005
Echocardiographic findings in patients meeting task force criteria for arrhythmogenic right ventricular dysplasia: new insights from the multidisciplinary study of right ventricular dysplasiaDanita M Yoerger, Frank Marcus, Duane Sherrill, et al.Molecular Vision|September 16, 2009
A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani familyMaleeha Azam, Rob W J Collin, Muhammad Imran Khan, et al.Pageof 33