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Analytical Methods : Advancing Methods and Applications|June 13, 2023
Point of care testing (POCT) of cholesterol in blood serum via a moving reaction boundary electrophoresis titration chipMuhammad Idrees Khan, Qiang Zhang, Youli Tian, et al.Virusdisease|January 2, 2018
Role of circulatory microRNAs in the pathogenesis of hepatitis C virusIqra Almas, Samia Afzal, Muhammad Idrees, et al.Journal of Infection in Developing Countries|July 6, 2011
Comparative sequence, antigenic and phylogenetic analysis of avian influenza (H9N2) surface proteins isolated in Pakistan between 1999 and 2008Azeem Mehmood Butt, Samerene Siddique, Shifa Tahir, et al.Journal of Molecular Graphics & Modelling|April 21, 2018
Allosteric ligands for the pharmacologically important Flavivirus target (NS5) from ZINC database based on pharmacophoric points, free energy calculations and dynamics correlationAbbas Khan, Shoaib Saleem, Muhammad Idrees, et al.Human Genome Variation|September 8, 2022
A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataractsBushra Irum, Firoz Kabir, Nadav Shoshany, et al.Human Genome Variation|December 6, 2016
Mutations in phosphodiesterase 6 identified in familial cases of retinitis pigmentosaInayat Ullah, Firoz Kabir, Clare Brooks S Gottsch, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 17, 2006
Metabolism of [14C]gemopatrilat after oral administration to rats, dogs, and humansJill C M Wait, Nimish Vaccharajani, James Mitroka, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2019
Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotoniaZafar Iqbal, Hasan Tawamie, Wei Ba, et al.Malaria Journal|September 10, 2014
PCR/RFLP-based analysis of genetically distinct Plasmodium vivax population of Pvmsp-3α and Pvmsp-3β genes in PakistanShahid Niaz Khan, Asif Khan, Sanaullah Khan, et al.Plos Genetics|September 17, 2013
An alteration in ELMOD3, an Arl2 GTPase-activating protein, is associated with hearing impairment in humansThomas J Jaworek, Elodie M Richard, Anna A Ivanova, et al.Pageof 72