Showing results (241-250 of 282) with videos related to
Sort By:
Pageof 29
Human Genetics|March 11, 2017
Genetic differentiation between upland and lowland populations shapes the Y-chromosomal landscape of West AsiaO Balanovsky, M Chukhryaeva, V Zaporozhchenko, et al.European Journal of Medicinal Chemistry|May 27, 2019
Synthesis, biological evaluation and computational study of novel isoniazid containing 4H-Pyrimido[2,1-b]benzothiazoles derivativesManoj N Bhoi, Mayuri A Borad, Divya J Jethava, et al.Journal of Biomolecular Structure & Dynamics|March 19, 2015
Molecular interaction of selected phytochemicals under the charged environment of Plasmodium falciparum chloroquine resistance transporter (PfCRT) modelSaumya K Patel, Vijay M Khedkar, Prakash C Jha, et al.JAMA Network Open|February 29, 2024
Telemedicine vs Telephone Consultations and Medication Prescribing Errors Among Referring Physicians: A Cluster Randomized Crossover TrialJames P Marcin, Monica K Lieng, Jamie Mouzoon, et al.AJNR. American Journal of Neuroradiology|January 14, 2017
Effects of Radiation Exposure on the Cost-Effectiveness of CT Angiography and Perfusion Imaging in Aneurysmal Subarachnoid HemorrhageJ Ivanidze, R A Charalel, I Shuryak, et al.Tetrahedron|August 9, 2011
Practical asymmetric synthesis of β-hydroxy γ-amino acids via complimentary aldol reactionsBhaumik A Pandya, Sivaraman Dandapani, Jeremy R Duvall, et al.Human Molecular Genetics|December 10, 1999
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing lossX Z Liu, X J Xia, L R Xu, et al.Nucleic Acids Research|November 17, 2007
A bioinformatic filter for improved base-call accuracy and polymorphism detection using the Affymetrix GeneChip whole-genome resequencing platformGagan A Pandya, Michael H Holmes, Sirisha Sunkara, et al.AJNR. American Journal of Neuroradiology|May 10, 2014
Cost-effectiveness of CT angiography and perfusion imaging for delayed cerebral ischemia and vasospasm in aneurysmal subarachnoid hemorrhageP C Sanelli, A Pandya, A Z Segal, et al.Human Molecular Genetics|April 1, 1996
Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?A Pandya, X J Xia, B L Landa, et al.Pageof 29