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Biochemical Pharmacology|August 18, 2016
Cooperativity between verapamil and ATP bound to the efflux transporter P-glycoproteinKaitlyn V Ledwitch, Morgan E Gibbs, Robert W Barnes, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2024
A bacterial TIR-based immune system senses viral capsids to initiate defenseCameron G Roberts, Chloe B Fishman, Dalton V Banh, et al.
Chemical Science|October 6, 2023
Deaminative ring contraction for the synthesis of polycyclic heteroaromatics: a concise total synthesis of toddaquinolineEmily K Kirkeby, Zachary T Schwartz, Myles A Lovasz, et al.
Genome Biology and Evolution|November 26, 2024
Multiple Displacement Amplification Facilitates SMRT Sequencing of Microscopic Animals and the Genome of the Gastrotrich Lepidodermella squamata (Dujardin 1841)Nickellaus G Roberts, Michael J Gilmore, Torsten H Struck, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|March 19, 2026
Semi-Empirical Model to Predict Blood Flow in an Extracorporeal Respiratory Support Circuit Driven by Ventricular Assist DevicesKalliope G Roberts, Umar Nasim, Yeahwa Hong, et al.
Genomics|November 24, 1999
The human family of Deafness/Dystonia peptide (DDP) related mitochondrial import proteinsH Jin, E Kendall, T C Freeman, et al.
British Medical Journal (Clinical Research Ed.)|July 10, 1982
Haemofiltration for profound dialysis-induced hypotension: removal of sodium and water without blood-pressure changeA M Davison, T G Roberts, B H Mascie-Taylor, et al.
Human Mutation|January 1, 1995
Protein truncation test: analysis of two novel point mutations at the carboxy-terminus of the human dystrophin gene associated with mental retardationS Tuffery, U Lenk, R G Roberts, et al.
Archives of Pediatrics & Adolescent Medicine|November 12, 1998
Aggressive approach in the treatment of acute lead encephalopathy with an extraordinarily high concentration of leadR A Gordon, G Roberts, Z Amin, et al.
Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.
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