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Science Translational Medicine|October 6, 2017
Rapid pathogen-specific phenotypic antibiotic susceptibility testing using digital LAMP quantification in clinical samplesNathan G Schoepp, Travis S Schlappi, Matthew S Curtis, et al.
ACS Applied Materials & Interfaces|December 19, 2017
Marine Antifouling Behavior of Lubricant-Infused Nanowrinkled Polymeric SurfacesCameron S Ware, Truis Smith-Palmer, Sam Peppou-Chapman, et al.
Ecology and Evolution|January 26, 2019
Behavioral classification of low-frequency acceleration and temperature data from a free-ranging small mammalEmily K Studd, Manuelle Landry-Cuerrier, Allyson K Menzies, et al.
Biochimica Et Biophysica Acta|February 12, 2014
Identification and validation of novel candidate protein biomarkers for the detection of human gastric cancerJulia M Humphries, Megan A S Penno, Florian Weiland, et al.
Genomics|October 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21G J Farrar, P McWilliam, E M Sharp, et al.
Genomics|November 1, 1992
Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigreeG J Farrar, P Kenna, S A Jordan, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 14, 2020
Clinical and Laboratory Standards Institute and European Committee on Antimicrobial Susceptibility Testing Position Statements on Polymyxin B and Colistin Clinical BreakpointsMichael J Satlin, James S Lewis, Melvin P Weinstein, et al.
BMC Pulmonary Medicine|October 24, 2025
Fibrotic and vascular abnormalities quantified by an AI-based model are associated with outcomes in patients with idiopathic pulmonary fibrosisJulien Guiot, Jonne Engelberts, Monique Henket, et al.
Infection Control and Hospital Epidemiology|December 19, 2022
Universal admission laboratory screening for severe acute respiratory coronavirus virus 2 (SARS-CoV-2) asymptomatic infection across a large health systemJennifer L Cihlar, Bryan D Harris, Patty W Wright, et al.
American Journal of Human Genetics|March 26, 1999
Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 geneF C Mansergh, S Millington-Ward, A Kennan, et al.
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