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Respiratory Research|January 23, 2019
Whole blood RNA sequencing reveals a unique transcriptomic profile in patients with ARDS following hematopoietic stem cell transplantationJoshua A Englert, Michael H Cho, Andrew E Lamb, et al.
JCI Insight|July 13, 2018
Circulating RIPK3 levels are associated with mortality and organ failure during critical illnessKevin C Ma, Edward J Schenck, Ilias I Siempos, et al.
The Journal of Urology|July 3, 2020
Pregnancy and Delivery in Women with Lower Urinary Tract Reconstruction: A National Multicenter Retrospective Study from the French-Speaking Neuro-Urology Study Group (GENULF) and the Neuro-Urology Committee of the French Association of UrologyE Bey, Q Manach, B Peyronnet, et al.
Cell Reports|April 6, 2022
ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of functionDesiree M Baron, Adam R Fenton, Sara Saez-Atienzar, et al.
Scientific Reports|April 5, 2022
A targetable 'rogue' neutrophil-subset, [CD11b+DEspR+] immunotype, is associated with severity and mortality in acute respiratory distress syndrome (ARDS) and COVID-19-ARDSVictoria L M Herrera, Allan J Walkey, Mai Q Nguyen, et al.
Science Translational Medicine|May 6, 2026
Lactate transport inhibition therapeutically reprograms fibroblast metabolism in experimental pulmonary fibrosisDavid R Ziehr, Fei Li, K Mark Parnell, et al.
Human Molecular Genetics|December 6, 2011
Identification of a chronic obstructive pulmonary disease genetic determinant that regulates HHIPXiaobo Zhou, Rebecca M Baron, Megan Hardin, et al.
Iscience|May 30, 2023
The upper and lower respiratory tract microbiome in severe aspiration pneumoniaGeorgios D Kitsios, Vi D Nguyen, Khaled Sayed, et al.
Research Square|September 21, 2021
Increased Neutrophil-Subset Associated With Severity/Mortality In ARDS And COVID19-ARDS Expresses The Dual Endothelin-1/VEGFsignal-Peptide Receptor (DEspR): An Actionable Therapeutic TargetVictoria L M Herrera, Allan J Walkey, Mai Q Nguyen, et al.
Nature Genetics|June 10, 2024
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's diseasePaul J Hop, Dongbing Lai, Pamela J Keagle, et al.
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