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Physiological Reports|March 1, 2018
P2X7 receptor antagonism ameliorates renal dysfunction in a rat model of sepsisNishkantha Arulkumaran, Marije L Sixma, Sean Pollen, et al.
Hypertension (Dallas, Tex. : 1979)|February 26, 2015
Design, characterization, and first-in-human study of the vascular actions of a novel biased apelin receptor agonistAimee L Brame, Janet J Maguire, Peiran Yang, et al.
Anesthesia and Analgesia|April 2, 2025
Metabolic Flexibility as a Candidate Mechanism for the Development of Postoperative MorbidityPietro Arina, John Whittle, Maciej R Kaczorek, et al.
Shock (Augusta, Ga.)|June 21, 2018
Part III: Minimum Quality Threshold in Preclinical Sepsis Studies (MQTiPSS) for Fluid Resuscitation and Antimicrobial Therapy EndpointsJudith Hellman, Soheyl Bahrami, Mihaly Boros, et al.
Frontiers in Physiology|June 7, 2018
Diabetes Worsens Skeletal Muscle Mitochondrial Function, Oxidative Stress, and Apoptosis After Lower-Limb Ischemia-Reperfusion: Implication of the RISK and SAFE Pathways?Julien Pottecher, Chris Adamopoulos, Anne Lejay, et al.
Alternatives to Laboratory Animals : ATLA|December 24, 2005
Opportunities to replace the use of animals in sepsis research. The report and recommendations of a Focus on Alternatives workshopChris Langley, Chris Brock, Gerard Brouwer, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|May 28, 2015
Bile duct-ligated mice exhibit multiple phenotypic similarities to acute decompensation patients despite histological differencesAlastair O'Brien, Louise China, Karen A Massey, et al.
Critical Care Medicine|March 2, 2022
The β 1 -Adrenergic Receptor Contributes to Sepsis-Induced Immunosuppression Through Modulation of Regulatory T-Cell Inhibitory FunctionManon Durand, Eugénie Hagimont, Huguette Louis, et al.
Computational and Structural Biotechnology Journal|December 11, 2020
Lipid metabolic signatures deviate in sepsis survivors compared to non-survivorsWaqas Khaliq, Peter Großmann, Sophie Neugebauer, et al.
Frontiers in Neuroscience|March 16, 2017
[Pyr1]Apelin-13(1-12) Is a Biologically Active ACE2 Metabolite of the Endogenous Cardiovascular Peptide [Pyr1]Apelin-13Peiran Yang, Rhoda E Kuc, Aimée L Brame, et al.
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