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Human Molecular Genetics|July 6, 2016
An enhanced Q175 knock-in mouse model of Huntington disease with higher mutant huntingtin levels and accelerated disease phenotypesAmber L Southwell, Amy Smith-Dijak, Chris Kay, et al.European Journal of Heart Failure|December 10, 2019
Imaging in patients with suspected acute heart failure: timeline approach position statement on behalf of the Heart Failure Association of the European Society of CardiologyJelena Čelutkienė, Mitja Lainscak, Lisa Anderson, et al.European Journal of Heart Failure|November 10, 2018
Innovative imaging methods in heart failure: a shifting paradigm in cardiac assessment. Position statement on behalf of the Heart Failure Association of the European Society of CardiologyJelena Čelutkienė, Carla M Plymen, Frank A Flachskampf, et al.Kidney International Reports|December 23, 2017
Rapid Biolayer Interferometry Measurements of Urinary CXCL9 to Detect Cellular Infiltrates Noninvasively After Kidney TransplantationIlaria Gandolfini, Cynthia Harris, Michael Abecassis, et al.Kidney International Reports|October 26, 2020
A Comprehensive Phenotypic and Functional Immune Analysis Unravels Circulating Anti-Phospholipase A2 Receptor Antibody Secreting Cells in Membranous Nephropathy PatientsChiara Cantarelli, Marta Jarque, Andrea Angeletti, et al.Transfusion|March 19, 2019
Therapeutic impact of red blood cell transfusion on anemic outpatients: the RETRO studyElizabeth St Lezin, Matthew S Karafin, Roberta Bruhn, et al.European Journal of Heart Failure|September 15, 2023
Practical algorithms for early diagnosis of heart failure and heart stress using NT-proBNP: A clinical consensus statement from the Heart Failure Association of the ESCAntoni Bayes-Genis, Kieran F Docherty, Mark C Petrie, et al.BMC Medical Genomics|July 25, 2018
Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritisElisabeth De Smit, Samuel W Lukowski, Lisa Anderson, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 17, 2019
A Rare Mutation in SMAD9 Associated With High Bone Mass Identifies the SMAD-Dependent BMP Signaling Pathway as a Potential Anabolic Target for OsteoporosisCelia L Gregson, Dylan J M Bergen, Paul Leo, et al.Bioinformatics (Oxford, England)|January 20, 2026
Aggregation of gene regulatory information and knowledge on FAIR principles enables discovery of pathogenic gene regulatory variantsKeyang Yu, Haoquan Zhao, Andrea Wilderman, et al.Pageof 15