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MicroRNA deep sequencing in two adult stem cell populations identifies miR-501 as a novel regulator of myosin heavy chain during muscle regeneration Development, 143, 4137–4148. https://doi.org/10.1242/dev.136051
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microRNA-29a in adult muscle stem cells controls skeletal muscle regeneration during injury and exercise downstream of fibroblast growth factor-2 Stem Cells, 34, 768–780. https://doi.org/10.1002/stem.2281
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New and emerging roles of small RNAs in neurodegeneration, muscle, cardiovascular and inflammatory diseases Swiss Medical Weekly, w14192. https://doi.org/10.4414/smw.2015.14192
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Aguzzi Group
ZORA Publication List
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Autoantibodies against the prion protein in individuals with PRNP mutations Neurology, 95, e2028–e2037. https://doi.org/10.1212/wnl.0000000000009183
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Ribosomal profiling during prion disease uncovers progressive translational derangement in glia but not in neurons ELife, 9, e62911. https://doi.org/10.7554/elife.62911
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Protective anti‐prion antibodies in human immunoglobulin repertoires EMBO Molecular Medicine, e12739. https://doi.org/10.15252/emmm.202012739
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Genome-wide transcriptomics identifies an early preclinical signature of prion infection PLoS Pathogens, 16, e1008653. https://doi.org/10.1371/journal.ppat.1008653
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NG2 glia are required for maintaining microglia homeostatic state Glia, glia.23721. https://doi.org/10.1002/glia.23721
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Enhanced detection of prion infectivity from blood by preanalytical enrichment with peptoid-conjugated beads PLoS ONE, 14, e0216013. https://doi.org/10.1371/journal.pone.0216013
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Unaltered prion disease in mice lacking developmental endothelial locus–1 Neurobiology of Aging, 76, 208–213. https://doi.org/10.1016/j.neurobiolaging.2019.01.003
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SARM1 deficiency up-regulates XAF1, promotes neuronal apoptosis, and accelerates prion disease Journal of Experimental Medicine, jem.20171885. https://doi.org/10.1084/jem.20171885
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Genome-Wide Identification of microRNAs Regulating the Human Prion Protein Brain Pathology, 29, 232–244. https://doi.org/10.1111/bpa.12679
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Lymphocyte activation gene 3 (Lag3) expression is increased in prion infections but does not modify disease progression Scientific Reports, 8, 14600. https://doi.org/10.1038/s41598-018-32712-8
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Toxic Protein Spread in Neurodegeneration: Reality versus Fantasy Trends in Molecular Medicine, 24, 1007–1020. https://doi.org/10.1016/j.molmed.2018.09.004
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Prion pathogenesis is unaltered in a mouse strain with a permeable blood-brain barrier PLoS Pathogens, 14, e1007424. https://doi.org/10.1371/journal.ppat.1007424
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Prions, prionoids and protein misfolding disorders Nature Reviews. Genetics, 19, 405–418. https://doi.org/10.1038/s41576-018-0011-4
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Intrinsic Toxicity of Antibodies to the Globular Domain of the Prion Protein Biological Psychiatry, 84, e51–e52. https://doi.org/10.1016/j.biopsych.2018.01.028
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Structural characterization of POM6 Fab and mouse prion protein complex identifies key regions for prions conformational conversion FEBS Journal, 285, 1701–1714. https://doi.org/10.1111/febs.14438
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GPR56/ADGRG1 regulates development and maintenance of peripheral myelin Journal of Experimental Medicine, 215, 941–961. https://doi.org/10.1084/jem.20161714
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Inhibition of group-I metabotropic glutamate receptors protects against prion toxicity PLoS Pathogens, 13, e1006733. https://doi.org/10.1371/journal.ppat.1006733
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Absolute Quantification of Amyloid Propagons by Digital Microfluidics Analytical Chemistry, 89, 12306–12313. https://doi.org/10.1021/acs.analchem.7b03279
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Prion pathogenesis is unaltered in the absence of SIRPα-mediated “don’t-eat-me” signaling. PLoS ONE, 12, e0177876. https://doi.org/10.1371/journal.pone.0177876
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The biological function of the cellular prion protein: an update BMC Biology, 15, 34. https://doi.org/10.1186/s12915-017-0375-5
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Modifiers of prion protein biogenesis and recycling identified by a highly-parallel endocytosis kinetics assay Journal of Biological Chemistry, 292, 8356–8368. https://doi.org/10.1074/jbc.M116.773283
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Protease resistance of infectious prions is suppressed by removal of a single atom in the cellular prion protein PLoS ONE, 12, e0170503. https://doi.org/10.1371/journal.pone.0170503
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Cystatin F is a biomarker of prion pathogenesis in mice PLoS ONE, 12, e0171923. https://doi.org/10.1371/journal.pone.0171923
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Neurotoxic antibodies against the prion protein do not trigger prion replication PLoS ONE, 11, e0163601. https://doi.org/10.1371/journal.pone.0163601
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The prion protein is an agonistic ligand of the G protein-coupled receptor Adgrg6 Nature, 536, 464–468. https://doi.org/10.1038/nature19312
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A neuroprotective role for microglia in prion diseases Journal of Experimental Medicine, 213, 1047–1059. https://doi.org/10.1084/jem.20151000
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Phase separation: linking cellular compartmentalization to disease Trends in Cell Biology, 26, 547–558. https://doi.org/10.1016/j.tcb.2016.03.004
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Homozygous Calreticulin mutations in patients with myelofibrosis lead to acquired myeloperoxidase deficiency Blood, 127, 3253–3259. https://doi.org/10.1182/blood-2016-02-696310
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Cell biology of prions and prionoids: a status report Trends in Cell Biology, 26, 40–51. https://doi.org/10.1016/j.tcb.2015.08.007
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Strictly co-isogenic C57BL/6J-Prnp−/−mice: A rigorous resource for prion science Journal of Experimental Medicine, 213, 313–327. https://doi.org/10.1084/jem.20151610
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Differential toxicity of antibodies to the prion protein PLoS Pathogens, 12, e1005401. https://doi.org/10.1371/journal.ppat.1005401
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Altered monoaminergic systems and depressive-like behavior in congenic prion protein nnock-out mice Journal of Biological Chemistry, 290, 26350. https://doi.org/10.1074/jbc.L115.689117
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Structure-based drug design identifies polythiophenes as antiprion compounds Science Translational Medicine, 7, 299ra123. https://doi.org/10.1126/scitranslmed.aab1923
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Prion infections and anti-PrP antibodies trigger converging neurotoxic pathways PLoS Pathogens, 11, e1004662. https://doi.org/10.1371/journal.ppat.1004662
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Neurodegeneration and unfolded-protein response in mice expressing a membrane-tethered flexible tail of PrP PLoS ONE, 10, e0117412. https://doi.org/10.1371/journal.pone.0117412
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Prion pathogenesis in the absence of NLRP3/ASC inflammasomes PLoS ONE, 10, e0117208. https://doi.org/10.1371/journal.pone.0117208
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Triggering receptor expressed on myeloid cells-2 is involved in prion-induced microglial activation but does not contribute to prion pathogenesis in mouse brains Neurobiology of Aging, 36, 1994–2003. https://doi.org/10.1016/j.neurobiolaging.2015.02.019
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Neurodegeneration: Alzheimer’s disease under strain. Nature, 512, 32–34. https://doi.org/10.1038/512032a
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The adaptor ASC has extracellular and “prionoid” activities that propagate inflammation. Nature Immunology, 15, 727–737. https://doi.org/10.1038/ni.2913
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The role of the NADPH oxidase NOX2 in prion pathogenesis PLoS Pathogens, 10, e1004531. https://doi.org/10.1371/journal.ppat.1004531
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Prions and lymphoid organs: Solved and remaining mysteries Prion, 7, 157–163. https://doi.org/10.4161/pri.23536
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The toxicity of antiprion antibodies is mediated by the flexible tail of the prion protein Nature, 501, 102–106. https://doi.org/10.1038/nature12402
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Microglia: scapegoat, saboteur, or something else? Science, 339, 156–161. https://doi.org/10.1126/science.1227901
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SIRPα polymorphisms, but not the prion protein, control phagocytosis of apoptotic cells Journal of Experimental Medicine, 210, 2539–2552. https://doi.org/10.1084/jem.20131274
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Efficient amyloid a clearance in the absence of immunoglobulins and complement factors American Journal of Pathology, 182, 1297–1307. https://doi.org/10.1016/j.ajpath.2012.12.035
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The immunobiology of prion diseases Nature Reviews. Immunology, 13, 888–902. https://doi.org/10.1038/nri3553
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Prions: protein aggregation and infectious diseases Physiological Reviews, 89, 1105–1152. https://doi.org/10.1152/physrev.00006.2009
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The POM monoclonals: a comprehensive set of antibodies to non-overlapping prion protein epitopes PLoS ONE, 3, e3872. https://doi.org/10.1371/journal.pone.0003872
Krützfeldt Group
ZORA Publication List
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Uncoupling protein 1 expression in adipocytes derived from skeletal muscle fibro/adipogenic progenitors is under genetic and hormonal control Journal of Cachexia, Sarcopenia and Muscle, 9, 384–399. https://doi.org/10.1002/jcsm.12277
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MicroRNA deep sequencing in two adult stem cell populations identifies miR-501 as a novel regulator of myosin heavy chain during muscle regeneration Development, 143, 4137–4148. https://doi.org/10.1242/dev.136051
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Strategies to use microRNAs as therapeutic targets Best Practice & Research : Clinical Endocrinology & Metabolism, 30, 551–561. https://doi.org/10.1016/j.beem.2016.07.004
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microRNA-29a in adult muscle stem cells controls skeletal muscle regeneration during injury and exercise downstream of fibroblast growth factor-2 Stem Cells, 34, 768–780. https://doi.org/10.1002/stem.2281
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Growth hormone replacement therapy regulates microRNA-29a and targets involved in insulin resistance Journal of Molecular Medicine, 93, 1369–1379. https://doi.org/10.1007/s00109-015-1322-y
Krützfeldt J, Rajewsky N, Braich R, Rajeev KG, Tuschl T, Manoharan M, Stoffel M. Silencing of microRNAs in vivo with 'antagomirs'. Nature. 2005 Dec 1;438(7068):685-9.
Krützfeldt J, Poy MN, Stoffel M. Strategies to determine the biological function of microRNAs. Nat Genet. 2006 Jun;38 Suppl 1:S14-9.
Krützfeldt J, Stoffel M. MicroRNAs: A new class of regulatory genes affecting metabolism. Cell Metab. 2006 Jul;4(1):9-12.
Krützfeldt J, Kuwajima S, Braich R, Rajeev KG, Pena J, Tuschl T, Manoharan M, Stoffel M. Specificity, duplex degradation and subcellular localization of antagomirs. Nucleic Acids Res. 2007 April; 35(9):2885-92.
Krützfeldt J, Rösch N, Hausser J, Manoharan M, Zavolan M, Stoffel M. MicroRNA-194 is a target of transcription factor 1 (Tcf1, Hnf1α) in adult liver and controls expression of frizzled-6. Hepatology. 2012 Jan;55(1):98-107.
Polymenidou Group
http://www.imls.uzh.ch/en/research/polymenidou/publ.html
ZORA Publication List
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Protease resistance of infectious prions is suppressed by removal of a single atom in the cellular prion protein PLoS ONE, 12, e0170503. https://doi.org/10.1371/journal.pone.0170503
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Prion-like propagation as a pathogenic principle in frontotemporal dementia Journal of Neurochemistry, 138 Supp, 163–183. https://doi.org/10.1111/jnc.13668
Polymenidou M*, Lagier-Tourenne C*, Hutt KR*, Huelga SC, Moran J, Liang TY, Ling SC, Sun E, Wancewicz E, Mazur C, Kordasiewicz H, Sedaghat Y, Donohue JP, Shiue L, Bennett CF, Yeo GW, Cleveland DW (2011) Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. Nature Neurosc, 14, 459–468 [*equal contribution]
Polymenidou M, Cleveland DW (2011) The Seeds of Neurodegeneration: Prion-like Spreading in ALS. Cell, 147, 498-508
Polymenidou M, Cleveland DW (2012) Prion-like spread of protein aggregates in neurodegeneration. Journal of Exp Med, 209, 889-93
Lagier-Tourenne C*, Polymenidou M*, Hutt KR*, Vu AQ, Clutario K, Baughn M, Huelga SC, Ling SC, Liang TY, Mazur C, Wancewicz E, Kim AS, Watt A, Freier S, Hicks GG, Donohue JP, Shiue L, Bennett CF, Ravits J, Cleveland DW and Yeo GW (2012) Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs. Nature Neurosc, 15, 1488-97 [*equal contribution]
Lagier-Tourenne C, Baughn M, Rigo F, Sun S, Liu P, Li HR, Jiang J, Watt AT, Chun S, Katz M, Qiu J, Sun Y, Ling S-C, Zhu Q, Polymenidou M, Drenner K, Artates JW, McAlonis-Downes M, Markmiller S, Hutt KR, Pizzo DP, Cady J, Harms MB, Baloh RH, Vandenberg SR, Yeo GW, Fu X-D, Bennett CF, Cleveland DW, Ravits J (2013) Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration. PNAS, 110, 47, E4530-39
Stoffel Group
LaPierre MP and Stoffel M (2017). MicroRNAs as stress regulators in pancreatic beta cells and diabetes. Molecular Metabolism 6:1010-1023.
Landmesser Group
ZORA Publication List
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2025 Focused Update of the 2019 ESC/EAS Guidelines for the management of dyslipidaemias European Heart Journal, 46, 4359–4378. https://doi.org/10.1093/eurheartj/ehaf190
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Vaccination as a new form of cardiovascular prevention: a European Society of Cardiology clinical consensus statement European Heart Journal, 46, 3518–3531. https://doi.org/10.1093/eurheartj/ehaf384
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Pharmacotherapy of cardiovascular diseases from herbs and pills to nucleic acids European Heart Journal, ehaf520. https://doi.org/10.1093/eurheartj/ehaf520
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Myocardial Inflammation in Cardiac Transthyretin Amyloidosis: Prevalence and Potential Prognostic Implications Circulation : Heart Failure, 18, e012146. https://doi.org/10.1161/circheartfailure.124.012146
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Hospitalization of Symptomatic Patients With Heart Failure and Moderate to Severe Functional Mitral Regurgitation Treated With MitraClip: Insights From RESHAPE-HF2 Journal of the American College of Cardiology, 84, 2347–2363. https://doi.org/10.1016/j.jacc.2024.08.027
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Transcatheter Valve Repair in Heart Failure with Moderate to Severe Mitral Regurgitation New England Journal of Medicine, 391, 1799–1809. https://doi.org/10.1056/NEJMoa2314328
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Quantitative flow ratio versus fractional flow reserve for coronary revascularisation guidance (FAVOR III Europe): a multicentre, randomised, non-inferiority trial The Lancet, 404, 1835–1846. https://doi.org/10.1016/S0140-6736(24)02175-5
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Prognostic impact of quantitative flow ratio (QFR)-consistent complete revascularization in patients with myocardial infarction and multivessel coronary artery disease American Heart Journal, 276, 22–30. https://doi.org/10.1016/j.ahj.2024.07.011
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Percutaneous repair of moderate-to-severe or severe functional mitral regurgitation in patients with symptomatic heart failure: Baseline characteristics of patients in the RESHAPE-HF2 trial and comparison to COAPT and MITRA-FR trials European Journal of Heart Failure, 26, 1608–1615. https://doi.org/10.1002/ejhf.3286
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Cholesterol crystals at the culprit lesion in patients with acute coronary syndrome are associated with worse cardiovascular outcomes at two years follow up - results from the translational OPTICO-ACS study program International Journal of Cardiology, 399, 131665. https://doi.org/10.1016/j.ijcard.2023.131665
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The inflammatory spectrum of cardiomyopathies Frontiers in Cardiovascular Medicine, 11, 1251780. https://doi.org/10.3389/fcvm.2024.1251780
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Coronary microevaginations characterize culprit plaques and their inflammatory microenvironment in a subtype of acute coronary syndrome with intact fibrous cap: results from the prospective translational OPTICO-ACS study European Heart Journal. Cardiovascular Imaging, 25, 175–184. https://doi.org/10.1093/ehjci/jead154
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Spotty calcium deposits within acute coronary syndrome (ACS)-causing culprit lesions impact inflammatory vessel-wall interactions and are associated with higher cardiovascular event rates at one year follow-up: Results from the prospective translational OPTICO-ACS study program Atherosclerosis, 385, 117284. https://doi.org/10.1016/j.atherosclerosis.2023.117284
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Clinical quantitative coronary artery stenosis and coronary atherosclerosis imaging: a Consensus Statement from the Quantitative Cardiovascular Imaging Study Group Nature Reviews. Cardiology, 20, 696–714. https://doi.org/10.1038/s41569-023-00880-4
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Prognostic impact of fractional flow reserve measurements in patients with acute coronary syndromes: a subanalysis of the FLORIDA study Heart and Vessels, 38, 1009–1018. https://doi.org/10.1007/s00380-023-02256-7
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Culprit plaque morphology determines inflammatory risk and clinical outcomes in acute coronary syndrome European Heart Journal, 44, 3911–3925. https://doi.org/10.1093/eurheartj/ehad334
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Large-scale microRNA functional high-throughput screening identifies miR-515-3p and miR-519e-3p as inducers of human cardiomyocyte proliferation IScience, 26, 106593. https://doi.org/10.1016/j.isci.2023.106593
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Quantitative flow ratio versus fractional flow reserve for guiding percutaneous coronary intervention: design and rationale of the randomised FAVOR III Europe Japan trial EuroIntervention, 18, e1358–e1364. https://doi.org/10.4244/EIJ-D-21-00214
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Coexistence of calcified- and lipid-containing plaque components and their association with incidental rupture points in acute coronary syndrome-causing culprit lesions: results from the prospective OPTICO-ACS study European Heart Journal. Cardiovascular Imaging, 23, 1598–1605. https://doi.org/10.1093/ehjci/jeab247
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Mammalian Target of Rapamycin Inhibition in Patients With ST-Segment Elevation Myocardial Infarction Journal of the American College of Cardiology, 80, 1802–1814. https://doi.org/10.1016/j.jacc.2022.08.747
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Gender-Specific Performance of One- Compared to Two-Catheter Concepts in Transradial Coronary Angiography - Insights From the Randomized UDDC-Radial-Trial Cardiovascular Revascularization Medicine, 43, 49–54. https://doi.org/10.1016/j.carrev.2022.05.001
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Vascular endothelial Tissue Factor contributes to trimethylamine N-oxide-enhanced arterial thrombosis Cardiovascular Research, 118, 2367–2384. https://doi.org/10.1093/cvr/cvab263
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Controlled-Level EVERolimus in Acute Coronary Syndrome (CLEVER-ACS) - A phase II, randomized, double-blind, multi-center, placebo-controlled trial American Heart Journal, 247, 33–41. https://doi.org/10.1016/j.ahj.2022.01.010
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Prognostic Impact of Pancoronary Quantitative Flow Ratio Assessment in Patients Undergoing Percutaneous Coronary Intervention for Acute Coronary Syndromes Circulation. Cardiovascular Interventions, 14, e010698. https://doi.org/10.1161/CIRCINTERVENTIONS.121.010698
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Reproducible Determination of High-Density Lipoprotein Proteotypes Journal of Proteome Research, 20, 4974–4984. https://doi.org/10.1021/acs.jproteome.1c00429
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Extracellular vesicle species differentially affect endothelial cell functions and differentially respond to exercise training in patients with chronic coronary syndromes European Journal of Preventive Cardiology, 28, 1467–1474. https://doi.org/10.1177/2047487320919894
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Cysteine-Rich Angiogenic Inducer 61 Improves Prognostic Accuracy of GRACE (Global Registry of Acute Coronary Events) 2.0 Risk Score in Patients With Acute Coronary Syndromes Journal of the American Heart Association, 10, e020488. https://doi.org/10.1161/JAHA.120.020488
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Feasibility and diagnostic reliability of quantitative flow ratio in the assessment of non-culprit lesions in acute coronary syndrome International Journal of Cardiovascular Imaging, 37, 1815–1823. https://doi.org/10.1007/s10554-021-02195-2
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Residual inflammatory risk at 12 months after acute coronary syndromes is frequent and associated with combined adverse events Atherosclerosis, 320, 31–37. https://doi.org/10.1016/j.atherosclerosis.2021.01.012
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Impact of real-time angiographic co-registered optical coherence tomography on percutaneous coronary intervention: the OPTICO-integration II trial Clinical Research in Cardiology, 110, 249–257. https://doi.org/10.1007/s00392-020-01739-1
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A randomised comparison of monoplane versus biplane fluoroscopy in patients undergoing percutaneous coronary intervention: the RAMBO trial EuroIntervention, 16, 672–679. https://doi.org/10.4244/EIJ-D-20-00217
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From traditional pharmacological towards nucleic acid-based therapies for cardiovascular diseases European Heart Journal, 41, 3884–3899. https://doi.org/10.1093/eurheartj/ehaa229
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Advancing RNA-targeted therapy for personalised prevention of coronary disease: focus on ANGPLT3 European Heart Journal, 41, 3946–3948. https://doi.org/10.1093/eurheartj/ehaa790
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Assessment of intermediate coronary lesions by fractional flow reserve and quantitative flow ratio in patients with small-vessel disease Catheterization and Cardiovascular Interventions, 96, 743–751. https://doi.org/10.1002/ccd.28531
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Differential immunological signature at the culprit site distinguishes acute coronary syndrome with intact from acute coronary syndrome with ruptured fibrous cap: results from the prospective translational OPTICO-ACS study European Heart Journal, 41, 3549–3560. https://doi.org/10.1093/eurheartj/ehaa703
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Myoglobin for Detection of High-Risk Patients with Acute Myocarditis Journal of Cardiovascular Translational Research, 13, 853–863. https://doi.org/10.1007/s12265-020-09957-8
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Association of left ventricular end-diastolic pressure with mortality in patients undergoing percutaneous coronary intervention for acute coronary syndromes Catheterization and Cardiovascular Interventions, 96, E439–E446. https://doi.org/10.1002/ccd.28839
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Virome Sequencing in Patients With Myocarditis Circulation : Heart Failure, 13, e007103. https://doi.org/10.1161/CIRCHEARTFAILURE.120.007103
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Clinical Presentation and Laboratory Findings in Men Versus Women with Myocarditis Journal of Women’s Health, 29, 193–199. https://doi.org/10.1089/jwh.2018.7618
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Structure-function relationships of HDL in diabetes and coronary heart disease Journal of Clinical Investigation Insight, 5, 131491. https://doi.org/10.1172/jci.insight.131491
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2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk European Heart Journal, 41, 111–188. https://doi.org/10.1093/eurheartj/ehz455
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Comparison of resting distal to aortic coronary pressure with angiography-based quantitative flow ratio International Journal of Cardiology, 279, 12–17. https://doi.org/10.1016/j.ijcard.2018.11.093
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Mechanical circulatory support with Impella versus intra-aortic balloon pump or medical treatment in cardiogenic shock-a critical appraisal of current data Clinical Research in Cardiology, 108, 1249–1257. https://doi.org/10.1007/s00392-019-01458-2
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Association of the body mass index with outcomes in elderly patients (≥80 years) undergoing percutaneous coronary intervention International Journal of Cardiology, 292, 73–77. https://doi.org/10.1016/j.ijcard.2019.06.044
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Systematic use of cardiac magnetic resonance imaging in MINOCA led to a five-fold increase in the detection rate of myocarditis: a retrospective study Swiss Medical Weekly, 149, w20098. https://doi.org/10.4414/smw.2019.20098
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Effect on Outcomes: Infections Complicating Percutaneous Coronary Interventions in Patients ≥80 Years of Age American Journal of Cardiology, 123, 1806–1811. https://doi.org/10.1016/j.amjcard.2019.03.003
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Pulmonary hypertension in patients with severe aortic stenosis: prognostic impact after transcatheter aortic valve replacement: pulmonary hypertension in patients undergoing TAVR JACC : Cardiovascular Imaging, 12, 591–601. https://doi.org/10.1016/j.jcmg.2018.02.015
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Gender and age differences in outcomes of patients with acute coronary syndromes referred for coronary angiography Catheterization and Cardiovascular Interventions, 93, 16–24. https://doi.org/10.1002/ccd.27712
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Impella versus IABP in acute myocardial infarction complicated by cardiogenic shock Open Heart, 6, e000987. https://doi.org/10.1136/openhrt-2018-000987
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Non-steroidal anti-inflammatory drug use in acute myopericarditis: 12-month clinical follow-up Open Heart, 6, e000990. https://doi.org/10.1136/openhrt-2018-000990
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Impact of acute kidney injury in elderly (≥80 years) patients undergoing percutaneous coronary intervention Journal of Interventional Cardiology, 31, 792–798. https://doi.org/10.1111/joic.12547
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Performance of One- Compared With Two-Catheter Concepts in Transradial Coronary Angiography (from the Randomized Use of Different Diagnostic Catheters-Radial-Trial) American Journal of Cardiology, 122, 1647–1651. https://doi.org/10.1016/j.amjcard.2018.07.039
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Predictive value of the age, creatinine, and ejection fraction (ACEF) score in patients with acute coronary syndromes International Journal of Cardiology, 270, 7–13. https://doi.org/10.1016/j.ijcard.2018.05.134
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Thrombus aspiration in acute coronary syndromes: prevalence, procedural success, change in serial troponin T levels and clinical outcomes in a contemporary Swiss cohort European Heart Journal: Acute Cardiovascular Care, 7, 522–531. https://doi.org/10.1177/2048872617706480
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Effect of Physical Disability on Mortality in Elderly Patients of ≥80 Years of Age Undergoing Percutaneous Coronary Intervention American Journal of Cardiology, 122, 537–541. https://doi.org/10.1016/j.amjcard.2018.04.055
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The danger lurks dastardly in the coronary vessel wall: spotlight on patients’ vulnerability. European Heart Journal, 39, 1656. https://doi.org/10.1093/eurheartj/ehy092
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The predictive value of a modified Carpentier classification in patients with coincidental mitral regurgitation undergoing TAVI for severe aortic valve stenosis1 Clinical Hemorheology and Microcirculation, 70, 15–25. https://doi.org/10.3233/CH-189906
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Reduction of low density lipoprotein-cholesterol and cardiovascular events with proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors and statins: an analysis of FOURIER, SPIRE, and the Cholesterol Treatment Trialists Collaboration European Heart Journal, 39, 2540–2545. https://doi.org/10.1093/eurheartj/ehx450
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Transcatheter Aortic Valve Replacement and Concomitant Mitral Regurgitation Frontiers in Cardiovascular Medicine, 5, 74. https://doi.org/10.3389/fcvm.2018.00074
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Left atrial appendage angiography is associated with the incidence and number of magnetic resonance imaging-detected brain lesions after percutaneous catheter-based left atrial appendage closure Heart Rhythm, 15, 3–8. https://doi.org/10.1016/j.hrthm.2017.11.015
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Cysteine-rich angiogenic inducer 61 (Cyr61): a novel soluble biomarker of acute myocardial injury improves risk stratification after acute coronary syndromes European Heart Journal, 38, 3493–3502. https://doi.org/10.1093/eurheartj/ehx640
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Left atrial appendage occlusion in patients with atrial fibrillation and previous major gastrointestinal bleeding (from the Amplatzer Cardiac Plug Multicenter Registry) American Journal of Cardiology, 120, 414–420. https://doi.org/10.1016/j.amjcard.2017.04.046
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Symmetric dimethylarginine, high-density lipoproteins and cardiovascular disease European Heart Journal, 38, 1597–1607. https://doi.org/10.1093/eurheartj/ehx118
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HDL cholesterol: reappraisal of its clinical relevance Clinical Research in Cardiology, 106, 663–675. https://doi.org/10.1007/s00392-017-1106-1
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The REMEDEE-OCT Study: An Evaluation of the Bioengineered COMBO Dual-Therapy CD34 Antibody-Covered Sirolimus-Eluting Coronary Stent Compared With a Cobalt-Chromium Everolimus-Eluting Stent in Patients With Acute Coronary Syndromes: Insights From Optical Coherence Tomography Imaging Analysis JACC. Cardiovascular Interventions, 10, 489–499. https://doi.org/10.1016/j.jcin.2016.11.040
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Intracoronary optical coherence tomography: clinical and research applications and intravascular imaging software overview Catheterization and Cardiovascular Interventions, 89, 679–689. https://doi.org/10.1002/ccd.26920
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Anacetrapib, but not evacetrapib, impairs endothelial function in CETP-transgenic mice in spite of marked HDL-C increase Atherosclerosis, 257, 186–194. https://doi.org/10.1016/j.atherosclerosis.2017.01.011
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Kyburz Group
Kyburz D, Karouzakis E, Ospelt C. Epigenetic changes: the missing link. Best Pract Res Clin Rheumatol. 2014 Aug;28(4):577-587.