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Dinser, L. ; Meisinger, C. ; Amann, U. ; Heier, M. ; Thilo, C.* ; Kuch, B.* ; Peters, A. ; Kirchberger, I.

Peripheral arterial disease is associated with higher mortality in patients with incident acute myocardial infarction.

Eur. J. Intern. Med. 51, 46-52 (2018)
Postprint DOI PMC
Open Access Green
Flatworms of the species Schmidtea mediterranea are immortal-adult animals contain a large pool of pluripotent stem cells that continuously differentiate into all adult cell types. Therefore, single-cell transcriptome profiling of adult animals should reveal mature and progenitor cells. By combining perturbation experiments, gene expression analysis, a computational method that predicts future cell states from transcriptional changes, and a lineage reconstruction method, we placed all major cell types onto a single lineage tree that connects all cells to a single stem cell compartment. We characterized gene expression changes during differentiation and discovered cell types important for regeneration. Our results demonstrate the importance of single-cell transcriptome analysis for mapping and reconstructing fundamental processes of developmental and regenerative biology at high resolution.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Peripheral Arterial Disease ; Acute Myocardial Infarction ; Long-term Mortality ; Short-term Case Fatality; Planarian Schmidtea-mediterranea; Stem-cells; Rna-seq; Gene-expression; Regeneration; Pluripotency; Trajectories; Organism; Tissues; System
Sprache englisch
Veröffentlichungsjahr 2018
HGF-Berichtsjahr 2018
ISSN (print) / ISBN 0953-6205
e-ISSN 1879-0828
Zeitschrift European Journal of Internal Medicine
Quellenangaben Band: 51, Heft: , Seiten: 46-52 Artikelnummer: , Supplement: ,
Verlag Pozzi
Verlagsort Roma
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Epidemiology (EPI)
POF Topic(s) 30202 - Environmental Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-504000-002
G-504000-006
G-504090-001
DOI 10.1016/j.ejim.2018.01.007
WOS ID WOS:000432488200025
Scopus ID 85040009348
PubMed ID 29310994
Erfassungsdatum 2018-02-28
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