Katalog der Deutschen Nationalbibliothek

Neuigkeiten

Leichte Bedienung, intuitive Suche: Die Betaversion unseres neuen Katalogs ist online! → Zur Betaversion des neuen DNB-Katalogs

 
Neuigkeiten 2. bis 5. Oktober 2025: Der Kartenlesesaal in Leipzig ist geschlossen. // 2 to 5 October 2025: The map reading room in Leipzig is closed.
 
 
 


Ergebnis der Suche nach: "173067964"
im Bestand: Gesamter Bestand

41 - 49 von 49
<< < > >>


Artikel 41 Serum microRNA-1233 is a specific biomarker for diagnosing acute pulmonary embolism
Enthalten in Journal of translational medicine Bd. 14, 5.5.2016, Nr. 1, date:12.2016: 1-10
Online Ressource
Artikel 42 Stimulators of the soluble guanylyl cyclase: promising functional insights from rare coding atherosclerosis-related GUCY1A3 variants
Enthalten in Basic research in cardiology Bd. 111, 24.6.2016, Nr. 4, date:7.2016: 1-13
Online Ressource
Artikel 43 The assertion that a G21V mutation in AGTR2 causes mental retardation is not supported by other studies
Enthalten in Human genetics Bd. 114, 13.1.2004, Nr. 4, date:3.2004: 396
Online Ressource
Artikel 44 The CAD risk locus 9p21 increases the risk of vascular calcification in an iPSC-derived VSMC model
Enthalten in Stem cell research & therapy Bd. 12, 6.3.2021, Nr. 1, date:12.2021: 1-12
Online Ressource
Artikel 45 The DZHK research platform: maximisation of scientific value by enabling access to health data and biological samples collected in cardiovascular clinical studies
Enthalten in Clinical research in cardiology Bd. 112, 8.3.2023, Nr. 7, date:7.2023: 923-941
Online Ressource
Artikel 46 The interleukin-11 receptor variant p.W307R results in craniosynostosis in humans
Enthalten in Scientific reports Bd. 13, 18.8.2023, Nr. 1, date:12.2023: 1-14
Online Ressource
Artikel 47 Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes
Enthalten in Basic research in cardiology Bd. 117, 17.2.2022, Nr. 1, date:12.2022: 1-20
Online Ressource
Artikel 48 What can we learn from common variants associated with unexpected phenotypes in rare genetic diseases?
Enthalten in Orphanet journal of rare diseases Bd. 16, 21.1.2021, Nr. 1, date:12.2021: 1-5
Online Ressource
Artikel 49 Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia
Enthalten in BMC cardiovascular disorders Bd. 14, 26.8.2014, Nr. 1, date:12.2014: 1-6
Online Ressource


41 - 49 von 49
<< < > >>


E-Mail-IconAdministration