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Artikel 601 Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Enthalten in Nature genetics Bd. 55, 25.9.2023, Nr. 10, date:10.2023: 1778-1779
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Artikel 602 Autogene cevumeran with or without atezolizumab in advanced solid tumors: a phase 1 trial
Enthalten in Nature medicine Bd. 31, 6.1.2025, Nr. 1, date:1.2025: 152-164
Online Ressource
Artikel 603 Bedarfe der Langzeitpflege in der COVID-19-Pandemie
Enthalten in Zeitschrift für Gerontologie und Geriatrie Bd. 53, 28.10.2020, Nr. 8, date:12.2020: 788-795
Online Ressource
Artikel 604 Behaviour of adipose-derived canine mesenchymal stem cells after superparamagnetic iron oxide nanoparticles labelling for magnetic resonance imaging
Enthalten in BMC veterinary research Bd. 13, 24.2.2017, Nr. 1, date:12.2016: 1-11
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Artikel 605 BepiColombo Science Investigations During Cruise and Flybys at the Earth, Venus and Mercury
Enthalten in Space science reviews Bd. 217, 11.2.2021, Nr. 1, date:2.2021: 1-81
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Artikel 606 Bone morphogenic protein-4 availability in the cardiac microenvironment controls inflammation and fibrosis in autoimmune myocarditis
Enthalten in Nature cardiovascular research Bd. 3, 19.2.2024, Nr. 3, date:3.2024: 301-316
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Artikel 607 Breast cancer risk factors and their effects on survival: a Mendelian randomisation study
Enthalten in BMC medicine Bd. 18, 17.11.2020, Nr. 1, date:12.2020: 1-10
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Artikel 608 Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Enthalten in Genome medicine Bd. 14, 18.5.2022, Nr. 1, date:12.2022: 1-17
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Artikel 609 Burnout among psychotherapists: a cross-cultural value survey among 12 European countries during the coronavirus disease pandemic
Enthalten in Scientific reports Bd. 12, 8.8.2022, Nr. 1, date:12.2022: 1-11
Online Ressource
Artikel 610 C4 nephritic factor in patients with immune-complex-mediated membranoproliferative glomerulonephritis and C3-glomerulopathy
Enthalten in Orphanet journal of rare diseases Bd. 14, 8.11.2019, Nr. 1, date:12.2019: 1-14
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