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Artikel 381 Prostate Cancer Stem Cells: Do They Have a Basal or Luminal Phenotype?
Enthalten in Hormones and cancer Bd. 2, 4.1.2011, Nr. 1, date:2.2011: 47-61
Online Ressource
Artikel 382 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Enthalten in Nature genetics Bd. 50, 22.12.2017, Nr. 1, date:1.2018: 26-41
Online Ressource
Artikel 383 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
Enthalten in Nature genetics Bd. 51, 18.2.2019, Nr. 3, date:3.2019: 452-469
Online Ressource
Artikel 384 PTHrP induces STAT5 activation, secretory differentiation and accelerates mammary tumor development
Enthalten in Breast cancer research Bd. 24, 19.4.2022, Nr. 1, date:12.2022: 1-23
Online Ressource
Artikel 385 Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Enthalten in Nature genetics Bd. 51, 3.6.2019, Nr. 7, date:7.2019: 1192-1193
Online Ressource
Artikel 386 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Enthalten in Nature genetics Bd. 51, 3.6.2019, Nr. 7, date:7.2019: 1191-1192
Online Ressource
Artikel 387 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Enthalten in Nature genetics Bd. 50, 16.3.2018, Nr. 5, date:5.2018: 766-767
Online Ressource
Artikel 388 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Enthalten in Nature genetics Bd. 50, 16.3.2018, Nr. 5, date:5.2018: 765-766
Online Ressource
Artikel 389 Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries
Enthalten in Nature Bd. 612, 14.11.2022, Nr. 7938, date:12.2022: E7
Online Ressource
Artikel 390 Rare coding variants in RCN3 are associated with blood pressure
Enthalten in BMC genomics Bd. 23, 19.2.2022, Nr. 1, date:12.2022: 1-18
Online Ressource


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