PuSH - Publication Server of Helmholtz Zentrum München

Journal browsing

342 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
Prorok, P.* et al.: Author Correction: Involvement of G-quadruplex regions in mammalian replication origin activity (Nature Communications, (2019), 10, 1, (3274), 10.1038/s41467-019-11104-0). Nat. Commun. 11:3058 (2020)
Qadir, M.M.F.* et al.: Long-term culture of human pancreatic slices as a model to study real-time islet regeneration. Nat. Commun. 11:3265 (2020)
Qadir, M.M.F.* et al.: Erratum: Publisher Correction: Long-term culture of human pancreatic slices as a model to study real-time islet regeneration (Nature communications (2020) 11 1 (3265)). Nat. Commun. 11:3742 (2020)
Sargurupremraj, M.* et al.: Cerebral small vessel disease genomics and its implications across the lifespan. Nat. Commun. 11:6285 (2020)
Schoppe, O. et al.: Deep learning-enabled multi-organ segmentation in whole-body mouse scans. Nat. Commun. 11:5626 (2020)
Seeger, M. et al.: Pushing the boundaries of optoacoustic microscopy by total impulse response characterization. Nat. Commun. 11:2910 (2020)
Strunz, M. et al.: Alveolar regeneration through a Krt8+transitional stem cell state that persists in human lung fibrosis. Nat. Commun. 11:3559 (2020)
Tetko, I.V. ; Karpov, P. ; Van Deursen, R.* & Godin, G.*: State-of-the-art augmented NLP transformer models for direct and single-step retrosynthesis. Nat. Commun. 11:5575 (2020)
Voigt, S. et al.: A central role of IKK2 and TPL2 in JNK activation and viral B-cell transformation. Nat. Commun. 11:685 (2020)
Zaghlool, S.B.* et al.: Epigenetics meets proteomics in an epigenome-wide association study with circulating blood plasma protein traits. Nat. Commun. 11:15 (2020)
Angelidis, I. et al.: An atlas of the aging lung mapped by single cell transcriptomics and deep tissue proteomics. Nat. Commun. 10:963 (2019)
Baumann, V.* et al.: Targeted removal of epigenetic barriers during transcriptional reprogramming. Nat. Commun. 10:2119 (2019)
Blok, L.S.* et al.: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018). Nat. Commun. 10:883 (2019)
Campagne, A.* et al.: BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation. Nat. Commun. 10:348 (2019)
Cho, J.J.* et al.: Hectd3 promotes pathogenic Th17 lineage through Stat3 activation and Malt1 signaling in neuroinflammation. Nat. Commun. 10:701 (2019)
Clark, D.W.* et al.: Associations of autozygosity with a broad range of human phenotypes. Nat. Commun. 10:4957 (2019)
Czamara, D.* et al.: Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nat. Commun. 10:2548 (2019)
Deelen, J.* et al.: A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals. Nat. Commun. 10:3346 (2019)
Eraslan, G. ; Simon, L. ; Mircea, M. ; Müller, N.S. & Theis, F.J.: Single-cell RNA-seq denoising using a deep count autoencoder. Nat. Commun. 10:390 (2019)
Fischer, C.* et al.: Long-term functional and structural preservation of precision-cut human myocardium under continuous electromechanical stimulation in vitro. Nat. Commun. 10:117 (2019)