UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Printing colour at the optical diffraction limit

Nature nanotechnology, 2012-09, Vol.7 (9), p.557-561

2012

Volltextzugriff (PDF)

A repository of assays to quantify 10,000 human proteins by SWATH-MS

Scientific data, 2014-09, Vol.1 (1), p.140031-140031, Article 140031

2014

Volltextzugriff (PDF)

Robust SNP-based prediction of rheumatoid arthritis through machine-learning-optimized polygenic risk score

Journal of translational medicine, 2023-02, Vol.21 (1), p.92-92, Article 92

2023

Volltextzugriff (PDF)

Cohort Profile: Growing Up in Singapore Towards healthy Outcomes (GUSTO) birth cohort study

International journal of epidemiology, 2014-10, Vol.43 (5), p.1401-1409

2014

Volltextzugriff (PDF)

Pan-cancer analysis of whole genomes

Nature (London), 2020-02, Vol.578 (7793), p.82-93

2020

Volltextzugriff (PDF)

Perioperative management of sarcopenia in patients undergoing major surgeries in Singapore: a modified Delphi consensus

International journal of surgery (London, England), 2024-08, Vol.110 (8), p.4552-4558

2024

Volltextzugriff (PDF)

A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

Nature communications, 2020-02, Vol.11 (1), p.728-12, Article 728

2020

Volltextzugriff (PDF)

In the critically ill patient, diabetes predicts mortality independent of statin therapy but is not associated with acute lung injury: A cohort study

Critical care medicine, 2012-06, Vol.40 (6), p.1835-1843

2012

Volltextzugriff (PDF)

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

Nature communications, 2023-12, Vol.14 (1), p.8077-18, Article 8077

2023

Volltextzugriff (PDF)

Robust Performance of Potentially Functional SNPs in Machine Learning Models for the Prediction of Atorvastatin-Induced Myalgia

Frontiers in pharmacology, 2021-04, Vol.12, p.605764-605764

2021

Volltextzugriff (PDF)

Divergent mutational processes distinguish hypoxic and normoxic tumours

Nature communications, 2020-02, Vol.11 (1), p.737-10, Article 737

2020

Volltextzugriff (PDF)

Hypothalamic Hamartomas: Evolving Understanding and Management

Neurology, 2021-11, Vol.97 (18), p.864-873

2021

Volltextzugriff (PDF)

Inferring structural variant cancer cell fraction

Nature communications, 2020-02, Vol.11 (1), p.730-730, Article 730

2020

Volltextzugriff (PDF)

Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig

Nature communications, 2020-02, Vol.11 (1), p.731-731, Article 731

2020

Volltextzugriff (PDF)

Early-onset sepsis in very preterm neonates in Australia and New Zealand, 2007–2018

Archives of disease in childhood. Fetal and neonatal edition, 2023-01, Vol.108 (1), p.31-37

2023

Volltextzugriff (PDF)

Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing

Nature genetics, 2023-06, Vol.55 (6), p.1076-1076

2023

Volltextzugriff (PDF)

Association of Socio-Economic Position with Technique Failure and Mortality in Australian Non-Indigenous Peritoneal Dialysis Patients

Peritoneal dialysis international, 2017-07, Vol.37 (4), p.397-406

2017

Volltextzugriff (PDF)

Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

Nature communications, 2022-12, Vol.13 (1), p.7573-7573, Article 7573

2022

Volltextzugriff (PDF)

Author Correction: Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig

Nature communications, 2022-12, Vol.13 (1), p.7567-7567, Article 7567

2022

Volltextzugriff (PDF)

Author Correction: Inferring structural variant cancer cell fraction

Nature communications, 2022-12, Vol.13 (1), p.7568-7568, Article 7568

2022

Volltextzugriff (PDF)

Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder

Journal of psychiatric research, 2016-11, Vol.82, p.126-135

2016

Volltextzugriff (PDF)

Author Correction: Divergent mutational processes distinguish hypoxic and normoxic tumours

Nature communications, 2022-12, Vol.13 (1), p.7569-7569, Article 7569

2022

Volltextzugriff (PDF)

TCL1 oncogene expression in B cell subsets from lymphoid hyperplasia and distinct classes of B cell lymphoma

Laboratory investigation, 2001-04, Vol.81 (4), p.555-564

2001

Volltextzugriff (PDF)

A Modeled Hydrophobic Domain on the TCL1 Oncoprotein Mediates Association with AKT at the Cytoplasmic Membrane

Biochemistry (Easton), 2002-05, Vol.41 (20), p.6376-6382

2002

Volltextzugriff (PDF)

1 – 25 von 27

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(25)
Mit Volltextzugriff
(21)

Publikationsform

Sprache

Englisch
(26)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Printing colour at the optical diffraction limit

A repository of assays to quantify 10,000 human proteins by SWATH-MS

Robust SNP-based prediction of rheumatoid arthritis through machine-learning-optimized polygenic risk score

Cohort Profile: Growing Up in Singapore Towards healthy Outcomes (GUSTO) birth cohort study

Pan-cancer analysis of whole genomes

Perioperative management of sarcopenia in patients undergoing major surgeries in Singapore: a modified Delphi consensus

Defining Benchmarks for Pelvic Exenteration Surgery: A Multicentre Analysis of Patients with Locally Advanced and Recurrent Rectal Cancer

A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

In the critically ill patient, diabetes predicts mortality independent of statin therapy but is not associated with acute lung injury: A cohort study

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

Robust Performance of Potentially Functional SNPs in Machine Learning Models for the Prediction of Atorvastatin-Induced Myalgia

Divergent mutational processes distinguish hypoxic and normoxic tumours

Hypothalamic Hamartomas: Evolving Understanding and Management

Inferring structural variant cancer cell fraction

Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig

Early-onset sepsis in very preterm neonates in Australia and New Zealand, 2007–2018

Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing

Association of Socio-Economic Position with Technique Failure and Mortality in Australian Non-Indigenous Peritoneal Dialysis Patients

Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

Author Correction: Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig

Author Correction: Inferring structural variant cancer cell fraction

Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder

Author Correction: Divergent mutational processes distinguish hypoxic and normoxic tumours

TCL1 oncogene expression in B cell subsets from lymphoid hyperplasia and distinct classes of B cell lymphoma

A Modeled Hydrophobic Domain on the TCL1 Oncoprotein Mediates Association with AKT at the Cytoplasmic Membrane

Suchergebnisse filtern