Results 151 to 160 of about 2,004,567 (296)
A urine‐based digital PCR assay targeting two hotspot TERT promoter variants detected bladder cancer with high sensitivity and no false positives in this case–control cohort. The streamlined AbsoluteQ workflow outperformed Sanger sequencing and supports non‐invasive molecular testing for bladder cancer detection.
Anna Nykel +12 more
wiley +1 more source
The NIH 2025 Public Access Policy: Immediate access, unequal costs. [PDF]
Ryus CR, Raymond King C, Melnick ER.
europepmc +1 more source
This study shows that lung adenocarcinomas exploit developmental branching morphogenesis to acquire a therapy resistant basal‐like tumour cell state. This process was found to be regulated by combined TP53 loss‐of‐function and type‐I interferon signalling, identifying a novel axis for biomarker and therapeutic target discovery.
Kamila J Bienkowska +13 more
wiley +1 more source
[Correspondence between Meyer Bodansky and Lea and Feibiger Publishers - 1926]
Correspondence between Dr. Meyer Bodansky and Lea and Feibiger Publishers dated September 29th, 1926, involving Dr. Bodansky asking permission to use information from Robertson's Principles of Biochemistry in his upcoming textbook.
Bodansky, Meyer, 1896-1941 +1 more
core
Combining osimertinib with the STING agonist ADU‐S100 activates innate and adaptive immunity to overcome the non‐inflamed microenvironment of Egfr‐mutant lung cancer. This combination increases NK and CD8+ T‐cell infiltration, associated with activation of the STING‐IRF3 pathway and local immunogenic cell death.
Jun Nishimura +19 more
wiley +1 more source
Acknowledgement to reviewers (June 2013 – March 2014)
Laura Fascio Pecetto
doaj +1 more source
Introducing COSIG: The Collection of Open Science Integrity Guides. [PDF]
Ozturk Y, Pirelli S, Richardson RAK.
europepmc +1 more source
Loss of IGF‐1R impairs DNA‐PKcs recruitment to chromatin leading to defective end‐joining
IGF‐1R promotes radioresistance by facilitating DNA‐PKcs recruitment to chromatin, enabling non‐homologous end‐joining (NHEJ) repair of double‐strand breaks. Inhibition or loss of IGF‐1R disrupts this recruitment to damage sites, driving compensatory reliance on microhomology‐mediated end‐joining (MMEJ) repair.
Matthew O. Ellis +3 more
wiley +1 more source
Editorial Staff Disclosure (2018)
Laura Fascio Pecetto
doaj +1 more source

