Results 191 to 200 of about 5,351,550 (365)
This study develops a semi‐supervised classifier integrating multi‐genomic data (1404 training/5893 validation samples) to improve homologous recombination deficiency (HRD) detection in breast cancer. Our method demonstrates prognostic value and predicts chemotherapy/PARP inhibitor sensitivity in HRD+ tumours.
Rong Zhu+12 more
wiley +1 more source
Letter comments on: "Twelve years of European cancer drug approval-a systematic investigation of the 'magnitude of clinical benefit'". [PDF]
Müller B, Estay R.
europepmc +1 more source
Anticancer Drug Development: Preclinical Screening, Clinical Trials and Approval [PDF]
David L. Selwood
openalex +1 more source
Pre-approval of Prescription Drug Advertisements in the Shadow of Central Hudson [PDF]
The article examines the effects of prescription drug advertising on patients and physicians, and explains how a requirement of pre-approval by the FDA for prescription drug advertisements could eliminate many of the problems such advertisements create ...
Ginn, Clifford M.
core
This nationwide study evaluated KRAS and NRAS mutations in 10 754 Turkish patients with metastatic colorectal cancer. The results revealed a mutation frequency of 51.1%, with 46.6% having KRAS mutations, 4.5% having NRAS mutations, and 48.5% being wild‐type for both.
Gozde Kavgaci+6 more
wiley +1 more source
Analysis of racial and ethnic disparities in multiple myeloma US FDA drug approval trials. [PDF]
Kanapuru B+11 more
europepmc +1 more source
US Food and Drug Administration Approval of Ciprofloxacin Hydrochloride for Management of Postexposure Inhalational Anthrax [PDF]
Allen S. Meyerhoff+5 more
openalex +1 more source
Landscape of BRAF transcript variants in human cancer
We investigate the annotation of BRAF variants, focusing on protein‐coding BRAF‐220 (formerly BRAF‐reference) and BRAF‐204 (BRAF‐X1). The IsoWorm pipeline allows us to quantify these variants in human cancer, starting from RNA‐sequencing data. BRAF‐204 is more abundant than BRAF‐220 and impacts patient survival.
Maurizio S. Podda+5 more
wiley +1 more source
Assessment of the impact of Japanese-specific long-term safety data on new drug approval. [PDF]
Uzu S, Sekine S, Asano J, Ikuma M.
europepmc +1 more source