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International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|October 1, 2021
ATHENA (GOG-3020/ENGOT-ov45): a randomized, phase III trial to evaluate rucaparib as monotherapy (ATHENA-MONO) and rucaparib in combination with nivolumab (ATHENA-COMBO) as maintenance treatment following frontline platinum-based chemotherapy in ovarian cancerBradley J Monk, Robert L Coleman, Keiichi Fujiwara, et al.
Clinical Pharmacology and Therapeutics|September 21, 2016
Essential competencies in prescribing: A first european cross-sectional study among 895 final-year medical studentsD J Brinkman, J Tichelaar, T Schutte, et al.
Gastroenterology|December 6, 2011
Hepatitis C virus infects the endothelial cells of the blood-brain barrierNicola F Fletcher, Garrick K Wilson, Jacinta Murray, et al.
Developmental Biology|September 13, 2006
A genomic view of the sea urchin nervous systemR D Burke, L M Angerer, M R Elphick, et al.
Elife|October 28, 2015
A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndromeJefferson J Doyle, Alexander J Doyle, Nicole K Wilson, et al.
The Journal of Physical Chemistry. A|June 1, 2023
Electronic Structure and Excited-State Dynamics of DNA-Templated Monomers and Aggregates of Asymmetric Polymethine DyesKatelyn M Duncan, Hannah M Byers, Madaline E Houdek, et al.
Genes, Chromosomes & Cancer|June 18, 2022
Infantile metastatic ependymoma with a novel molecular profile and favorable outcome to intensive chemotherapy without irradiation: Case-based reviewFlavia Watusi De Faria, Kathleen M Schieffer, Christopher R Pierson, et al.
Nature Genetics|January 31, 2012
Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomasGang Wu, Alberto Broniscer, Troy A McEachron, et al.
Brain : a Journal of Neurology|May 28, 2021
PTEN somatic mutations contribute to spectrum of cerebral overgrowthDaniel C Koboldt, Katherine E Miller, Anthony R Miller, et al.
Leukemia|February 28, 2013
Clonal diversity of recurrently mutated genes in myelodysplastic syndromesM J Walter, D Shen, J Shao, et al.
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