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Clinical Genetics|June 19, 2023
Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq programKatherine E Bonini, Amanda Thomas-Wilson, Priya N Marathe, et al.
Melanoma Research|March 10, 2015
High-throughput oncogene mutation profiling shows demographic differences in BRAF mutation rates among melanoma patientsKarin van den Hurk, Balazs Balint, Sinead Toomey, et al.
HGG Advances|June 26, 2024
Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual populationPriya N Marathe, Sabrina A Suckiel, Katherine E Bonini, et al.
Nature Medicine|June 2, 2015
Epigenetic activation of a cryptic TBC1D16 transcript enhances melanoma progression by targeting EGFRMiguel Vizoso, Humberto J Ferreira, Paula Lopez-Serra, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 3, 2021
GUÍA: a digital platform to facilitate result disclosure in genetic counselingSabrina A Suckiel, Jaqueline A Odgis, Katie M Gallagher, et al.
Nature Communications|October 7, 2018
Copy number load predicts outcome of metastatic colorectal cancer patients receiving bevacizumab combination therapyDominiek Smeets, Ian S Miller, Darran P O'Connor, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 25, 2018
Loss of Chromosome 18q11.2-q12.1 Is Predictive for Survival in Patients With Metastatic Colorectal Cancer Treated With BevacizumabErik van Dijk, Hedde D Biesma, Martijn Cordes, et al.
Journal of the American Chemical Society|March 19, 2021
Design of BET Inhibitor Bottlebrush Prodrugs with Superior Efficacy and Devoid of Systemic ToxicitiesFarrukh Vohidov, Jannik N Andersen, Kyriakos D Economides, et al.
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