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Molecular Psychiatry|September 10, 2014
Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneityJ Ellegood, E Anagnostou, B A Babineau, et al.
Blood Cancer Discovery|July 15, 2022
Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid LeukemiaJune Takeda, Kenichi Yoshida, Masahiro M Nakagawa, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|March 4, 2021
The International Association for the Study of Lung Cancer Global Survey on Programmed Death-Ligand 1 Testing for NSCLCMari Mino-Kenudson, Nolwenn Le Stang, Jillian B Daigneault, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|December 25, 2019
PD-L1 Testing for Lung Cancer in 2019: Perspective From the IASLC Pathology CommitteeSylvie Lantuejoul, Ming Sound-Tsao, Wendy A Cooper, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|June 12, 2020
The Promises and Challenges of Tumor Mutation Burden as an Immunotherapy Biomarker: A Perspective from the International Association for the Study of Lung Cancer Pathology CommitteeLynette M Sholl, Fred R Hirsch, David Hwang, et al.
The Lancet. Global Health|June 22, 2023
Description of the first global outbreak of mpox: an analysis of global surveillance dataHenry Laurenson-Schafer, Nikola Sklenovská, Ana Hoxha, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|November 30, 2017
Prevalence and clinical association of gene mutations through multiplex mutation testing in patients with NSCLC: results from the ETOP Lungscape ProjectK M Kerr, U Dafni, K Schulze, et al.
Nature Communications|December 8, 2022
Epithelial TGFβ engages growth-factor signalling to circumvent apoptosis and drive intestinal tumourigenesis with aggressive featuresDustin J Flanagan, Raheleh Amirkhah, David F Vincent, et al.
Nature Reviews. Genetics|July 12, 2018
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statementAntonie D Kline, Joanna F Moss, Angelo Selicorni, et al.
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