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Showing results (811-820 of 866) with videos related to

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Nature Communications|October 22, 2016
Genomic heterogeneity of multiple synchronous lung cancerYu Liu, Jianjun Zhang, Lin Li, et al.
Nature|December 18, 2009
A small-cell lung cancer genome with complex signatures of tobacco exposureErin D Pleasance, Philip J Stephens, Sarah O'Meara, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|May 12, 2020
Programmed Death-Ligand 1 Heterogeneity and Its Impact on Benefit From Immune Checkpoint Inhibitors in NSCLCLingzhi Hong, Marcelo V Negrao, Seyedeh S Dibaj, et al.
American Journal of Human Genetics|August 2, 2007
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMichael Field, Patrick S Tarpey, Raffaella Smith, et al.
Nature Communications|July 7, 2019
Multi-region exome sequencing reveals genomic evolution from preneoplasia to lung adenocarcinomaXin Hu, Junya Fujimoto, Lisha Ying, et al.
Nature|January 21, 2011
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinomaIgnacio Varela, Patrick Tarpey, Keiran Raine, et al.
Nature Genetics|October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusPatrick Tarpey, Shery Thomas, Nagini Sarvananthan, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
Science Translational Medicine|August 9, 2013
Genome-wide mutational signatures of aristolochic acid and its application as a screening toolSong Ling Poon, See-Tong Pang, John R McPherson, et al.
Nature Biotechnology|June 8, 2017
The promise of organ and tissue preservation to transform medicineSebastian Giwa, Jedediah K Lewis, Luis Alvarez, et al.
Pageof 87

Showing results (811-820 of 866) with videos related to

Sort By:
Pageof 87
Nature Communications|October 22, 2016
Genomic heterogeneity of multiple synchronous lung cancerYu Liu, Jianjun Zhang, Lin Li, et al.
Nature|December 18, 2009
A small-cell lung cancer genome with complex signatures of tobacco exposureErin D Pleasance, Philip J Stephens, Sarah O'Meara, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|May 12, 2020
Programmed Death-Ligand 1 Heterogeneity and Its Impact on Benefit From Immune Checkpoint Inhibitors in NSCLCLingzhi Hong, Marcelo V Negrao, Seyedeh S Dibaj, et al.
American Journal of Human Genetics|August 2, 2007
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMichael Field, Patrick S Tarpey, Raffaella Smith, et al.
Nature Communications|July 7, 2019
Multi-region exome sequencing reveals genomic evolution from preneoplasia to lung adenocarcinomaXin Hu, Junya Fujimoto, Lisha Ying, et al.
Nature|January 21, 2011
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinomaIgnacio Varela, Patrick Tarpey, Keiran Raine, et al.
Nature Genetics|October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusPatrick Tarpey, Shery Thomas, Nagini Sarvananthan, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
Science Translational Medicine|August 9, 2013
Genome-wide mutational signatures of aristolochic acid and its application as a screening toolSong Ling Poon, See-Tong Pang, John R McPherson, et al.
Nature Biotechnology|June 8, 2017
The promise of organ and tissue preservation to transform medicineSebastian Giwa, Jedediah K Lewis, Luis Alvarez, et al.
Pageof 87