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Richard W Tothill

Showing results (41-50 of 69) with videos related to

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Endocrine-Related Cancer|April 7, 2020
A xenograft and cell line model of SDH-deficient pheochromocytoma derived from Sdhb+/- ratsJames F Powers, Brent Cochran, James D Baleja, et al.
Endocrine-Related Cancer|August 30, 2020
A xenograft and cell line model of SDH-deficient pheochromocytoma derived from Sdhb+/- ratsJames F Powers, Brent Cochran, James D Baleja, et al.
Cancer Research|May 19, 2005
An expression-based site of origin diagnostic method designed for clinical application to cancer of unknown originRichard W Tothill, Adam Kowalczyk, Danny Rischin, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 9, 2013
BRAF/NRAS wild-type melanomas have a high mutation load correlating with histologic and molecular signatures of UV damageVictoria J Mar, Stephen Q Wong, Jason Li, et al.
Ebiomedicine|October 11, 2020
CUP-AI-Dx: A tool for inferring cancer tissue of origin and molecular subtype using RNA gene-expression data and artificial intelligenceYue Zhao, Ziwei Pan, Sandeep Namburi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 14, 2008
Novel molecular subtypes of serous and endometrioid ovarian cancer linked to clinical outcomeRichard W Tothill, Anna V Tinker, Joshy George, et al.
Plos Genetics|October 3, 2012
Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility allelesElla R Thompson, Maria A Doyle, Georgina L Ryland, et al.
Nature Communications|January 9, 2023
Author Correction: Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironmentMagnus Zethoven, Luciano Martelotto, Andrew Pattison, et al.
Plos One|April 23, 2014
Bioinformatics pipelines for targeted resequencing and whole-exome sequencing of human and mouse genomes: a virtual appliance approach for instant deploymentJason Li, Maria A Doyle, Isaam Saeed, et al.
Nature Communications|October 21, 2022
Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironmentMagnus Zethoven, Luciano Martelotto, Andrew Pattison, et al.
Pageof 7

Showing results (41-50 of 69) with videos related to

Sort By:
Pageof 7
Endocrine-Related Cancer|April 7, 2020
A xenograft and cell line model of SDH-deficient pheochromocytoma derived from Sdhb+/- ratsJames F Powers, Brent Cochran, James D Baleja, et al.
Endocrine-Related Cancer|August 30, 2020
A xenograft and cell line model of SDH-deficient pheochromocytoma derived from Sdhb+/- ratsJames F Powers, Brent Cochran, James D Baleja, et al.
Cancer Research|May 19, 2005
An expression-based site of origin diagnostic method designed for clinical application to cancer of unknown originRichard W Tothill, Adam Kowalczyk, Danny Rischin, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 9, 2013
BRAF/NRAS wild-type melanomas have a high mutation load correlating with histologic and molecular signatures of UV damageVictoria J Mar, Stephen Q Wong, Jason Li, et al.
Ebiomedicine|October 11, 2020
CUP-AI-Dx: A tool for inferring cancer tissue of origin and molecular subtype using RNA gene-expression data and artificial intelligenceYue Zhao, Ziwei Pan, Sandeep Namburi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 14, 2008
Novel molecular subtypes of serous and endometrioid ovarian cancer linked to clinical outcomeRichard W Tothill, Anna V Tinker, Joshy George, et al.
Plos Genetics|October 3, 2012
Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility allelesElla R Thompson, Maria A Doyle, Georgina L Ryland, et al.
Nature Communications|January 9, 2023
Author Correction: Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironmentMagnus Zethoven, Luciano Martelotto, Andrew Pattison, et al.
Plos One|April 23, 2014
Bioinformatics pipelines for targeted resequencing and whole-exome sequencing of human and mouse genomes: a virtual appliance approach for instant deploymentJason Li, Maria A Doyle, Isaam Saeed, et al.
Nature Communications|October 21, 2022
Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironmentMagnus Zethoven, Luciano Martelotto, Andrew Pattison, et al.
Pageof 7