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W Ellison

Showing results (511-520 of 574) with videos related to

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Acta Neuropathologica|February 24, 2012
Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomasMarcel Kool, Andrey Korshunov, Marc Remke, et al.
Genome Announcements|May 14, 2016
Complete Genome Sequences of Zika Virus Strains Isolated from the Blood of Patients in Thailand in 2014 and the Philippines in 2012D W Ellison, J T Ladner, R Buathong, et al.
Cold Spring Harbor Molecular Case Studies|October 13, 2019
Enrichment of heterozygous germline <i>RECQL4</i> loss-of-function variants in pediatric osteosarcomaJamie L Maciaszek, Ninad Oak, Wenan Chen, et al.
Nature|July 20, 2010
Cross-species genomics matches driver mutations and cell compartments to model ependymomaRobert A Johnson, Karen D Wright, Helen Poppleton, et al.
Nature Communications|September 29, 2018
Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptomeMichael Rusch, Joy Nakitandwe, Sheila Shurtleff, et al.
Human Mutation|July 24, 2013
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delaysAndrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Nature Genetics|March 10, 2009
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastomaPaul A Northcott, Yukiko Nakahara, Xiaochong Wu, et al.
The Journal of Investigative Dermatology|October 1, 2014
The genomic landscape of childhood and adolescent melanomaCharles Lu, Jinghui Zhang, Panduka Nagahawatte, et al.
Cancer Cell|December 24, 2014
Combined MYC and P53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable diseaseRebecca M Hill, Sanne Kuijper, Janet C Lindsey, et al.
Acta Neuropathologica|May 17, 2018
Molecularly defined diffuse leptomeningeal glioneuronal tumor (DLGNT) comprises two subgroups with distinct clinical and genetic featuresMaximilian Y Deng, Martin Sill, Jason Chiang, et al.
Pageof 58

Showing results (511-520 of 574) with videos related to

Sort By:
Pageof 58
Acta Neuropathologica|February 24, 2012
Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomasMarcel Kool, Andrey Korshunov, Marc Remke, et al.
Genome Announcements|May 14, 2016
Complete Genome Sequences of Zika Virus Strains Isolated from the Blood of Patients in Thailand in 2014 and the Philippines in 2012D W Ellison, J T Ladner, R Buathong, et al.
Cold Spring Harbor Molecular Case Studies|October 13, 2019
Enrichment of heterozygous germline <i>RECQL4</i> loss-of-function variants in pediatric osteosarcomaJamie L Maciaszek, Ninad Oak, Wenan Chen, et al.
Nature|July 20, 2010
Cross-species genomics matches driver mutations and cell compartments to model ependymomaRobert A Johnson, Karen D Wright, Helen Poppleton, et al.
Nature Communications|September 29, 2018
Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptomeMichael Rusch, Joy Nakitandwe, Sheila Shurtleff, et al.
Human Mutation|July 24, 2013
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delaysAndrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Nature Genetics|March 10, 2009
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastomaPaul A Northcott, Yukiko Nakahara, Xiaochong Wu, et al.
The Journal of Investigative Dermatology|October 1, 2014
The genomic landscape of childhood and adolescent melanomaCharles Lu, Jinghui Zhang, Panduka Nagahawatte, et al.
Cancer Cell|December 24, 2014
Combined MYC and P53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable diseaseRebecca M Hill, Sanne Kuijper, Janet C Lindsey, et al.
Acta Neuropathologica|May 17, 2018
Molecularly defined diffuse leptomeningeal glioneuronal tumor (DLGNT) comprises two subgroups with distinct clinical and genetic featuresMaximilian Y Deng, Martin Sill, Jason Chiang, et al.
Pageof 58