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Peter Collins

Showing results (321-330 of 349) with videos related to

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Human Molecular Genetics|November 22, 2002
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsPatrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, et al.
Haematologica|August 2, 2016
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defectsBen Johnson, Gillian C Lowe, Jane Futterer, et al.
Oncotarget|September 18, 2015
Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older ageAdam M Fontebasso, Margret Shirinian, Dong-Anh Khuong-Quang, et al.
Acta Neuropathologica|February 14, 2013
Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutationsDavid E Reuss, Rosario M Piro, David T W Jones, et al.
American Journal of Epidemiology|December 15, 2015
The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International ConsortiumE Susan Amirian, Georgina N Armstrong, Renke Zhou, et al.
Human Mutation|September 29, 2019
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variantsLoredana Bury, Karyn Megy, Jonathan C Stephens, et al.
Nature|February 21, 2012
Clonal selection drives genetic divergence of metastatic medulloblastomaXiaochong Wu, Paul A Northcott, Adrian Dubuc, et al.
Cell|May 28, 2013
The eEF2 kinase confers resistance to nutrient deprivation by blocking translation elongationGabriel Leprivier, Marc Remke, Barak Rotblat, et al.
Acta Neuropathologica|January 27, 2016
Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphologyIbrahim Qaddoumi, Wilda Orisme, Ji Wen, et al.
Cancer Cell|November 5, 2013
Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomasSebastian Bender, Yujie Tang, Anders M Lindroth, et al.
Pageof 35

Showing results (321-330 of 349) with videos related to

Sort By:
Pageof 35
Human Molecular Genetics|November 22, 2002
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsPatrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, et al.
Haematologica|August 2, 2016
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defectsBen Johnson, Gillian C Lowe, Jane Futterer, et al.
Oncotarget|September 18, 2015
Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older ageAdam M Fontebasso, Margret Shirinian, Dong-Anh Khuong-Quang, et al.
Acta Neuropathologica|February 14, 2013
Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutationsDavid E Reuss, Rosario M Piro, David T W Jones, et al.
American Journal of Epidemiology|December 15, 2015
The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International ConsortiumE Susan Amirian, Georgina N Armstrong, Renke Zhou, et al.
Human Mutation|September 29, 2019
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variantsLoredana Bury, Karyn Megy, Jonathan C Stephens, et al.
Nature|February 21, 2012
Clonal selection drives genetic divergence of metastatic medulloblastomaXiaochong Wu, Paul A Northcott, Adrian Dubuc, et al.
Cell|May 28, 2013
The eEF2 kinase confers resistance to nutrient deprivation by blocking translation elongationGabriel Leprivier, Marc Remke, Barak Rotblat, et al.
Acta Neuropathologica|January 27, 2016
Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphologyIbrahim Qaddoumi, Wilda Orisme, Ji Wen, et al.
Cancer Cell|November 5, 2013
Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomasSebastian Bender, Yujie Tang, Anders M Lindroth, et al.
Pageof 35