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Nancy F Hansen

Showing results (21-30 of 53) with videos related to

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European Journal of Human Genetics : EJHG|December 8, 2011
Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegenerationTyler Mark Pierson, Dimitre R Simeonov, Murat Sincan, et al.
BMC Genomics|January 13, 2010
Effort required to finish shotgun-generated genome sequences differs significantly among vertebratesRobert W Blakesley, Nancy F Hansen, Jyoti Gupta, et al.
BMC Cancer|November 28, 2014
Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1Meghan L Rudd, Hassan Mohamed, Jessica C Price, et al.
Nature Genetics|October 30, 2012
Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genesMatthieu Le Gallo, Andrea J O'Hara, Meghan L Rudd, et al.
Neurology|June 8, 2012
Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM1-gangliosidosisTyler Mark Pierson, David A Adams, Thomas Markello, et al.
Molecular Genetics and Metabolism|July 20, 2011
Personalized genomic medicine: lessons from the exomeBenjamin D Solomon, Daniel E Pineda-Alvarez, Donald W Hadley, et al.
Neuro-Oncology|February 6, 2019
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define premalignant neurofibromatosis type 1-associated atypical neurofibromasAlexander Pemov, Nancy F Hansen, Sivasish Sindiri, et al.
Cancer|May 10, 2017
Somatic mutation profiles of clear cell endometrial tumors revealed by whole exome and targeted gene sequencingMatthieu Le Gallo, Meghan L Rudd, Mary Ellen Urick, et al.
Plos One|June 12, 2013
Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11AJessica C Price, Lana M Pollock, Meghan L Rudd, et al.
BMC Genomics|June 26, 2010
Light whole genome sequence for SNP discovery across domestic cat breedsJames C Mullikin, Nancy F Hansen, Lei Shen, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
European Journal of Human Genetics : EJHG|December 8, 2011
Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegenerationTyler Mark Pierson, Dimitre R Simeonov, Murat Sincan, et al.
BMC Genomics|January 13, 2010
Effort required to finish shotgun-generated genome sequences differs significantly among vertebratesRobert W Blakesley, Nancy F Hansen, Jyoti Gupta, et al.
BMC Cancer|November 28, 2014
Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1Meghan L Rudd, Hassan Mohamed, Jessica C Price, et al.
Nature Genetics|October 30, 2012
Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genesMatthieu Le Gallo, Andrea J O'Hara, Meghan L Rudd, et al.
Neurology|June 8, 2012
Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM1-gangliosidosisTyler Mark Pierson, David A Adams, Thomas Markello, et al.
Molecular Genetics and Metabolism|July 20, 2011
Personalized genomic medicine: lessons from the exomeBenjamin D Solomon, Daniel E Pineda-Alvarez, Donald W Hadley, et al.
Neuro-Oncology|February 6, 2019
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define premalignant neurofibromatosis type 1-associated atypical neurofibromasAlexander Pemov, Nancy F Hansen, Sivasish Sindiri, et al.
Cancer|May 10, 2017
Somatic mutation profiles of clear cell endometrial tumors revealed by whole exome and targeted gene sequencingMatthieu Le Gallo, Meghan L Rudd, Mary Ellen Urick, et al.
Plos One|June 12, 2013
Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11AJessica C Price, Lana M Pollock, Meghan L Rudd, et al.
BMC Genomics|June 26, 2010
Light whole genome sequence for SNP discovery across domestic cat breedsJames C Mullikin, Nancy F Hansen, Lei Shen, et al.
Pageof 6