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Adam Butler

Showing results (51-60 of 76) with videos related to

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Nature|January 8, 2010
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genesGillian L Dalgliesh, Kyle Furge, Chris Greenman, et al.
Nature|December 18, 2009
A comprehensive catalogue of somatic mutations from a human cancer genomeErin D Pleasance, R Keira Cheetham, Philip J Stephens, et al.
American Journal of Human Genetics|January 20, 2007
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorPatrick S Tarpey, F Lucy Raymond, Sarah O'Meara, et al.
Nature Genetics|March 18, 2014
Recurrent PTPRB and PLCG1 mutations in angiosarcomaSam Behjati, Patrick S Tarpey, Helen Sheldon, et al.
Genes, Chromosomes & Cancer|September 22, 2005
Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adultsGraham Bignell, Raffaella Smith, Chris Hunter, et al.
Cancer Research|April 19, 2006
A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapyChris Hunter, Raffaella Smith, Daniel P Cahill, et al.
Genome Research|January 30, 2019
The circular RNome of primary breast cancerMarcel Smid, Saskia M Wilting, Katharina Uhr, et al.
Nature Genetics|August 21, 2007
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationPatrick S Tarpey, F Lucy Raymond, Lam S Nguyen, et al.
Nature Genetics|March 22, 2023
Author Correction: Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotranspositionBernardo Rodriguez-Martin, Eva G Alvarez, Adrian Baez-Ortega, et al.
Nature Genetics|May 13, 2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentLeanne M Dibbens, Patrick S Tarpey, Kim Hynes, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
Nature|January 8, 2010
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genesGillian L Dalgliesh, Kyle Furge, Chris Greenman, et al.
Nature|December 18, 2009
A comprehensive catalogue of somatic mutations from a human cancer genomeErin D Pleasance, R Keira Cheetham, Philip J Stephens, et al.
American Journal of Human Genetics|January 20, 2007
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorPatrick S Tarpey, F Lucy Raymond, Sarah O'Meara, et al.
Nature Genetics|March 18, 2014
Recurrent PTPRB and PLCG1 mutations in angiosarcomaSam Behjati, Patrick S Tarpey, Helen Sheldon, et al.
Genes, Chromosomes & Cancer|September 22, 2005
Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adultsGraham Bignell, Raffaella Smith, Chris Hunter, et al.
Cancer Research|April 19, 2006
A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapyChris Hunter, Raffaella Smith, Daniel P Cahill, et al.
Genome Research|January 30, 2019
The circular RNome of primary breast cancerMarcel Smid, Saskia M Wilting, Katharina Uhr, et al.
Nature Genetics|August 21, 2007
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationPatrick S Tarpey, F Lucy Raymond, Lam S Nguyen, et al.
Nature Genetics|March 22, 2023
Author Correction: Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotranspositionBernardo Rodriguez-Martin, Eva G Alvarez, Adrian Baez-Ortega, et al.
Nature Genetics|May 13, 2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentLeanne M Dibbens, Patrick S Tarpey, Kim Hynes, et al.
Pageof 8