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David Jones

Showing results (491-500 of 531) with videos related to

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Nature Genetics|October 25, 2022
Multiomics study of nonalcoholic fatty liver diseaseGardar Sveinbjornsson, Magnus O Ulfarsson, Rosa B Thorolfsdottir, et al.
Journal of Hepatology|July 1, 2022
Liver stiffness measurement by vibration-controlled transient elastography improves outcome prediction in primary biliary cholangitisChristophe Corpechot, Fabrice Carrat, Farid Gaouar, 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 31, 2025
The complexity of tobacco smoke-induced mutagenesis in head and neck cancerLaura Torrens, Sarah Moody, Ana Carolina de Carvalho, et al.
Nature|January 8, 2010
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genesGillian L Dalgliesh, Kyle Furge, Chris Greenman, 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.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
The Complexity of Tobacco Smoke-Induced Mutagenesis in Head and Neck CancerLaura Torrens, Sarah Moody, Ana Carolina de Carvalho, et al.
Nature Genetics|October 19, 2021
Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidenceSarah Moody, Sergey Senkin, S M Ashiqul Islam, 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.
Pageof 54

Showing results (491-500 of 531) with videos related to

Sort By:
Pageof 54
Nature Genetics|October 25, 2022
Multiomics study of nonalcoholic fatty liver diseaseGardar Sveinbjornsson, Magnus O Ulfarsson, Rosa B Thorolfsdottir, et al.
Journal of Hepatology|July 1, 2022
Liver stiffness measurement by vibration-controlled transient elastography improves outcome prediction in primary biliary cholangitisChristophe Corpechot, Fabrice Carrat, Farid Gaouar, 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 31, 2025
The complexity of tobacco smoke-induced mutagenesis in head and neck cancerLaura Torrens, Sarah Moody, Ana Carolina de Carvalho, et al.
Nature|January 8, 2010
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genesGillian L Dalgliesh, Kyle Furge, Chris Greenman, 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.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
The Complexity of Tobacco Smoke-Induced Mutagenesis in Head and Neck CancerLaura Torrens, Sarah Moody, Ana Carolina de Carvalho, et al.
Nature Genetics|October 19, 2021
Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidenceSarah Moody, Sergey Senkin, S M Ashiqul Islam, 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.
Pageof 54