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E R Maher

Showing results (101-110 of 171) with videos related to

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Genomics|August 1, 1991
Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysisE R Maher, E Bentley, J R Yates, et al.
American Journal of Human Genetics|April 1, 1997
Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumorsA H Prowse, A R Webster, F M Richards, et al.
Journal of Medical Genetics|May 1, 1997
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndromeD Catchpoole, W W Lam, D Valler, et al.
The British Journal of Ophthalmology|November 12, 2003
Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2)M Michaelides, I A Aligianis, G E Holder, et al.
Genes, Chromosomes & Cancer|August 10, 1999
Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 and VBP1) mutation and loss in renal-cell carcinoma developmentS C Clifford, S Walsh, K Hewson, et al.
Oncogene|February 16, 2010
Identification of candidate tumour suppressor genes frequently methylated in renal cell carcinomaM R Morris, C Ricketts, D Gentle, et al.
Journal of Medical Genetics|December 1, 1996
Microsatellite instability in early onset and familial colorectal cancerC Brassett, J A Joyce, N J Froggatt, et al.
British Journal of Cancer|March 31, 2005
Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumourD Astuti, F Latif, K Wagner, et al.
JAMA|October 11, 1995
Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type IIH P Neumann, C Eng, L M Mulligan, et al.
British Journal of Cancer|January 16, 2008
Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinomaM R Morris, D Gentle, M Abdulrahman, et al.
Pageof 18

Showing results (101-110 of 171) with videos related to

Sort By:
Pageof 18
Genomics|August 1, 1991
Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysisE R Maher, E Bentley, J R Yates, et al.
American Journal of Human Genetics|April 1, 1997
Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumorsA H Prowse, A R Webster, F M Richards, et al.
Journal of Medical Genetics|May 1, 1997
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndromeD Catchpoole, W W Lam, D Valler, et al.
The British Journal of Ophthalmology|November 12, 2003
Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2)M Michaelides, I A Aligianis, G E Holder, et al.
Genes, Chromosomes & Cancer|August 10, 1999
Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 and VBP1) mutation and loss in renal-cell carcinoma developmentS C Clifford, S Walsh, K Hewson, et al.
Oncogene|February 16, 2010
Identification of candidate tumour suppressor genes frequently methylated in renal cell carcinomaM R Morris, C Ricketts, D Gentle, et al.
Journal of Medical Genetics|December 1, 1996
Microsatellite instability in early onset and familial colorectal cancerC Brassett, J A Joyce, N J Froggatt, et al.
British Journal of Cancer|March 31, 2005
Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumourD Astuti, F Latif, K Wagner, et al.
JAMA|October 11, 1995
Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type IIH P Neumann, C Eng, L M Mulligan, et al.
British Journal of Cancer|January 16, 2008
Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinomaM R Morris, D Gentle, M Abdulrahman, et al.
Pageof 18