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R B Jenkins

Showing results (121-130 of 159) with videos related to

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Cancer Research|May 1, 1992
Molecular analysis of deletions of the short arm of chromosome 9 in human gliomasO I Olopade, R B Jenkins, D T Ransom, et al.
American Journal of Medical Genetics|August 28, 1995
Uniparental disomy in congenital disorders: a prospective studyN M Lindor, P S Karnes, V V Michels, et al.
Cancer Genetics and Cytogenetics|July 11, 1992
Cytogenetic analysis of six renal oncocytomas and a chromophobe cell renal carcinoma. Evidence that -Y, -1 may be a characteristic anomaly in renal oncocytomasT B Crotty, K M Lawrence, C A Moertel, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 1, 1996
Absence of mutations in DNA mismatch repair genes in sporadic endometrial tumors with microsatellite instabilityP C Lim, D Tester, W Cliby, et al.
Genetic Testing|September 12, 2001
Papillary renal cell carcinoma: analysis of germline mutations in the MET proto-oncogene in a clinic-based populationN M Lindor, C B Dechet, M H Greene, et al.
Genes, Chromosomes & Cancer|November 1, 1992
Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomasD T Ransom, S R Ritland, D W Kimmel, et al.
Cancer|September 15, 1990
Frequent occurrence of cytogenetic abnormalities in sporadic nonmedullary thyroid carcinomaR B Jenkins, I D Hay, J F Herath, et al.
Journal of Neuropathology and Experimental Neurology|September 1, 1996
The glial and mesenchymal elements of gliosarcomas share similar genetic alterationsR H Boerman, K Anderl, J Herath, et al.
American Journal of Clinical Pathology|December 10, 1999
Detection of p16, RB, CDK4, and p53 gene deletion and amplification by fluorescence in situ hybridization in 96 gliomasA Perry, K Anderl, T J Borell, et al.
Genomics|February 16, 2000
EHD2, EHD3, and EHD4 encode novel members of a highly conserved family of EH domain-containing proteinsU Pohl, J S Smith, I Tachibana, et al.
Pageof 16

Showing results (121-130 of 159) with videos related to

Sort By:
Pageof 16
Cancer Research|May 1, 1992
Molecular analysis of deletions of the short arm of chromosome 9 in human gliomasO I Olopade, R B Jenkins, D T Ransom, et al.
American Journal of Medical Genetics|August 28, 1995
Uniparental disomy in congenital disorders: a prospective studyN M Lindor, P S Karnes, V V Michels, et al.
Cancer Genetics and Cytogenetics|July 11, 1992
Cytogenetic analysis of six renal oncocytomas and a chromophobe cell renal carcinoma. Evidence that -Y, -1 may be a characteristic anomaly in renal oncocytomasT B Crotty, K M Lawrence, C A Moertel, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 1, 1996
Absence of mutations in DNA mismatch repair genes in sporadic endometrial tumors with microsatellite instabilityP C Lim, D Tester, W Cliby, et al.
Genetic Testing|September 12, 2001
Papillary renal cell carcinoma: analysis of germline mutations in the MET proto-oncogene in a clinic-based populationN M Lindor, C B Dechet, M H Greene, et al.
Genes, Chromosomes & Cancer|November 1, 1992
Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomasD T Ransom, S R Ritland, D W Kimmel, et al.
Cancer|September 15, 1990
Frequent occurrence of cytogenetic abnormalities in sporadic nonmedullary thyroid carcinomaR B Jenkins, I D Hay, J F Herath, et al.
Journal of Neuropathology and Experimental Neurology|September 1, 1996
The glial and mesenchymal elements of gliosarcomas share similar genetic alterationsR H Boerman, K Anderl, J Herath, et al.
American Journal of Clinical Pathology|December 10, 1999
Detection of p16, RB, CDK4, and p53 gene deletion and amplification by fluorescence in situ hybridization in 96 gliomasA Perry, K Anderl, T J Borell, et al.
Genomics|February 16, 2000
EHD2, EHD3, and EHD4 encode novel members of a highly conserved family of EH domain-containing proteinsU Pohl, J S Smith, I Tachibana, et al.
Pageof 16