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D I Smith

Showing results (131-140 of 166) with videos related to

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Cytogenetic and Genome Research|September 2, 2008
Differential loss of expression of common fragile site genes between oral tongue and oropharyngeal squamous cell carcinomasC Soderberg, D S Perez, O C Ukpo, et al.
Genomics|September 1, 1991
Localization of 616 human chromosome 3-specific cosmids using a somatic cell hybrid deletion mapping panelD I Smith, W Liu, D Ginzinger, et al.
The Prostate|April 30, 1999
Mutation and expression analysis of the p73 gene in prostate cancerA Yokomizo, M Mai, D G Bostwick, et al.
Breast Cancer Research and Treatment|January 14, 2000
p73 mutations are not detected in sporadic and hereditary breast cancerD I Schwartz, N M Lindor, C Walsh-Vockley, et al.
Oncogene|August 26, 1998
Differential loss of heterozygosity at 7q31.2 in follicular and papillary thyroid tumorsJ S Zhang, M Nelson, B McIver, et al.
Genomics|January 15, 1994
Characterization of a microdissection library from human chromosome region 3p14W Bardenheuer, S Szymanski, A Lux, et al.
Genomics|September 1, 1991
A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndromeR M Gemmill, M Varella-Garcia, D I Smith, et al.
American Journal of Respiratory Cell and Molecular Biology|May 2, 1998
Macrophage-stimulating protein and its receptor in non-small-cell lung tumors: induction of receptor tyrosine phosphorylation and cell migrationC G Willett, M H Wang, R L Emanuel, et al.
Cancer Research|October 1, 1996
Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumorsR Shridhar, V Shridhar, X Wang, et al.
Journal of Medical Genetics|October 1, 1996
Precise localisation of 3p25 breakpoints in four patients with the 3p-syndromeT Drumheller, B C McGillivray, D Behrner, et al.
Pageof 17

Showing results (131-140 of 166) with videos related to

Sort By:
Pageof 17
Cytogenetic and Genome Research|September 2, 2008
Differential loss of expression of common fragile site genes between oral tongue and oropharyngeal squamous cell carcinomasC Soderberg, D S Perez, O C Ukpo, et al.
Genomics|September 1, 1991
Localization of 616 human chromosome 3-specific cosmids using a somatic cell hybrid deletion mapping panelD I Smith, W Liu, D Ginzinger, et al.
The Prostate|April 30, 1999
Mutation and expression analysis of the p73 gene in prostate cancerA Yokomizo, M Mai, D G Bostwick, et al.
Breast Cancer Research and Treatment|January 14, 2000
p73 mutations are not detected in sporadic and hereditary breast cancerD I Schwartz, N M Lindor, C Walsh-Vockley, et al.
Oncogene|August 26, 1998
Differential loss of heterozygosity at 7q31.2 in follicular and papillary thyroid tumorsJ S Zhang, M Nelson, B McIver, et al.
Genomics|January 15, 1994
Characterization of a microdissection library from human chromosome region 3p14W Bardenheuer, S Szymanski, A Lux, et al.
Genomics|September 1, 1991
A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndromeR M Gemmill, M Varella-Garcia, D I Smith, et al.
American Journal of Respiratory Cell and Molecular Biology|May 2, 1998
Macrophage-stimulating protein and its receptor in non-small-cell lung tumors: induction of receptor tyrosine phosphorylation and cell migrationC G Willett, M H Wang, R L Emanuel, et al.
Cancer Research|October 1, 1996
Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumorsR Shridhar, V Shridhar, X Wang, et al.
Journal of Medical Genetics|October 1, 1996
Precise localisation of 3p25 breakpoints in four patients with the 3p-syndromeT Drumheller, B C McGillivray, D Behrner, et al.
Pageof 17