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J K Cowell

Showing results (51-60 of 131) with videos related to

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International Journal of Molecular Medicine|December 16, 1998
Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisationR G Grundy, R Aledo, J K Cowell
International Journal of Molecular Medicine|April 14, 2000
A new region of synteny between human chromosome 1p22 and mouse chromosome 5D M Chelsea, T Roberts, J K Cowell
Annals of Human Genetics|January 1, 1997
Fine structure physical mapping of a 1.9 Mb region of chromosome 13q12I H Still, T Roberts, J K Cowell
Annals of Human Genetics|May 1, 1996
Characterisation of a human chromosome 1 somatic cell hybrid mapping panel and regional assignment of 6 novel STST Roberts, R S Mead, J K Cowell
Proceedings of the National Academy of Sciences of the United States of America|September 18, 1997
Direct isolation of human transcribed sequences from yeast artificial chromosomes through the application of RNA fingerprintingI H Still, P Vince, J K Cowell
Genomics|June 15, 1999
The third member of the transforming acidic coiled coil-containing gene family, TACC3, maps in 4p16, close to translocation breakpoints in multiple myeloma, and is upregulated in various cancer cell linesI H Still, P Vince, J K Cowell
International Journal of Molecular Medicine|April 11, 2001
Fine mapping of the PTGFR gene to 1p31 region and mutation analysis in human breast cancerK Sossey-Alaoui, E Kitamura, J K Cowell
British Journal of Cancer|June 1, 1994
Molecular genetic analysis of chromosome 11p in familial Wilms tumourP N Baird, J Pritchard, J K Cowell
Oncogene|January 26, 2016
WASF3 provides the conduit to facilitate invasion and metastasis in breast cancer cells through HER2/HER3 signalingY Teng, W Pi, Y Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1993
Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastomaA Hogg, B Bia, Z Onadim, et al.
Pageof 14

Showing results (51-60 of 131) with videos related to

Sort By:
Pageof 14
International Journal of Molecular Medicine|December 16, 1998
Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisationR G Grundy, R Aledo, J K Cowell
International Journal of Molecular Medicine|April 14, 2000
A new region of synteny between human chromosome 1p22 and mouse chromosome 5D M Chelsea, T Roberts, J K Cowell
Annals of Human Genetics|January 1, 1997
Fine structure physical mapping of a 1.9 Mb region of chromosome 13q12I H Still, T Roberts, J K Cowell
Annals of Human Genetics|May 1, 1996
Characterisation of a human chromosome 1 somatic cell hybrid mapping panel and regional assignment of 6 novel STST Roberts, R S Mead, J K Cowell
Proceedings of the National Academy of Sciences of the United States of America|September 18, 1997
Direct isolation of human transcribed sequences from yeast artificial chromosomes through the application of RNA fingerprintingI H Still, P Vince, J K Cowell
Genomics|June 15, 1999
The third member of the transforming acidic coiled coil-containing gene family, TACC3, maps in 4p16, close to translocation breakpoints in multiple myeloma, and is upregulated in various cancer cell linesI H Still, P Vince, J K Cowell
International Journal of Molecular Medicine|April 11, 2001
Fine mapping of the PTGFR gene to 1p31 region and mutation analysis in human breast cancerK Sossey-Alaoui, E Kitamura, J K Cowell
British Journal of Cancer|June 1, 1994
Molecular genetic analysis of chromosome 11p in familial Wilms tumourP N Baird, J Pritchard, J K Cowell
Oncogene|January 26, 2016
WASF3 provides the conduit to facilitate invasion and metastasis in breast cancer cells through HER2/HER3 signalingY Teng, W Pi, Y Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1993
Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastomaA Hogg, B Bia, Z Onadim, et al.
Pageof 14