Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J K Cowell

Showing results (81-90 of 131) with videos related to

Pageof 14
Sort By:
Oncogene|July 1, 1992
Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencingA Hogg, Z Onadim, P N Baird, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1992
Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotypeZ Onadim, A Hogg, P N Baird, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Regional localisation of tri- and tetranucleotide repeat sequence-containing cosmids on chromosome 13L A Hawthorn, B Kapanadse, N Yankovsky, et al.
Oncogene|June 1, 1993
The consistent 13q14 translocation breakpoint seen in chronic B-cell leukaemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition geneL A Hawthorn, R Chapman, D Oscier, et al.
British Journal of Cancer|November 20, 1998
Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumourR G Grundy, J Pritchard, P Scambler, et al.
Human Genetics|April 1, 1990
Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid libraryR B Wadey, P F Little, J Pritchard, et al.
Human Genetics|May 1, 1989
The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11J K Cowell, R B Wadey, B B Buckle, et al.
Genes, Chromosomes & Cancer|March 10, 1998
Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridizationO Chernova, I Still, M Kalaycio, et al.
European Journal of Cancer (Oxford, England : 1990)|June 1, 1997
The use of SCID mice for the growth of retinoblastoma cell lines and for the establishment of xenografts from primary tumoursJ K Cowell, P Ramani, Y Song, et al.
Cancer Genetics and Cytogenetics|September 22, 2001
Molecular characterization of the breakpoint region associated with a constitutional t(2;15)(q34;q26) in a patient with multiple myelomaE Kitamura, B A Kuemerle, O B Chernova, et al.
Pageof 14

Showing results (81-90 of 131) with videos related to

Sort By:
Pageof 14
Oncogene|July 1, 1992
Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencingA Hogg, Z Onadim, P N Baird, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1992
Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotypeZ Onadim, A Hogg, P N Baird, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Regional localisation of tri- and tetranucleotide repeat sequence-containing cosmids on chromosome 13L A Hawthorn, B Kapanadse, N Yankovsky, et al.
Oncogene|June 1, 1993
The consistent 13q14 translocation breakpoint seen in chronic B-cell leukaemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition geneL A Hawthorn, R Chapman, D Oscier, et al.
British Journal of Cancer|November 20, 1998
Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumourR G Grundy, J Pritchard, P Scambler, et al.
Human Genetics|April 1, 1990
Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid libraryR B Wadey, P F Little, J Pritchard, et al.
Human Genetics|May 1, 1989
The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11J K Cowell, R B Wadey, B B Buckle, et al.
Genes, Chromosomes & Cancer|March 10, 1998
Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridizationO Chernova, I Still, M Kalaycio, et al.
European Journal of Cancer (Oxford, England : 1990)|June 1, 1997
The use of SCID mice for the growth of retinoblastoma cell lines and for the establishment of xenografts from primary tumoursJ K Cowell, P Ramani, Y Song, et al.
Cancer Genetics and Cytogenetics|September 22, 2001
Molecular characterization of the breakpoint region associated with a constitutional t(2;15)(q34;q26) in a patient with multiple myelomaE Kitamura, B A Kuemerle, O B Chernova, et al.
Pageof 14