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

T B Shows

Showing results (111-120 of 381) with videos related to

Pageof 39
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1983
Polymorphic gene for human carbonic anhydrase II: a molecular disease marker located on chromosome 8P J Venta, T B Shows, P J Curtis, et al.
Cytogenetics and Cell Genetics|January 1, 1995
The kinase insert domain receptor gene (KDR) has been relocated to chromosome 4q11-->q12S N Sait, M Dougher-Vermazen, T B Shows, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1984
Assignment of the gene for methylthioadenosine phosphorylase to human chromosome 9 by mouse-human somatic cell hybridizationC J Carrera, R L Eddy, T B Shows, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1985
Variable numbers of pepsinogen genes are located in the centromeric region of human chromosome 11 and determine the high-frequency electrophoretic polymorphismR T Taggart, T K Mohandas, T B Shows, et al.
Cytogenetics and Cell Genetics|January 1, 1985
The 1985 Catalog of Mapped Genes and report of the Nomenclature CommitteeP J McAlpine, T B Shows, R L Miller, et al.
Cytogenetics and Cell Genetics|January 1, 1975
Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridizationM C Rattazzi, J A Brown, R G Davidson, et al.
Biochemical Genetics|October 1, 1970
Biochemical polymorphisms in feral and inbred mice (mus musculus)T H Roderick, F H Ruddle, V M Chapman, et al.
Cytogenetics and Cell Genetics|January 1, 1992
The KDR gene maps to human chromosome 4q31.2----q32, a locus which is distinct from locations for other type III growth factor receptor tyrosine kinasesB I Terman, S Jani-Sait, M E Carrion, et al.
Molecular and Cellular Biology|February 11, 1991
Different forms of Go alpha mRNA arise by alternative splicing of transcripts from a single gene on human chromosome 16J J Murtagh, R Eddy, T B Shows, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1987
Cloning of the chromosome translocation breakpoint junction of the t(14;19) in chronic lymphocytic leukemiaT W McKeithan, J D Rowley, T B Shows, et al.
Pageof 39

Showing results (111-120 of 381) with videos related to

Sort By:
Pageof 39
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1983
Polymorphic gene for human carbonic anhydrase II: a molecular disease marker located on chromosome 8P J Venta, T B Shows, P J Curtis, et al.
Cytogenetics and Cell Genetics|January 1, 1995
The kinase insert domain receptor gene (KDR) has been relocated to chromosome 4q11-->q12S N Sait, M Dougher-Vermazen, T B Shows, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1984
Assignment of the gene for methylthioadenosine phosphorylase to human chromosome 9 by mouse-human somatic cell hybridizationC J Carrera, R L Eddy, T B Shows, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1985
Variable numbers of pepsinogen genes are located in the centromeric region of human chromosome 11 and determine the high-frequency electrophoretic polymorphismR T Taggart, T K Mohandas, T B Shows, et al.
Cytogenetics and Cell Genetics|January 1, 1985
The 1985 Catalog of Mapped Genes and report of the Nomenclature CommitteeP J McAlpine, T B Shows, R L Miller, et al.
Cytogenetics and Cell Genetics|January 1, 1975
Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridizationM C Rattazzi, J A Brown, R G Davidson, et al.
Biochemical Genetics|October 1, 1970
Biochemical polymorphisms in feral and inbred mice (mus musculus)T H Roderick, F H Ruddle, V M Chapman, et al.
Cytogenetics and Cell Genetics|January 1, 1992
The KDR gene maps to human chromosome 4q31.2----q32, a locus which is distinct from locations for other type III growth factor receptor tyrosine kinasesB I Terman, S Jani-Sait, M E Carrion, et al.
Molecular and Cellular Biology|February 11, 1991
Different forms of Go alpha mRNA arise by alternative splicing of transcripts from a single gene on human chromosome 16J J Murtagh, R Eddy, T B Shows, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1987
Cloning of the chromosome translocation breakpoint junction of the t(14;19) in chronic lymphocytic leukemiaT W McKeithan, J D Rowley, T B Shows, et al.
Pageof 39