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

S L Naylor

Showing results (121-130 of 137) with videos related to

Pageof 14
Sort By:
Human Molecular Genetics|July 1, 1997
Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 geneJ O Winberg, N Hammami-Hauasli, O Nilssen, et al.
Genomics|September 16, 1999
An evolutionary rearrangement of the Xp11.3-11.23 region in 3p21.3, a region frequently deleted in a variety of cancersT Timmer, P Terpstra, A van den Berg, et al.
Oncogene|September 27, 2006
PHC3, a component of the hPRC-H complex, associates with E2F6 during G0 and is lost in osteosarcoma tumorsA M Deshpande, J D Akunowicz, X T Reveles, et al.
Genomics|September 15, 1994
Characterization of the mouse loricrin gene: linkage with profilaggrin and the flaky tail and soft coat mutant loci on chromosome 3J A Rothnagel, M A Longley, D S Bundman, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
Characterization, mapping, and expression of the human ceruloplasmin geneF Yang, S L Naylor, J B Lum, et al.
Oncogene|July 1, 1994
Two novel human serine/threonine kinases with homologies to the cell cycle regulating Xenopus MO15, and NIMA kinases: cloning and characterization of their expression patternE N Levedakou, M He, E W Baptist, et al.
Genomics|February 1, 1989
Loss of heterozygosity on chromosome 10 in human glioblastoma multiformeM Fujimoto, D W Fults, G A Thomas, et al.
Nature|November 17, 1983
A polymorphic DNA marker genetically linked to Huntington's diseaseJ F Gusella, N S Wexler, P M Conneally, et al.
Genomics|February 15, 1996
Isolation of the human semaphorin III/F gene (SEMA3F) at chromosome 3p21, a region deleted in lung cancerR H Xiang, C H Hensel, D K Garcia, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3T Timmer, P Terpstra, A van den Berg, et al.
Pageof 14

Showing results (121-130 of 137) with videos related to

Sort By:
Pageof 14
Human Molecular Genetics|July 1, 1997
Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 geneJ O Winberg, N Hammami-Hauasli, O Nilssen, et al.
Genomics|September 16, 1999
An evolutionary rearrangement of the Xp11.3-11.23 region in 3p21.3, a region frequently deleted in a variety of cancersT Timmer, P Terpstra, A van den Berg, et al.
Oncogene|September 27, 2006
PHC3, a component of the hPRC-H complex, associates with E2F6 during G0 and is lost in osteosarcoma tumorsA M Deshpande, J D Akunowicz, X T Reveles, et al.
Genomics|September 15, 1994
Characterization of the mouse loricrin gene: linkage with profilaggrin and the flaky tail and soft coat mutant loci on chromosome 3J A Rothnagel, M A Longley, D S Bundman, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
Characterization, mapping, and expression of the human ceruloplasmin geneF Yang, S L Naylor, J B Lum, et al.
Oncogene|July 1, 1994
Two novel human serine/threonine kinases with homologies to the cell cycle regulating Xenopus MO15, and NIMA kinases: cloning and characterization of their expression patternE N Levedakou, M He, E W Baptist, et al.
Genomics|February 1, 1989
Loss of heterozygosity on chromosome 10 in human glioblastoma multiformeM Fujimoto, D W Fults, G A Thomas, et al.
Nature|November 17, 1983
A polymorphic DNA marker genetically linked to Huntington's diseaseJ F Gusella, N S Wexler, P M Conneally, et al.
Genomics|February 15, 1996
Isolation of the human semaphorin III/F gene (SEMA3F) at chromosome 3p21, a region deleted in lung cancerR H Xiang, C H Hensel, D K Garcia, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3T Timmer, P Terpstra, A van den Berg, et al.
Pageof 14