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

L B RUSSELL

Showing results (151-160 of 162) with videos related to

Pageof 17
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
A molecular model for the genetic and phenotypic characteristics of the mouse lethal yellow (Ay) mutationE J Michaud, S J Bultman, M L Klebig, et al.
Nature Genetics|December 1, 1995
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cellsK B Avraham, T Hasson, K P Steel, et al.
Progress in Nucleic Acid Research and Molecular Biology|January 1, 1989
A retroviral insertion in the dilute (d) locus provides molecular access to this region of mouse chromosome 9N A Jenkins, M C Strobel, P K Seperack, et al.
Genetics|April 30, 1998
Molecular genetic dissection of mouse unconventional myosin-VA: head region mutationsJ D Huang, M J Cope, V Mermall, et al.
Oncogene|March 1, 1988
Genetic analysis and developmental regulation of testis-specific RNA expression of Mos, Abl, actin and Hox-1.4F Propst, M P Rosenberg, M K Oskarsson, et al.
The Journal of Experimental Medicine|April 5, 2000
Self-tolerance to the murine homologue of a tyrosinase-derived melanoma antigen: implications for tumor immunotherapyT A Colella, T N Bullock, L B Russell, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
A mutation in Rab27a causes the vesicle transport defects observed in ashen miceS M Wilson, R Yip, D A Swing, et al.
The EMBO Journal|November 15, 1996
The semidominant Mi(b) mutation identifies a role for the HLH domain in DNA binding in addition to its role in protein dimerizationE Steingrímsson, A Nii, D E Fisher, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990
Molecular and genetic characterization of a radiation-induced structural rearrangement in mouse chromosome 2 causing mutations at the limb deformity and agouti lociR P Woychik, W M Generoso, L B Russell, et al.
Nature|February 22, 1996
Disruption of the nuclear hormone receptor RORalpha in staggerer miceB A Hamilton, W N Frankel, A W Kerrebrock, et al.
Pageof 17

Showing results (151-160 of 162) with videos related to

Sort By:
Pageof 17
Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
A molecular model for the genetic and phenotypic characteristics of the mouse lethal yellow (Ay) mutationE J Michaud, S J Bultman, M L Klebig, et al.
Nature Genetics|December 1, 1995
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cellsK B Avraham, T Hasson, K P Steel, et al.
Progress in Nucleic Acid Research and Molecular Biology|January 1, 1989
A retroviral insertion in the dilute (d) locus provides molecular access to this region of mouse chromosome 9N A Jenkins, M C Strobel, P K Seperack, et al.
Genetics|April 30, 1998
Molecular genetic dissection of mouse unconventional myosin-VA: head region mutationsJ D Huang, M J Cope, V Mermall, et al.
Oncogene|March 1, 1988
Genetic analysis and developmental regulation of testis-specific RNA expression of Mos, Abl, actin and Hox-1.4F Propst, M P Rosenberg, M K Oskarsson, et al.
The Journal of Experimental Medicine|April 5, 2000
Self-tolerance to the murine homologue of a tyrosinase-derived melanoma antigen: implications for tumor immunotherapyT A Colella, T N Bullock, L B Russell, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
A mutation in Rab27a causes the vesicle transport defects observed in ashen miceS M Wilson, R Yip, D A Swing, et al.
The EMBO Journal|November 15, 1996
The semidominant Mi(b) mutation identifies a role for the HLH domain in DNA binding in addition to its role in protein dimerizationE Steingrímsson, A Nii, D E Fisher, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990
Molecular and genetic characterization of a radiation-induced structural rearrangement in mouse chromosome 2 causing mutations at the limb deformity and agouti lociR P Woychik, W M Generoso, L B Russell, et al.
Nature|February 22, 1996
Disruption of the nuclear hormone receptor RORalpha in staggerer miceB A Hamilton, W N Frankel, A W Kerrebrock, et al.
Pageof 17