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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) mutation
E 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 cells
K 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 9
N A Jenkins, M C Strobel, P K Seperack, et al.
Genetics
|
April 30, 1998
Molecular genetic dissection of mouse unconventional myosin-VA: head region mutations
J 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-1.4
F 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 immunotherapy
T 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 mice
S 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 dimerization
E 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 loci
R P Woychik, W M Generoso, L B Russell, et al.
Nature
|
February 22, 1996
Disruption of the nuclear hormone receptor RORalpha in staggerer mice
B A Hamilton, W N Frankel, A W Kerrebrock, et al.
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of 17
Search research articles
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Showing results (151-160 of 162) with videos related to
Sort By:
Page
of 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) mutation
E 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 cells
K 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 9
N A Jenkins, M C Strobel, P K Seperack, et al.
Genetics
|
April 30, 1998
Molecular genetic dissection of mouse unconventional myosin-VA: head region mutations
J 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-1.4
F 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 immunotherapy
T 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 mice
S 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 dimerization
E 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 loci
R P Woychik, W M Generoso, L B Russell, et al.
Nature
|
February 22, 1996
Disruption of the nuclear hormone receptor RORalpha in staggerer mice
B A Hamilton, W N Frankel, A W Kerrebrock, et al.
Page
of 17