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Annals of the New York Academy of Sciences
|
January 1, 1991
Reverse genetics in the mouse and its application to the study of deafness
E M Rinchik, D K Johnson, F L Margolis, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 19, 2001
Genetic and environmental factors modify bovine spongiform encephalopathy incubation period in mice
K Manolakou, J Beaton, I McConnell, et al.
The EMBO Journal
|
February 1, 1992
A second tyrosinase-related protein, TRP-2, maps to and is mutated at the mouse slaty locus
I J Jackson, D M Chambers, K Tsukamoto, et al.
Nucleic Acids Research
|
January 24, 1981
The absence of introns within a human fibroblast interferon gene
M Houghton, I J Jackson, A G Porter, et al.
Human Molecular Genetics
|
October 1, 1996
The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma
P Valverde, E Healy, S Sikkink, et al.
Human Molecular Genetics
|
October 13, 2000
Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation
N Flanagan, E Healy, A Ray, et al.
Lancet (London, England)
|
April 1, 2000
Melanocortin-1-receptor gene and sun sensitivity in individuals without red hair
E Healy, N Flannagan, A Ray, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1990
Genetic and molecular analysis of chlorambucil-induced germ-line mutations in the mouse
E M Rinchik, J W Bangham, P R Hunsicker, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 22, 1999
Melanocortin 1 receptor variation in the domestic dog
J M Newton, A L Wilkie, L He, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 22, 1999
A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23
E H Simpson, R Suffolk, J A Bell, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 94) with videos related to
Sort By:
Page
of 10
Annals of the New York Academy of Sciences
|
January 1, 1991
Reverse genetics in the mouse and its application to the study of deafness
E M Rinchik, D K Johnson, F L Margolis, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 19, 2001
Genetic and environmental factors modify bovine spongiform encephalopathy incubation period in mice
K Manolakou, J Beaton, I McConnell, et al.
The EMBO Journal
|
February 1, 1992
A second tyrosinase-related protein, TRP-2, maps to and is mutated at the mouse slaty locus
I J Jackson, D M Chambers, K Tsukamoto, et al.
Nucleic Acids Research
|
January 24, 1981
The absence of introns within a human fibroblast interferon gene
M Houghton, I J Jackson, A G Porter, et al.
Human Molecular Genetics
|
October 1, 1996
The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma
P Valverde, E Healy, S Sikkink, et al.
Human Molecular Genetics
|
October 13, 2000
Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation
N Flanagan, E Healy, A Ray, et al.
Lancet (London, England)
|
April 1, 2000
Melanocortin-1-receptor gene and sun sensitivity in individuals without red hair
E Healy, N Flannagan, A Ray, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1990
Genetic and molecular analysis of chlorambucil-induced germ-line mutations in the mouse
E M Rinchik, J W Bangham, P R Hunsicker, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 22, 1999
Melanocortin 1 receptor variation in the domestic dog
J M Newton, A L Wilkie, L He, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 22, 1999
A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23
E H Simpson, R Suffolk, J A Bell, et al.
Page
of 10