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M T Davisson

Showing results (111-120 of 139) with videos related to

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Progress in Clinical and Biological Research|January 1, 1993
Segmental trisomy as a mouse model for Down syndromeM T Davisson, C Schmidt, R H Reeves, et al.
American Journal of Human Genetics|September 28, 2001
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4J M Newton, O Cohen-Barak, N Hagiwara, et al.
Cytogenetics and Cell Genetics|January 1, 1979
Report of the committee on comparative mappingP L Pearson, T H Roderick, M T Davisson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1995
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophyD S Rice, R W Williams, P Ward-Bailey, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Comparative map for mice and humansJ H Nadeau, M T Davisson, D P Doolittle, et al.
Birth Defects Original Article Series|January 1, 1980
Report of the committee on comparative mappingP L Pearson, T H Roderick, M T Davisson, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Report of the committee on comparative mappingP A Lalley, M T Davisson, J A Graves, et al.
The Journal of Biological Chemistry|May 15, 1989
The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activitiesC A Langner, E H Birkenmeier, O Ben-Zeev, et al.
Genomics|July 20, 1995
RNA expression and chromosomal location of the mouse long-chain acyl-CoA dehydrogenase geneM E Hinsdale, S C Farmer, K R Johnson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 29, 2000
Grey intense: a new mouse mutation affecting pigmentationM T Davisson, K R Johnson, R T Bronson, et al.
Pageof 14

Showing results (111-120 of 139) with videos related to

Sort By:
Pageof 14
Progress in Clinical and Biological Research|January 1, 1993
Segmental trisomy as a mouse model for Down syndromeM T Davisson, C Schmidt, R H Reeves, et al.
American Journal of Human Genetics|September 28, 2001
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4J M Newton, O Cohen-Barak, N Hagiwara, et al.
Cytogenetics and Cell Genetics|January 1, 1979
Report of the committee on comparative mappingP L Pearson, T H Roderick, M T Davisson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1995
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophyD S Rice, R W Williams, P Ward-Bailey, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Comparative map for mice and humansJ H Nadeau, M T Davisson, D P Doolittle, et al.
Birth Defects Original Article Series|January 1, 1980
Report of the committee on comparative mappingP L Pearson, T H Roderick, M T Davisson, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Report of the committee on comparative mappingP A Lalley, M T Davisson, J A Graves, et al.
The Journal of Biological Chemistry|May 15, 1989
The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activitiesC A Langner, E H Birkenmeier, O Ben-Zeev, et al.
Genomics|July 20, 1995
RNA expression and chromosomal location of the mouse long-chain acyl-CoA dehydrogenase geneM E Hinsdale, S C Farmer, K R Johnson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 29, 2000
Grey intense: a new mouse mutation affecting pigmentationM T Davisson, K R Johnson, R T Bronson, et al.
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