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Biochemical Genetics
|
December 1, 1982
Pleiotropic and other genetic effects influencing the activities of brain and liver enzymes in congenic lines of C57BL/6J mice with defined electrophoretic variant markers
R J Feuers, J B Bishop, L J McGarrity, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
September 25, 2001
Maximum life spans in mice are extended by wild strain alleles
S Klebanov, C M Astle, T H Roderick, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
August 1, 1987
Mapping X-linked ophthalmic diseases. III. Provisional assignment of the locus for blue cone monochromacy to Xq28
R A Lewis, J D Holcomb, W C Bromley, et al.
Biochemical Genetics
|
August 1, 1976
Evolution of mammalian carbonic anhydrase loci by tanden duplication: close linkage of Car-1 and Car-2 to the centromere region of chromosome 3 of the mouse
E M Eicher, R H Stern, J E Womack, et al.
Genetica
|
January 5, 2002
Heritability of life span in mice and its implication for direct and indirect selection for longevity
S Klebanov, K Flurkey, T H Roderick, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1991
Comparative map for mice and humans
J H Nadeau, M T Davisson, D P Doolittle, et al.
Molecular Vision
|
September 24, 1999
Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse
B Chang, N L Hawes, T H Roderick, et al.
Investigative Ophthalmology & Visual Science
|
March 1, 1994
Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis
B Chang, R T Bronson, N L Hawes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 1995
Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15
J R Heckenlively, B Chang, L C Erway, et al.
Investigative Ophthalmology & Visual Science
|
February 1, 1996
Corn1: a mouse model for corneal surface disease and neovascularization
R S Smith, N L Hawes, S D Kuhlmann, et al.
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of 9
Search research articles
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Showing results (51-60 of 82) with videos related to
Sort By:
Page
of 9
Biochemical Genetics
|
December 1, 1982
Pleiotropic and other genetic effects influencing the activities of brain and liver enzymes in congenic lines of C57BL/6J mice with defined electrophoretic variant markers
R J Feuers, J B Bishop, L J McGarrity, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
September 25, 2001
Maximum life spans in mice are extended by wild strain alleles
S Klebanov, C M Astle, T H Roderick, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
August 1, 1987
Mapping X-linked ophthalmic diseases. III. Provisional assignment of the locus for blue cone monochromacy to Xq28
R A Lewis, J D Holcomb, W C Bromley, et al.
Biochemical Genetics
|
August 1, 1976
Evolution of mammalian carbonic anhydrase loci by tanden duplication: close linkage of Car-1 and Car-2 to the centromere region of chromosome 3 of the mouse
E M Eicher, R H Stern, J E Womack, et al.
Genetica
|
January 5, 2002
Heritability of life span in mice and its implication for direct and indirect selection for longevity
S Klebanov, K Flurkey, T H Roderick, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1991
Comparative map for mice and humans
J H Nadeau, M T Davisson, D P Doolittle, et al.
Molecular Vision
|
September 24, 1999
Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse
B Chang, N L Hawes, T H Roderick, et al.
Investigative Ophthalmology & Visual Science
|
March 1, 1994
Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis
B Chang, R T Bronson, N L Hawes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 1995
Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15
J R Heckenlively, B Chang, L C Erway, et al.
Investigative Ophthalmology & Visual Science
|
February 1, 1996
Corn1: a mouse model for corneal surface disease and neovascularization
R S Smith, N L Hawes, S D Kuhlmann, et al.
Page
of 9