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Investigative Ophthalmology & Visual Science
|
October 1, 1992
Autosomal dominant mouse cataract (Lop-10). Consistent differences of expression in heterozygotes
P E Runge, N L Hawes, J R Heckenlively, et al.
Pharmacology, Biochemistry, and Behavior
|
July 1, 1987
Different genes specify hyporesponsiveness to seizures induced by caffeine and the benzodiazepine inverse agonist, DMCM
T W Seale, K A Abla, T H Roderick, et al.
Genetical Research
|
October 1, 1990
The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15
M T Davisson, T H Roderick, E C Akeson, et al.
American Journal of Ophthalmology
|
March 1, 1984
Prevalence of retinitis pigmentosa in Maine
C H Bunker, E L Berson, W C Bromley, et al.
Birth Defects Original Article Series
|
January 1, 1982
Report of the committee on comparative mapping
P L Pearson, T H Roderick, M T Davisson, et al.
Science (New York, N.Y.)
|
December 20, 1985
Rapid mutations in mice?
M C Green, D W Bailey, E L Green, et al.
Biology of Reproduction
|
May 1, 1988
Juvenile spermatogonial depletion (jsd): a genetic defect of germ cell proliferation of male mice
W G Beamer, T L Cunliffe-Beamer, K L Shultz, et al.
Pharmacology, Biochemistry, and Behavior
|
May 1, 1986
Complex genetic determinants of susceptibility to methylxanthine-induced locomotor activity changes
T W Seale, T H Roderick, P Johnson, et al.
Biochemical Genetics
|
February 1, 1989
Organic aciduria and butyryl CoA dehydrogenase deficiency in BALB/cByJ mice
S P Schiffer, M Prochazka, P F Jezyk, et al.
Genomics
|
August 15, 1996
Chromosomal localization of a new mouse lens opacity gene (lop18)
B Chang, N L Hawes, R S Smith, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 82) with videos related to
Sort By:
Page
of 9
Investigative Ophthalmology & Visual Science
|
October 1, 1992
Autosomal dominant mouse cataract (Lop-10). Consistent differences of expression in heterozygotes
P E Runge, N L Hawes, J R Heckenlively, et al.
Pharmacology, Biochemistry, and Behavior
|
July 1, 1987
Different genes specify hyporesponsiveness to seizures induced by caffeine and the benzodiazepine inverse agonist, DMCM
T W Seale, K A Abla, T H Roderick, et al.
Genetical Research
|
October 1, 1990
The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15
M T Davisson, T H Roderick, E C Akeson, et al.
American Journal of Ophthalmology
|
March 1, 1984
Prevalence of retinitis pigmentosa in Maine
C H Bunker, E L Berson, W C Bromley, et al.
Birth Defects Original Article Series
|
January 1, 1982
Report of the committee on comparative mapping
P L Pearson, T H Roderick, M T Davisson, et al.
Science (New York, N.Y.)
|
December 20, 1985
Rapid mutations in mice?
M C Green, D W Bailey, E L Green, et al.
Biology of Reproduction
|
May 1, 1988
Juvenile spermatogonial depletion (jsd): a genetic defect of germ cell proliferation of male mice
W G Beamer, T L Cunliffe-Beamer, K L Shultz, et al.
Pharmacology, Biochemistry, and Behavior
|
May 1, 1986
Complex genetic determinants of susceptibility to methylxanthine-induced locomotor activity changes
T W Seale, T H Roderick, P Johnson, et al.
Biochemical Genetics
|
February 1, 1989
Organic aciduria and butyryl CoA dehydrogenase deficiency in BALB/cByJ mice
S P Schiffer, M Prochazka, P F Jezyk, et al.
Genomics
|
August 15, 1996
Chromosomal localization of a new mouse lens opacity gene (lop18)
B Chang, N L Hawes, R S Smith, et al.
Page
of 9