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Archives of Neurology
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October 1, 1973
Fetal globoid cell leukocystrophy (Krabbe disease). Pathological and biochemical examination
W G Ellis, E L Schneider, J R McCulloch, et al.
Stroke
|
November 1, 1990
Reduced neurotoxicity in transgenic mice overexpressing human copper-zinc-superoxide dismutase
P H Chan, L Chu, S F Chen, et al.
Science (New York, N.Y.)
|
October 4, 1974
Human chromosome 21 dosage: effect on the expression of the interferon induced antiviral state
Y H Tan, E L Schneider, J Tischfield, et al.
Annals of Neurology
|
April 1, 1997
Midbrain dopaminergic neuronal degeneration in a transgenic mouse model of familial amyotrophic lateral sclerosis
V Kostic, M E Gurney, H X Deng, et al.
Brain Research Bulletin
|
June 1, 1991
Quantitative autoradiographic distribution of [3H]-MPTP binding in the brains of superoxide dismutase transgenic mice
S Przedborski, V Kostic, V Jackson-Lewis, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
May 1, 1994
Prolonged expression of hsp70 mRNA following transient focal cerebral ischemia in transgenic mice overexpressing CuZn-superoxide dismutase
H Kamii, H Kinouchi, F R Sharp, et al.
Annals of Neurology
|
September 28, 1998
Overexpression of copper/zinc superoxide dismutase: a novel cause of murine muscular dystrophy
T A Rando, R S Crowley, E J Carlson, et al.
Genesis (New York, N.Y. : 2000)
|
September 6, 2001
Cardiomyopathy in mice with paternal uniparental disomy for chromosome 12
A J Villar, E J Carlson, A M Gillespie, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1990
Down syndrome: toward a molecular definition of the phenotype
J R Korenberg, H Kawashima, S M Pulst, et al.
American Journal of Human Genetics
|
September 1, 1977
The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?
E F Neufeld, I Liebaers, C J Epstein, et al.
Page
of 30
Search research articles
Search
Showing results (181-190 of 299) with videos related to
Sort By:
Page
of 30
Archives of Neurology
|
October 1, 1973
Fetal globoid cell leukocystrophy (Krabbe disease). Pathological and biochemical examination
W G Ellis, E L Schneider, J R McCulloch, et al.
Stroke
|
November 1, 1990
Reduced neurotoxicity in transgenic mice overexpressing human copper-zinc-superoxide dismutase
P H Chan, L Chu, S F Chen, et al.
Science (New York, N.Y.)
|
October 4, 1974
Human chromosome 21 dosage: effect on the expression of the interferon induced antiviral state
Y H Tan, E L Schneider, J Tischfield, et al.
Annals of Neurology
|
April 1, 1997
Midbrain dopaminergic neuronal degeneration in a transgenic mouse model of familial amyotrophic lateral sclerosis
V Kostic, M E Gurney, H X Deng, et al.
Brain Research Bulletin
|
June 1, 1991
Quantitative autoradiographic distribution of [3H]-MPTP binding in the brains of superoxide dismutase transgenic mice
S Przedborski, V Kostic, V Jackson-Lewis, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
May 1, 1994
Prolonged expression of hsp70 mRNA following transient focal cerebral ischemia in transgenic mice overexpressing CuZn-superoxide dismutase
H Kamii, H Kinouchi, F R Sharp, et al.
Annals of Neurology
|
September 28, 1998
Overexpression of copper/zinc superoxide dismutase: a novel cause of murine muscular dystrophy
T A Rando, R S Crowley, E J Carlson, et al.
Genesis (New York, N.Y. : 2000)
|
September 6, 2001
Cardiomyopathy in mice with paternal uniparental disomy for chromosome 12
A J Villar, E J Carlson, A M Gillespie, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1990
Down syndrome: toward a molecular definition of the phenotype
J R Korenberg, H Kawashima, S M Pulst, et al.
American Journal of Human Genetics
|
September 1, 1977
The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?
E F Neufeld, I Liebaers, C J Epstein, et al.
Page
of 30