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The Journal of Biological Chemistry
|
January 17, 2002
Urea-selective concentrating defect in transgenic mice lacking urea transporter UT-B
Baoxue Yang, Lise Bankir, Annemarie Gillespie, et al.
Free Radical Biology & Medicine
|
March 2, 2010
Enhanced expression of mitochondrial superoxide dismutase leads to prolonged in vivo cell cycle progression and up-regulation of mitochondrial thioredoxin
Aekyong Kim, Suman Joseph, Aslam Khan, et al.
The Journal of Comparative Neurology
|
August 1, 2007
Synaptic and cognitive abnormalities in mouse models of Down syndrome: exploring genotype-phenotype relationships
Pavel V Belichenko, Alexander M Kleschevnikov, Ahmad Salehi, et al.
American Journal of Medical Genetics
|
February 13, 2002
Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome
Joan T Richtsmeier, Ann Zumwalt, Elaine J Carlson, et al.
Aging Cell
|
December 17, 2008
The overexpression of major antioxidant enzymes does not extend the lifespan of mice
Viviana I Pérez, Holly Van Remmen, Alex Bokov, et al.
Digestive Diseases and Sciences
|
March 26, 2002
Reactive oxygen species and vascular cell adhesion molecule-1 in distant organ failure following bile duct obstruction in mice
Zenichi Morise, Masakazu Ueda, Masaki Kitajima, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
August 28, 2009
Enlarged brain ventricles and impaired neurogenesis in the Ts1Cje and Ts2Cje mouse models of Down syndrome
Keiichi Ishihara, Kenji Amano, Eiichi Takaki, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 17, 2004
Hippocampal long-term potentiation suppressed by increased inhibition in the Ts65Dn mouse, a genetic model of Down syndrome
Alexander M Kleschevnikov, Pavel V Belichenko, Angela J Villar, et al.
Human Molecular Genetics
|
May 13, 2004
Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome
Kenji Amano, Haruhiko Sago, Chiharu Uchikawa, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 30, 2005
Identification and characterization of a new Down syndrome model, Ts[Rb(12.1716)]2Cje, resulting from a spontaneous Robertsonian fusion between T(171)65Dn and mouse chromosome 12
Angela J Villar, Pavel V Belichenko, Anne Marie Gillespie, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 49) with videos related to
Sort By:
Page
of 5
The Journal of Biological Chemistry
|
January 17, 2002
Urea-selective concentrating defect in transgenic mice lacking urea transporter UT-B
Baoxue Yang, Lise Bankir, Annemarie Gillespie, et al.
Free Radical Biology & Medicine
|
March 2, 2010
Enhanced expression of mitochondrial superoxide dismutase leads to prolonged in vivo cell cycle progression and up-regulation of mitochondrial thioredoxin
Aekyong Kim, Suman Joseph, Aslam Khan, et al.
The Journal of Comparative Neurology
|
August 1, 2007
Synaptic and cognitive abnormalities in mouse models of Down syndrome: exploring genotype-phenotype relationships
Pavel V Belichenko, Alexander M Kleschevnikov, Ahmad Salehi, et al.
American Journal of Medical Genetics
|
February 13, 2002
Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome
Joan T Richtsmeier, Ann Zumwalt, Elaine J Carlson, et al.
Aging Cell
|
December 17, 2008
The overexpression of major antioxidant enzymes does not extend the lifespan of mice
Viviana I Pérez, Holly Van Remmen, Alex Bokov, et al.
Digestive Diseases and Sciences
|
March 26, 2002
Reactive oxygen species and vascular cell adhesion molecule-1 in distant organ failure following bile duct obstruction in mice
Zenichi Morise, Masakazu Ueda, Masaki Kitajima, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
August 28, 2009
Enlarged brain ventricles and impaired neurogenesis in the Ts1Cje and Ts2Cje mouse models of Down syndrome
Keiichi Ishihara, Kenji Amano, Eiichi Takaki, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 17, 2004
Hippocampal long-term potentiation suppressed by increased inhibition in the Ts65Dn mouse, a genetic model of Down syndrome
Alexander M Kleschevnikov, Pavel V Belichenko, Angela J Villar, et al.
Human Molecular Genetics
|
May 13, 2004
Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome
Kenji Amano, Haruhiko Sago, Chiharu Uchikawa, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 30, 2005
Identification and characterization of a new Down syndrome model, Ts[Rb(12.1716)]2Cje, resulting from a spontaneous Robertsonian fusion between T(171)65Dn and mouse chromosome 12
Angela J Villar, Pavel V Belichenko, Anne Marie Gillespie, et al.
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