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I Dragatsis

Showing results (11-20 of 15) with videos related to

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Genes, Brain, and Behavior|February 6, 2010
α8-integrins are required for hippocampal long-term potentiation but not for hippocampal-dependent learningC-S Chan, H Chen, A Bradley, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 22, 2001
Neurons lacking huntingtin differentially colonize brain and survive in chimeric miceA Reiner, N Del Mar, C A Meade, et al.
Human Molecular Genetics|February 3, 2000
Huntingtin is required for normal hematopoiesisM Metzler, C D Helgason, I Dragatsis, et al.
Neurobiology of Disease|December 25, 2017
Effect of early embryonic deletion of huntingtin from pyramidal neurons on the development and long-term survival of neurons in cerebral cortex and striatumI Dragatsis, P Dietrich, H Ren, et al.
Neurobiology of Disease|November 26, 2008
CAG repeat lengths > or =335 attenuate the phenotype in the R6/2 Huntington's disease transgenic mouseI Dragatsis, D Goldowitz, N Del Mar, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Genes, Brain, and Behavior|February 6, 2010
α8-integrins are required for hippocampal long-term potentiation but not for hippocampal-dependent learningC-S Chan, H Chen, A Bradley, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 22, 2001
Neurons lacking huntingtin differentially colonize brain and survive in chimeric miceA Reiner, N Del Mar, C A Meade, et al.
Human Molecular Genetics|February 3, 2000
Huntingtin is required for normal hematopoiesisM Metzler, C D Helgason, I Dragatsis, et al.
Neurobiology of Disease|December 25, 2017
Effect of early embryonic deletion of huntingtin from pyramidal neurons on the development and long-term survival of neurons in cerebral cortex and striatumI Dragatsis, P Dietrich, H Ren, et al.
Neurobiology of Disease|November 26, 2008
CAG repeat lengths > or =335 attenuate the phenotype in the R6/2 Huntington's disease transgenic mouseI Dragatsis, D Goldowitz, N Del Mar, et al.
Pageof 2