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Peter L Oliver

Showing results (51-60 of 82) with videos related to

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Iscience|October 11, 2021
Zfhx3-mediated genetic ablation of the SCN abolishes light entrainable circadian activity while sparing food anticipatory activityAshleigh G Wilcox, R Sonia Bains, Debbie Williams, et al.
Plos Genetics|December 10, 2009
Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxaPeter L Oliver, Leo Goodstadt, Joshua J Bayes, et al.
Antioxidants (Basel, Switzerland)|June 27, 2024
Neuroinflammation and Lysosomal Abnormalities Characterise the Essential Role for Oxidation Resistance 1 in the Developing and Adult CerebellumEboni M V Bucknor, Errin Johnson, Stephanie Efthymiou, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2009
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker miceEsther B E Becker, Peter L Oliver, Maike D Glitsch, et al.
Neuron|August 27, 2011
A transcriptomic atlas of mouse neocortical layersT Grant Belgard, Ana C Marques, Peter L Oliver, et al.
Neurobiology of Disease|October 6, 2018
Single-copy expression of an amyotrophic lateral sclerosis-linked TDP-43 mutation (M337V) in BAC transgenic mice leads to altered stress granule dynamics and progressive motor dysfunctionDavid Gordon, Ruxandra Dafinca, Jakub Scaber, et al.
Biological Psychiatry|December 18, 2007
Human-mouse quantitative trait locus concordance and the dissection of a human neuroticism locusJanice M Fullerton, Saffron A G Willis-Owen, Binnaz Yalcin, et al.
Brain : a Journal of Neurology|January 12, 2026
Enhanced mGluR1 function causes motor deficits and region-specific Purkinje cell dysfunctionMohamed F Ibrahim, Sevda Boyanova, Yin Chun Cheng, et al.
Behavioural Brain Research|October 16, 2015
Circadian profiling in two mouse models of lysosomal storage disorders; Niemann Pick type-C and Sandhoff diseaseKatie Richardson, Achilleas Livieratos, Richard Dumbill, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2007
A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouseAlexander F Jeans, Peter L Oliver, Reuben Johnson, et al.
Pageof 9

Showing results (51-60 of 82) with videos related to

Sort By:
Pageof 9
Iscience|October 11, 2021
Zfhx3-mediated genetic ablation of the SCN abolishes light entrainable circadian activity while sparing food anticipatory activityAshleigh G Wilcox, R Sonia Bains, Debbie Williams, et al.
Plos Genetics|December 10, 2009
Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxaPeter L Oliver, Leo Goodstadt, Joshua J Bayes, et al.
Antioxidants (Basel, Switzerland)|June 27, 2024
Neuroinflammation and Lysosomal Abnormalities Characterise the Essential Role for Oxidation Resistance 1 in the Developing and Adult CerebellumEboni M V Bucknor, Errin Johnson, Stephanie Efthymiou, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2009
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker miceEsther B E Becker, Peter L Oliver, Maike D Glitsch, et al.
Neuron|August 27, 2011
A transcriptomic atlas of mouse neocortical layersT Grant Belgard, Ana C Marques, Peter L Oliver, et al.
Neurobiology of Disease|October 6, 2018
Single-copy expression of an amyotrophic lateral sclerosis-linked TDP-43 mutation (M337V) in BAC transgenic mice leads to altered stress granule dynamics and progressive motor dysfunctionDavid Gordon, Ruxandra Dafinca, Jakub Scaber, et al.
Biological Psychiatry|December 18, 2007
Human-mouse quantitative trait locus concordance and the dissection of a human neuroticism locusJanice M Fullerton, Saffron A G Willis-Owen, Binnaz Yalcin, et al.
Brain : a Journal of Neurology|January 12, 2026
Enhanced mGluR1 function causes motor deficits and region-specific Purkinje cell dysfunctionMohamed F Ibrahim, Sevda Boyanova, Yin Chun Cheng, et al.
Behavioural Brain Research|October 16, 2015
Circadian profiling in two mouse models of lysosomal storage disorders; Niemann Pick type-C and Sandhoff diseaseKatie Richardson, Achilleas Livieratos, Richard Dumbill, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2007
A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouseAlexander F Jeans, Peter L Oliver, Reuben Johnson, et al.
Pageof 9