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Lucie Vizor

Showing results (1-10 of 13) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|June 9, 2009
Dedicated mouse production and husbandryLucie Vizor, Sara Wells
Journal of Biological Rhythms|August 18, 2017
Inducible Knockout of Mouse Zfhx3 Emphasizes Its Key Role in Setting the Pace and Amplitude of the Adult Circadian ClockAshleigh G Wilcox, Lucie Vizor, Michael J Parsons, et al.
Journal of Cell Science|September 4, 2008
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal developmentTom R Webb, Sally H Cross, Lisa McKie, et al.
Molecular and Cellular Neurosciences|October 3, 2002
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathyAdrian M Isaacs, Alexander Jeans, Peter L Oliver, et al.
Frontiers in Physiology|September 12, 2022
A <i>Wars2</i> mutant mouse shows a sex and diet specific change in fat distribution, reduced food intake and depot-specific upregulation of WAT browningMilan Mušo, Liz Bentley, Lucie Vizor, et al.
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.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 2, 2007
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2Tertius A Hough, Monika Polewski, Kristen Johnson, et al.
Plos Genetics|October 27, 2011
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutantsMichael T Cheeseman, Hayley E Tyrer, Debbie Williams, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
Comparative and Functional Genomics|July 17, 2008
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouseVicky Tsipouri, John A Curtin, Pat M Nolan, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|June 9, 2009
Dedicated mouse production and husbandryLucie Vizor, Sara Wells
Journal of Biological Rhythms|August 18, 2017
Inducible Knockout of Mouse Zfhx3 Emphasizes Its Key Role in Setting the Pace and Amplitude of the Adult Circadian ClockAshleigh G Wilcox, Lucie Vizor, Michael J Parsons, et al.
Journal of Cell Science|September 4, 2008
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal developmentTom R Webb, Sally H Cross, Lisa McKie, et al.
Molecular and Cellular Neurosciences|October 3, 2002
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathyAdrian M Isaacs, Alexander Jeans, Peter L Oliver, et al.
Frontiers in Physiology|September 12, 2022
A <i>Wars2</i> mutant mouse shows a sex and diet specific change in fat distribution, reduced food intake and depot-specific upregulation of WAT browningMilan Mušo, Liz Bentley, Lucie Vizor, et al.
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.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 2, 2007
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2Tertius A Hough, Monika Polewski, Kristen Johnson, et al.
Plos Genetics|October 27, 2011
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutantsMichael T Cheeseman, Hayley E Tyrer, Debbie Williams, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
Comparative and Functional Genomics|July 17, 2008
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouseVicky Tsipouri, John A Curtin, Pat M Nolan, et al.
Pageof 2