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Methods in Molecular Biology (Clifton, N.J.)
|
June 9, 2009
Dedicated mouse production and husbandry
Lucie 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 Clock
Ashleigh 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 development
Tom 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 neuropathy
Adrian 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 browning
Milan 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 activity
Ashleigh 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 Akp2
Tertius 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 mutants
Michael 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 mouse
Adrian 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 mouse
Vicky Tsipouri, John A Curtin, Pat M Nolan, et al.
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Showing results (1-10 of 13) with videos related to
Sort By:
Page
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Methods in Molecular Biology (Clifton, N.J.)
|
June 9, 2009
Dedicated mouse production and husbandry
Lucie 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 Clock
Ashleigh 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 development
Tom 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 neuropathy
Adrian 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 browning
Milan 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 activity
Ashleigh 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 Akp2
Tertius 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 mutants
Michael 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 mouse
Adrian 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 mouse
Vicky Tsipouri, John A Curtin, Pat M Nolan, et al.
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of 2