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The Journal of Biological Chemistry
|
October 5, 2010
Neurodegenerative mutation in cytoplasmic dynein alters its organization and dynein-dynactin and dynein-kinesin interactions
Wenhan Deng, Caroline Garrett, Benjamin Dombert, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
September 15, 2023
A missense mutation in zinc finger homeobox-3 (ZFHX3) impedes growth and alters metabolism and hypothalamic gene expression in mice
Patrick M Nolan, Gareth Banks, Nora Bourbia, et al.
Neurobiology of Aging
|
September 3, 2014
Genetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep
Gareth Banks, Ines Heise, Becky Starbuck, 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.
Disease Models & Mechanisms
|
August 26, 2025
Multi-modal comparative phenotyping of knock-in mouse models of frontotemporal dementia/amyotrophic lateral sclerosis
Sevda Boyanova, Gareth Banks, Tatiana V Lipina, et al.
Mechanisms of Ageing and Development
|
October 6, 2018
Modelling physical resilience in ageing mice
Markus Schosserer, Gareth Banks, Soner Dogan, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 12, 2021
Zfhx3 modulates retinal sensitivity and circadian responses to light
Steven Hughes, Jessica K Edwards, Ashleigh G Wilcox, et al.
The Journal of Biological Chemistry
|
April 13, 2010
The legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease
Ali Morsi El-Kadi, Virginie Bros-Facer, Wenhan Deng, et al.
Disease Models & Mechanisms
|
January 30, 2019
Loss of <i>Frrs1l</i> disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities
Michelle Stewart, Petrina Lau, Gareth Banks, et al.
International Journal of Molecular Sciences
|
January 21, 2022
Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-Oxidation
Youssef Khalil, Sara Carrino, Fujun Lin, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
The Journal of Biological Chemistry
|
October 5, 2010
Neurodegenerative mutation in cytoplasmic dynein alters its organization and dynein-dynactin and dynein-kinesin interactions
Wenhan Deng, Caroline Garrett, Benjamin Dombert, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
September 15, 2023
A missense mutation in zinc finger homeobox-3 (ZFHX3) impedes growth and alters metabolism and hypothalamic gene expression in mice
Patrick M Nolan, Gareth Banks, Nora Bourbia, et al.
Neurobiology of Aging
|
September 3, 2014
Genetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep
Gareth Banks, Ines Heise, Becky Starbuck, 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.
Disease Models & Mechanisms
|
August 26, 2025
Multi-modal comparative phenotyping of knock-in mouse models of frontotemporal dementia/amyotrophic lateral sclerosis
Sevda Boyanova, Gareth Banks, Tatiana V Lipina, et al.
Mechanisms of Ageing and Development
|
October 6, 2018
Modelling physical resilience in ageing mice
Markus Schosserer, Gareth Banks, Soner Dogan, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 12, 2021
Zfhx3 modulates retinal sensitivity and circadian responses to light
Steven Hughes, Jessica K Edwards, Ashleigh G Wilcox, et al.
The Journal of Biological Chemistry
|
April 13, 2010
The legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease
Ali Morsi El-Kadi, Virginie Bros-Facer, Wenhan Deng, et al.
Disease Models & Mechanisms
|
January 30, 2019
Loss of <i>Frrs1l</i> disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities
Michelle Stewart, Petrina Lau, Gareth Banks, et al.
International Journal of Molecular Sciences
|
January 21, 2022
Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-Oxidation
Youssef Khalil, Sara Carrino, Fujun Lin, et al.
Page
of 3