1-10 of 10
Elizabeth M. C. Fisher
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles

Taf1 knockout is lethal in embryonic male mice and heterozygous females show weight and movement disorders

In collection:
Tools and Resources for Mouse Studies
Elisa M. Crombie, Andrea J. Korecki, Karen Cleverley, Bethany A. Adair, Thomas J. Cunningham, Weaverly Colleen Lee, Tess C. Lengyell, Cheryl Maduro, Victor Mo, Liam M. Slade, Ines Zouhair, Elizabeth M. C. Fisher, Elizabeth M. Simpson
Journal: Disease Models & Mechanisms
Dis Model Mech (2024) 17 (7): dmm050741.
https://doi.org/10.1242/dmm.050741
Published: 10 July 2024
View article titled, Taf1 knockout is lethal in embryonic male mice and heterozygous females show weight and movement disorders
Open the PDF for Taf1 knockout is lethal in embryonic male mice and heterozygous females show weight and movement disorders in another window
Includes: Supplementary data
Journal Articles

Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations

In collection:
Neurodegenerative Disorders
Zeinab Ali, Juan M. Godoy-Corchuelo, Aurea B. Martins-Bach, Irene Garcia-Toledo, Luis C. Fernández-Beltrán, Remya R. Nair, Shoshana Spring, Brian J. Nieman, Irene Jimenez-Coca, Rasneer S. Bains, Hamish Forrest, Jason P. Lerch, Karla L. Miller, Elizabeth M. C. Fisher, Thomas J. Cunningham, Silvia Corrochano
Journal: Disease Models & Mechanisms
Dis Model Mech (2023) 16 (10): dmm050200.
https://doi.org/10.1242/dmm.050200
Published: 23 October 2023
View article titled, Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations
Open the PDF for Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations in another window
Includes: Supplementary data
Journal Articles

Genetic dissection of triplicated chromosome 21 orthologs yields varying skeletal traits in Down syndrome model mice

In collection:
Developmental Disorders
Kourtney Sloan, Jared Thomas, Matthew Blackwell, Deanna Voisard, Eva Lana-Elola, Sheona Watson-Scales, Daniel L. Roper, Joseph M. Wallace, Elizabeth M. C. Fisher, Victor L. J. Tybulewicz, Randall J. Roper
Journal: Disease Models & Mechanisms
Dis Model Mech (2023) 16 (4): dmm049927.
https://doi.org/10.1242/dmm.049927
Published: 26 April 2023
View article titled, Genetic dissection of triplicated chromosome 21 orthologs yields varying skeletal traits in Down syndrome model mice
Open the PDF for Genetic dissection of triplicated chromosome 21 orthologs yields varying skeletal traits in Down syndrome model mice in another window
Includes: Supplementary data
Journal Articles

Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes

In collection:
Developmental Disorders , Human Genetic Disease
Eva Lana-Elola, Heather Cater, Sheona Watson-Scales, Simon Greenaway, Jennifer Müller-Winkler, Dorota Gibbins, Mihaela Nemes, Amy Slender, Tertius Hough, Piia Keskivali-Bond, Cheryl L. Scudamore, Eleanor Herbert, Gareth T. Banks, Helene Mobbs, Tara Canonica, Justin Tosh, Suzanna Noy, Miriam Llorian, Patrick M. Nolan, Julian L. Griffin, Mark Good, Michelle Simon, Ann-Marie Mallon, Sara Wells, Elizabeth M. C. Fisher, Victor L. J. Tybulewicz
Journal: Disease Models & Mechanisms
Dis Model Mech (2021) 14 (10): dmm049157.
https://doi.org/10.1242/dmm.049157
Published: 18 October 2021
View article titled, Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes
Open the PDF for Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes in another window
Includes: Supplementary data
Journal Articles

Transgenic and physiological mouse models give insights into different aspects of amyotrophic lateral sclerosis

Francesca De Giorgio, Cheryl Maduro, Elizabeth M. C. Fisher, Abraham Acevedo-Arozena
Journal: Disease Models & Mechanisms
Dis Model Mech (2019) 12 (1): dmm037424.
https://doi.org/10.1242/dmm.037424
Published: 2 January 2019
View article titled, Transgenic and physiological mouse models give insights into different aspects of amyotrophic lateral sclerosis
Open the PDF for Transgenic and physiological mouse models give insights into different aspects of amyotrophic lateral sclerosis in another window
Journal Articles

Rodent models in Down syndrome research: impact and future opportunities

Yann Herault, Jean M. Delabar, Elizabeth M. C. Fisher, Victor L. J. Tybulewicz, Eugene Yu, Veronique Brault
Journal: Disease Models & Mechanisms
Dis Model Mech (2017) 10 (10): 1165–1186.
https://doi.org/10.1242/dmm.029728
Published: 1 October 2017
View article titled, Rodent models in Down syndrome research: impact and future opportunities
Open the PDF for Rodent models in Down syndrome research: impact and future opportunities in another window
Journal Articles

Down syndrome: searching for the genetic culprits

Eva Lana-Elola, Sheona D. Watson-Scales, Elizabeth M. C. Fisher, Victor L. J. Tybulewicz
Journal: Disease Models & Mechanisms
Dis Model Mech (2011) 4 (5): 586–595.
https://doi.org/10.1242/dmm.008078
Published: 1 September 2011
View article titled, Down syndrome: searching for the genetic culprits
Open the PDF for Down syndrome: searching for the genetic culprits in another window
Journal Articles

A comprehensive assessment of the SOD1 G93A low-copy transgenic mouse, which models human amyotrophic lateral sclerosis

Abraham Acevedo-Arozena, Bernadett Kalmar, Shafa Essa, Thomas Ricketts, Peter Joyce, Rosie Kent, Claire Rowe, Andy Parker, Anna Gray, Majid Hafezparast, Julian R. Thorpe, Linda Greensmith, Elizabeth M. C. Fisher
Journal: Disease Models & Mechanisms
Dis Model Mech (2011) 4 (5): 686–700.
https://doi.org/10.1242/dmm.007237
Published: 1 September 2011
View article titled, A comprehensive assessment of the SOD1 G93A low-copy transgenic mouse, which models human amyotrophic lateral sclerosis
Open the PDF for A comprehensive assessment of the SOD1 G93A low-copy transgenic mouse, which models human amyotrophic lateral sclerosis in another window
Includes: Supplementary data
Journal Articles

New approaches for modelling sporadic genetic disease in the mouse

Elizabeth M. C. Fisher, Eva Lana-Elola, Sheona D. Watson, George Vassiliou, Victor L. J. Tybulewicz
Journal: Disease Models & Mechanisms
Dis Model Mech (2009) 2 (9-10): 446–453.
https://doi.org/10.1242/dmm.001644
Published: 2 September 2009
View article titled, New approaches for modelling sporadic genetic disease in the mouse
Open the PDF for New approaches for modelling sporadic genetic disease in the mouse in another window
Journal Articles

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy

Francesca Achilli, Virginie Bros-Facer, Hazel P. Williams, Gareth T. Banks, Mona AlQatari, Ruth Chia, Valter Tucci, Michael Groves, Carole D. Nickols, Kevin L. Seburn, Rachel Kendall, Muhammed Z. Cader, Kevin Talbot, Jan van Minnen, Robert W. Burgess, Sebastian Brandner, Joanne E. Martin, Martin Koltzenburg, Linda Greensmith, Patrick M. Nolan, Elizabeth M. C. Fisher
Journal: Disease Models & Mechanisms
Dis Model Mech (2009) 2 (7-8): 359–373.
https://doi.org/10.1242/dmm.002527
Published: 24 June 2009
View article titled, An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy
Open the PDF for An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy in another window
Includes: Multimedia, Supplementary data