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Author Details

Michelle Stewart
Mary Lyon Centre at Medical Research Council
2007
45
18
PMIDPaper TitleJournal TitlePublished Year
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
37283649A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (<i>NFIX</i>) Gene Has Phenotypic Features of Marshall-Smith Syndrome.JBMR Plus2023
37035623Longitudinal home-cage automated assessment of climbing behavior shows sexual dimorphism and aging-related decrease in C57BL/6J healthy mice and allows early detection of motor impairment in the N171-82Q mouse model of Huntington's disease.Front Behav Neurosci2023
36280881Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice.Orphanet J Rare Dis2022
35416977An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation.Hum Mol Genet2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
33446734Maternal and offspring high-fat diet leads to platelet hyperactivation in male mice offspring.Sci Rep2021
33713180A novel knockout mouse for the small EDRK-rich factor 2 (Serf2) showing developmental and other deficits.Mamm Genome2021
33729479Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2.Hum Mol Genet2021
32542000The occurrence of tarsal injuries in male mice of C57BL/6N substrains in multiple international mouse facilities.PLoS One2020
33103030Calcilytic NPSP795 Increases Plasma Calcium and PTH in an Autosomal Dominant Hypocalcemia Type 1 Mouse Model.JBMR Plus2020
32213617<i>Mylk3</i> null C57BL/6N mice develop cardiomyopathy, whereas <i>Nnt</i> null C57BL/6J mice do not.Life Sci Alliance2020
30692144Loss of <i>Frrs1l</i> disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities.Dis Model Mech2019
31338999Abcc5 Knockout Mice Have Lower Fat Mass and Increased Levels of Circulating GLP-1.Obesity (Silver Spring)2019
31593567Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.PLoS Biol2019
31479441Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.PLoS Biol2019
30854487Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.Commun Biol2019
29203346FTO demethylase activity is essential for normal bone growth and bone mineralization in mice.Biochim Biophys Acta Mol Basis Dis2018
29925374Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants.BMC Biol2018
29764981Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis.EMBO J2018
29509900A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.Hum Mol Genet2018
27307423Does age matter? The impact of rodent age on study outcomes.Lab Anim2017
28363792Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control.Methods2017
28194447Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy.JCI Insight2017
29479578N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (<i>Ap2s1</i>) Mutations Establish <i>Ap2s1</i> Loss-of-Function Mice.JBMR Plus2017
29053787Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in 'FUSDelta14' knockin mice.Brain2017
29046478Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation.JCI Insight2017
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
28575322Mutant Mice With Calcium-Sensing Receptor Activation Have Hyperglycemia That Is Rectified by Calcilytic Therapy.Endocrinology2017
27236917Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy.Am J Hum Genet2016
26604141Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.Hum Mol Genet2016
25468678A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity.Hum Mol Genet2015
26432886Loss of arylformamidase with reduced thymidine kinase expression leads to impaired glucose tolerance.Biol Open2015
26214591Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.Nat Genet2015
25140802Reducing Igf-1r levels leads to paradoxical and sexually dimorphic effects in HD mice.PLoS One2014
25348630Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.Brain2014
25091723Functional analysis of a novel ENU-induced PHD finger 11 (Phf11) mouse mutant.Mamm Genome2014
22010050α-Synuclein levels modulate Huntington's disease in mice.Hum Mol Genet2012
22771245The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of Dishevelled.Dev Biol2012
22363567Brainstem respiratory oscillators develop independently of neuronal migration defects in the Wnt/PCP mouse mutant looptail.PLoS One2012
20457824Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cages.Lab Anim2010
18987059Analysis of breeding and pathology helps refine management practices of a large-scale N'-ethyl-N'-nitrosourea mouse mutagenesis programme.Lab Anim2009
19476720Urethral obstruction by seminal coagulum is associated with medetomidine-ketamine anesthesia in male mice on C57BL/6J and mixed genetic backgrounds.J Am Assoc Lab Anim Sci2009
19223390Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway.Hum Mol Genet2009
17487951A new coat color mouse line for testing germline transmission of embryonic stem cells while retaining an inbred genetic background.J Am Assoc Lab Anim Sci2007
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Collaborators

Sara Wells
Mary Lyon Centre at Medical Research Council
Co-authored papers 28
Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 13
Gemma F Codner
Medical Research Council Harwell Institute
Co-authored papers 8
Jacqueline K White
Wellcome Trust Sanger Institute
Co-authored papers 6
Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 6
Colin McKerlie
The Hospital for Sick Children
Co-authored papers 6
Lauryl M J Nutter
The Hospital for Sick Children
Co-authored papers 6
Ann-Marie Mallon
The Turing Institute
Co-authored papers 5
Luis Santos
The Turing Institute
Co-authored papers 5
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 5
Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 5
Kent C Lloyd
University of California davis
Co-authored papers 4
John R Seavitt
Baylor College of Medicine
Co-authored papers 4
Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 4
Lynette Bower
University of California davis
Co-authored papers 4
Stephen A Murray
Columbia University.
Co-authored papers 4
Wolfgang Wurst
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 3
Robert E Braun
University of Maine
Co-authored papers 3
Valerie Gailus-Durner
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 3
Helen Parkinson
European Bioinformatics Institute
Co-authored papers 3
Natasha A Karp
Wellcome Sanger Institute
Co-authored papers 3
Je Kyung Seong
Seoul National University
Co-authored papers 3
Glauco P Tocchini-Valentini
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 3
Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 3
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 3
Tania Sorg
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
Co-authored papers 3
Monica J Justice
The Hospital for Sick Children
Co-authored papers 2
Philip L Beales
UCL Great Ormond Street Institute of Child Health, University College London
Co-authored papers 2
Juan Gallegos
Baylor College of Medicine
Co-authored papers 2
Simon Greenaway
Harwell Institute
Co-authored papers 2
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