Muriel T. Davisson

Marietta Memorial Hospital — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

62h-index15.6kcitations237works0.02yr avg
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Research Topics

Animal Genetics and Reproduction(31), Down syndrome and intellectual disability research(24), Retinal Development and Disorders(19), Genetics and Neurodevelopmental Disorders(16), Chromosomal and Genetic Variations(15)

Publications235 total

Exploring Submaximal Effort Using Isometric Testing: Potential Implications in the Determination of Client Effort During Clinical Evaluation
American Journal of Occupational Therapy·2025
Centralized mouse repositories
UNC Libraries·2020Open Access
The Jackson Laboratory Mouse Mutant Resource
2020· 23 cited
Age exacerbates abnormal protein expression in a mouse model of Down syndrome
Neurobiology of Aging·2017· 19 cited
Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis
American Journal of Physiology-Renal Physiology·2015· 2 citedOpen Access
A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers
Kidney International·2014· 51 citedOpen Access
Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease
Human Molecular Genetics·2013· 58 cited
Centralized mouse repositories
Mammalian Genome·2012· 27 citedOpen Access
Discovery Genetics: The History and Future of Spontaneous Mutation Research
Current Protocols in Mouse Biology·2012· 22 citedOpen Access
Abstract 5267: Mouse models of cancer at The Jackson Laboratory Repository
Cancer Research·2012
Loss of Correlations among Proteins in Brains of the Ts65Dn Mouse Model of Down Syndrome
Journal of Proteome Research·2012· 39 cited
Historical Foundations
Elsevier eBooks·2012· 3 cited
Strains, Stocks and Mutant Mice
Elsevier eBooks·2012· 26 cited
A Spontaneous Mutation in Contactin 1 in the Mouse
PLoS ONE·2011· 19 citedOpen Access
Erratum to: Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn
Mammalian Genome·2011Open Access
Hypothalamic mitochondrial dysfunction associated with anorexia in the <i>anx/anx</i> mouse
Proceedings of the National Academy of Sciences·2011· 68 citedOpen Access
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn
Mammalian Genome·2011· 186 cited
Embryonic Stem Cells from a Mouse Down Syndrome Model Have Impaired Proliferation and Increased Oxidative Stress.
Biology of Reproduction·2011
The Mouse Model of Down Syndrome Ts65Dn Presents Visual Deficits as Assessed by Pattern Visual Evoked Potentials
Investigative Ophthalmology & Visual Science·2010· 32 citedOpen Access
ZFP191 is required by oligodendrocytes for CNS myelination
Genes & Development·2010· 82 citedOpen Access
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Frequent Co-authors

Bo Chang(11), John R. Heckenlively(11), Norman L. Hawes(9), Hope O. Sweet(8), Cecilia Schmidt(7), Thomas H. Roderick(7), Steven Nusinowitz(6), Susan A. Cook(5), Ellen C. Akeson(5), Roderick T. Bronson(5), Simon W. M. John(4), Richard S. Smith(3), Dan Goldowitz(3), Katheleen Gardiner(3), Ronald E. Hurd(3), James E. Womack(3), Nicholas G. Irving(2), R.E. Hurd(2), Olga V. Savinova(2), Michael G. Anderson(2)