David Stuss, MSc - Publications
Affiliations: | Biology | University of Victoria, Victoria, British Columbia, Canada |
Area:
Rett SyndromeYear | Citation | Score | |||
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2015 | Rietveld L, Stuss DP, McPhee D, Delaney KR. Genotype-specific effects of Mecp2 loss-of-function on morphology of Layer V pyramidal neurons in heterozygous female Rett syndrome model mice. Frontiers in Cellular Neuroscience. 9: 145. PMID 25941473 DOI: 10.3389/fncel.2015.00145 | 0.561 | |||
2015 | Rietveld L, Stuss DP, McPhee D, Delaney KR. Genotype-specific effects of Mecp2 loss-of-function on morphology of layer V pyramidal neurons in heterozygous female Rett syndrome model mice Frontiers in Cellular Neuroscience. 9. DOI: 10.3389/fncel.2015.00145 | 0.517 | |||
2013 | Stuss DP, Cheema M, Ng MK, Martinez de Paz A, Williamson B, Missiaen K, Cosman JD, McPhee D, Esteller M, Hendzel M, Delaney K, Ausió J. Impaired in vivo binding of MeCP2 to chromatin in the absence of its DNA methyl-binding domain. Nucleic Acids Research. 41: 4888-900. PMID 23558747 DOI: 10.1093/Nar/Gkt213 | 0.456 | |||
2012 | Stuss DP, Boyd JD, Levin DB, Delaney KR. MeCP2 mutation results in compartment-specific reductions in dendritic branching and spine density in layer 5 motor cortical neurons of YFP-H mice. Plos One. 7: e31896. PMID 22412847 DOI: 10.1371/journal.pone.0031896 | 0.532 | |||
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