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David Stuss, MSc - Publications

Affiliations: 
Biology University of Victoria, Victoria, British Columbia, Canada 
Area:
Rett Syndrome
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4 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.518
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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