Carl O. Olson

University of Manitoba — Canada

Biochemistry, Genetics and Molecular Biology · Life Sciences

18h-index1.4kcitations25works3.02yr avg
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Research Topics

Connexins and lens biology(10), Genetics and Neurodevelopmental Disorders(9), Epigenetics and DNA Methylation(7), Neuroscience and Neuropharmacology Research(3), Autism Spectrum Disorder Research(3)

Publications25 total

Mutation of MeCP2 at T158M Leads to Distinct Molecular and Phenotypic Abnormalities in Male and Female Mice
Cells·2025· 1 citedOpen Access
Transcriptional Inhibition of the Mecp2 Promoter by MeCP2E1 and MeCP2E2 Isoforms Suggests Negative Auto-Regulatory Feedback that can be Moderated by Metformin
Journal of Molecular Neuroscience·2024· 5 cited
DNA Methylation Contributes to the Differential Expression Levels of Mecp2 in Male Mice Neurons and Astrocytes
International Journal of Molecular Sciences·2019· 34 citedOpen Access
Genome-Wide Transcriptome Landscape of Embryonic Brain-Derived Neural Stem Cells Exposed to Alcohol with Strain-Specific Cross-Examination in BL6 and CD1 Mice
Scientific Reports·2019· 27 citedOpen Access
MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients
Frontiers in Genetics·2018· 55 citedOpen Access
Protective effects of gabapentin against the seizure susceptibility and comorbid behavioral abnormalities in the early socially isolated mice
European Journal of Pharmacology·2017· 16 cited
Attenuation of oxidative and nitrosative stress in cortical area associates with antidepressant-like effects of tropisetron in male mice following social isolation stress
Brain Research Bulletin·2016· 54 cited
Involvement of D1 and D2 dopamine receptors in the antidepressant-like effects of selegiline in maternal separation model of mouse
Physiology & Behavior·2016· 73 cited
Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome
Human Molecular Genetics·2014· 10 citedOpen Access
Brain Region-Specific Expression of MeCP2 Isoforms Correlates with DNA Methylation within Mecp2 Regulatory Elements
PLoS ONE·2014· 114 citedOpen Access
Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome
Human Molecular Genetics·2013· 81 citedOpen Access
Dynamic expression of MEIS1 homeoprotein in E14.5 forebrain and differentiated forebrain-derived neural stem cells
Annals of Anatomy - Anatomischer Anzeiger·2013· 39 cited
Novel MeCP2 Isoform-Specific Antibody Reveals the Endogenous MeCP2E1 Expression in Murine Brain, Primary Neurons and Astrocytes
PLoS ONE·2012· 71 citedOpen Access
Connexin45-Containing Neuronal Gap Junctions in Rodent Retina Also Contain Connexin36 in Both Apposing Hemiplaques, Forming Bihomotypic Gap Junctions, with Scaffolding Contributed by Zonula Occludens-1
Journal of Neuroscience·2008· 119 citedOpen Access
Connexin36 vs. connexin32, “miniature” neuronal gap junctions, and limited electrotonic coupling in rodent suprachiasmatic nucleus
Neuroscience·2007· 81 citedOpen Access
Identification of connexin36 in gap junctions between neurons in rodent locus coeruleus
Neuroscience·2007· 87 citedOpen Access
Association of connexin36 and zonula occludens-1 with zonula occludens-2 and the transcription factor zonula occludens-1-associated nucleic acid-binding protein at neuronal gap junctions in rodent retina
Neuroscience·2006· 52 citedOpen Access
Ultrastructural localization of connexins (Cx36, Cx43, Cx45), glutamate receptors and aquaporin-4 in rodent olfactory mucosa, olfactory nerve and olfactory bulb
Journal of Neurocytology·2005· 102 citedOpen Access
Neuronal connexin36 association with zonula occludens‐1 protein (ZO‐1) in mouse brain and interaction with the first PDZ domain of ZO‐1
European Journal of Neuroscience·2004· 144 citedOpen Access
High-resolution proteomic mapping in the vertebrate central nervous system: Close proximity of connexin35 to NMDA glutamate receptor clusters and co-localization of connexin36 with immunoreactivity for zonula occludens protein-1 (ZO-1)
Journal of Neurocytology·2004· 67 citedOpen Access
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Frequent Co-authors

Mojgan Rastegar(13), J.I. Nagy(10), Thomas Yasumura(8), John E. Rash(8), Naomi Kamasawa(7), Kimberly G. V. Davidson(6), Xinbo Li(5), Robby M. Zachariah(5), Vichithra R. B. Liyanage(4), Shayan Amiri(4), Marjorie Buist(4), Shijun Lu(3), Hossein Amini-Khoei(3), Arya Haj‐Mirzaian(3), Maryam Rahimi-Balaei(3), C. Ciolofan(2), Chinelo Ezeonwuka(2), Christophe Furman(2), Dag H. Yasui(2), Janine M. LaSalle(2)