Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Carl O. Olson"'
Autor:
Carl O. Olson, Shervin Pejhan, Daniel Kroft, Kimia Sheikholeslami, David Fuss, Marjorie Buist, Annan Ali Sher, Marc R. Del Bigio, Yehezkel Sztainberg, Victoria Mok Siu, Lee Cyn Ang, Marianne Sabourin-Felix, Tom Moss, Mojgan Rastegar
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Rett syndrome (RTT) is a severe and rare neurological disorder that is caused by mutations in the X-linked MECP2 (methyl CpG-binding protein 2) gene. MeCP2 protein is an important epigenetic factor in the brain and in neurons. In Mecp2-deficient neur
Externí odkaz:
https://doaj.org/article/d5ec5417e1f1402e90cc3f8fa5bb1e26
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 8, p 1845 (2019)
Methyl CpG binding protein-2 (MeCP2) isoforms (E1 and E2) are important epigenetic regulators in brain cells. Accordingly, MeCP2 loss- or gain-of-function mutation causes neurodevelopmental disorders, including Rett syndrome (RTT), MECP2 duplication
Externí odkaz:
https://doaj.org/article/d7f136ad28c64ac9b4d1fd967bf2d291
Autor:
Carl O. Olson, Robby M. Zachariah, Geoffrey G. Hicks, Wayne Xu, Romina D. Levy, Aaron MacAulay, James R. Davie, Kyle Curtis, Marjorie Buist, Shayan Amiri, Mojgan Rastegar, Vichithra R. B. Liyanage
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-17 (2019)
Scientific Reports
Scientific Reports
We have previously reported the deregulatory impact of ethanol on global DNA methylation of brain-derived neural stem cells (NSC). Here, we conducted a genome-wide RNA-seq analysis in differentiating NSC exposed to different modes of ethanol exposure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faa709a92ef5bb0aa0aa4cfe884c2607
http://link.springer.com/article/10.1038/s41598-018-36059-y
http://link.springer.com/article/10.1038/s41598-018-36059-y
Autor:
Annan Ali Sher, Marjorie Buist, Marc R. Del Bigio, Victoria Mok Siu, Shervin Pejhan, Marianne Sabourin-Felix, Mojgan Rastegar, Tom Moss, Carl O. Olson, David Fuss, Lee Cyn Ang, Daniel Kroft, Kimia Sheikholeslami, Yehezkel Sztainberg
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Frontiers in Genetics
Frontiers in Genetics
Rett syndrome (RTT) is a severe and rare neurological disorder that is caused by mutations in the X-linked MECP2 (methyl CpG-binding protein 2) gene. MeCP2 protein is an important epigenetic factor in the brain and in neurons. In Mecp2-deficient neur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dff5424731a528dfec9f575f3d09dbb2
Autor:
Carl O. Olson, Hossein Amini-Khoei, Shayan Amiri, Sakineh Alijanpour, Ali Razmi, Ali Mohammadi-Asl, Mehdi Mehdizadeh, Mojgan Rastegar, Maryam Rahimi-Balaei, Arya Haj-Mirzaian, Mohammad-Reza Zarrindast
Publikováno v:
Physiology & Behavior. 163:107-114
Mother-infant interactions are known to be associated with the psychological well-being of an individual in adulthood. It is well accepted that emotional stress in early life, such as maternal separation (MS), leads to alterations in the neurotransmi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6803998c7c9400df02c0f7f0d49244
https://doi.org/10.1016/j.physbeh.2016.04.052
https://doi.org/10.1016/j.physbeh.2016.04.052
Autor:
Arya Haj-Mirzaian, Armin Shirzadian, Mohammad-Reza Zarrindast, Maryam Rahimi-Balaei, Shayan Amiri, Arman Mohsenzadeh, Carl O. Olson, Ali Razmi, Hossein Amini-Khoei, Mojgan Rastegar, Mahmoud Ghazi-Khansari
Publikováno v:
European journal of pharmacology. 797
Adolescence is a pivotal period of brain development during lifespan, which is sensitive to stress exposure. Early social isolation stress (SIS) is known to provoke a variety of psychiatric comorbidities as well as seizure risk. Psychiatric comorbidi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::712e3e7a5fe5e48e9488b47a32bbaaf7
https://pubmed.ncbi.nlm.nih.gov/28115172
https://pubmed.ncbi.nlm.nih.gov/28115172
Autor:
N. Kamasawa, James I. Nagy, Carl O. Olson, John E. Rash, Thomas Yasumura, Kimberly G. V. Davidson
Publikováno v:
Neuroscience. 147:938-956
Locus coeruleus neurons are strongly coupled during early postnatal development, and it has been proposed that these neurons are linked by extraordinarily abundant gap junctions consisting of connexin32 and connexin26, and that those same connexins a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29d1a9b9dde5650bb4219e3f0ca1f414
https://doi.org/10.1016/j.neuroscience.2007.04.061
https://doi.org/10.1016/j.neuroscience.2007.04.061
Autor:
John E. Rash, F.E. Dudek, Carl O. Olson, Alberto E. Pereda, Kimberly G. V. Davidson, James I. Nagy, N. Kamasawa, Xinbo Li, C. S. Furman, Thomas Yasumura
Publikováno v:
Journal of Neurocytology. 33:131-151
Combined confocal microscopy and freeze-fracture replica immunogold labeling (FRIL) were used to examine the connexin identity at electrical synapses in goldfish brain and rat retina, and to test for "co-localization" vs. "close proximity" of connexi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cc54ff538f9088cb7eee039f2803139
https://doi.org/10.1023/b:neur.0000029653.34094.0b
https://doi.org/10.1023/b:neur.0000029653.34094.0b
Autor:
B.D. Lynn, Carl O. Olson, James I. Nagy, John E. Rash, Carola Meier, Thomas Yasumura, Xinbo Li, Kimberly G. V. Davidson
Publikováno v:
European Journal of Neuroscience. 16:795-806
The recently discovered connexin29 (Cx29) was reported to be present in the central and peripheral nervous systems (CNS and PNS), and its mRNA was found in particular abundance in peripheral nerve. The expression and localization of Cx29 protein in s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61a8ac02e5c86f1e42ed7aba3ade2130
https://doi.org/10.1046/j.1460-9568.2002.02149.x
https://doi.org/10.1046/j.1460-9568.2002.02149.x
Autor:
Justin O. Aflatooni, Dag H. Yasui, N. Carolyn Schanen, Mari S. Golub, John B. Vincent, Daniel J. Hu, Florence K. Crary, Michael L. Gonzales, Mojgan Rastegar, Bryant J. Gavino, Carl O. Olson, Janine M. LaSalle
Publikováno v:
Human molecular genetics. 23(9)
Mutations in MECP2 cause the neurodevelopmental disorder Rett syndrome (RTT OMIM 312750). Alternative inclusion of MECP2/Mecp2 exon 1 with exons 3 and 4 encodes MeCP2-e1 or MeCP2-e2 protein isoforms with unique amino termini. While most MECP2 mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd01a8e0894ebb2fda60a48f24dd85ea
https://pubmed.ncbi.nlm.nih.gov/24352790
https://pubmed.ncbi.nlm.nih.gov/24352790