Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Gregory C. Carlson"'
Autor:
Russell G. Port, Christopher Gajewski, Elizabeth Krizman, Holly C. Dow, Shinji Hirano, Edward S. Brodkin, Gregory C. Carlson, Michael B. Robinson, Timothy P.L. Roberts, Steven J. Siegel
Publikováno v:
Neurobiology of Disease, Vol 108, Iss , Pp 324-338 (2017)
Approximately one in 45 children have been diagnosed with Autism Spectrum Disorder (ASD), which is characterized by social/communication impairments. Recent studies have linked a subset of familial ASD to mutations in the Protocadherin 10 (Pcdh10) ge
Externí odkaz:
https://doaj.org/article/d8f49ff3a72541078ce2a0f414937b67
Autor:
Steven E. Arnold, Irwin Lucki, Bethany R. Brookshire, Gregory C. Carlson, Caroline A. Browne, Hala Kazi, Sookhee Bang, Bo-Ran Choi, Yong Chen, Mary F. McMullen, Sangwon F. Kim
Publikováno v:
Neurobiology of Disease, Vol 67, Iss , Pp 79-87 (2014)
Insulin resistance and other features of the metabolic syndrome are increasingly recognized for their effects on cognitive health. To ascertain mechanisms by which this occurs, we fed mice a very high fat diet (60% kcal by fat) for 17 days or a moder
Externí odkaz:
https://doaj.org/article/0f2c69c70c3044f080016390788f6f49
Autor:
Timothy P.L. Roberts, Edward S. Brodkin, Steven J. Siegel, Holly C. Dow, Russell G. Port, Elizabeth N. Krizman, Michael B. Robinson, Shinji Hirano, Christopher R. Gajewski, Gregory C. Carlson
Publikováno v:
Neurobiology of Disease, Vol 108, Iss, Pp 324-338 (2017)
Approximately one in 45 children have been diagnosed with Autism Spectrum Disorder (ASD), which is characterized by social/communication impairments. Recent studies have linked a subset of familial ASD to mutations in the Protocadherin 10 (Pcdh10) ge
Autor:
Sangwon F. Kim, Bethany R. Brookshire, Rachel S. White, Yong Chen, Irwin Lucki, Robert Lin, Steve J. Siegel, Gregory C. Carlson
Publikováno v:
Neuroscience. 322:408-415
Dexras1 is a novel GTPase that acts at a confluence of signaling mechanisms associated with psychiatric and neurological disease including NMDA receptors, NOS1AP and nNOS. Recent work has shown that Dexras1 mediates iron trafficking and NMDA-dependen
Autor:
Gregory C. Carlson
Publikováno v:
Christian Education Journal: Research on Educational Ministry. 13:81-84
Autor:
Bryant Lance Horowitz, Konrad Talbot, W. Bailey Glen, Gregory C. Carlson, Antonieta Lavin, J. David Jentsch, Tyrone D. Cannon
Publikováno v:
Hippocampus. 24:204-213
Genetic variants in DTNBP1 encoding the protein dysbindin-1 have often been associated with schizophrenia and with the cognitive deficits prominent in that disorder. Because impaired function of the hippocampus is thought to play a role in these memo
SOCIABILITY DEFICITS AND ALTERED AMYGDALA CIRCUITS IN MICE LACKING Pcdh10, AN AUTISM ASSOCIATED GENE
Autor:
Hyong Kim, Hannah Schoch, Holly C. Dow, Rachel S. White, Lucero Cordero, Dirk Feldmeyer, Warren B. Bilker, Ashley A. Pallathra, Russell G. Port, Robert T. Schultz, Shinji Hirano, Dominique Bohorquez, Anamika Banerjee, Hongzhe Li, Sarah L. Ferri, Arati S. Kreibich, Edward S. Brodkin, Ted Abel, Chang-Gyu Hahn, Gregory C. Carlson, Karin E. Borgmann-Winter
Background Behavioral symptoms in individuals with autism spectrum disorder (ASD) have been attributed to abnormal neuronal connectivity, but the molecular bases of these behavioral and brain phenotypes are largely unknown. Human genetic studies have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::326765a704bc20ebecb4e2cc235685a6
https://europepmc.org/articles/PMC5161717/
https://europepmc.org/articles/PMC5161717/
Autor:
Hassan A, Liao W, Julia Chartove, Gregory C. Carlson, Mary F. McMullen, Rachel S. White, Seha Kim
Rett syndrome (RTT) has a complex developmental course over childhood and adolescence. Patients with RTT often have a pre-symptomatic period with no or little outward signs of the disorder, followed by developmental arrest and regression. Following r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3bc908fb2a9c288e026ea7f7351fcb2
https://doi.org/10.1101/034835
https://doi.org/10.1101/034835
Autor:
Le Zhang, Linda Hu, Julie A. Blendy, Darren Goffin, Steve J. Siegel, Zhaolan Zhou, Megan Allen, Arith-Ruth S. Reyes, Caroline Ong, Michael E. Greenberg, I-Ting Judy Wang, Sonia Cohen, Gregory C. Carlson, Maria João Amorim, Amy Mercado-Berton
Publikováno v:
Nature neuroscience
Mutations in the MECP2 gene cause the autism spectrum disorder Rett syndrome (RTT). One of the most common MeCP2 mutations associated with RTT occurs at threonine 158, converting it to methionine (T158M) or alanine (T158A). To understand the role of
Autor:
Florian Weissinger, Cuiyong Yue, Chyze Whee Ang, Fu-Chun Hsu, Hajime Takano, Douglas A. Coulter, Ethan M. Goldberg, Gregory C. Carlson
Publikováno v:
The Journal of Physiology. 589:1893-1903
Mammalian cortical structures are endowed with the capacity for plasticity, which emerges from a combination of the dynamics of circuit connectivity and function, and the intrinsic function of the neurons within the circuit. However, this capacity is