Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Michael C Pride"'
Autor:
Brian C Trainor, Michael C Pride, Rosalina Villalon Landeros, Nicholas W Knoblauch, Elizabeth Y Takahashi, Andrea L Silva, Katie K Crean
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e17405 (2011)
Stressful life experiences are known to be a precipitating factor for many mental disorders. The social defeat model induces behavioral responses in rodents (e.g. reduced social interaction) that are similar to behavioral patterns associated with moo
Externí odkaz:
https://doaj.org/article/27be523da17545d0bad52386bf464e03
Autor:
Michael C. Pride, Jason P. Lerch, Pamela J. Lein, Jill L. Silverman, Timothy A. Fenton, Carolyn Klocke, Stela P. Petkova, Ben Waldau, Jacob Ellegood, Jeannine White
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-16 (2020)
Scientific reports, vol 10, iss 1
Scientific Reports
Scientific reports, vol 10, iss 1
Scientific Reports
Neurobehavioral studies have produced contradictory findings concerning the function of neurogenesis in the adult dentate gyrus. Previous studies have proved inconsistent across several behavioral endpoints thought to be dependent on dentate neurogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1a73aa5c40697aee31aa40b06ed8421
http://link.springer.com/article/10.1038/s41598-020-65090-1
http://link.springer.com/article/10.1038/s41598-020-65090-1
Autor:
Anthony S. Wexler, Keith J. Bein, Michael C. Pride, Pamela J. Lein, Jill L. Silverman, Stela P. Petkova, Kelley T. Patten, Elizabeth L. Berg, Christopher Wallis, Anthony Valenzuela, Lauren R. Pedersen
Publikováno v:
Translational psychiatry, vol 10, iss 1
Translational Psychiatry, Vol 10, Iss 1, Pp 1-16 (2020)
Translational Psychiatry
Translational Psychiatry, Vol 10, Iss 1, Pp 1-16 (2020)
Translational Psychiatry
Epidemiological studies consistently implicate traffic-related air pollution (TRAP) and/or proximity to heavily trafficked roads as risk factors for developmental delays and neurodevelopmental disorders (NDDs); however, there are limited preclinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd3bce0a40fe718b58ced2394bde19f0
https://escholarship.org/uc/item/5jz6f3dw
https://escholarship.org/uc/item/5jz6f3dw
Autor:
Michael C. Pride, Ulrika Beitnere, Brian J. Nieman, Edwin J. Weeber, Nycole A. Copping, Melinda M. Peters, Anna Adhikari, Jill L. Silverman, Heather A. Born, Peter Deng, Stela P. Petkova, Scott V. Dindot, Markus Wöhr, David J. Segal, Jason P. Lerch, Timothy A. Fenton, R. D. Lee, L. S. Noakes, Y. Shen, Kevin Nash, Elizabeth L. Berg, Kyle D. Fink, Henriette O'Geen, L. R. Pedersen, Sarah E. Harris, David Cameron, Jacob Ellegood, Anne E. Anderson
Publikováno v:
Translational psychiatry, vol 10, iss 1
Translational Psychiatry
Translational Psychiatry, Vol 10, Iss 1, Pp 1-16 (2020)
Translational Psychiatry
Translational Psychiatry, Vol 10, Iss 1, Pp 1-16 (2020)
Angelman syndrome (AS) is a rare neurodevelopmental disorder characterized by developmental delay, impaired communication, motor deficits and ataxia, intellectual disabilities, microcephaly, and seizures. The genetic cause of AS is the loss of expres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edfec6dabf457b6daed8b3f4902607dc
https://escholarship.org/uc/item/4wd513f2
https://escholarship.org/uc/item/4wd513f2
Autor:
Michael C. Pride, Karen L. Jones, Mu Yang, Jill L. Silverman, Judy Van de Water, Elizabeth Edmiston, Jacqueline N. Crawley
Publikováno v:
Molecular psychiatry
Immune dysregulation has been noted consistently in individuals with autism spectrum disorder (ASD) and their families, including the presence of autoantibodies reactive to fetal brain proteins in nearly a quarter of mothers of children with ASD vers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d139d58e55da8320831bdbc3c57b2d0d
https://doi.org/10.1038/s41380-018-0126-1
https://doi.org/10.1038/s41380-018-0126-1
Autor:
Lyndsey M. Kirk, Kyle R. Puhger, David J. Speca, Michael C. Pride, Jill L. Silverman, Yael Stern-Bach, Lucas Matt, Johannes W. Hell, Jacqueline N. Crawley, Elva D Diaz, Tomer Haham, George Chenaux, Kristopher E. Plambeck, Mohammad Qneibi
Publikováno v:
Cell Reports, Vol 22, Iss 9, Pp 2246-2253 (2018)
Cell reports, vol 22, iss 9
Cell reports, vol 22, iss 9
Summary: Altering AMPA receptor (AMPAR) content at synapses is a key mechanism underlying the regulation of synaptic strength during learning and memory. Previous work demonstrated that SynDIG1 (synapse differentiation-induced gene 1) encodes a trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56020d04c650ac22e8787f3f96585560
http://www.sciencedirect.com/science/article/pii/S2211124718301943
http://www.sciencedirect.com/science/article/pii/S2211124718301943
Autor:
Hala Harony-Nicolas, Nycole A. Copping, Melissa D. Bauman, Elizabeth L. Berg, Pamela J. Lein, Jacob Ellegood, Jill L. Silverman, Michael C. Pride, Joseph D. Buxbaum, Markus Wöhr, Josef K. Rivera, Milo Careaga, Jason P. Lerch, Robert F. Berman
Publikováno v:
Autism Research. 11:587-601
Author(s): Berg, Elizabeth L; Copping, Nycole A; Rivera, Josef K; Pride, Michael C; Careaga, Milo; Bauman, Melissa D; Berman, Robert F; Lein, Pamela J; Harony-Nicolas, Hala; Buxbaum, Joseph D; Ellegood, Jacob; Lerch, Jason P; Wohr, Markus; Silverman,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9ae2dd3063530b8396e584b25e3e4fa
https://doi.org/10.1002/aur.1925
https://doi.org/10.1002/aur.1925
Autor:
Nycole A. Copping, Sarah G. B. Christian, Dylan J Ritter, Elizabeth L. Berg, Nathalie Buscher, Jason P. Lerch, Janine M. LaSalle, M. Saharul Islam, Dorota Zolkowska, Lawrence T. Reiter, Jill L. Silverman, Michael C. Pride, Scott V. Dindot, Jacob Ellegood
Publikováno v:
Human molecular genetics, vol 26, iss 20
Maternally derived copy number gains of human chromosome 15q11.2-q13.3 (Dup15q syndrome or Dup15q) cause intellectual disability, epilepsy, developmental delay, hypotonia, speech impairments, and minor dysmorphic features. Dup15q syndrome is one of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::232c40670c942fc06c44c5d0ceca1bc3
https://doi.org/10.1093/hmg/ddx289
https://doi.org/10.1093/hmg/ddx289
Autor:
Axel Visel, Michael C. Pride, Konstantinos Zarbalis, Diane E. Dickel, Tyler W. Stradleigh, Nycole A. Copping, Linda Su-Feher, Gaurav Kaushik, Veena Afzal, Alexander Nord, Rinaldo Catta-Preta, Len A. Pennacchio, Melanie D. Schaffler, Jacqueline N. Crawley, Ingrid Plajzer-Frick, A. Ayanna Wade, M. Asrafuzzaman Riyadh, Shreya Louis, Jacob Ellegood, Iva Zdilar, Brandon J. Mannion, Andrea Gompers, Jill L. Silverman, Jason P. Lerch
Publikováno v:
Gompers, AL; Su-Feher, L; Ellegood, J; Copping, NA; Riyadh, MA; Stradleigh, TW; et al.(2017). Germline Chd8 haploinsufficiency alters brain development in mouse. Nature Neuroscience, 20(8), 1062-1073. doi: 10.1038/nn.4592. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/0ck9n78k
Nature neuroscience, vol 20, iss 8
Nature neuroscience, vol 20, iss 8
© 2017 Nature America, Inc., part of Springer Nature. All rights reserved. The chromatin remodeling gene CHD8 represents a central node in neurodevelopmental gene networks implicated in autism. We examined the impact of germline heterozygous framesh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ea7a52fba27ddece54bc5897f6dee0c
https://doi.org/10.1038/nn.4592
https://doi.org/10.1038/nn.4592
Autor:
Meron Azage, David B. Everman, Brooke T. Smith, Steffen Syrbe, Stephen W. Scherer, Jennifer Keller-Ramey, Gregory M. Cooper, Verónica Martínez-Cerdeño, Susan M. Hiatt, Mathew J Wallis, Dmitriy Niyazov, Benjamin Büttner, Rami Abou Jamra, Ryan K. C. Yuen, Johannes R. Lemke, Natasha J Brown, Amber Begtrup, Richard E. Person, Barbara Kellam, Chloé Quélin, Heinrich Sticht, Laurence J. Walsh, Angelo Harlan De Crescenzo, Konstantinos Zarbalis, Jonathan B. Strober, Susan Walker, Alexios A Panoutsopoulos, Shuxi Liu, Diana Le Duc, Urania Kotzaeridou, Michael S. Hildebrand, Michael C. Pride, Eleonora Napoli, Jacqueline N. Crawley, Francis Jeshira Reynoso Santos, Katelyn Payne, Renee Bend, Sandra Yang, Megan T. Cho, Evdokia Anagnostou, Cecilia R Giulivi, Rhonda E. Schnur, Lori Orosco, Andreas Ziegler, Jan H Doering, Christèle Dubourg, Jill L. Silverman
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2019, 142 (9), pp.2617-2630. ⟨10.1093/brain/awz198⟩
Brain : a journal of neurology, vol 142, iss 9
Brain-A Journal of Neurology, 2019, 142 (9), pp.2617-2630. ⟨10.1093/brain/awz198⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2019, 142 (9), pp.2617-2630. ⟨10.1093/brain/awz198⟩
Brain : a journal of neurology, vol 142, iss 9
Brain-A Journal of Neurology, 2019, 142 (9), pp.2617-2630. ⟨10.1093/brain/awz198⟩
The underpinnings of mild to moderate neurodevelopmental delay remain elusive, often leading to late diagnosis and interventions. Here, we present data on exome and genome sequencing as well as array analysis of 13 individuals that point to pathogeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb2df3be07639a893ba2d310d80a7739
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02309674
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02309674