Search Results - "Pride, Michael C"

Sex differences in social interaction behavior following social defeat stress in the monogamous California mouse (Peromyscus californicus) by Trainor, Brian C, Pride, Michael C, Villalon Landeros, Rosalina, Knoblauch, Nicholas W, Takahashi, Elizabeth Y, Silva, Andrea L, Crean, Katie K

“…Stressful life experiences are known to be a precipitating factor for many mental disorders. The social defeat model induces behavioral responses in rodents…”
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Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism by Dhamne, Sameer C, Silverman, Jill L, Super, Chloe E, Lammers, Stephen H T, Hameed, Mustafa Q, Modi, Meera E, Copping, Nycole A, Pride, Michael C, Smith, Daniel G, Rotenberg, Alexander, Crawley, Jacqueline N, Sahin, Mustafa

“…Autism spectrum disorder (ASD) is a clinically and biologically heterogeneous condition characterized by social, repetitive, and sensory behavioral…”
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Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndrome by Copping, Nycole A, Christian, Sarah G B, Ritter, Dylan J, Islam, M Saharul, Buscher, Nathalie, Zolkowska, Dorota, Pride, Michael C, Berg, Elizabeth L, LaSalle, Janine M, Ellegood, Jacob, Lerch, Jason P, Reiter, Lawrence T, Silverman, Jill L, Dindot, Scott V

“…Maternally derived copy number gains of human chromosome 15q11.2-q13.3 (Dup15q syndrome or Dup15q) cause intellectual disability, epilepsy, developmental…”
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Developmental social communication deficits in the Shank3 rat model of phelan‐mcdermid syndrome and autism spectrum disorder by 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., Wöhr, Markus, Silverman, Jill L.

“…Mutations in the SHANK3 gene have been discovered in autism spectrum disorder (ASD), and the intellectual disability, Phelan‐McDermid Syndrome. This study…”
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Early motor phenotype detection in a female mouse model of Rett syndrome is improved by cross-fostering by Vogel Ciernia, Annie, Pride, Michael C, Durbin-Johnson, Blythe, Noronha, Adriana, Chang, Alene, Yasui, Dag H, Crawley, Jacqueline N, LaSalle, Janine M

“…Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutations in the gene encoding methyl CpG binding protein 2 (MeCP2) that occur…”
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SynDIG4/Prrt1 Is Required for Excitatory Synapse Development and Plasticity Underlying Cognitive Function by Matt, Lucas, Kirk, Lyndsey M., Chenaux, George, Speca, David J., Puhger, Kyle R., Pride, Michael C., Qneibi, Mohammad, Haham, Tomer, Plambeck, Kristopher E., Stern-Bach, Yael, Silverman, Jill L., Crawley, Jacqueline N., Hell, Johannes W., Díaz, Elva

“…Altering AMPA receptor (AMPAR) content at synapses is a key mechanism underlying the regulation of synaptic strength during learning and memory. Previous work…”
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Effects of kappa opioid receptors on conditioned place aversion and social interaction in males and females by Robles, Cindee F., McMackin, Marissa Z., Campi, Katharine L., Doig, Ian E., Takahashi, Elizabeth Y., Pride, Michael C., Trainor, Brian C.

“…•Low doses of kappa opioid receptor agonist induced place aversion in females but not males.•Acute effects of kappa agonist on social interaction behavior are…”
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Developmental exposure to near roadway pollution produces behavioral phenotypes relevant to neurodevelopmental disorders in juvenile rats by Berg, Elizabeth L., Pedersen, Lauren R., Pride, Michael C., Petkova, Stela P., Patten, Kelley T., Valenzuela, Anthony E., Wallis, Christopher, Bein, Keith J., Wexler, Anthony, Lein, Pamela J., Silverman, Jill L.

“…Epidemiological studies consistently implicate traffic-related air pollution (TRAP) and/or proximity to heavily trafficked roads as risk factors for…”
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Autism-specific maternal autoantibodies produce behavioral abnormalities in an endogenous antigen-driven mouse model of autism by Jones, Karen L., Pride, Michael C., Edmiston, Elizabeth, Yang, Mu, Silverman, Jill L., Crawley, Jacqueline N., Van de Water, Judy

“…Immune dysregulation has been noted consistently in individuals with autism spectrum disorder (ASD) and their families, including the presence of…”
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Germline Chd8 haploinsufficiency alters brain development in mouse by Gompers, Andrea L, Su-Feher, Linda, Ellegood, Jacob, Copping, Nycole A, Riyadh, M Asrafuzzaman, Stradleigh, Tyler W, Pride, Michael C, Schaffler, Melanie D, Wade, A Ayanna, Catta-Preta, Rinaldo, Zdilar, Iva, Louis, Shreya, Kaushik, Gaurav, Mannion, Brandon J, Plajzer-Frick, Ingrid, Afzal, Veena, Visel, Axel, Pennacchio, Len A, Dickel, Diane E, Lerch, Jason P, Crawley, Jacqueline N, Zarbalis, Konstantinos S, Silverman, Jill L, Nord, Alex S

“…Strong genetic evidence points to a significant role for heterozygous mutations to general chromatin remodeling factors, such as CHD8, in autism. Gompers et al…”
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Cognitive deficits in the Snord116 deletion mouse model for Prader-Willi syndrome by Adhikari, Anna, Copping, Nycole A., Onaga, Beth, Pride, Michael C., Coulson, Rochelle L., Yang, Mu, Yasui, Dag H., LaSalle, Janine M., Silverman, Jill L.

“…•A lack of the gene cluster SNORD116 may be responsible for some aspects of PWS.•Heterozygous Snord116 mutation mice had learning and memory deficits in three…”
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Surgical restabilization reduces the progression of post-traumatic osteoarthritis initiated by ACL rupture in mice by Lin, Yu-Yang, Jbeily, Elias H., Tjandra, Priscilla M., Pride, Michael C., Lopez-Torres, Michael, Elmankabadi, Seif B., Delman, Connor M., Biris, Kristin K., Bang, Heejung, Silverman, Jill L., Lee, Cassandra A., Christiansen, Blaine A.

“…People who sustain joint injuries such as anterior cruciate ligament (ACL) rupture often develop post-traumatic osteoarthritis (PTOA). In human patients, ACL…”
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Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size by Le Duc, Diana, Giulivi, Cecilia, Hiatt, Susan M, Napoli, Eleonora, Panoutsopoulos, Alexios, Harlan De Crescenzo, Angelo, Kotzaeridou, Urania, Syrbe, Steffen, Anagnostou, Evdokia, Azage, Meron, Bend, Renee, Begtrup, Amber, Brown, Natasha J, Büttner, Benjamin, Cho, Megan T, Cooper, Gregory M, Doering, Jan H, Dubourg, Christèle, Everman, David B, Hildebrand, Michael S, Santos, Francis Jeshira Reynoso, Kellam, Barbara, Keller-Ramey, Jennifer, Lemke, Johannes R, Liu, Shuxi, Niyazov, Dmitriy, Payne, Katelyn, Person, Richard, Quélin, Chloé, Schnur, Rhonda E, Smith, Brooke T, Strober, Jonathan, Walker, Susan, Wallis, Mathew, Walsh, Laurence, Yang, Sandra, Yuen, Ryan K C, Ziegler, Andreas, Sticht, Heinrich, Pride, Michael C, Orosco, Lori, Martínez-Cerdeño, Verónica, Silverman, Jill L, Crawley, Jacqueline N, Scherer, Stephen W, Zarbalis, Konstantinos S, Jamra, Rami

“…The underpinnings of mild to moderate neurodevelopmental delay remain elusive, often leading to late diagnosis and interventions. Here, we present data on…”
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MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndrome by Vogel Ciernia, Annie, Yasui, Dag H, Pride, Michael C, Durbin-Johnson, Blythe, Noronha, Adriana B, Chang, Alene, Knotts, Trina A, Rutkowsky, Jennifer R, Ramsey, Jon J, Crawley, Jacqueline N, LaSalle, Janine M

“…Abstract Mutations in the X-linked gene MECP2 cause the majority of Rett syndrome (RTT) cases. Two differentially spliced isoforms of exons 1 and 2 (MeCP2-e1…”
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