Search Results - "PAYLOR, R"

Altered anxiety‐related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome by Spencer, C. M., Alekseyenko, O., Serysheva, E., Yuva‐Paylor, L. A., Paylor, R.

“…The loss of fragile X mental retardation (FMR1) gene function causes fragile X syndrome (FXS), a common mental retardation syndrome. Anxiety and abnormal…”
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Estimating Surface/Subsurface Sediment Mixing in Karst Settings Using 7Be Isotopes by Wicks, C. M., Paylor, R. L., Bentley, S. J.

“…This study shows that the cosmogenic radionuclide beryllium‐7 can be used to track sediment movement through caves. The activities of beryllium‐7 and…”
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The use of behavioral test batteries, II: Effect of test interval by Paylor, Richard, Spencer, Corinne M., Yuva-Paylor, Lisa A., Pieke-Dahl, Sandra

“…Test batteries are commonly used to assess the behavioral phenotype of genetically modified and inbred strains of mice. However, few systematic studies have…”
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Inbred strain differences in prepulse inhibition of the mouse startle response by Paylor, R, Crawley, J N

“…Prepulse inhibition is the phenomenon in which a weak prepulse stimulus suppresses the response to a startling stimulus. Patients with schizophrenia have…”
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Mouse genetic models for prepulse inhibition: an early review by GEYER, M. A, MCLLWAIN, K. L, PAYLOR, R

“…Prepulse inhibition (PPI) is the phenomenon in which a weak prepulse stimulus attenuates the response to a subsequent startling stimulus. Patients with…”
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Fmr1 knockout mice are impaired in a leverpress escape/avoidance task by Brennan, F. X., Albeck, D. S., Paylor, R.

“…Fragile X syndrome (FXS) is the most common form of inherited mental retardation (MR). FXS is typically caused by a mutation of the Fmr1 gene (Verkerk et al…”
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Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments by PAYLOR, Richard, MCILWAIN, Kellie L, MCANINCH, Robin, NELLIS, Anna, YUVA-PAYLOR, Lisa A, BALDINI, Antonio, LINDSAY, Elizabeth A

“…Del22q11 syndrome is caused by heterozygous deletion of an approximately 3 Mb segment of chromosome 22q11.2. Children diagnosed with del22q11 syndrome commonly…”
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Expanded characterization of the social interaction abnormalities in mice lacking Dvl1 by Long, J. M., LaPorte, P., Paylor, R., Wynshaw‐Boris, A.

“…Dvl1 is one of three murine Dishevelled genes widely expressed in embryonic development and in the adult central nervous system. Dishevelled proteins are a…”
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Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies by Crawley, J N, Belknap, J K, Collins, A, Crabbe, J C, Frankel, W, Henderson, N, Hitzemann, R J, Maxson, S C, Miner, L L, Silva, A J, Wehner, J M, Wynshaw-Boris, A, Paylor, R

“…Choosing the best genetic strains of mice for developing a new knockout or transgenic mouse requires extensive knowledge of the endogenous traits of inbred…”
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Role of neuronal nicotinic receptors in the effects of nicotine and ethanol on contextual fear conditioning by Wehner, J.M., Keller, J.J., Keller, A.B., Picciotto, M.R., Paylor, R., Booker, T.K., Beaudet, A., Heinemann, S.F., Balogh, S.A.

“…Nicotine can enhance contextual learning while ethanol impairs some forms of learning. Nicotine can overcome some of the impairing effects of ethanol when the…”
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Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity by Fletcher, Colin F., Tottene, Angelita, Lennon, Vanda A., Wilson, Scott M., Dubel, Stefan J., Paylor, Richard, Hosford, David A., Tessarollo, Lino, McEnery, Maureen W., Pietrobon, Daniela, Copeland, Neal G., Jenkins, Nancy A.

“…ABSTRACT P/Q‐type voltage‐dependent calcium channel CACNA1A mutations cause dominantly inherited migraine, episodic ataxia, and cerebellar atrophy in humans…”
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Impaired passive avoidance learning in mice lacking central neuronal nicotinic acetylcholine receptors by Marubio, L.M., Paylor, R.

“…The nicotinic cholinergic system influences cognition, anxiety, locomotion, and addiction by acting upon nicotinic acetylcholine receptors (nAChRs). To date,…”
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The DBA/2J strain and prepulse inhibition of startle: a model system to test antipsychotics? by Olivier, B, Leahy, C, Mullen, T, Paylor, R, Groppi, V E, Sarnyai, Z, Brunner, D

“…Prepulse inhibition (PPI) of the startle response in mice is increasingly used as a paradigm of sensory gating with potential predictive and construct validity…”
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Mutant Mice Lacking the γ Isoform of Protein Kinase C Show Decreased Behavioral Actions of Ethanol and Altered Function of γ-Aminobutyrate Type A Receptors by Harris, R. Adron, McQuilkin, Susan J., Paylor, Richard, Abeliovich, Asa, Tonegawa, Susumu, Wehner, Jeanne M.

“…Calcium/phospholipid-dependent protein kinase (protein kinase C, PKC) has been suggested to play a role in the sensitivity of γ-aminobutyrate type A (GABAA)…”
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DBA/2 and C57BL/6 Mice Differ in Contextual Fear but Not Auditory Fear Conditioning by Paylor, Richard, Tracy, Ryan, Wehner, Jeanne, Rudy, Jerry W

“…It has been proposed that DBA/2 and C57BL/6 mice perform differently on some learning and memory tasks because of functional differences in the hippocampal…”
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Deletion of 150 kb in the Minimal Digeorge/Velocardiofacial Syndrome Critical Region in Mouse by Kimber, Wendy L., Hsieh, Patrick, Hirotsune, Shinji, Yuva-Paylor, Lisa, Sutherland, Helen F., Chen, Amy, Ruiz-Lozano, Pilar, Hoogstraten-Miller, Shelley L., Chien, Kenneth R., Paylor, Richard, Scambler, Peter J., Wynshaw-Boris, Anthony

“…Deletions or rearrangements of human chromosome 22q11 lead to a variety of related clinical syndromes such as DiGeorge syndrome (DGS) and velocardiofacial…”
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Estimating Surface/Subsurface Sediment Mixing in Karst Settings Using 7 Be Isotopes by Wicks, C. M., Paylor, R. L., Bentley, S. J.

“…Abstract This study shows that the cosmogenic radionuclide beryllium‐7 can be used to track sediment movement through caves. The activities of beryllium‐7 and…”
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Pitfalls in the interpretation of genetic and pharmacological effects on anxiety-like behaviour in rodents by Bouwknecht, Jan Adriaan, Paylor, Richard

“…Over the last 15 years, genetically modified mice have added important data to our knowledge on psychiatric diseases including anxiety. This has produced many…”
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Acute Toxic Leukoencephalopathy: Potential for Reversibility Clinically and on MRI With Diffusion-Weighted and FLAIR Imaging by McKinney, Alexander M, Kieffer, Stephen A, Paylor, Rogerich T, SantaCruz, Karen S, Kendi, Ayse, Lucato, Leandro

“…Toxic leukoencephalopathy may present acutely or subacutely with symmetrically reduced diffusion in the periventricular and supraventricular white matter,…”
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Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome by Moretti, Paolo, Bouwknecht, J. Adriaan, Teague, Ryan, Paylor, Richard, Zoghbi, Huda Y.

“…Rett syndrome (RTT) is an autistic spectrum disorder with a known genetic basis. RTT is caused by loss of function mutations in the X-linked gene MECP2 and is…”
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