Items where authors include "Clapcote, SJ"

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Number of items: 25.

Article

Clapcote, SJ orcid.org/0000-0002-6662-5690 (2022) How can we obtain truly translational mouse models to improve clinical outcomes in schizophrenia? Disease Models & Mechanisms, 15 (11). dmm049970. ISSN 1754-8403

Al-Amri, AH, Armstrong, P orcid.org/0000-0001-8735-3762, Amici, M et al. (22 more authors) (2022) PDZD8 Disruption Causes Cognitive Impairment in Humans, Mice and Fruit Flies. Biological Psychiatry, 92 (4). pp. 323-334. ISSN 0006-3223

Hughes, RB, Whittingham-Dowd, J, Clapcote, SJ orcid.org/0000-0002-6662-5690 et al. (2 more authors) (2022) Altered medial prefrontal cortex and dorsal raphé activity predict genotype and correlate with abnormal learning behavior in a mouse model of autism-associated 2p16.3 deletion. Autism research : official journal of the International Society for Autism Research, 15 (4). pp. 614-627. ISSN 1939-3792

Wilkinson, ID, Mahmood, T, Yasmin, SF et al. (11 more authors) (2022) In memory of Professor Iain Wilkinson: cognitive and neuroimaging endophenotypes in a consanguineous schizophrenia multiplex family. Psychological Medicine. PII S0033291721005250. ISSN 0033-2917

Ng, HWY, Ogbeta, JA and Clapcote, SJ orcid.org/0000-0002-6662-5690 (2021) Genetically altered animal models for ATP1A3-related disorders. Disease Models and Mechanisms, 14 (10). dmm048938. ISSN 1754-8403

Hosalli, P, Cardno, A orcid.org/0000-0002-6136-5965, Brewin, A et al. (4 more authors) (2021) Risk of psychosis in Yorkshire African, Caribbean and Mixed Ethnic communities. Journal of Psychiatric Intensive Care, 17 (2). pp. 107-111. ISSN 1742-6464

Cole, BA, Clapcote, SJ, Muench, SP et al. (1 more author) (2021) Targeting KNa1.1 channels in KCNT1-associated epilepsy. Trends in Pharmacological Sciences. ISSN 0165-6147

Mahmood, T, El-Asrag, ME, Poulter, JA orcid.org/0000-0003-2048-5693 et al. (19 more authors) (2020) A recessively inherited risk locus on chromosome 13q22-31 conferring susceptibility to schizophrenia. Schizophrenia Bulletin. ISSN 0586-7614

Hughes, RB, Whittingham-Dowd, J, Simmons, RE et al. (3 more authors) (2020) Ketamine Restores Thalamic-Prefrontal Cortex Functional Connectivity in a Mouse Model of Neurodevelopmental Disorder-Associated 2p16.3 Deletion. Cerebral Cortex, 30 (4). pp. 2358-2371. ISSN 1047-3211

Al-Amri, AH, Al Saegh, A, Al-Mamari, W et al. (10 more authors) (2019) LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics, 62 (12). 103592. ISSN 1769-7212

Pervolaraki, E, Tyson, AL, Pibiri, F et al. (7 more authors) (2019) The within-subject application of diffusion tensor MRI and CLARITY reveals brain structural changes in Nrxn2 deletion mice. Molecular Autism, 10 (1). ARTN 8. ISSN 2040-2392

Alsaady, I, Tedford, E, Alsaad, M et al. (8 more authors) (2019) Downregulation of the central noradrenergic system by Toxoplasma gondii infection. Infection and Immunity, 87 (2). e00789-18. ISSN 0019-9567

Timothy, JWS, Klas, N, Sanghani, HR et al. (8 more authors) (2018) Circadian Disruptions in the Myshkin Mouse Model of Mania Are Independent of Deficits in Suprachiasmatic Molecular Clock Function. Biological Psychiatry, 84 (11). pp. 827-837. ISSN 0006-3223

Cheung, SY, Henrot, M, Al-Saad, M et al. (17 more authors) (2018) TRPC4/TRPC5 channels mediate adverse reaction to the cancer cell cytotoxic agent (-)-Englerin A. Oncotarget, 9 (51). pp. 29634-29643. ISSN 1949-2553

Al-Amri, A, Saegh, AA, Al-Mamari, W et al. (6 more authors) (2016) Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. American Journal of Medical Genetics Part A, 170 (7). pp. 1826-1831. ISSN 1552-4825

Kirshenbaum, GS, Idris, NF, Dachtler, J et al. (2 more authors) (2016) Deficits in social behavioral tests in a mouse model of alternating hemiplegia of childhood. Journal of Neurogenetics, 30 (1). pp. 42-49. ISSN 0167-7063

McGirr, A, Lipina, TV, Mun, HS et al. (11 more authors) (2016) Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition. Neuropsychopharmacology, 41. pp. 1080-1092. ISSN 0893-133X

Dachtler, J, Elliott, C, Rodgers, RJ et al. (2 more authors) (2016) Missense mutation in DISC1 C-terminal coiled-coil has GSK3β signaling and sex-dependent behavioral effects in mice. Scientific Reports, 6. 18748. ISSN 2045-2322

Kirshenbaum, GS, Dachtler, JD, Roder, JC et al. (1 more author) (2016) Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood. Neurogenetics, 17 (1). pp. 57-63. ISSN 1364-6745

Kirshenbaum, GS, Dachtler, J, Roder, JC et al. (1 more author) (2015) Characterization of Cognitive Deficits in Mice with an Alternating Hemiplegia-Linked Mutation. Behavioral Neuroscience, 129 (6). pp. 822-831. ISSN 0735-7044

Dachtler, J, Ivorra, JL, Rowland, TE et al. (3 more authors) (2015) Heterozygous Deletion of α-Neurexin I or α-Neurexin II Results in Behaviors Relevant to Autism and Schizophrenia. Behavioral Neuroscience, 129 (6). 765 - 776. ISSN 0735-7044

Dachtler, J, Glasper, J, Cohen, RN et al. (6 more authors) (2014) Deletion of α-neurexin II results in autism-related behaviors in mice. Translational Psychiatry, 4 (11). e484. e484 - ?. ISSN 2158-3188

Chandran, JS, Kazanis, I, Clapcote, SJ et al. (4 more authors) (2014) Disc1 variation leads to specific alterations in adult neurogenesis. PLoS ONE, 9 (10). ARTN e108088. ISSN 1932-6203

Ritchie, DJ and Clapcote, SJ (2013) Disc1 deletion is present in Swiss-derived inbred mouse strains: implications for transgenic studies of learning and memory. Laboratory Animals, 47 (3). 162 - 167. ISSN 0023-6772

Edwards, IJ, Bruce, G, Lawrenson, C et al. (4 more authors) (2013) Na+/K+ ATPase α1 and α3 Isoforms Are Differentially Expressed in α- and γ-Motoneurons. Journal of Neuroscience, 33 (24). 9913 - 9919. ISSN 0270-6474

This list was generated on Sat Mar 23 11:37:22 2024 GMT.