Peter Kind
Affiliations: | University of Edinburgh, Edinburgh, Scotland, United Kingdom |
Area:
Developmental NeuroscienceGoogle:
"Peter Kind"Mean distance: 13.38 (cluster 6) | S | N | B | C | P |
Parents
Sign in to add mentor| Colin Blakemore | grad student | 1993 | Oxford |
| Susan J. Hockfield | post-doc | 1993-1997 | Yale |
| Colin Blakemore | post-doc | 1997-2000 | Oxford |
Children
Sign in to add trainee| Daniel Giffney | research assistant | Edinburgh | |
| Tommas J. Ellender | research assistant | 2003-2004 | Edinburgh |
| Chih-Yuan Chiang | grad student | 2011- | Edinburgh |
| Sally Till | post-doc | 2006- | Edinburgh |
Collaborators
Sign in to add collaboratorSumantra ShonaChattarji |
collaborator | Edinburgh | |
| Anis Contractor | collaborator | Northwestern | |
| Kathryn M. Murphy | collaborator | McMaster University | |
| Frank Sengpiel | collaborator |
BETA: Related publications
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Publications
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| Zoupi L, Booker SA, Eigel D, et al. (2021) Selective vulnerability of inhibitory networks in multiple sclerosis. Acta Neuropathologica |
| Wong H, Hooper AWM, Niibori Y, et al. (2020) Sexually dimorphic patterns in electroencephalography power spectrum and autism-related behaviors in a rat model of fragile X syndrome. Neurobiology of Disease. 105118 |
| Booker SA, Simões de Oliveira L, Anstey NJ, et al. (2020) Input-Output Relationship of CA1 Pyramidal Neurons Reveals Intact Homeostatic Mechanisms in a Mouse Model of Fragile X Syndrome. Cell Reports. 32: 107988 |
| Das Sharma S, Pal R, Reddy BK, et al. (2020) Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patterns. Molecular Autism. 11: 52 |
| Mastro TL, Preza A, Basu S, et al. (2020) A sex difference in the response of the rodent postsynaptic density to synGAP haploinsufficiency. Elife. 9 |
| Booker SA, Domanski APF, Dando OR, et al. (2019) Altered dendritic spine function and integration in a mouse model of fragile X syndrome. Nature Communications. 10: 4813 |
| Domanski APF, Booker SA, Wyllie DJA, et al. (2019) Cellular and synaptic phenotypes lead to disrupted information processing in Fmr1-KO mouse layer 4 barrel cortex. Nature Communications. 10: 4814 |
| Asiminas A, Jackson AD, Louros SR, et al. (2019) Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X Syndrome. Science Translational Medicine. 11 |
| Strehlow V, Heyne HO, Vlaskamp DRM, et al. (2018) GRIN2A-related disorders: genotype and functional consequence predict phenotype. Brain : a Journal of Neurology |
| McKay S, Ryan TJ, McQueen J, et al. (2018) The Developmental Shift of NMDA Receptor Composition Proceeds Independently of GluN2 Subunit-Specific GluN2 C-Terminal Sequences. Cell Reports. 25: 841-851.e4 |