Esther B E Becker

Affiliations: 
University of Oxford, Oxford, United Kingdom 
Area:
Cerebellum, Development, Ataxia, Autism
Website:
http://www.dpag.ox.ac.uk/academic_staff/esther_becker/
Google:
"Esther Becker"
Mean distance: 16.05 (cluster 28)
 
SNBCP

Parents

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Azad Bonni grad student 2000-2005 Harvard
 (Signaling mechanisms regulating neuronal apoptosis.)
Kay Elizabeth Davies post-doc 2006-2010 Oxford

Children

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Norbert Lidzba research assistant 2012- Oxford
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Publications

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Clifford H, Dulneva A, Ponting CP, et al. (2019) A gene expression signature in developing Purkinje cells predicts autism and intellectual disability co-morbidity status. Scientific Reports. 9: 485
Bruchhage MMK, Bucci MP, Becker EBE. (2018) Cerebellar involvement in autism and ADHD. Handbook of Clinical Neurology. 155: 61-72
Wei WC, Huang WC, Lin YP, et al. (2017) Functional expression of calcium-permeable Canonical Transient Receptor Potential 4-containing channels promotes migration of medulloblastoma cells. The Journal of Physiology
Leto K, Arancillo M, Becker EB, et al. (2015) Consensus Paper: Cerebellar Development. Cerebellum (London, England)
Wei WC, Jacobs B, Becker EB, et al. (2015) Reciprocal regulation of two G protein-coupled receptors sensing extracellular concentrations of Ca2+ and H. Proceedings of the National Academy of Sciences of the United States of America
Hanson SM, Sansom MS, Becker EB. (2015) Modeling Suggests TRPC3 Hydrogen Bonding and Not Phosphorylation Contributes to the Ataxia Phenotype of the Moonwalker Mouse. Biochemistry. 54: 4033-41
Dulneva A, Lee S, Oliver PL, et al. (2015) The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellum. Human Molecular Genetics. 24: 4114-25
Fogel BL, Hanson SM, Becker EB. (2015) Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans? Movement Disorders : Official Journal of the Movement Disorder Society. 30: 284-6
Sekerková G, Kim JA, Nigro MJ, et al. (2013) Early onset of ataxia in moonwalker mice is accompanied by complete ablation of type II unipolar brush cells and Purkinje cell dysfunction. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 19689-94
Németh AH, Kwasniewska AC, Lise S, et al. (2013) Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model. Brain : a Journal of Neurology. 136: 3106-18
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