Esther B. E. Becker

发表

Autism spectrum disorder and the cerebellum.

Catherine J. Stoodley, C. Stoodley, Esther B. E. Becker, 2013, International review of neurobiology.

JNK Phosphorylation and Activation of BAD Couples the Stress-activated Signaling Pathway to the Cell Death Machinery*

Esther B. E. Becker, A. Bonni, Y. Konishi, 2002, The Journal of Biological Chemistry.

A gene expression signature in developing Purkinje cells predicts autism and intellectual disability co-morbidity status

Harry W. Clifford, C. Ponting, W. Haerty, 2019, Scientific Reports.

Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model

Jiannis Ragoussis, Andrea H. Németh, David Buck, 2013, Brain : a journal of neurology.

p38 MAP Kinase Mediates Apoptosis through Phosphorylation of BimEL at Ser-65*

Azad Bonni, Esther B. E. Becker, A. Bonni, 2006, Journal of Biological Chemistry.

A Conserved MST-FOXO Signaling Pathway Mediates Oxidative-Stress Responses and Extends Life Span

Judit Villén, Maria K. Lehtinen, Azad Bonni, 2006, Cell.

Consensus Paper: Cerebellar Development

Richard J. T. Wingate, William B. Dobyns, Roy V. Sillitoe, 2015, The Cerebellum.

Modeling Suggests TRPC3 Hydrogen Bonding and Not Phosphorylation Contributes to the Ataxia Phenotype of the Moonwalker Mouse

Sonya M. Hanson, Esther B. E. Becker, M. Sansom, 2015, Biochemistry.

Cerebellar involvement in autism and ADHD.

Esther B. E. Becker, M. Bucci, M. Bruchhage, 2018, Handbook of clinical neurology.

Functional expression of calcium‐permeable canonical transient receptor potential 4‐containing channels promotes migration of medulloblastoma cells

Esther B. E. Becker, V. Flockerzi, Yu-ping Lin, 2017, The Journal of physiology.

Induced pluripotent stem cell technology for modelling and therapy of cerebellar ataxia

Esther B. E. Becker, L. Watson, M. M. Wong, 2015, Open Biology.

From Mice to Men: TRPC3 in Cerebellar Ataxia

Esther B. E. Becker, 2015, The Cerebellum.

Reciprocal regulation of two G protein-coupled receptors sensing extracellular concentrations of Ca2+ and H+

Esther B. E. Becker, M. Glitsch, B. Jacobs, 2015, Proceedings of the National Academy of Sciences.

TRPC3 is a major contributor to functional heterogeneity of cerebellar Purkinje cells

Esther B. E. Becker, C. D. De Zeeuw, M. Schonewille, 2019, eLife.

TRPC3 is essential for functional heterogeneity of cerebellar Purkinje cells

C. I. Zeeuw, Esther B. E. Becker, M. Schonewille, 2018, bioRxiv.

Apoptosis Induced by p75NTR Overexpression Requires Jun Kinase-Dependent Phosphorylation of Bad

Esther B. E. Becker, P. Barker, A. Bonni, 2003, The Journal of Neuroscience.

Early Onset of Ataxia in Moonwalker Mice Is Accompanied by Complete Ablation of Type II Unipolar Brush Cells and Purkinje Cell Dysfunction

E. Mugnaini, M. Martina, Esther B. E. Becker, 2013, The Journal of Neuroscience.

Purkinje Cell Patterning—Insights from Single-Cell Sequencing

Esther B. E. Becker, Elizabeth J. Apsley, Elizabeth J Apsley, 2022, Cells.

Activation of FOXO1 by Cdk1 in Cycling Cells and Postmitotic Neurons

Esther B. E. Becker, Zengqiang Yuan, A. Bonni, 2008, Science.

Pin1 Mediates Neural-Specific Activation of the Mitochondrial Apoptotic Machinery

Esther B. E. Becker, A. Bonni, 2006, Neuron.

A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex

Z. Molnár, A. Hoerder-Suabedissen, Esther B. E. Becker, 2016, Neuron.

Contactin-associated protein-2 antibodies in non-paraneoplastic cerebellar ataxia

Esther B. E. Becker, A. Vincent, F. Sobott, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

Cerebellar Modelling Using Human Induced Pluripotent Stem

Esther B. E. Becker, S. Nayler, J. Jacob, 2022, Neuromethods.

Cell cycle regulation of neuronal apoptosis in development and disease

Esther B. E. Becker, A. Bonni, 2004, Progress in Neurobiology.

A JIP3-Regulated GSK3β/DCX Signaling Pathway Restricts Axon Branching

Esther B. E. Becker, O. Reiner, A. Bonni, 2010, The Journal of Neuroscience.

The Use of Stem Cell-Derived Neurons for Understanding Development and Disease of the Cerebellum

Esther B. E. Becker, S. Nayler, 2018, Front. Neurosci..

Beyond proliferation--cell cycle control of neuronal survival and differentiation in the developing mammalian brain.

Esther B. E. Becker, A. Bonni, 2005, Seminars in cell & developmental biology.

Recent advances in modelling of cerebellar ataxia using induced pluripotent stem cells

Esther B. E. Becker, L. Watson, M. M. Wong, 2017, Journal of neurology & neuromedicine.

High-resolution transcriptional landscape of xeno-free human induced pluripotent stem cell-derived cerebellar organoids

Esther B. E. Becker, R. Bowden, S. Nayler, 2021, Scientific Reports.

Single-cell sequencing of human iPSC-derived cerebellar organoids shows recapitulation of cerebellar development

Esther B. E. Becker, R. Bowden, S. Nayler, 2020, bioRxiv.

Pin1 in Neuronal Apoptosis

Esther B. E. Becker, A. Bonni, 2007, Cell cycle.

Oxr1 Is Essential for Protection against Oxidative Stress-Induced Neurodegeneration

K. Davies, P. Oliver, Esther B. E. Becker, 2011, PLoS genetics.

A gene expression signature in developing Purkinje cells predicts autism and intellectual disability co-morbidity status

Harry W. Clifford, C. Ponting, W. Haerty, 2019, Scientific Reports.

The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellum

K. Davies, P. Oliver, Esther B. E. Becker, 2015, Human molecular genetics.

Bim Regulation of Lumen Formation in Cultured Mammary Epithelial Acini Is Targeted by Oncogenes

Esther B. E. Becker, J. Brugge, A. Bonni, 2005, Molecular and Cellular Biology.

Characterization of the c-Jun N-Terminal Kinase-BimEL Signaling Pathway in Neuronal Apoptosis

Esther B. E. Becker, P. Barker, A. Bonni, 2004, The Journal of Neuroscience.

Deconstructing cerebellar development cell by cell

Esther B. E. Becker, S. Nayler, J. Jacob, 2020, PLoS genetics.

The Moonwalker Mouse: New Insights into TRPC3 Function, Cerebellar Development, and Ataxia

Esther B. E. Becker, 2014, The Cerebellum.

Caspr2 interacts with type 1 inositol 1,4,5-trisphosphate receptor in the developing cerebellum and regulates Purkinje cell morphology

Esther B. E. Becker, Abby L. Olsen, E. Lancaster, 2020, The Journal of Biological Chemistry.

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44

David Sims, Andrea H. Németh, Yvonne Wallis, 2017, American journal of human genetics.

A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice

E. Fisher, K. Davies, P. Oliver, 2009, Proceedings of the National Academy of Sciences.

AJIP3-RegulatedGSK3/DCXSignalingPathwayRestricts AxonBranching

Esther B. E. Becker, Parizad M. Bilimoria, 2010 .

Neurodegeneration in SCA14 is associated with increased PKCγ kinase activity, mislocalization and aggregation

Esther B. E. Becker, K. Talbot, G. Fuller, 2018, Acta Neuropathologica Communications.

A Simplified Method for Generating Purkinje Cells from Human-Induced Pluripotent Stem Cells

Esther B. E. Becker, L. Watson, S. Cowley, 2018, The Cerebellum.

Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?

Sonya M. Hanson, Esther B. E. Becker, B. Fogel, 2015, Movement disorders : official journal of the Movement Disorder Society.

Moonwalker Mouse

Esther B. E. Becker, 2021, Handbook of the Cerebellum and Cerebellar Disorders.

Genotype‐phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14

Esther B. E. Becker, N. Wood, S. Efthymiou, 2018, Movement disorders : official journal of the Movement Disorder Society.

TRPC 3 is a major contributor to functional heterogeneity of 1 cerebellar Purkinje cells 2 3

Esther B. E. Becker, M. Schonewille, H. Boele, 2022 .

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44

Esther B. E. Becker, P. Clouston, H. Houlden, 2017, American Journal of Human Genetics.

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44

Esther B. E. Becker, P. Clouston, H. Houlden, 2017, American journal of human genetics.

Candidate Screening of the TRPC3 Gene in Cerebellar Ataxia

D. Geschwind, K. Davies, Esther B. E. Becker, 2011, The Cerebellum.

PTCH1 mutant human cerebellar organoids are associated with altered neural development and early pathways of medulloblastoma oncogenesis

Esther B. E. Becker, S. Cowley, J. Jacob, 2023, bioRxiv.

Recent advances in modelling of cerebellar ataxia using induced pluripotent stem cells

Esther B. E. Becker, L. Watson, M. M. Wong, 2017, Journal of neurology & neuromedicine.

Cerebellar involvement in autism and ADHD.

Esther B. E. Becker, M. Bucci, M. Bruchhage, 2018, Handbook of clinical neurology.

Strathprints Institutional Repository (2016) a Transient Translaminar Gabaergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal a Transient Translaminar Gabaergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex a Transient Tran

A. Hoerder-Suabedissen, Esther B. E. Becker, S. Butt, 2022 .

Mutation of the Murine Ataxia Gene TRPC3 Causes Cerebellar Ataxia in Humans (P1.009)

Sonya M. Hanson, Esther B. E. Becker, B. Fogel, 2016, Neurology.