Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Publications

TRPC3 signalling contributes to the biogenesis of extracellular vesicles

BECKER E., (2024), Journal of Extracellular Biology

PTCH1-mutant human cerebellar organoids exhibit altered neural development and recapitulate early medulloblastoma tumorigenesis.

van Essen MJ. et al, (2024), Dis Model Mech, 17

Detailed Analysis of ITPR1 Missense Variants Guides Diagnostics and Therapeutic Design.

Tolonen JP. et al, (2023), Mov Disord

Modulation and Regulation of Canonical Transient Receptor Potential 3 (TRPC3) Channels.

Cole BA. and Becker EBE., (2023), Cells, 12

PTCH1mutant human cerebellar organoids are associated with altered neural development and early pathways of medulloblastoma oncogenesis

van Essen MJ. et al, (2023)

Moonwalker Mouse

Ibrahim MF. and Becker EBE., (2023), Essentials of Cerebellum and Cerebellar Disorders: A Primer For Graduate Students, Second Edition, 441 - 447

Purkinje Cell Patterning-Insights from Single-Cell Sequencing.

Apsley EJ. and Becker EBE., (2022), Cells, 11

Cerebellar Modelling Using Human Induced Pluripotent Stem Cells

van Essen MJ. et al, (2022), Neuromethods, 177, 1 - 21

MODELLING SHH-MEDULLOBLASTOMA USING CEREBELLAR ORGANOIDS

van Essen M. et al, (2022), NEURO-ONCOLOGY, 24, 2 - 2

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

Nayler S. et al, (2021), Scientific Reports, 11

Moonwalker Mouse

Becker EBE., (2021), Handbook of the Cerebellum and Cerebellar Disorders: Second Edition: Volume 3, 1773 - 1788

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

Argent L. et al, (2020), J Biol Chem, 295, 12716 - 12726

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

Nayler S. et al, (2020)

Deconstructing cerebellar development cell by cell

Van Essen M. et al, (2020), PLoS Genetics

Deconstructing cerebellar development cell by cell.

van Essen MJ. et al, (2020), PLoS Genet, 16

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

Wu B. et al, (2019), Elife, 8

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

Clifford H. et al, (2019), Sci Rep, 9

TRPC3 is essential for functional heterogeneity of cerebellar Purkinje cells

Wu B. et al, (2018)

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

Wong MMK. et al, (2018), Acta Neuropathol Commun, 6

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

Watson LM. et al, (2018), Cerebellum, 17, 419 - 427

Load More

Include forthcoming?