Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jessie W. Brunner"'
Autor:
Marieke Meijer, Kristina Rehbach, Jessie W. Brunner, Jessica A. Classen, Hanna C.A. Lammertse, Lola A. van Linge, Desiree Schut, Tamara Krutenko, Matthias Hebisch, L. Niels Cornelisse, Patrick F. Sullivan, Michael Peitz, Ruud F. Toonen, Oliver Brüstle, Matthijs Verhage
Publikováno v:
Cell Reports, Vol 27, Iss 7, Pp 2199-2211.e6 (2019)
Summary: Synaptic dysfunction is associated with many brain disorders, but robust human cell models to study synaptic transmission and plasticity are lacking. Instead, current in vitro studies on human neurons typically rely on spontaneous synaptic e
Externí odkaz:
https://doaj.org/article/20c05e78a6744a9bb42bc89f2c5fbe99
Autor:
Jessie W, Brunner, Hanna C A, Lammertse, Annemiek A, van Berkel, Frank, Koopmans, Ka Wan, Li, August B, Smit, Ruud F, Toonen, Matthijs, Verhage, Sophie, van der Sluis
Publikováno v:
Molecular psychiatry.
Studies using induced pluripotent stem cells (iPSCs) are gaining momentum in brain disorder modelling, but optimal study designs are poorly defined. Here, we compare commonly used designs and statistical analysis for different research aims. Furtherm
Autor:
Jessie W. Brunner, Hanna C. A. Lammertse, Annemiek A. van Berkel, Frank Koopmans, Ka Wan Li, August B. Smit, Ruud F. Toonen, Matthijs Verhage, Sophie van der Sluis
Publikováno v:
Molecular Psychiatry. Nature Publishing Group
Molecular Psychiatry, 28(4), 1-12. Nature Publishing Group
Brunner, J W, Lammertse, H C A, van Berkel, A A, Koopmans, F, Li, K W, Smit, A B, Toonen, R F, Verhage, M & van der Sluis, S 2022, ' Power and optimal study design in iPSC-based brain disease modelling ', Molecular Psychiatry . https://doi.org/10.1038/s41380-022-01866-3
Brunner, J W, Lammertse, H C A, van Berkel, A A, Koopmans, F, Li, K W, Smit, A B, Toonen, R F, Verhage, M & van der Sluis, S 2022, ' Power and optimal study design in iPSC-based brain disease modelling ', Molecular Psychiatry, vol. 28, no. 4, pp. 1-12 . https://doi.org/10.1038/s41380-022-01866-3
Molecular Psychiatry, 28(4), 1-12. Nature Publishing Group
Brunner, J W, Lammertse, H C A, van Berkel, A A, Koopmans, F, Li, K W, Smit, A B, Toonen, R F, Verhage, M & van der Sluis, S 2022, ' Power and optimal study design in iPSC-based brain disease modelling ', Molecular Psychiatry . https://doi.org/10.1038/s41380-022-01866-3
Brunner, J W, Lammertse, H C A, van Berkel, A A, Koopmans, F, Li, K W, Smit, A B, Toonen, R F, Verhage, M & van der Sluis, S 2022, ' Power and optimal study design in iPSC-based brain disease modelling ', Molecular Psychiatry, vol. 28, no. 4, pp. 1-12 . https://doi.org/10.1038/s41380-022-01866-3
Studies using induced pluripotent stem cells (iPSCs) are gaining momentum in brain disorder modelling, but optimal study designs are poorly defined. Here, we compare commonly used designs and statistical analysis for different research aims. Furtherm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd5a644e41b17aed3c3d99f59d054545
https://research.vumc.nl/en/publications/4ea06ae6-37eb-47d8-a72c-3e93968cbb63
https://research.vumc.nl/en/publications/4ea06ae6-37eb-47d8-a72c-3e93968cbb63
Autor:
Ka Wan Li, Fatima Farzana, Frank Koopmans, August B. Smit, Jessie W. Brunner, Silvia Oldani, Matthijs Verhage, Marinka Brouwer, Ruud F. Toonen, Ning Chen, Jan R.T. van Weering
Publikováno v:
Brouwer, M, Farzana, F, Koopmans, F, Chen, N, Brunner, J W, Oldani, S, Li, K W, van Weering, J R T, Smit, A B, Toonen, R F & Verhage, M 2019, ' SALM1 controls synapse development by promoting F-actin/PIP2-dependent Neurexin clustering ', EMBO Journal, vol. 38, no. 17, e101289 . https://doi.org/10.15252/embj.2018101289
EMBO Journal, 38(17):e101289, 1-20. Nature Publishing Group
EMBO Journal, 38(17):e101289. Wiley-Blackwell
Brouwer, M, Farzana, F, Koopmans, F, Chen, N, Brunner, J W, Oldani, S, Li, K W, van Weering, J R, Smit, A B, Toonen, R F & Verhage, M 2019, ' SALM1 controls synapse development by promoting F-actin/PIP2-dependent Neurexin clustering ', EMBO Journal, vol. 38, no. 17, e101289, pp. 1-20 . https://doi.org/10.15252/embj.2018101289
The EMBO Journal
EMBO Journal, 38(17):e101289, 1-20. Nature Publishing Group
EMBO Journal, 38(17):e101289. Wiley-Blackwell
Brouwer, M, Farzana, F, Koopmans, F, Chen, N, Brunner, J W, Oldani, S, Li, K W, van Weering, J R, Smit, A B, Toonen, R F & Verhage, M 2019, ' SALM1 controls synapse development by promoting F-actin/PIP2-dependent Neurexin clustering ', EMBO Journal, vol. 38, no. 17, e101289, pp. 1-20 . https://doi.org/10.15252/embj.2018101289
The EMBO Journal
Synapse development requires spatiotemporally regulated recruitment of synaptic proteins. In this study, we describe a novel presynaptic mechanism of cis‐regulated oligomerization of adhesion molecules that controls synaptogenesis. We identified sy
Autor:
L. Niels Cornelisse, Hanna C.A. Lammertse, Ruud F. Toonen, Oliver Brüstle, Tamara Krutenko, Marieke Meijer, Kristina Rehbach, Jessie W. Brunner, Jessica Classen, Patrick F. Sullivan, Desiree Schut, Matthias Hebisch, Matthijs Verhage, Michael Peitz, Lola A. van Linge
Publikováno v:
Cell Reports
Cell Reports, Vol 27, Iss 7, Pp 2199-2211.e6 (2019)
Cell Reports, 27(7), 2199-2211.e6. Cell Press
Meijer, M, Rehbach, K, Brunner, J W, Classen, J A, Lammertse, H C A, van Linge, L A, Schut, D, Krutenko, T, Hebisch, M, Cornelisse, L N, Sullivan, P F, Peitz, M, Toonen, R F, Brüstle, O & Verhage, M 2019, ' A Single-Cell Model for Synaptic Transmission and Plasticity in Human iPSC-Derived Neurons ', Cell Reports, vol. 27, no. 7, pp. 2199-2211.e6 . https://doi.org/10.1016/j.celrep.2019.04.058
Cell Reports, Vol 27, Iss 7, Pp 2199-2211.e6 (2019)
Cell Reports, 27(7), 2199-2211.e6. Cell Press
Meijer, M, Rehbach, K, Brunner, J W, Classen, J A, Lammertse, H C A, van Linge, L A, Schut, D, Krutenko, T, Hebisch, M, Cornelisse, L N, Sullivan, P F, Peitz, M, Toonen, R F, Brüstle, O & Verhage, M 2019, ' A Single-Cell Model for Synaptic Transmission and Plasticity in Human iPSC-Derived Neurons ', Cell Reports, vol. 27, no. 7, pp. 2199-2211.e6 . https://doi.org/10.1016/j.celrep.2019.04.058
Summary: Synaptic dysfunction is associated with many brain disorders, but robust human cell models to study synaptic transmission and plasticity are lacking. Instead, current in vitro studies on human neurons typically rely on spontaneous synaptic e