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Hanna C A Lammertse

Showing results (1-10 of 7) with videos related to

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Journal of Cell Science|October 17, 2022
Reduced dynamin-1 levels in neurons lacking MUNC18-1Hanna C A Lammertse, Alessandro Moro, Ingrid Saarloos, et al.
Brain : a Journal of Neurology|December 20, 2019
Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmissionHanna C A Lammertse, Annemiek A van Berkel, Michele Iacomino, et al.
Frontiers in Molecular Neuroscience|June 13, 2020
Dysregulated Prefrontal Cortex Inhibition in Prepubescent and Adolescent Fragile X Mouse ModelIoannis Kramvis, Rhodé van Westen, Hanna C A Lammertse, et al.
Molecular Psychiatry|March 4, 2026
Phenotypic diversity is caused by non-linear genetic interactions between two SNAREopathy genesJovana Kovačević, Sébastien Houy, Johny Pires, et al.
Molecular Psychiatry|November 17, 2022
Power and optimal study design in iPSC-based brain disease modellingJessie W Brunner, Hanna C A Lammertse, Annemiek A van Berkel, et al.
Cell Reports|May 16, 2019
A Single-Cell Model for Synaptic Transmission and Plasticity in Human iPSC-Derived NeuronsMarieke Meijer, Kristina Rehbach, Jessie W Brunner, et al.
Frontiers in Physiology|January 10, 2022
<i>STXBP1</i> Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEGSimon J Houtman, Hanna C A Lammertse, Annemiek A van Berkel, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of Cell Science|October 17, 2022
Reduced dynamin-1 levels in neurons lacking MUNC18-1Hanna C A Lammertse, Alessandro Moro, Ingrid Saarloos, et al.
Brain : a Journal of Neurology|December 20, 2019
Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmissionHanna C A Lammertse, Annemiek A van Berkel, Michele Iacomino, et al.
Frontiers in Molecular Neuroscience|June 13, 2020
Dysregulated Prefrontal Cortex Inhibition in Prepubescent and Adolescent Fragile X Mouse ModelIoannis Kramvis, Rhodé van Westen, Hanna C A Lammertse, et al.
Molecular Psychiatry|March 4, 2026
Phenotypic diversity is caused by non-linear genetic interactions between two SNAREopathy genesJovana Kovačević, Sébastien Houy, Johny Pires, et al.
Molecular Psychiatry|November 17, 2022
Power and optimal study design in iPSC-based brain disease modellingJessie W Brunner, Hanna C A Lammertse, Annemiek A van Berkel, et al.
Cell Reports|May 16, 2019
A Single-Cell Model for Synaptic Transmission and Plasticity in Human iPSC-Derived NeuronsMarieke Meijer, Kristina Rehbach, Jessie W Brunner, et al.
Frontiers in Physiology|January 10, 2022
<i>STXBP1</i> Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEGSimon J Houtman, Hanna C A Lammertse, Annemiek A van Berkel, et al.
Pageof 1