Kim H, Lee K, Yoo K, Kim J, Kim H, Lim C
Mol Neurobiol. 2025; .
PMID: 39920439
DOI: 10.1007/s12035-025-04734-7.
Wang W, Williams D, Teoh J, Soundararajan D, Zuberi A, Lutz C
Proc Natl Acad Sci U S A. 2024; 121(42):e2400709121.
PMID: 39374387
PMC: 11494352.
DOI: 10.1073/pnas.2400709121.
Patt L, Tascio D, Domingos C, Timmermann A, Jabs R, Henneberger C
Int J Mol Sci. 2023; 24(17).
PMID: 37686294
PMC: 10488269.
DOI: 10.3390/ijms241713490.
de Rosa R, Valastro S, Cambria C, Barbiero I, Puricelli C, Tramarin M
Int J Mol Sci. 2023; 24(1).
PMID: 36613509
PMC: 9820583.
DOI: 10.3390/ijms24010068.
Imam N, Choudhury S, Hemmen K, Heinze K, Schindelin H
Biophys Rep (N Y). 2022; 2(4):100079.
PMID: 36425671
PMC: 9680708.
DOI: 10.1016/j.bpr.2022.100079.
Activity-Induced Cortical Glutamatergic Neuron Nascent Proteins.
Schiapparelli L, Xie Y, Sharma P, McClatchy D, Ma Y, Yates 3rd J
J Neurosci. 2022; 42(42):7900-7920.
PMID: 36261270
PMC: 9617616.
DOI: 10.1523/JNEUROSCI.0707-22.2022.
Differential modulation of collybistin conformational dynamics by the closely related GTPases Cdc42 and TC10.
Imam N, Choudhury S, Heinze K, Schindelin H
Front Synaptic Neurosci. 2022; 14:959875.
PMID: 35989712
PMC: 9386560.
DOI: 10.3389/fnsyn.2022.959875.
Gene Therapy: Novel Approaches to Targeting Monogenic Epilepsies.
Goodspeed K, Bailey R, Prasad S, Sadhu C, Cardenas J, Holmay M
Front Neurol. 2022; 13:805007.
PMID: 35847198
PMC: 9284605.
DOI: 10.3389/fneur.2022.805007.
Human ARHGEF9 intellectual disability syndrome is phenocopied by a mutation that disrupts collybistin binding to the GABA receptor α2 subunit.
Hines D, Contreras A, Garcia B, Barker J, Boren A, El Achkar C
Mol Psychiatry. 2022; 27(3):1729-1741.
PMID: 35169261
PMC: 9095487.
DOI: 10.1038/s41380-022-01468-z.
Gephyrin-Lacking PV Synapses on Neocortical Pyramidal Neurons.
Kuljis D, Micheva K, Ray A, Wegner W, Bowman R, Madison D
Int J Mol Sci. 2021; 22(18).
PMID: 34576197
PMC: 8467468.
DOI: 10.3390/ijms221810032.
A proline-rich motif in the large intracellular loop of the glycine receptor α1 subunit interacts with the Pleckstrin homology domain of collybistin.
Breitinger U, Weinlander K, Pechmann Y, Langlhofer G, Enz R, Becker C
J Adv Res. 2021; 29:95-106.
PMID: 33842008
PMC: 8020344.
DOI: 10.1016/j.jare.2020.09.009.
Plasticity in the Hippocampus, Neurogenesis and Drugs of Abuse.
Avchalumov Y, Mandyam C
Brain Sci. 2021; 11(3).
PMID: 33810204
PMC: 8004884.
DOI: 10.3390/brainsci11030404.
The role of GABAergic signalling in neurodevelopmental disorders.
Tang X, Jaenisch R, Sur M
Nat Rev Neurosci. 2021; 22(5):290-307.
PMID: 33772226
PMC: 9001156.
DOI: 10.1038/s41583-021-00443-x.
Neuroligin-2 dependent conformational activation of collybistin reconstituted in supported hybrid membranes.
Schafer J, Forster L, Mey I, Papadopoulos T, Brose N, Steinem C
J Biol Chem. 2020; 295(52):18604-18613.
PMID: 33127642
PMC: 7939476.
DOI: 10.1074/jbc.RA120.015347.
Quantitative Synaptic Biology: A Perspective on Techniques, Numbers and Expectations.
Reshetniak S, Fernandez-Busnadiego R, Muller M, Rizzoli S, Tetzlaff C
Int J Mol Sci. 2020; 21(19).
PMID: 33023247
PMC: 7582872.
DOI: 10.3390/ijms21197298.
Impaired Glycine Receptor Trafficking in Neurological Diseases.
Schaefer N, Roemer V, Janzen D, Villmann C
Front Mol Neurosci. 2018; 11:291.
PMID: 30186111
PMC: 6110938.
DOI: 10.3389/fnmol.2018.00291.
Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system.
Gamlin C, Yu W, Wong R, Hoon M
Neural Dev. 2018; 13(1):12.
PMID: 29875009
PMC: 5991458.
DOI: 10.1186/s13064-018-0109-6.
Common Ribs of Inhibitory Synaptic Dysfunction in the Umbrella of Neurodevelopmental Disorders.
Ali Rodriguez R, Joya C, Hines R
Front Mol Neurosci. 2018; 11:132.
PMID: 29740280
PMC: 5928253.
DOI: 10.3389/fnmol.2018.00132.
Synaptic Plasticity and Excitation-Inhibition Balance in the Dentate Gyrus: Insights from Recordings in Neuroligin-1, Neuroligin-2, and Collybistin Knockouts.
Jedlicka P, Muellerleile J, Schwarzacher S
Neural Plast. 2018; 2018:6015753.
PMID: 29670649
PMC: 5835277.
DOI: 10.1155/2018/6015753.
ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation.
Wang J, Zhou P, Wang J, Tang B, Su T, Liu X
Neurogenetics. 2017; 19(1):9-16.
PMID: 29130122
DOI: 10.1007/s10048-017-0528-2.