PubMed for id: 20910

Year	Number of Results
1995	4
1996	2
1998	2
1999	1
2000	3
2001	4
2002	5
2003	6
2004	9
2005	11
2006	10
2007	9
2008	2
2009	5
2010	5
2011	3
2012	7
2013	8
2014	5
2015	5
2016	6
2017	9
2018	10
2019	4
2020	11
2021	7
2022	4
2023	4
2024	2

1

Microcircuit failure in STXBP1 encephalopathy leads to hyperexcitability.

Dos Santos AB, Larsen SD, Guo L, Barbagallo P, Montalant A, Verhage M, Sørensen JB, Perrier JF. Dos Santos AB, et al. Cell Rep Med. 2023 Dec 19;4(12):101308. doi: 10.1016/j.xcrm.2023.101308. Epub 2023 Dec 11. Cell Rep Med. 2023. PMID: 38086378 Free PMC article.

2

Excitatory and inhibitory receptors utilize distinct post- and trans-synaptic mechanisms in vivo.

Miyazaki T, Morimoto-Tomita M, Berthoux C, Konno K, Noam Y, Yamasaki T, Verhage M, Castillo PE, Watanabe M, Tomita S. Miyazaki T, et al. Elife. 2021 Oct 18;10:e59613. doi: 10.7554/eLife.59613. Elife. 2021. PMID: 34658339 Free PMC article.

3

Targeted stabilization of Munc18-1 function via pharmacological chaperones.

Abramov D, Guiberson NGL, Daab A, Na Y, Petsko GA, Sharma M, Burré J. Abramov D, et al. EMBO Mol Med. 2021 Jan 11;13(1):e12354. doi: 10.15252/emmm.202012354. Epub 2020 Dec 17. EMBO Mol Med. 2021. PMID: 33332765 Free PMC article.

4

Loss of MUNC18-1 leads to retrograde transport defects in neurons.

van Berkel AA, Santos TC, Shaweis H, van Weering JRT, Toonen RF, Verhage M. van Berkel AA, et al. J Neurochem. 2021 May;157(3):450-466. doi: 10.1111/jnc.15256. Epub 2020 Dec 12. J Neurochem. 2021. PMID: 33259669 Free PMC article.

5

Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmission.

Lammertse HCA, van Berkel AA, Iacomino M, Toonen RF, Striano P, Gambardella A, Verhage M, Zara F. Lammertse HCA, et al. Brain. 2020 Feb 1;143(2):441-451. doi: 10.1093/brain/awz391. Brain. 2020. PMID: 31855252 Free PMC article.

6

Mechanism-based rescue of Munc18-1 dysfunction in varied encephalopathies by chemical chaperones.

Guiberson NGL, Pineda A, Abramov D, Kharel P, Carnazza KE, Wragg RT, Dittman JS, Burré J. Guiberson NGL, et al. Nat Commun. 2018 Sep 28;9(1):3986. doi: 10.1038/s41467-018-06507-4. Nat Commun. 2018. PMID: 30266908 Free PMC article.

7

Munc18-1 haploinsufficiency impairs learning and memory by reduced synaptic vesicular release in a model of Ohtahara syndrome.

Orock A, Logan S, Deak F. Orock A, et al. Mol Cell Neurosci. 2018 Apr;88:33-42. doi: 10.1016/j.mcn.2017.12.002. Epub 2017 Dec 5. Mol Cell Neurosci. 2018. PMID: 29217410 Free PMC article.

8

Tyrosine phosphorylation of Munc18-1 inhibits synaptic transmission by preventing SNARE assembly.

Meijer M, Dörr B, Lammertse HC, Blithikioti C, van Weering JR, Toonen RF, Söllner TH, Verhage M. Meijer M, et al. EMBO J. 2018 Jan 17;37(2):300-320. doi: 10.15252/embj.201796484. Epub 2017 Nov 17. EMBO J. 2018. PMID: 29150433 Free PMC article.

9

Munc18-1 redistributes in nerve terminals in an activity- and PKC-dependent manner.

Cijsouw T, Weber JP, Broeke JH, Broek JA, Schut D, Kroon T, Saarloos I, Verhage M, Toonen RF. Cijsouw T, et al. J Cell Biol. 2014 Mar 3;204(5):759-75. doi: 10.1083/jcb.201308026. J Cell Biol. 2014. PMID: 24590174 Free PMC article.

10

Munc18-1 haploinsufficiency results in enhanced anxiety-like behavior as determined by heart rate responses in mice.

Hager T, Maroteaux G, Pont Pd, Julsing J, van Vliet R, Stiedl O. Hager T, et al. Behav Brain Res. 2014 Mar 1;260:44-52. doi: 10.1016/j.bbr.2013.11.033. Epub 2013 Dec 1. Behav Brain Res. 2014. PMID: 24304718

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