Year |
Citation |
Score |
2016 |
Selten MM, Meyer F, Ba W, Vallès A, Maas DA, Negwer M, Eijsink VD, van Vugt RW, van Hulten JA, van Bakel NH, Roosen J, van der Linden RJ, Schubert D, Verheij MM, Kasri NN, et al. Increased GABAB receptor signaling in a rat model for schizophrenia. Scientific Reports. 6: 34240. PMID 27687783 DOI: 10.1038/Srep34240 |
0.679 |
|
2016 |
Ba W, Nadif Kasri N. RhoGTPases at the synapse: An embarrassment of choice. Small Gtpases. 1-8. PMID 27492682 DOI: 10.1080/21541248.2016.1206352 |
0.776 |
|
2016 |
Benevento M, Iacono G, Selten M, Ba W, Oudakker A, Frega M, Keller J, Mancini R, Lewerissa E, Kleefstra T, Stunnenberg HG, Zhou H, van Bokhoven H, Nadif Kasri N. Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling. Neuron. PMID 27373831 DOI: 10.1016/J.Neuron.2016.06.003 |
0.632 |
|
2016 |
Ba W, Selten MM, van der Raadt J, van Veen H, Li LL, Benevento M, Oudakker AR, Lasabuda RS, Letteboer SJ, Roepman R, van Wezel RJ, Courtney MJ, van Bokhoven H, Nadif Kasri N. ARHGAP12 Functions as a Developmental Brake on Excitatory Synapse Function. Cell Reports. PMID 26854232 DOI: 10.1016/J.Celrep.2016.01.037 |
0.64 |
|
2015 |
Ba W, Yan Y, Reijnders MR, Schuurs-Hoeijmakers JH, Feenstra I, Bongers EM, Bosch DG, de Leeuw N, Pfundt R, Gilissen C, de Vries PF, Veltman JA, Hoischen A, Mefford HC, Eichler EE, et al. TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function. Human Molecular Genetics. PMID 26721934 DOI: 10.1093/Hmg/Ddv618 |
0.73 |
|
2015 |
Olde Loohuis NF, Ba W, Stoerchel PH, Kos A, Jager A, Schratt G, Martens GJ, van Bokhoven H, Nadif Kasri N, Aschrafi A. MicroRNA-137 Controls AMPA-Receptor-Mediated Transmission and mGluR-Dependent LTD. Cell Reports. 11: 1876-84. PMID 26095359 DOI: 10.1016/J.Celrep.2015.05.040 |
0.647 |
|
2014 |
Willemsen MH, Ba W, Wissink-Lindhout WM, de Brouwer AP, Haas SA, Bienek M, Hu H, Vissers LE, van Bokhoven H, Kalscheuer V, Nadif Kasri N, Kleefstra T. Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function. Journal of Medical Genetics. 51: 487-94. PMID 24812067 DOI: 10.1136/Jmedgenet-2013-102182 |
0.709 |
|
2013 |
Ba W, van der Raadt J, Nadif Kasri N. Rho GTPase signaling at the synapse: implications for intellectual disability. Experimental Cell Research. 319: 2368-74. PMID 23769912 DOI: 10.1016/j.yexcr.2013.05.033 |
0.687 |
|
Show low-probability matches. |