_id,doi,title
10301,10.7554/elife.71575,Control of protein synthesis and memory by GluN3A-NMDA receptors through inhibition of GIT1/mTORC1 assembly
9953,10.1016/j.bbi.2021.07.022,Microglial-glucocorticoid receptor depletion alters the response of hippocampal microglia and neurons in a chronic unpredictable mild stress paradigm in female mice
7800,10.1101/2020.01.10.902064 ,Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development
7877,10.1016/j.celrep.2020.107647,MAU2 and NIPBL variants impair the heterodimerization of the cohesin loader subunits and cause Cornelia de Lange syndrome
7957,10.1016/j.tins.2020.05.004,Neurodevelopmental disorders: From genetics to functional pathways
8131,10.1016/j.gde.2020.06.004,Molecular mechanisms for targeted ASD treatments
8620,10.15479/AT:ISTA:8620,Illuminating the role of Cul3 in autism spectrum disorder pathogenesis
7149,10.1111/cge.13674,Chromatinopathies: A focus on Cornelia de Lange syndrome
7488,10.3390/ijms21031042,Evaluating Face2Gene as a tool to identify Cornelia de Lange syndrome by facial phenotypes
7586,10.15252/embj.2019103358,Uncoupling endosomal CLC chloride/proton exchange causes severe neurodegeneration
6896,10.1016/j.brainres.2019.146458,Modeling cell-cell interactions in the brain using cerebral organoids
7414,10.1016/j.euroneuro.2019.09.039,S.16.03 A homozygous missense mutation in SLC7A5 leads to autism spectrum disorder and microcephaly
7415,10.1016/j.euroneuro.2019.09.040,S.16.05 Illuminating the role of the e3 ubiquitin ligase cullin3 in brain development and autism
6074,10.15479/AT:ISTA:6074,"Supplementary data for the research paper ""Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition"""
6088,10.1021/acs.molpharmaceut.8b01217,Inhibition of ABCB1 and ABCG2 at the mouse blood-brain barrier with marketed drugs to improve brain delivery of the model ABCB1/ABCG2 substrate [11C]erlotinib
6470,10.1113/JP277681,Improved spike inference accuracy by estimating the peak amplitude of unitary [Ca2+] transients in weakly GCaMP6f-expressing hippocampal pyramidal cells
105,10.1038/s41431-018-0231-2,CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63
3,10.1038/s41593-018-0266-2,Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition
691,10.1136/jmedgenet-2017-104627,A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features
456,10.1126/scitranslmed.aar7514,Zika-associated microcephaly: Reduce the stress and race for the treatment