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Cadherin 8 regulates proliferation of cortical interneuron progenitors

https://doi.org/10.1007/s00429-018-1772-4
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1096-9861(19971020)387:2<291::aid-cne10>3.0.co;2-yopenalex-snapshot
Expression of cadherin-8 mRNA in the developing mouse central nervous system
inferredcites →https://doi.org/10.1002/(sici)1097-0177(199702)208:2<178::aid-aja5>3.0.co;2-fopenalex-snapshot
Restricted expression of cadherin-8 in segmental and functional subdivisions of the embryonic mouse brain
inferredcites →https://doi.org/10.1002/aur.1456openalex-snapshot
T‐Brain‐1 – A Potential Master Regulator in Autism Spectrum Disorders
inferredcites →https://doi.org/10.1002/cne.10905openalex-snapshot
Green fluorescent protein expression and colocalization with calretinin, parvalbumin, and somatostatin in the GAD67‐GFP knock‐in mouse
inferredcites →https://doi.org/10.1002/cne.20141openalex-snapshot
Expression ofDbx1,Neurogenin 2,Semaphorin 5A,Cadherin 8, andEmx1distinguish ventral and lateral pallial histogenetic divisions in the developing mouse claustroamygdaloid complex
inferredcites →https://doi.org/10.1002/cne.22271openalex-snapshot
Differential gene expression in migrating cortical interneurons during mouse forebrain development
inferredcites →https://doi.org/10.1002/cne.22801openalex-snapshot
Comparative analysis of type II classic cadherin mRNA distribution patterns in the developing and adult mouse somatosensory cortex and hippocampus suggests significant functional redundancy
inferredcites →https://doi.org/10.1002/cne.23666openalex-snapshot
Cadherin‐8 expression, synaptic localization, and molecular control of neuronal form in prefrontal corticostriatal circuits
inferredcites →https://doi.org/10.1002/hipo.20395openalex-snapshot
Cadherin‐8 and N‐cadherin differentially regulate pre‐ and postsynaptic development of the hippocampal mossy fiber pathway
inferredcites →https://doi.org/10.1002/hipo.20859openalex-snapshot
Synaptic loss and retention of different classic cadherins with LTP‐associated synaptic structural remodeling in vivo
inferredcites →https://doi.org/10.1006/exnr.1998.6909openalex-snapshot
Heterogeneity of Cadherin-8 Expression in the Neonatal Rat Striatum: Comparison with Striatal Compartments
inferredcites →https://doi.org/10.1006/geno.1997.5152openalex-snapshot
Molecular Properties and Chromosomal Location of Cadherin-8
inferredcites →https://doi.org/10.1006/mcne.2000.0849openalex-snapshot
Loss of Cadherin-11 Adhesion Receptor Enhances Plastic Changes in Hippocampal Synapses and Modifies Behavioral Responses
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/s00429-017-1418-yopenalex-snapshot
Protective role of Cadherin 13 in interneuron development
inferredcites →https://doi.org/10.1016/j.celrep.2014.08.063openalex-snapshot
Cadherin-7 Regulates Mossy Fiber Connectivity in the Cerebellum
inferredcites →https://doi.org/10.1016/j.ijdevneu.2012.12.002openalex-snapshot
Morphology of the facial motor nuclei in a rat model of autism during early development
inferredcites →https://doi.org/10.1016/j.neuron.2011.06.019openalex-snapshot
Cadherin-9 Regulates Synapse-Specific Differentiation in the Developing Hippocampus
inferredcites →https://doi.org/10.1016/j.neuron.2011.07.006openalex-snapshot
Cadherin-6 Mediates Axon-Target Matching in a Non-Image-Forming Visual Circuit
inferredcites →https://doi.org/10.1016/j.tcb.2013.12.001openalex-snapshot
Decision making during interneuron migration in the developing cerebral cortex
inferredcites →https://doi.org/10.1016/j.tins.2004.11.011openalex-snapshot
Multiple facets of GABAergic neurons and synapses: multiple fates of GABA signalling in epilepsies
inferredcites →https://doi.org/10.1016/s0306-4522(98)00077-3openalex-snapshot
Cadherin-8 protein expression in gray matter structures and nerve fibers of the neonatal and adult mouse brain
inferredcites →https://doi.org/10.1016/s0893-133x(01)00225-1openalex-snapshot
GABAergic Interneurons Implications for Understanding Schizophrenia and Bipolar Disorder
inferredcites →https://doi.org/10.1038/36285openalex-snapshot
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
inferredcites →https://doi.org/10.1038/nature10989openalex-snapshot
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
inferredcites →https://doi.org/10.1038/nature11011openalex-snapshot
Patterns and rates of exonic de novo mutations in autism spectrum disorders
inferredcites →https://doi.org/10.1038/nature11523openalex-snapshot
Intrinsically determined cell death of developing cortical interneurons
inferredcites →https://doi.org/10.1038/nn.3626openalex-snapshot
Tbr1 haploinsufficiency impairs amygdalar axonal projections and results in cognitive abnormality
inferredcites →https://doi.org/10.1038/nrn2043openalex-snapshot
The cadherin superfamily in neuronal connections and interactions
inferredcites →https://doi.org/10.1093/cercor/7.4.293openalex-snapshot
Basic fibroblast growth factor prolongs the proliferation of rat cortical progenitor cells in vitro without altering their cell cycle parameters
inferredcites →https://doi.org/10.1111/ejn.12225openalex-snapshot
Cellular and molecular mechanisms controlling the migration of neocortical interneurons
inferredcites →https://doi.org/10.1111/j.1460-9568.2011.07896.xopenalex-snapshot
Differential gene expression in migratory streams of cortical interneurons
inferredcites →https://doi.org/10.1111/j.1528-1167.2008.01725.xopenalex-snapshot
Decreased number of interneurons and increased seizures in neuropilin 2 deficient mice: Implications for autism and epilepsy
inferredcites →https://doi.org/10.1126/science.1227764openalex-snapshot
Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
inferredcites →https://doi.org/10.1126/science.278.5337.474openalex-snapshot
Interneuron Migration from Basal Forebrain to Neocortex: Dependence on Dlx Genes
inferredcites →https://doi.org/10.1128/mcb.00011-09openalex-snapshot
The Protocadherin Gene Celsr3 Is Required for Interneuron Migration in the Mouse Forebrain
inferredcites →https://doi.org/10.1136/jmg.2010.079426openalex-snapshot
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
inferredcites →https://doi.org/10.1152/physrev.00014.2011openalex-snapshot
Cadherins in Brain Morphogenesis and Wiring
inferredcites →https://doi.org/10.1159/000334489openalex-snapshot
Neurons on the Move: Migration and Lamination of Cortical Interneurons
inferredcites →https://doi.org/10.1159/000444713openalex-snapshot
Epigenetic Regulations of GABAergic Neurotransmission: Relevance for Neurological Disorders and Epigenetic Therapy
inferredcites →https://doi.org/10.1177/1179069518760783openalex-snapshot
Single-Cell Transcriptomics Reveals Regulators of Neuronal Migration and Maturation During Brain Development
inferredcites →https://doi.org/10.1242/bio.20133202openalex-snapshot
Limk2 mediates semaphorin signalling in cortical interneurons migrating through the subpallium
inferredcites →https://doi.org/10.1242/dev.02354openalex-snapshot
Classic cadherins regulate tangential migration of precerebellar neurons in the caudal hindbrain
inferredcites →https://doi.org/10.1242/dev.042457openalex-snapshot
Cadherin-7 and cadherin-6B differentially regulate the growth, branching and guidance of cranial motor axons
inferredcites →https://doi.org/10.1242/dev.063362openalex-snapshot
VEGF signalling controls GnRH neuron survival via NRP1 independently of KDR and blood vessels
inferredcites →https://doi.org/10.1242/dev.102988openalex-snapshot
Cadherin-based adhesions in the apical endfoot are required for active Notch signaling to control neurogenesis in vertebrates
inferredcites →https://doi.org/10.1242/dev.125.15.2963openalex-snapshot
Neural crest emigration from the neural tube depends on regulated cadherin expression
inferredcites →https://doi.org/10.1242/dev.127.24.5297openalex-snapshot
Control of the migratory pathway of facial branchiomotor neurones
inferredcites →https://doi.org/10.1242/dev.128.4.561openalex-snapshot
Role of cadherins in maintaining the compartment boundary between the cortex and striatum during development
inferredcites →https://doi.org/10.1371/journal.pmed.0030467openalex-snapshot
A Gene Expression Signature Predicts Survival of Patients with Stage I Non-Small Cell Lung Cancer
inferredcites →https://doi.org/10.1523/jneurosci.0243-07.2007openalex-snapshot
Cadherin-8 Is Required for the First Relay Synapses to Receive Functional Inputs from Primary Sensory Afferents for Cold Sensation
inferredcites →https://doi.org/10.1523/jneurosci.0593-13.2013openalex-snapshot
N-Cadherin Sustains Motility and Polarity of Future Cortical Interneurons during Tangential Migration
inferredcites →https://doi.org/10.1523/jneurosci.1245-04.2004openalex-snapshot
Lhx6 Regulates the Migration of Cortical Interneurons from the Ventral Telencephalon But Does Not Specify their GABA Phenotype
inferredcites →https://doi.org/10.1523/jneurosci.17-03-01075.1997openalex-snapshot
Apoptosis and Its Relation to the Cell Cycle in the Developing Cerebral Cortex
inferredcites →https://doi.org/10.1523/jneurosci.1793-14.2014openalex-snapshot
Proliferative Defects and Formation of a Double Cortex in Mice Lacking Mltt4 and Cdh2 in the Dorsal Telencephalon
inferredcites →https://doi.org/10.1523/jneurosci.22-17-07617.2002openalex-snapshot
Targeting Axons to Specific Fiber TractsIn Vivoby Altering Cadherin Expression
inferredcites →https://doi.org/10.1523/jneurosci.5464-10.2011openalex-snapshot
Robo1 Regulates Semaphorin Signaling to Guide the Migration of Cortical Interneurons through the Ventral Forebrain
inferredcites →https://doi.org/10.3892/or.2013.2597openalex-snapshot
CHD8 is an independent prognostic indicator that regulates Wnt/β-catenin signaling and the cell cycle in gastric cancer

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.5281/zenodo.5658141openalex-extracted
Dynamics of Brain Structure and its Genetic Architecture over the Lifespan
inferred← citeshttps://doi.org/10.1002/alz.14461openalex-snapshot
Sex‐stratified genome‐wide meta‐analysis identifies novel loci for cognitive decline in older adults
inferred← citeshttps://doi.org/10.1007/s00429-017-1418-yopenalex-snapshot
Protective role of Cadherin 13 in interneuron development
inferred← citeshttps://doi.org/10.1016/j.expneurol.2019.113055openalex-snapshot
Zfhx3 is required for the differentiation of late born D1-type medium spiny neurons
inferred← citeshttps://doi.org/10.1016/j.isci.2023.108002openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-026-41177-zopenalex-snapshot
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Epigenome-wide association study of perceived discrimination in the Multi-Ethnic Study of Atherosclerosis (MESA)
inferred← citeshttps://doi.org/10.1101/2020.04.24.031138openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2021.01.13.426600openalex-snapshot
New Gene Embedding Learned from Biomedical Literature and Its Application in Identifying Cancer Drivers
inferred← citeshttps://doi.org/10.1101/2023.11.27.568858openalex-snapshot
Expansion of the neocortex and protection from neurodegeneration by in vivo transient reprogramming
inferred← citeshttps://doi.org/10.1387/ijdb.210139idopenalex-snapshot
Birth and death of neurons in the developing and mature mammalian brain
inferred← citeshttps://doi.org/10.3389/fonc.2019.00381openalex-snapshot
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