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A role for Bicaudal-D2 in radial cerebellar granule cell migration
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1098-1136(20010101)33:1<72::aid-glia1007>3.0.co;2-aopenalex-snapshot
GFAP promoter-controlled EGFP-expressing transgenic mice: A tool to visualize astrocytes and astrogliosis in living brain tissue
inferredcites →https://doi.org/10.1002/dneu.20850openalex-snapshot
The role of Rho GTPase proteins in CNS neuronal migration
inferredcites →https://doi.org/10.1002/dvg.20226openalex-snapshot
Nestin‐Cre transgenic mouse line Nes‐Cre1 mediates highly efficient Cre/loxP mediated recombination in the nervous system, kidney, and somite‐derived tissues
inferredcites →https://doi.org/10.1002/gene.10008openalex-snapshot
hGFAP‐cre transgenic mice for manipulation of glial and neuronal function in vivo
inferredcites →https://doi.org/10.1002/glia.21154openalex-snapshot
Loss of adenomatous polyposis coli in Bergmann glia disrupts their unique architecture and leads to cell nonautonomous neurodegeneration of cerebellar Purkinje neurons
inferredcites →https://doi.org/10.1007/s12035-013-8405-yopenalex-snapshot
Bergmann Glia Function in Granule Cell Migration During Cerebellum Development
inferredcites →https://doi.org/10.1016/0092-8674(89)90611-9openalex-snapshot
Structure of the Drosophila BicaudalD protein and its role in localizing the posterior determinant nanos
inferredcites →https://doi.org/10.1016/j.aanat.2005.07.004openalex-snapshot
BicD-dependent localization processes: from Drosophilia development to human cell biology
inferredcites →https://doi.org/10.1016/j.ajhg.2013.04.011openalex-snapshot
Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy
inferredcites →https://doi.org/10.1016/j.ajhg.2013.04.013openalex-snapshot
Molecular Defects in the Motor Adaptor BICD2 Cause Proximal Spinal Muscular Atrophy with Autosomal-Dominant Inheritance
inferredcites →https://doi.org/10.1016/j.ajhg.2013.04.018openalex-snapshot
Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia
inferredcites →https://doi.org/10.1016/j.cell.2013.08.024openalex-snapshot
Dynein Recruitment to Nuclear Pores Activates Apical Nuclear Migration and Mitotic Entry in Brain Progenitor Cells
inferredcites →https://doi.org/10.1016/j.conb.2012.04.010openalex-snapshot
Sticky situations: recent advances in control of cell adhesion during neuronal migration
inferredcites →https://doi.org/10.1016/j.devcel.2007.06.010openalex-snapshot
Rab6 Regulates Transport and Targeting of Exocytotic Carriers
inferredcites →https://doi.org/10.1016/j.mcn.2006.06.013openalex-snapshot
Integrin-linked kinase regulates Bergmann glial differentiation during cerebellar development
inferredcites →https://doi.org/10.1016/j.neuron.2005.08.028openalex-snapshot
Math1 Is Expressed in Temporally Discrete Pools of Cerebellar Rhombic-Lip Neural Progenitors
inferredcites →https://doi.org/10.1016/j.neuron.2010.09.027openalex-snapshot
Genetic Mosaic Dissection of Lis1 and Ndel1 in Neuronal Migration
inferredcites →https://doi.org/10.1016/j.neuron.2011.02.008openalex-snapshot
An Isoform-Specific SnoN1-FOXO1 Repressor Complex Controls Neuronal Morphogenesis and Positioning in the Mammalian Brain
inferredcites →https://doi.org/10.1016/j.pneurobio.2013.08.001openalex-snapshot
Origin, lineage and function of cerebellar glia
inferredcites →https://doi.org/10.1016/j.tins.2010.01.004openalex-snapshot
Should I stay or should I go? Becoming a granule cell
inferredcites →https://doi.org/10.1016/j.tins.2010.08.003openalex-snapshot
Compartmentalization from the outside: the extracellular matrix and functional microdomains in the brain
inferredcites →https://doi.org/10.1016/j.ydbio.2009.02.011openalex-snapshot
Neuron-derived FGF9 is essential for scaffold formation of Bergmann radial fibers and migration of granule neurons in the cerebellum
inferredcites →https://doi.org/10.1016/j.ymgme.2003.08.019openalex-snapshot
Development and malformations of the cerebellum in mice
inferredcites →https://doi.org/10.1016/s0896-6273(00)80346-3openalex-snapshot
Neuregulin and erbB Receptors Play a Critical Role in Neuronal Migration
inferredcites →https://doi.org/10.1016/s0945-053x(00)00106-2openalex-snapshot
Tenascin-C in development and disease: gene regulation and cell function
inferredcites →https://doi.org/10.1038/316146a0openalex-snapshot
The J1 glycoprotein—a novel nervous system cell adhesion molecule of the L2/HNK-1 family
inferredcites →https://doi.org/10.1038/414611aopenalex-snapshot
Conserved signals and machinery for RNA transport in Drosophila oogenesis and embryogenesis
inferredcites →https://doi.org/10.1038/nature05453openalex-snapshot
Genome-wide atlas of gene expression in the adult mouse brain
inferredcites →https://doi.org/10.1038/ncb891openalex-snapshot
Bicaudal-D regulates COPI-independent Golgi–ER transport by recruiting the dynein–dynactin motor complex
inferredcites →https://doi.org/10.1038/ng954openalex-snapshot
Targeted mutation of Cyln2 in the Williams syndrome critical region links CLIP-115 haploinsufficiency to neurodevelopmental abnormalities in mice
inferredcites →https://doi.org/10.1038/nn1153openalex-snapshot
RNAi reveals doublecortin is required for radial migration in rat neocortex
inferredcites →https://doi.org/10.1038/nn2064openalex-snapshot
Plexin-A2 and its ligand, Sema6A, control nucleus-centrosome coupling in migrating granule cells
inferredcites →https://doi.org/10.1073/pnas.82.23.8075openalex-snapshot
Cytotactin, an extracellular matrix protein of neural and non-neural tissues that mediates glia-neuron interaction.
inferredcites →https://doi.org/10.1083/jcb.104.2.331openalex-snapshot
Sequential expression and differential function of multiple adhesion molecules during the formation of cerebellar cortical layers.
inferredcites →https://doi.org/10.1083/jcb.116.6.1475openalex-snapshot
Tenascin promotes cerebellar granule cell migration and neurite outgrowth by different domains in the fibronectin type III repeats.
inferredcites →https://doi.org/10.1083/jcb.200309025openalex-snapshot
Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration
inferredcites →https://doi.org/10.1091/mbc.e12-03-0210openalex-snapshot
BICD2, dynactin, and LIS1 cooperate in regulating dynein recruitment to cellular structures
inferredcites →https://doi.org/10.1093/emboj/20.15.4041openalex-snapshot
Mammalian Golgi‐associated Bicaudal‐D2 functions in the dynein–dynactin pathway by interacting with these complexes
inferredcites →https://doi.org/10.1093/emboj/cdg592openalex-snapshot
Bicaudal D induces selective dynein‐mediated microtubule minus end‐directed transport
inferredcites →https://doi.org/10.1093/hmg/ddn182openalex-snapshot
A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice
inferredcites →https://doi.org/10.1101/cshperspect.a004960openalex-snapshot
Tenascins and the Importance of Adhesion Modulation
inferredcites →https://doi.org/10.1146/annurev.neuro.051508.135600openalex-snapshot
The Glial Nature of Embryonic and Adult Neural Stem Cells
inferredcites →https://doi.org/10.1146/annurev.neuro.22.1.511openalex-snapshot
CENTRAL NERVOUS SYSTEM NEURONAL MIGRATION
inferredcites →https://doi.org/10.1242/dev.008078openalex-snapshot
Rab6 and the secretory pathway affect oocyte polarity inDrosophila
inferredcites →https://doi.org/10.1242/dev.01891openalex-snapshot
PTEN deletion in Bergmann glia leads to premature differentiation and affects laminar organization
inferredcites →https://doi.org/10.1242/dev.02821openalex-snapshot
Rab6 mediates membrane organization and determinant localization duringDrosophilaoogenesis
inferredcites →https://doi.org/10.1242/dev.128.16.3133openalex-snapshot
Pax6regulates granule cell polarization during parallel fiber formation in the developing cerebellum
inferredcites →https://doi.org/10.1242/dev.129.4.965openalex-snapshot
Mice that lack astrotactin have slowed neuronal migration
inferredcites →https://doi.org/10.1371/journal.pbio.1000350openalex-snapshot
Bicaudal D2, Dynein, and Kinesin-1 Associate with Nuclear Pore Complexes and Regulate Centrosome and Nuclear Positioning during Mitotic Entry
inferredcites →https://doi.org/10.1523/jneurosci.12-03-00736.1992openalex-snapshot
Expression of tenascin in the developing and adult cerebellar cortex
inferredcites →https://doi.org/10.1523/jneurosci.1282-12.2012openalex-snapshot
Ric-8a, a Guanine Nucleotide Exchange Factor for Heterotrimeric G Proteins, Regulates Bergmann Glia-Basement Membrane Adhesion during Cerebellar Foliation
inferredcites →https://doi.org/10.1523/jneurosci.15-02-01110.1995openalex-snapshot
Dynamics of granule cell migration: a confocal microscopic study in acute cerebellar slice preparations
inferredcites →https://doi.org/10.1523/jneurosci.19-14-06017.1999openalex-snapshot
Migration Defects ofcdk5−/−Neurons in the Developing Cerebellum is Cell Autonomous
inferredcites →https://doi.org/10.1523/jneurosci.22-15-06309.2002openalex-snapshot
Cortical Excitatory Neurons and Glia, But Not GABAergic Neurons, Are Produced in the Emx1-Expressing Lineage
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/advs.202101329openalex-snapshot
The m 6 A Readers YTHDF1 and YTHDF2 Synergistically Control Cerebellar Parallel Fiber Growth by Regulating Local Translation of the Key Wnt5a Signaling Components in Axons
inferred← citeshttps://doi.org/10.1007/978-3-319-39468-8_21openalex-snapshot
Evolution of the Molecules Coupling mRNA Transport with Translational Control in Metazoans
inferred← citeshttps://doi.org/10.1016/b978-0-12-809470-9.00011-4openalex-snapshot
The use of mouse models to probe cytoplasmic dynein function
inferred← citeshttps://doi.org/10.1016/bs.vh.2016.11.005openalex-snapshot
Neuronal Roles of the Bicaudal D Family of Motor Adaptors
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.03.054openalex-snapshot
Structural basis for cargo binding and autoinhibition of Bicaudal-D1 by a parallel coiled-coil with homotypic registry
inferred← citeshttps://doi.org/10.1016/j.cub.2020.05.091openalex-snapshot
Nesprin-2 Recruitment of BicD2 to the Nuclear Envelope Controls Dynein/Kinesin-Mediated Neuronal Migration In Vivo
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.04.022openalex-snapshot
Cdk1 Activates Pre-mitotic Nuclear Envelope Dynein Recruitment and Apical Nuclear Migration in Neural Stem Cells
inferred← citeshttps://doi.org/10.1016/j.foodchem.2020.128672openalex-snapshot
Prevention properties on cerebral ischemia reperfusion of medicine food homologous Dioscorea yam-derived diosgenin based on mediation of potential targets
inferred← citeshttps://doi.org/10.1016/j.ibneur.2024.06.004openalex-snapshot
Alchornea laxiflora (Benth.) Pax & K. Hoffman extract protects against lead-induced neurodegeneration in cockerel chickens
inferred← citeshttps://doi.org/10.1016/j.ibror.2020.07.004openalex-snapshot
The ameliorative effects of a phenolic derivative of Moringa oleifera leave against vanadium-induced neurotoxicity in mice
inferred← citeshttps://doi.org/10.1016/j.jprot.2019.03.008openalex-snapshot
What if? Mouse proteomics after gene inactivation
inferred← citeshttps://doi.org/10.1016/j.neulet.2021.135796openalex-snapshot
Roles of the multivalent dynein adaptors BicD2 and RILP in neurons
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2025.110793openalex-snapshot
Antisense oligonucleotide of cargo adaptor BICD2 long-term effectively alleviates neuropathic pain via activation of PSD95 in the mouse spinal dorsal horn
inferred← citeshttps://doi.org/10.1016/j.nmd.2021.07.399openalex-snapshot
Neurogenic arthrogryposis and the power of phenotyping
inferred← citeshttps://doi.org/10.1016/j.tcb.2016.01.001openalex-snapshot
Bicaudal D Family of Motor Adaptors: Linking Dynein Motility to Cargo Binding
inferred← citeshttps://doi.org/10.1038/ncomms5380openalex-snapshot
Correction: Corrigendum: A role for Bicaudal-D2 in radial cerebellar granule cell migration
inferred← citeshttps://doi.org/10.1038/nn.4531openalex-snapshot
Cerebellar granule cells acquire a widespread predictive feedback signal during motor learning
inferred← citeshttps://doi.org/10.1038/s10038-022-01060-xopenalex-snapshot
A homozygous loss-of-function variant in BICD2 is associated with lissencephaly and cerebellar hypoplasia
inferred← citeshttps://doi.org/10.1038/s41419-018-1027-6openalex-snapshot
MARVELD1 depletion leads to dysfunction of motor and cognition via regulating glia-dependent neuronal migration during brain development
inferred← citeshttps://doi.org/10.1038/s42003-026-09924-0openalex-snapshot
PACS1 syndrome mutation disrupts dynein-mediated cargo transport via HDAC6 and BICD2
inferred← citeshttps://doi.org/10.1038/tp.2015.147openalex-snapshot
Early-life serotonin dysregulation affects the migration and positioning of cortical interneuron subtypes
inferred← citeshttps://doi.org/10.1073/pnas.1620141114openalex-snapshot
DYNC1H1 mutations associated with neurological diseases compromise processivity of dynein–dynactin–cargo adaptor complexes
inferred← citeshttps://doi.org/10.1073/pnas.2201967119openalex-snapshot
Elevated BICD2 DNA methylation in blood of major depressive disorder patients and reduction of depressive-like behaviors in hippocampal Bicd2 -knockdown mice
inferred← citeshttps://doi.org/10.1083/jcb.201703201openalex-snapshot
Disease-associated mutations in human BICD2 hyperactivate motility of dynein–dynactin
inferred← citeshttps://doi.org/10.1083/jcb.201908040openalex-snapshot
Microtubules and motor proteins support zebrafish neuronal migration by directing cargo
inferred← citeshttps://doi.org/10.1093/hmg/ddy086openalex-snapshot
Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development
inferred← citeshttps://doi.org/10.1093/schizbullopen/sgac047openalex-snapshot
DNA Hyper-methylation Associated With Schizophrenia May Lead to Increased Levels of Autoantibodies
inferred← citeshttps://doi.org/10.1101/854711openalex-snapshot
Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophy
inferred← citeshttps://doi.org/10.1111/ene.12914openalex-snapshot
Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD 2
inferred← citeshttps://doi.org/10.1146/annurev-neuro-072116-031437openalex-snapshot
Lessons from Worm Dendritic Patterning
inferred← citeshttps://doi.org/10.1159/000487797openalex-snapshot
Intrauterine Growth Restriction Affects Cerebellar Granule Cells in the Developing Guinea Pig Brain
inferred← citeshttps://doi.org/10.1186/s12920-022-01349-yopenalex-snapshot
Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy
inferred← citeshttps://doi.org/10.1186/s12920-023-01472-4openalex-snapshot
Muscle and bone characteristics of a Chinese family with spinal muscular atrophy, lower extremity predominant 1 (SMALED1) caused by a novel missense DYNC1H1 mutation
inferred← citeshttps://doi.org/10.1186/s13148-018-0457-4openalex-snapshot
Epigenome-wide analysis in newborn blood spots from monozygotic twins discordant for cerebral palsy reveals consistent regional differences in DNA methylation
inferred← citeshttps://doi.org/10.1186/s40478-019-0827-yopenalex-snapshot
Dynein activating adaptor BICD2 controls radial migration of upper-layer cortical neurons in vivo
inferred← citeshttps://doi.org/10.1186/s40478-020-00909-6openalex-snapshot
Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophy
inferred← citeshttps://doi.org/10.1186/s40478-020-00971-0openalex-snapshot
Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation
inferred← citeshttps://doi.org/10.1242/jcs.261935openalex-snapshot
Widespread nuclear lamina injuries defeat proteostatic purposes of α-synuclein amyloid inclusions
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010642openalex-snapshot
Role of Nesprin-2 and RanBP2 in BICD2-associated brain developmental disorders
inferred← citeshttps://doi.org/10.1523/jneurosci.2133-14.2015openalex-snapshot
Loss of the Neuron-Specific F-Box Protein FBXO41 Models an Ataxia-Like Phenotype in Mice with Neuronal Migration Defects and Degeneration in the Cerebellum
inferred← citeshttps://doi.org/10.15252/embj.201387579openalex-snapshot
Bicaudal‐D1 regulates the intracellular sorting and signalling of neurotrophin receptors
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1693689/v1openalex-snapshot
Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy
inferred← citeshttps://doi.org/10.21203/rs.3.rs-645110/v1openalex-snapshot
DNA hyper-methylation associated with schizophrenia may lead to breakdown of self-tolerance
inferred← citeshttps://doi.org/10.3389/fnins.2015.00397openalex-snapshot
Cytoplasmic dynein and its regulatory proteins in Golgi pathology in nervous system disorders
inferred← citeshttps://doi.org/10.3389/fnins.2015.00401openalex-snapshot
Dominant spinal muscular atrophy is caused by mutations in BICD2, an important golgin protein
inferred← citeshttps://doi.org/10.3892/ijmm.2021.4871openalex-snapshot
The role of the Golgi apparatus in disease (Review)
inferred← citeshttps://doi.org/10.47081/njn2021.12.4/002openalex-snapshot
Effects of in-vivo Vanadium-Induced Neurotoxicity and Withdrawal on Three Consecutive Generations of Mice Brains: A Neurobehavioural and Histo-Immunohistochemical Study
inferred← citeshttps://doi.org/10.6084/m9.figshare.11998476openalex-snapshot
Additional file 1 of Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophy
inferred← citeshttps://doi.org/10.6084/m9.figshare.12655510openalex-snapshot
Additional file 1 of Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation
inferred← citeshttps://doi.org/10.6084/m9.figshare.12655513openalex-snapshot
Additional file 2 of Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation
inferred← citeshttps://doi.org/10.6084/m9.figshare.12655516openalex-snapshot
Additional file 3 of Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation
inferred← citeshttps://doi.org/10.6084/m9.figshare.21009581openalex-snapshot
Additional file 1 of Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy
inferred← citeshttps://doi.org/10.6084/m9.figshare.21009584openalex-snapshot
Additional file 2 of Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy
inferred← citeshttps://doi.org/10.6084/m9.figshare.21009587openalex-snapshot
Additional file 3 of Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy
inferred← citeshttps://doi.org/10.6084/m9.figshare.21009590openalex-snapshot
Additional file 4 of Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy
inferred← citeshttps://doi.org/10.6084/m9.figshare.21009593openalex-snapshot
Additional file 5 of Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy
inferred← citeshttps://doi.org/10.70675/df8a63dbz73adz4ab8zb455z6d9ab4fdec6fopenalex-snapshot
Étude des bases moléculaires et cellulaires de la vulnérabilité des neurones moteurs dans l'amyotrophie spinale distale des membres inférieurs
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