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Paper Details

Postnatal Conditional Deletion of <i>Bcl11b</i> in Striatal Projection Neurons Mimics the Transcriptional Signature of Huntington's Disease.
Biomedicines
1
2022
BCL11B, DARPP-32, HD, HDAC, Huntington's Disease, Huntington's disease, MSNs, Parkinson's disease, Striatal Projection Neurons, Striatal medium spiny neurons, X-, XDP, addiction, adult MSNs, autism, calcium, dopamine, dopamine D2 receptor, dopaminergic, human, linked dystonia-parkinsonism, mature MSNs, mice, mouse, postnatal MSNs, schizophrenia, striatal gene
Author NameAffiliation
Sean D MooneyUniversity of Washington
Sean D MooneyUniversity of Washington
Lisa M EllerbyBuck Institute for Research on Aging
Lisa M EllerbyUniversity of Southern California
Michelle E EhrlichIcahn School of Medicine at Mount Sinai
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Datasets

Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink