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A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype.
Dwyer, Noelle D; Manning, Danielle K; Moran, Jennifer L; Mudbhary, Raksha; Fleming, Michael S; Favero, Carlita B; Vock, Vita M; O'Leary, Dennis D M; Walsh, Christopher A; Beier, David R.
Affiliation
  • Dwyer ND; Howard Hughes Medical Institute, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, USA. ndwyer@virginia.edu
Neural Dev ; 6: 3, 2011 Jan 07.
Article in En | MEDLINE | ID: mdl-21214893

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Axons / Thalamus / Transcription Factors / Cerebral Cortex / Homeodomain Proteins / Gene Expression Regulation, Developmental / Mutation Type of study: Prognostic_studies Language: En Journal: Neural Dev Year: 2011 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Axons / Thalamus / Transcription Factors / Cerebral Cortex / Homeodomain Proteins / Gene Expression Regulation, Developmental / Mutation Type of study: Prognostic_studies Language: En Journal: Neural Dev Year: 2011 Document type: Article Affiliation country: United States Country of publication: United kingdom