Shared and distinct functional effects of patient-specific Tbr1 mutations on cortical development | bioRxiv
TBR1 Gene - GeneCards | TBR1 Protein | TBR1 Antibody
A de novo frameshift pathogenic variant in TBR1 identified in autism without intellectual disability
TBR1 - Wikipedia
Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex | PNAS
TBR1 Gene - GeneCards | TBR1 Protein | TBR1 Antibody
Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex | PNAS
Down-regulation of rostral marker genes in Tbr1 mutant cortex. ( A – D... | Download Scientific Diagram
TBR1 syndrome
Shared and distinct functional effects of patient-specific Tbr1 mutations on cortical development | bioRxiv
TBR1 acts as an immediate early gene to induce Grin2b expression during... | Download Scientific Diagram
Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex | PNAS
Generation and basic characterization of Tbr1 +/K228E and Tbr1... | Download Scientific Diagram
TBR1 Gene - GeneCards | TBR1 Protein | TBR1 Antibody
Frontiers | A TBR1-K228E Mutation Induces Tbr1 Upregulation, Altered Cortical Distribution of Interneurons, Increased Inhibitory Synaptic Transmission, and Autistic-Like Behavioral Deficits in Mice
Tbr1 and Fezf2 Regulate Alternate Corticofugal Neuronal Identities during Neocortical Development | Journal of Neuroscience
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature | European Journal of Human Genetics
TBR1 Gene - GeneCards | TBR1 Protein | TBR1 Antibody
Frontiers | A TBR1-K228E Mutation Induces Tbr1 Upregulation, Altered Cortical Distribution of Interneurons, Increased Inhibitory Synaptic Transmission, and Autistic-Like Behavioral Deficits in Mice
Top autism gene may rewire brain by altering expression of other genes | Spectrum | Autism Research News
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature | European Journal of Human Genetics
Expression of Pax6, Tbr2, and Tbr1 protein in E14.5 cortex (coronal... | Download Scientific Diagram
Mutations in TBR1 gene leads to cortical malformations and intellectual disability - ScienceDirect