The tumor suppressor Brat controls neuronal stem cell lineages by inhibiting Deadpan and Zelda | EMBO reports
RCSB PDB - 1Q7F: Brain Tumor NHL domain
Erblicher Brust- und Eierstockkrebs.pdf - genteQ
Genetic Mapping and Exome Sequencing Identify Variants Associated with Five Novel Diseases | PLOS ONE
The V62E mutation in BRAT1-mutated patient cells impairs BRAT1... | Download Scientific Diagram
Proposed model for the function of BRAT1 and BRP1 in DNA... | Download Scientific Diagram
Compound heterozygous BRAT1 mutations cause familial Ohtahara syndrome with hypertonia and microcephaly | Journal of Human Genetics
Cureus | A Rare Case of Lethal Neonatal Rigidity and Multi-Focal Seizure Syndrome | Article
The Crystal Structure of the NHL Domain in Complex with RNA Reveals the Molecular Basis of Drosophila Brain-Tumor-Mediated Gene Regulation - ScienceDirect
Glioblastoma: Current Status, Emerging Targets, and Recent Advances | Journal of Medicinal Chemistry
Mutation-based clustering and classification analysis reveals distinctive age groups and age-related biomarkers for glioma | BMC Medical Informatics and Decision Making | Full Text
Hirntumordiagnostik: Neue Entwicklungen und Zukunftsperspektiven
PDF) cIMPACT-NOW update 5: recommended grading criteria and terminologies for IDH-mutant astrocytomas. (2020) | Daniel J. Brat | 136 Citations
Biomedicines | Free Full-Text | Detection of TERT Promoter Mutations as a Prognostic Biomarker in Gliomas: Methodology, Prospects, and Advances
An intronic variant in BRAT1 creates a cryptic splice site, causing epileptic encephalopathy without prominent rigidity | SpringerLink
Asymmetric Segregation of the Tumor Suppressor Brat Regulates Self-Renewal in Drosophila Neural Stem Cells: Cell
Brat Is a Miranda Cargo Protein that Promotes Neuronal Differentiation and Inhibits Neuroblast Self-Renewal - ScienceDirect
BRAT1 Gene - GeneCards | BRAT1 Protein | BRAT1 Antibody
BRCA1 185delAG Mutation Enhances Interleukin-1β Expression in Ovarian Surface Epithelial Cells
BRAT1 mutations are associated with infantile epileptic encephalopathy, mitochondrial dysfunction, and survival into childhood - Horn - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
Frontiers | Novel Biallelic Variant in the BRAT1 Gene Caused Nonprogressive Cerebellar Ataxia Syndrome
BRAT1 in Brain Function
Frontiers | Novel Biallelic Variant in the BRAT1 Gene Caused Nonprogressive Cerebellar Ataxia Syndrome
Locations of various BRAT1 mutations within the exon or splicing... | Download Scientific Diagram
BRAT1 in Brain Function
