HLA-B gene
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| HLA-B | expressed_in | frontal cortex | — | 1 |
| HLA-B | associated_with | mood disorders | — | 1 |
Mentioned in (35)
Papers in which this entity is mentioned.
- Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
- Immune selection determines tumor antigenicity and influences response to checkpoint inhibitors. (2023)
- Rapid genotype imputation from sequence with reference panels. (2021)
- Neuronal ApoE upregulates MHC-I expression to drive selective neurodegeneration in Alzheimer's disease. (2021)
- Pan-cancer analysis of longitudinal metastatic tumors reveals genomic alterations and immune landscape dynamics associated with pembrolizumab sensitivity. (2021)
- B cells and tertiary lymphoid structures promote immunotherapy response. (2020)
- Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype. (2019)
- HLA-VBSeq v2: improved HLA calling accuracy with full-length Japanese class-I panel. (2019)
- Whole-exome sequencing of cervical carcinomas identifies activating ERBB2 and PIK3CA mutations as targets for combination therapy. (2019)
- Genome-Informed Targeted Therapy for Osteosarcoma. (2019)
- Best practices for bioinformatic characterization of neoantigens for clinical utility. (2019)
- Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
- Immune diversity sheds light on missing variation in worldwide genetic diversity panels. (2018)
- The Immune Landscape of Cancer. (2018)
- Nanopore sequencing and assembly of a human genome with ultra-long reads. (2018)
- Predicting T cell recognition of MHC class I restricted neoepitopes. (2018)
- Fast and accurate HLA typing from short-read next-generation sequence data with xHLA. (2017)
- Allele-Specific HLA Loss and Immune Escape in Lung Cancer Evolution. (2017)
- Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors. (2017)
- High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs. (2016)
- The IPD and IMGT/HLA database: allele variant databases. (2015)
- HLAreporter: a tool for HLA typing from next generation sequencing data. (2015)
- Profiling tissue-resident T cell repertoires by RNA sequencing. (2015)
- HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data. (2015)
- Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads. (2014)
- OptiType: precision HLA typing from next-generation sequencing data. (2014)
- DNA methylation contributes to natural human variation. (2013)
- HLA typing from 1000 genomes whole genome and whole exome illumina data. (2013)
- Properties of MHC class I presented peptides that enhance immunogenicity. (2013)
- HLA typing from RNA-Seq sequence reads. (2012)
- Novel roles for immune molecules in neural development: implications for neurodevelopmental disorders. (2010)
- Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (2009)
- Common and rare variants in multifactorial susceptibility to common diseases. (2008)
- The HLA system: genetics, immunology, clinical testing, and clinical implications. (2007)
- A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. (2006)
Merged raw entities (1)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| hla-b | gene | 35 | 124 |