[PMID 22472607] Translocator protein (18?kDa) polymorphism (rs6971) explains in-vivo brain binding affinity of the PET radioligand [(18)F]-FEPPA


[PMID 18389087] Rarity of Somatic Mutation and Frequency of Normal Sequence Variation Detected in Sporadic Colon Adenocarcinoma Using High-Throughput cDNA Sequencing.


[PMID 22251896] Identifying improved TSPO PET imaging probes through biomathematics: the impact of multiple TSPO binding sites in vivo.


[PMID 22895910] Whole Body Biodistribution and Radiation Dosimetry in Humans of a New PET Ligand, [(18)F]-FEPPA, to Image Translocator Protein (18 kDa)




[PMID 23785173] Influence of TSPO Genotype on 11C-PBR28 Standardized Uptake Values


[PMID 23942012] Bipolar Disorder is associated with the rs6971 polymorphism in the gene encoding 18kDa Translocator Protein (TSPO)


[PMID 24071511] Quantification of the Specific Translocator Protein Signal of 18F-PBR111 in Healthy Humans: A Genetic Polymorphism Effect on In Vivo Binding


[PMID 22968319] A genetic polymorphism for translocator protein 18 kDa affects both in vitro and in vivo radioligand binding in human brain to this putative biomarker of neuroinflammation.


[PMID 24904112] In Vivo Assessment of Brain White Matter Inflammation in Multiple Sclerosis with 18F-PBR111 PET


[PMID 25707397] In-vivo imaging of grey and white matter neuroinflammation in Alzheimer's disease: a positron emission tomography study with a novel radioligand, [(18)F]-FEPPA


[PMID 25833352] (11)C-PBR28 imaging in multiple sclerosis patients and healthy controls: test-retest reproducibility and focal visualization of active white matter areas


[PMID 26472628] Microglial Activity in People at Ultra High Risk of Psychosis and in Schizophrenia: An [(11)C]PBR28 PET Brain Imaging Study

rs6971

Parent Gene: TSPO

Importance: 1
Less common allele: A = 17%
More common allele: G = 83%
My Genotype: Log In