Add to ORKGBackground: A rare variant in the Triggering Receptor Expressed on Myeloid cells 2 (TREM2) gene has been reported to be a genetic risk factor for Alzheimer's disease by two independent groups (Odds ratio between 2.9-4.5). Given the key role of TREM2 in th
AbstractTREM and TREM-like receptors are a structurally similar protein family encoded by genes clus...
Background: Triggering receptor expressed on myeloid cells 2 (TREM2) is an important modulator of in...
Summary Alzheimer's disease is a genetically complex disorder; rare variants in the triggering rece...
Abstract Background A rare variant in the Triggering Receptor Expressed on Myeloid cells 2 (TREM2) g...
A rare variant in TREM2 (p.R47H, rs75932628) was recently reported to increase the risk of Alzheimer...
A rare variant in TREM2 (p.R47H, rs75932628) was recently reported to increase the risk of Alzheimer...
The triggering receptor expressed on myeloid 2 (TREM2) is an immune phagocytic receptor expressed on...
BACKGROUND: Homozygous loss-of-function mutations in TREM2, encoding the triggering receptor express...
BACKGROUND: Homozygous loss-of-function mutations in TREM2, encoding the triggering receptor expres...
Recent evidence suggests that rare genetic variants within the TREM2 gene are associated with increa...
the role of the TREM2 p.R47H variant as a risk factor for Alzheimer’s disease and frontotemporal dem...
Abstract Background The R47H variant of Triggering Receptor Expressed on Myeloid cells 2 (TREM2) con...
Homozygous mutations in exon 2 of TREM2, a gene involved in Nasu-Hakola disease, can cause frontotem...
Rare variation in TREM2 has been associated with greater risk for Alzheimer's disease (AD). TREM2 en...
OBJECTIVES: Recently, 2 independent studies reported that a rare missense variant, rs75932628 (R47H)...
AbstractTREM and TREM-like receptors are a structurally similar protein family encoded by genes clus...
Background: Triggering receptor expressed on myeloid cells 2 (TREM2) is an important modulator of in...
Summary Alzheimer's disease is a genetically complex disorder; rare variants in the triggering rece...
Abstract Background A rare variant in the Triggering Receptor Expressed on Myeloid cells 2 (TREM2) g...
A rare variant in TREM2 (p.R47H, rs75932628) was recently reported to increase the risk of Alzheimer...
A rare variant in TREM2 (p.R47H, rs75932628) was recently reported to increase the risk of Alzheimer...
The triggering receptor expressed on myeloid 2 (TREM2) is an immune phagocytic receptor expressed on...
BACKGROUND: Homozygous loss-of-function mutations in TREM2, encoding the triggering receptor express...
BACKGROUND: Homozygous loss-of-function mutations in TREM2, encoding the triggering receptor expres...
Recent evidence suggests that rare genetic variants within the TREM2 gene are associated with increa...
the role of the TREM2 p.R47H variant as a risk factor for Alzheimer’s disease and frontotemporal dem...
Abstract Background The R47H variant of Triggering Receptor Expressed on Myeloid cells 2 (TREM2) con...
Homozygous mutations in exon 2 of TREM2, a gene involved in Nasu-Hakola disease, can cause frontotem...
Rare variation in TREM2 has been associated with greater risk for Alzheimer's disease (AD). TREM2 en...
OBJECTIVES: Recently, 2 independent studies reported that a rare missense variant, rs75932628 (R47H)...
AbstractTREM and TREM-like receptors are a structurally similar protein family encoded by genes clus...
Background: Triggering receptor expressed on myeloid cells 2 (TREM2) is an important modulator of in...
Summary Alzheimer's disease is a genetically complex disorder; rare variants in the triggering rece...