5xFAD |
Transgenic mouse model carrying APP KM670/671NL (Swedish), APP I716V (Florida), APP V717I (London), PSEN1 M146L (A>C), PSEN1 L286V mutations |
AAO |
Age at onset |
ABCA7 |
ATP-binding cassette subfamily A member 7 |
ACE |
Angiotensin I-converting enzyme |
AD |
Alzheimer’s disease |
ADAD |
Autosomal dominant Alzheimer’s disease |
ADAM10 |
ADAM metallopeptidase domain 10 |
ALS |
Amyotrohpic lateral sclerosis |
ANK1 |
Ankyrin 1 |
APOE |
Apolipoprotein E |
APP |
Amyloid precursor protein |
APPNL-G-F
|
Knock-in mice model carrying the APP KM670/671NL (Swedish), APP I716F (Iberian), APP E693G (Arctic) mutations |
APPswe/PS1dE9 |
Transgenic mouse model carrying APP KM670/671NL (Swedish), PSEN1: deltaE9 mutations |
APPPS1-21 |
Transgenic mouse model carrying APP KM670/671NL (Swedish), PSEN1 L166P |
ASO |
Antisense oligonucleotides |
Aβ |
Amyloid β |
BACE |
β secretase, also known as β-site Amyloid precursor protein Ceaving Enzyme |
BBB |
Blood-brain barrier |
BV2 |
Immortalized murine microglial cell line |
CD2AP |
CD2-associated protein |
CD33 |
Myeloid cell surface antigen CD33 |
CDR |
Clinical dementia ratio |
CE |
Cholesterol ester |
CERAD |
Consortium to Establish a Registry for Alzheimer’s Disease |
CELF1 |
CUGBP Elav-like family member 1 |
CLU |
Clusterin |
CNS |
Central nervous system |
CNV |
Copy number variant |
CR1 |
Complement C3b/C4b receptor 1 (Knops blood group) |
CSF |
Cerebrospinal fluid |
CT |
Computerized tomography |
DAM |
Disease-associated microglia |
DIAN |
Dominantly inherited network |
DLB |
Dementia with Levy bodies |
EMP |
Erithro-myeloid progenitor |
EAAT |
Excitatory amino acid-mediated transporters |
EOAD |
Early onset Alzheimer’s disease |
EPHA1 |
EPH receptor A1 |
ERK |
Extracellular signal-regulated kinase |
ETA
|
Endothelin A receptor |
EWAs |
Epigenome-wide association studies |
fAD |
Familial Alzheimer’s disease |
fLOAD |
Familial late-onset Alzheimer’s disease |
FDR |
False discovery rate |
FTD |
Frontotemporal dementia |
GWA |
Genome-wide association |
H3K9ac |
Histone 3 lysine 9 acetylation |
H4K16ac |
Histone 4 lysine 16 acetylation |
HD |
Huntington’s disease |
HSPG |
Heparan sulfate proteoglycan |
iPSC |
Induced pluripotent stem cells |
ITAM |
Immunoreceptor tyrosine-based activation motif |
LDLR |
Low-density lipoprotein receptor |
LOAD |
Late-onset Alzheimer’s disease |
LRP1 |
LDL (low-density lipoprotein) receptor-related protein 1 |
MAP |
Memory and aging project |
MAPK |
Mitogen-activated protein kinases (formerly known as ERK) |
MAPT |
Microtubule-associated protein tau |
MCI |
Mild cognitive impairment |
MDMi |
Monocyte-derived microglia-like cells |
MKK7 |
MAPK kinase 7 |
MMSE |
Mini-mental state examination |
MOca |
Montreal Cognitive Assessment |
MRI |
Magnetic resonance imaging |
MS4A |
Membrane spanning 4 |
MS4A4A |
Membrane spanning 4-domains A4A |
mTOR |
Mechanistic target of rapamycin |
NfL |
Neurofilament Ligtht |
NFTs |
Neuro fibrillary tangles |
NGRN |
Neurogranin |
NLRP3 |
Nucleotide-binding domain (NOD)-like receptor protein 3 |
NOX4 |
NADPH oxidase 4 |
NT |
Neuropil threads |
p38MAPK |
p38 mitogen-activated protein kinase |
PD |
Parkinson’s disease |
PET |
Positron emission tomography |
PGRN |
Progranulin |
PI3K |
Phosphatidylinositol-3-kinase |
PIB |
Pittsburgh compound B |
PICALM |
Phosphatidylinositol-binding clathrin assembly protein |
PPAR |
Peroxisome proliferator-activated receptor |
PRS |
Polygenic Risk Score |
PS19 |
Transgenic mouse model carrying MAPT P301S mutation |
PSEN1 |
Presenilin 1 |
PSEN2 |
Presenilin 2 |
ROS |
Religious Order Study |
sAD |
Sporadic Alzheimer’s disease |
sLOAD |
Sporadic late-onset Alzheimer’s disease |
SNPs |
Single nucleotide polymorphism |
sPDGFRβ |
Soluble platelet-derived growth factor receptor-β |
SPI1 |
Spi-1 proto-oncogene |
TLRs |
Toll-like receptors |
TMEM106B |
Transmembrane protein 106B |
TREM2 |
Triggering receptor expressed on myeloid cells 2 |
TWAs |
Transcriptome-wide association studies |
TYROBP |
Transmembrane immune signaling adaptor TYROBP |
VD |
Vascular dementia |
VILIP1 |
Visinin-like 1 |