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. 2019 Dec 16;24(24):4604. doi: 10.3390/molecules24244604
AD Alzheimer’s disease
AGEs Advanced glycation end-product
AICD Amyloid precursor protein intracellular domain
ALS Amyotrophic lateral sclerosis
ANP Atrial natriuretic peptide
APP Amyloid precursor protein
Asn Asparagine
Amyloid beta
BACE-1 β-Site APP-cleaving enzyme 1
CAG Glutamine-coding
CCI4 Carbon tetrachloride
CMD Congenital muscular dystrophy
CML N-carboxymethyl-lysine
CN Caudate nucleus
CNS Central nervous system
COX-2 Cyclooxygenase-2
CSF Cerebrospinal fluid
CTF C-terminal fragments
CTLA-4 Cytotoxic T lymphocyte antigen 4
dolichol-P Dolichol-phosphate
DON 6-Diazo-5-oxo-L-norleucine
ECM Extracellular matrix
ELISA Enzyme-linked immunosorbent assay
ER Endoplasmic reticulum
ERAD ER-associated degradation
ErkFDA Extracellular signal-regulated kinasesFood and Drug Administration
GlcNAc N-acetylglucosamine
GlcNAc-1-P N-acetylglucosamine-1-phosphate
GlcNAc6ST1 A carbohydrate sulfotransferase
GM1 Monosialotetrahexosylganglioside
GM2 Monosialic ganglioside
GM3 Monosialodihexosylganglioside
GSLs Glycosphingolipids
HD Huntington’s disease
HMGB1 High mobility group box 1 protein
HNK-1 Human natural killer-1 glycan antigen
HSAS X-linked hydrocephalus with stenosis of the aqueduct of sylvius
I-R Ischemia–reperfusion
IgG Immunoglobulin G
IL-6 Interleukin 6
L-DOPA Levodopa
L1CAM Neural cell adhesion molecule L1
LacCer Lactosylceramide
Lewy bodies α-Synuclein aggregates
LeX LewisX
LIGA-20 A blood–brain barrier-permeable GM1 analogue
MALDI-TOF Matrix-assisted Laser Desorption/Ionization
MASA syndrome A rare X-linked recessive neurological disorder on the L1 disorder spectrum
MEB Muscle–eye–brain disease
mHtt Mutant huntingtin
MS Multiple Sclerosis
NCAM Neural cell adhesion molecule
NeuGc N-glycolylneuraminic acid
NF-kβ Nuclear factor kappa-light-chain-enhancer of activated B cells
NO Nitric oxide
NSPC Neural stem and progenitor cells
NTD Neural tube defect
O-GlcNAc O-linked β-N-acetylglucosamine
OGA O-GlcNAcase
OGT O-GlcNAc transferase
P0 Myelin protein zero
p3 peptide 3-kDa fragments of amino-terminal truncated Aβ peptides
PD Parkinson’s disease
PHFs Paired helical filaments
PNS Peripheral nervous system
pRb Etinoblastoma protein
PS Presenilin
PSA Polysialic acid
PST ST8Sia IV
PTM Post-translational modification
RAGE Receptor for advanced glycation end-products
ROS Reactive oxygen species
Ser Serine
Sirt1 NAD-dependent deacetylase sirtuin-1
sLeX Sialyl LewisX
SOD1 Superoxide dismutase 1
sRAGE Soluble receptor for advanced glycation end-products
ST Sialyltransferase
STAT3 Signal transducer and activator of transcription 3
STX ST8Sia II
Thr Threonine
TNF-α Tumor necrosis factor alpha
UA Ursolic acid
UDP Uridine diphosphate
α-Sp22 A glycosylated form of α-synuclein