Gene Ontology annotation through association of InterPro records with GO terms

Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity

Annotation inferences using phylogenetic trees

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

Automatic Gene Ontology annotation based on Rhea mapping

Electronic Gene Ontology annotations created by ARBA machine learning models

Combined Automated Annotation using Multiple IEA Methods

Use of fluorescent substrates for characterization of Gaucher disease mutations.

Analyses of variant acid beta-glucosidases: effects of Gaucher disease mutations.

Structure of acid beta-glucosidase with pharmacological chaperone provides insight into Gaucher disease.

Integral and associated lysosomal membrane proteins.

LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase.

Acid beta-glucosidase 1 counteracts p38delta-dependent induction of interleukin-6: possible role for ceramide as an anti-inflammatory lipid.

Involvement of acid beta-glucosidase 1 in the salvage pathway of ceramide formation.

Decreased glucocerebrosidase activity in Gaucher disease parallels quantitative enzyme loss due to abnormal interaction with TCP1 and c-Cbl.

Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies.

Beta-glucosidase 1 (GBA1) is a second bile acid β-glucosidase in addition to β-glucosidase 2 (GBA2). Study in β-glucosidase deficient mice and humans.

In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.

Loss of β-glucocerebrosidase activity does not affect alpha-synuclein levels or lysosomal function in neuronal cells.

Functional analysis of 11 novel GBA alleles.

Structure of LIMP-2 provides functional insights with implications for SR-BI and CD36.

Cholesterol glucosylation is catalyzed by transglucosylation reaction of β-glucosidase 1.

The LIMP-2/SCARB2 binding motif on acid β-glucosidase: basic and applied implications for Gaucher disease and associated neurodegenerative diseases.

iPSC-derived dopamine neurons reveal differences between monozygotic twins discordant for Parkinson's disease.

Identification of miRNAs that modulate glucocerebrosidase activity in Gaucher disease cells.

Mitochondrial dysfunction associated with glucocerebrosidase deficiency.

Glucocerebrosidase gene therapy prevents α-synucleinopathy of midbrain dopamine neurons.

Glucosylated cholesterol in mammalian cells and tissues: formation and degradation by multiple cellular β-glucosidases.

Autophagic lysosome reformation dysfunction in glucocerebrosidase deficient cells: relevance to Parkinson disease.

Progranulin Recruits HSP70 to β-Glucocerebrosidase and Is Therapeutic Against Gaucher Disease.

Cryo-TEM structure of β-glucocerebrosidase in complex with its transporter LIMP-2.

Effect of saposins A and C on the enzymatic hydrolysis of liposomal glucosylceramide.

GBA1:SAPC hydrolyzes GlcCer