Unexpected consequences of combined glucocerebrosidase and acid sphingomyelinase deficiency in a model of Parkinson’s disease - - GEO DataSets

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Unexpected consequences of combined glucocerebrosidase and acid sphingomyelinase deficiency in a model of Parkinson’s disease

(Submitter supplied) Heterozygous variants in GBA1, encoding glucocerebrosidase (GCase), are the most common genetic risk factor for Parkinson’s disease (PD). Moreover, sporadic PD patients also have a substantial reduction of GCase activity. Genetic variants of SMPD1 are also overrepresented in PD cohorts, whereas a reduction of its encoded enzyme (acid sphingomyelinase or ASM) activity is linked to an earlier age of PD onset. more...

Organism:: Danio rerio

Type:: Expression profiling by high throughput sequencing

Platform:: GPL18413
16 Samples

Download data: SF

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Accession:: GSE229995

ID:: 200229995

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Unexpected consequences of combined glucocerebrosidase and acid sphingomyelinas...
Unexpected consequences of combined glucocerebrosidase and acid sphingomyelinase deficiency in a model of Parkinson’s disease
Accession: GSE229995

GEO DataSets
Ruminococcus sp. AM32-17LB AM32-17LB.Scaf1, whole genome shotgun sequence
Ruminococcus sp. AM32-17LB AM32-17LB.Scaf1, whole genome shotgun sequence
gi|1472580683|gb|QUIY01000001.1||gn :QUIY01|AM32-17LB.Scaf1

Nucleotide

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