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UnknownAn adaptable luminescence resonance energy transfer assay for measuring and screening protein-protein interactions and their inhibition.
Not available
S-EPMC3729432 | biostudies-literature
UnknownHypermanganesemia with Dystonia 1: A Novel Mutation and Response to Iron Supplementation.
Not available
S-EPMC6962664 | biostudies-literature
ProteomicsNovel protein biomarkers of monoamine metabolism defects correlate with disease severity
Background: Genetic defects of monoamine neurotransmitters are rare neurological diseases amenable to treatment with variable response. They are major causes of early parkinsonism and other spectrum of movement disorders including dopa-responsive dystonia. Objectives: To conduct proteomic studies i...
ORGANISM(S): Homo sapiens (Human) 
2020-11-16 | PXD021642 | Pride
Proteomics Monoamine metabolism defects 
UnknownStructures of holo wild-type human cellular retinol-binding protein II (hCRBPII) bound to retinol and retinal.
Not available
S-EPMC4257620 | biostudies-literature
UnknownDecreased psychiatric symptomatology after the onset of COVID-19 in a longitudinal college mental health study.
Not available
S-EPMC9589876 | biostudies-literature
UnknownHomozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome.
Not available
S-EPMC4276403 | biostudies-literature
UnknownTuning the electronic absorption of protein-embedded all-trans-retinal.
Not available
S-EPMC4046837 | biostudies-literature
UnknownAbnormal red cell structure and function in neuroacanthocytosis.
Not available
S-EPMC4416783 | biostudies-literature
UnknownHigh frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease.
Not available
S-EPMC3381985 | biostudies-literature
UnknownEverolimus dosing recommendations for tuberous sclerosis complex-associated refractory seizures.
Not available
S-EPMC6033043 | biostudies-literature
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