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GenomicsNext Generation Sequencing Approaches to Childhood Neurological Diseases
Next Generation Sequencing Approaches to Childhood Neurological Diseases
PRJNA314925 | ENA
ProteomicsEnabling phenotypic drug discovery for neurological mitochondrial DNA disorders with patient-derived neural progenitor cells
Mitochondrial DNA (mtDNA) mutations predominantly cause neurological diseases. Searching for therapeutic strategies is hindered by the absence of viable neural model systems due to the challenges of engineering mtDNA. We demonstrate that neural progenitor cells (NPCs), rapidly obtained from human in...
ORGANISM(S): Homo Sapiens (ncbitaxon:9606) 
2017-03-31 | MSV000080849 | MassIVE
GenomicsParoxysmal neurological disorders
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAS00001000048 | EGA
GenomicsParoxysmal neurological Disorders
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAS00001000386 | EGA
GenomicsParoxysmal Neurological Disorders 2
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAS00001000190 | EGA
GenomicsIdentifying autosomal recessive mutations causing neurological disorders
The objective of this study is to resequence of targeted intervals containing autosomal recessive variants causing neurological disorders in consanguineous pedigrees. Using homozygosity mapping, three intervals of very different sizes have previously been unambiguously mapped for three different neu...
EGAS00001000023 | EGA
GenomicsParoxysmal Neurological Disorders rare epilepsies
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of EuroEPINOMICS. Most cases have a strong family history. The study sample will include both cases and controls.
EGAS00001000421 | EGA
UnknownImaging of brain barrier inflammation and brain fluid drainage in human neurological diseases.
Not available
S-EPMC10838199 | biostudies-literature
ProteomicsMagnetic Transferrin Assay (MTA) as a novel approach for discovering serum exosome derived protein biomarkers in neurological diseases
We developed TF-based MNPs (TF-MNPs) to isolate blood-derived exosome in this study and isolated the blood-derived exosomes of patients with neuroinflammatory diseases, such as dementia, Parkinson’s disease and multiple sclerosis via this strategy and then evaluated the proteomic profiling of these ...
ORGANISM(S): Homo sapiens (Human) 
2023-02-20 | PXD038555 | Pride
Human Serum exosome Lc-msms Dementia Multiple sclerosis Parkinson Neurological disease 
UnknownTransporters as Drug Targets in Neurological Diseases.
Not available
S-EPMC5056151 | biostudies-literature
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