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UnknownRituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome.
Not available
S-EPMC3968490 | biostudies-literature
GenomicsNeuroblastoma Genome-Wide Association Study (NBL-GWAS)

Neuroblastoma is a malignancy of the developing sympathetic nervous system that most commonly affects young children and is often lethal. The etiology of this embryonal cancer is not known.

We have performed a whole genome scan for association of neuroblastoma with SNP genotypes an...

phs000124.v2.p1 | EGA
MetabolomicsNMR-based metabolomic profile of hypercholesterolemic human sera: Relationship with in vitro gene expression?
Hypercholesterolaemia is considered an important cause of atherosclerotic cardiovascular disease. In a previous investigation, we demonstrated that cultured hepatoma cells treated with hypercholesterolaemic sera compared with cells treated with normocholesterolaemic sera show overexpression of mRNAs...
2020-05-26 | MTBLS1416 | MetaboLights
TranscriptomicsAn 18 gene expression-based score classifier predicts the clinical outcome in stage 4 neuroblastoma
The prognosis of children with metastatic stage 4 neuroblastoma (NB) has remained poor in the past decade. Using microarray analyses of 342 primary tumors, we here developed and validated an easy to use gene expression-based risk score including 18 genes, which can robustly predict the outcome of st...
ORGANISM(S): Homo sapiens 
2016-04-05 | E-GEOD-79910 | biostudies-arrayexpress
TranscriptomicsGene expression profiling in neuroblastoma cells upon CHAF1A silencing
We used an inducible ShRNA system and microarrays to detail the global programme of gene expression underlying neuroblastoma differentiation upon CHAF1A silencing . CHAF1A is a subunit of the Chromatin Assembly Factor-1 (CAF1) and regulates H3K9-trimethylation. High expression of CHAF1A strongly cor...
ORGANISM(S): Homo sapiens 
2013-11-01 | E-GEOD-51978 | biostudies-arrayexpress
UnknownATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion.
Not available
S-EPMC4775342 | biostudies-literature
UnknownHFE p.H63D polymorphism does not influence ALS phenotype and survival.
Not available
S-EPMC5183653 | biostudies-literature
UnknownThe European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results.
Not available
S-EPMC8173879 | biostudies-literature
UnknownNeuropeptide Y as a risk factor for cardiorenal disease and cognitive dysfunction in chronic kidney disease: translational opportunities and challenges.
Not available
S-EPMC8713155 | biostudies-literature
TranscriptomicsTargeting ATP2B1 impairs PI3K/Akt/Forkhead box (Fox) transcription factor signaling and reduces SARS-COV-2 infection and replication
RNA-seq of human cells Edited using CRISPR vs parental and Unedited control. We identified a rare homozygous intronic variant in the ATP2B1 locus (rs111337717; chr12:89643729, T>C) that is associated with the severity of COVID-19 (i.e., symptomatic versus asymptomatic patients). Next, we employed ...
ORGANISM(S): Homo sapiens 
2024-05-13 | E-MTAB-13916 | biostudies-arrayexpress
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