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UnknownItalian screening protocol and genotypes characterization for HCV elimination (2022-2023) in Ferrara's province: a real-world study.
Not available
S-EPMC11890607 | biostudies-literature
TranscriptomicsDietary titanium dioxide (E171) increases systemic ROS levels and alters the colon transcriptome – Evidence from a human dietary intervention study
This study provides critical insights into the adverse effects of titanium dioxide (E171) on human gastrointestinal health and its potential molecular mechanisms of action, marking a significant advancement in food toxicology. Through a human dietary intervention study involving 31 participants cons...
ORGANISM(S): Homo sapiens 
2025-09-30 | E-MTAB-15089 | biostudies-arrayexpress
UnknownCase Report: Laboratory detection of a thrombotic tendency in a family with hypodysfibrinogenemia and a novel FGG mutation.
Not available
S-EPMC11518780 | biostudies-literature
TranscriptomicsTranscription profiling of human mesenchymal stromal cells to reveal senescence associated gene expression changes
Transcription profiling of human mesenchymal cells (MSCs) after ex vivo expansion under culture conditions supporting extensive cell proliferation. Highly efficient cell expansion within short time (~40 days) and comparison of gene expression profiles from MSCs after primary seeding, defined as earl...
ORGANISM(S): Homo sapiens 
2009-12-31 | E-MEXP-1997 | biostudies-arrayexpress
TranscriptomicsWhole-genome methylation analysis (450k) of school aged children prenatally exposed to alcohol vs controls
We tested a hypothesis that prenatal alcohol exposure may lead to epigenetic alterations to the DNA resulting in attentional and cognitive alterations of the children. 6-9 year old children school children of the Franconian Cognition and Emotion Studies (FRANCES) cohort which were tested for an obj...
ORGANISM(S): Homo sapiens 
2018-05-12 | E-MTAB-6730 | biostudies-arrayexpress
UnknownGP64-pseudotyped lentiviral vectors target liver endothelial cells and correct hemophilia A mice
Not available
S-SCDT-10_1038-S44321-024-00072-8 | biostudies-other
GenomicsCopy Number Variation in Congenital Kidney Malformations

We report a study of large rare, copy number variants (CNVs) in 192 patients with renal hypodysplasia (RHD). Congenital malformations of the kidney and urinary tract are present in 3 to 7 per 1,000 births, accounting for 16% of birth defects. These malformations account for 40-50% of pediatric an...

phs000565.v1.p1 | EGA
TranscriptomicsIntegrative single-cell RNA-Seq and ATAC-Seq analysis of human foetal liver and bone marrow haematopoiesis (scRNA-Seq)
This is plate-based (SmartSeq2-Seq) single-cell transcriptome data set from 15 human foetal livers and bone marrow (17-22 PCW). It includes 5,867 cells with an average of 3,074 genes per cell before QC and 4,504 cells with an average of 3,642 genes per cell after QC.
ORGANISM(S): Homo sapiens 
2020-05-25 | E-MTAB-9067 | biostudies-arrayexpress
UnknownIntermittent fasting enhances cisplatin-metformin efficacy in therapy-resistant ovarian cancer PDXs.
Not available
S-EPMC12803865 | biostudies-literature
UnknownATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion.
Not available
S-EPMC4775342 | biostudies-literature
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