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UnknownEffectiveness and safety of first-generation protease inhibitors in clinical practice: Hepatitis C virus patients with advanced fibrosis.
Not available
S-EPMC4533049 | biostudies-literature
GenomicsIIS - Fundacion Jimenez Diaz Data Access Committee
Data Access Committee EGAC00001002010
EGAC00001002010 | EGA
TranscriptomicsExpression data from control and Phospholipid dependent kinase 1 (PDK1) null cytotoxic T-lymphocytes (CTL) and from control and Akt inhibitor treated CTL
In cytotoxic T cells (CTL), Protein Kinase B /Akt is activated by the T cell antigen receptor (TCR) and the cytokine Interleukin 2 (IL2), in part by phosophorylation of Akt by Phospholipid dependent kinase 1 (PDK1). The role of PDK1 and Akt in CTL has however not been fully defined. In order to expl...
ORGANISM(S): Mus musculus 
2011-02-01 | E-GEOD-26290 | biostudies-arrayexpress
UnknownAcute Pancreatitis Associated with Propofol in a Patient with End-Stage Renal Disease: Diagnostic Challenges and Confounding Factors
Not available
S-EPMC12935577 | biostudies-literature
Genomics58747723-e185-4df8-aac6-8e65d2b0f0d3 - samples
In the context of research, this dataset contains 423 IRD samples; 411 of them analyzed with Clinical Exome Sequencing solutions, and 12 with Whole Exome Sequencing.
EGAD00001007022 | EGA
GenomicsGenetic landscape of inherited retinal dystrophies affected cases in Spain
Inherited retinal diseases (IRDs), defined by dysfunction or progressive loss of photoreceptors, are disorders characterized by elevated heterogeneity, both at the clinical and genetic levels. Our main goal was to address the genetic landscape of IRD in a Spanish cohort of patients. A retrospective ...
EGAS00001005104 | EGA
UnknownNoninvasive Ventilation for Pediatric Acute Respiratory Distress Syndrome: Experience From the 2016/2017 Pediatric Acute Respiratory Distress Syndrome Incidence and Epidemiology Prospective Cohort Study.
Not available
S-EPMC10524424 | biostudies-literature
UnknownLiver status and outcomes in patients without previous known liver disease receiving anticoagulant therapy for venous thromboembolism.
Not available
S-EPMC8501936 | biostudies-literature
TranscriptomicsA human ESC model for MLL-AF4 reveals an impaired early human hemato-endothelial specification
The MLL-AF4 fusion gene is a hallmark genomic aberration in high-risk acute lymphoblastic leukemia in infants. Although it is well-established that MLL-AF4 arises pre-natally during human development, its effects on hematopoietic development in utero remains unexplored. We have created a human-spec...
ORGANISM(S): Homo sapiens 
2011-06-09 | E-GEOD-29869 | biostudies-arrayexpress
TranscriptomicsGene Expression in Whole Blood of Atopic Eczema and Healthy Children at 4 years
We studied genes that are related to atopic diseases [i.e., atopic eczema (AE)]. Immunological factors and principal genes involved in the biosynthesis of polyunsaturated fatty acids were included. We analyzed whether expression of genes encoding key enzymes of LC-PUFA synthesis (FADS1, FADS2 and EL...
ORGANISM(S): Homo sapiens 
2013-06-29 | E-GEOD-48310 | biostudies-arrayexpress
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