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TranscriptomicsLEOPARD Syndrome iPS, BJ iPS and Fibroblasts
Expression data from LEOPARD Syndrome-iPS clones, BJ-iPS cells and parental Fibroblasts 9 samples in total are analyzed. Among 22011 genes in expression data, there are 3657 genes with at least 2 fold expression change between the average of the three fibroblast lines versus all of the iPS lines/HE...
ORGANISM(S): Homo sapiens 
2010-06-24 | E-GEOD-20473 | biostudies-arrayexpress
UnknownRapid Genome Sequencing Compared to a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic Evaluation.
Not available
S-EPMC12036383 | biostudies-literature
GenomicsGenome-wide maps of Runx3 bound regions in splenic CD8+ T cells.
ChIP-seq was conducted using freshly isolated (resting) splenic WT CD8+ T cells with anti-Runx3 antibody (Ab), anti-H3K4me1 Ab and non-immune serum (NIS) as control. Two biological Runx3 and two NIS IP repeats from splenic CD8+ T cells isolated by positive selection on anti-CD8 magnetic beads, coll...
ORGANISM(S): Mus musculus 
2013-11-18 | E-GEOD-50130 | biostudies-arrayexpress
UnknownAutomated Identification of Germline de novo Mutations in Family Trios: A Consensus-Based Informatic Approach.
Not available
S-EPMC10979888 | biostudies-literature
UnknownEfficient identification of de novo mutations in family trios: a consensus-based informatic approach.
Not available
S-EPMC11953573 | biostudies-literature
GenomicsThe transcription program of Runx3 in natural killer cells and CD8+ T cells
This SuperSeries is composed of the SubSeries listed below. Refer to individual Series
ORGANISM(S): Mus musculus 
2013-11-18 | E-GEOD-50131 | biostudies-arrayexpress
UnknownMechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency.
Not available
S-EPMC8048381 | biostudies-literature
UnknownNovel Variant Findings and Challenges Associated With the Clinical Integration of Genomic Testing: An Interim Report of the Genomic Medicine for Ill Neonates and Infants (GEMINI) Study.
Not available
S-EPMC7885094 | biostudies-literature
ProteomicsIntegration of Protein Interactome Data with Congenital Heart Disease Variants Reveals Disease Genes
Congenital Heart Disease (CHD) accounts for 1% of birth defects, and while large-scale genetic studies have uncovered genes associated with CHDs, identifying causal mutations remains a challenge. We hypothesized that genetic determinants for CHDs could be found in the protein interactomes of GATA4 a...
ORGANISM(S): Homo sapiens (Human) 
2022-07-05 | PXD022091 | Pride
Congenital heart disease Cardiomyocytes Ap-ms 
GenomicsGenome-wide maps of Runx3 bound regions in splenic IL-2-activated CD8+ T cells
ChIP-seq was conducted on isolated splenic WT CD8+ T cells, TCR-activated and cultured with IL-2 using anti-Runx3 antibodies (Ab), anti-H3K4me1 Ab and non-immune serum (NIS) as control. Two biological Runx3 and two NIS IP repeats from TCR-activated and IL-2 cultured splenic CD8+ T cells isolated by ...
ORGANISM(S): Mus musculus 
2013-11-18 | E-GEOD-50128 | biostudies-arrayexpress
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