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UnknownSpatially-Resolved Proteomics: Rapid Quantitative Analysis of Laser Capture Microdissected Alveolar Tissue Samples.
Not available
S-EPMC5177886 | biostudies-literature
UnknownSpatial distribution of marker gene activity in the mouse lung during alveolarization.
Not available
S-EPMC6307338 | biostudies-literature
TranscriptomicsCandidate driver genes in focal chromosomal aberrations of stage II colon cancer
Chromosomal instable colorectal cancer is marked by specific large chromosomal copy number aberrations. Recently, focal aberrations of 3Mb or smaller have been identified as a common phenomenon in cancer. Inherent to their limited size, these aberrations harbour one or few genes. The aim of this stu...
ORGANISM(S): Homo sapiens 
2010-04-19 | E-GEOD-17047 | biostudies-arrayexpress
TranscriptomicsTranscriptome comparison of bat (Miniopterus natalensis) forelimb and hindlimb autopods at developmental stages CS16 and CS17 and E13.5 mouse forelimb autopods
The bat offers an alternative paradigm to the standard mouse and chick model of limb development as it has extremely divergent forelimbs (long digits supporting a wing) and hindlimbs (short digits and claws) due the distinct requirements of both aerial and terrestrial locomotion. We used a cross-spe...
ORGANISM(S): Mus musculus 
2014-02-15 | E-GEOD-51042 | biostudies-arrayexpress
TranscriptomicsirCLIP of SRSF3 in a mouse epicardial cell line
This experiment aims to map SRSF3 binding to the global transcriptome in a mouse epicardial cell line
ORGANISM(S): Mus musculus 
2022-12-31 | E-MTAB-11853 | biostudies-arrayexpress
Genomicsena-DATASET-UCAM-GEL-15-04-2015-15:15:23:555-345 - samples
Whole exome sequencing BAM files for samples from the BRIDGE Consortium with pathogenic or likely pathogenic variants on genes linked to bleeding or platelet disorders.
EGAD00001001333 | EGA
GenomicsSequencing of heritable Bleeding and Platelet Disorders
The BRIDGE-BPD study aims to discover new causal genes for Bleeding and Platelet Disorders (BPD) by high throughput sequencing using cluster analyses based on improved and standardized deep phenotyping of cases. BPD is one of the 13 Rare Disease projects under the NIHR BioResource Rare Diseases BRID...
EGAS00001001172 | EGA
GenomicsNIHR BioResource DAC
Data Access Committee EGAC00001000259
EGAC00001000259 | EGA
UnknownSomatic mutation and selection at population scale.
Not available
S-EPMC12611758 | biostudies-literature
TranscriptomicsMolecular profiling of blastic plasmacytoid dendritic cell neoplasm reveals a unique pattern and suggests selective sensitivity to nf-kb pathway inhibition
Molecular profiling of blastic plasmacytoid dendritic cell neoplasm reveals a unique pattern and suggests selective sensitivity to nf-kb pathway inhibition To better understand the pathobiology of BPDCN and discover new targets for effective therapies, the gene expression profile (GEP) of 25 BPDCN s...
ORGANISM(S): Homo sapiens 
2014-10-03 | E-GEOD-62014 | biostudies-arrayexpress
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