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UnknownA randomized, double-blind, placebo-controlled trial of intravenous alpha-1 antitrypsin for ARDS secondary to COVID-19.
Not available
S-EPMC8913266 | biostudies-literature
UnknownClinical and Genetic Risk Factors for Acute Pancreatitis in Patients With Acute Lymphoblastic Leukemia.
Not available
S-EPMC4962704 | biostudies-literature
TranscriptomicsRNA-sequencing TS23 humerus and associated joints
RNA-sequencing profiling analysis was performed on TS23 humerus tissue from control mice(splotch-delayed). The purpose of this profiling analysis was to identify the transcriptome and expression profile of the developing humerus rudiment and associated joints at embryonic theiler stage 23 (E14.5) du...
ORGANISM(S): Mus musculus 
2014-01-23 | E-MTAB-1745 | biostudies-arrayexpress
TranscriptomicsRNA-sequencing DE Spd (humerus)
RNA-sequencing profiling analysis was performed on TS23 humerus tissue from muscle-less mutant (splotch-delayed) mice and compared to control littermates. The purpose of this profiling analysis was to identify differentially expressed genes between muscle-less and control embryonic (TS23) humerus ti...
ORGANISM(S): Mus musculus 
2014-01-23 | E-MTAB-1746 | biostudies-arrayexpress
TranscriptomicsComparative genomic hybridization of human samples with deletions of 16p11.2p12.2 or duplication/triplication of 16p11.2p12.2 to identify the breakpoints
Array CGH was performed to identify the breakpoints in 3 cases with deletions of 16p11.2p12.2 and 1 case with a duplication/triplication of 16p11.2p12.2.
ORGANISM(S): Homo sapiens 
2007-09-01 | E-TABM-286 | biostudies-arrayexpress
TranscriptomicsGenotyping of two patients with microdeletions of 16p11.2p12.2 to refine the breakpoint locations
Whole genome genoyping/copy-number analysis was performed on two patients with microdeletions of 16p11.2p12.2 to refine the breakpoint locations.
ORGANISM(S): Homo sapiens 
2007-09-01 | E-MEXP-1148 | biostudies-arrayexpress
GenomicsGenome-Wide Analysis of Hypodiploid Acute Lymphoblastic Leukemia

Hypodiploid acute lymphoblastic leukemia (ALL) is an aggressive form of leukemia characterized by multiple whole chromosomal losses and very poor outcome. Here we report an integrative genomic analysis that identifies multiple subtypes of hypodiploid ALL characterized by variation in the degree o...

phs000341.v1.p1 | EGA
GenomicsWhole Genome Sequencing of a Triple Negative Breast Cancer Patient: Matched Primary Tumor, Normal, Metastasis and Xenograft samples

Breast Cancer Subject Participant ID 700064 (Source Sample names: 6888 and 206). We used massively parallel DNA sequencing technologies to screen entire genomes, in an unbiased manner, for genetic changes associated with tumor growth and metastasis. We describe the complete genome sequence ...

phs000245.v1.p1 | EGA
GenomicsPCGP Ph-likeALL RNASeq - samples
DATA FILES FOR SJPhLike-RNASeq
EGAD00001001016 | EGA
GenomicsPCGP Ph-likeALL SNP6 - samples
PCGP Ph-likeALL SNP6
EGAD00010000598 | EGA
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