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UnknownThe adaptive immune and immune checkpoint landscape of neoadjuvant treated esophageal adenocarcinoma using digital pathology quantitation.
Not available
S-EPMC7268770 | biostudies-literature
UnknownLack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies.
Not available
S-EPMC10648441 | biostudies-literature
UnknownIdentification of a prognostic signature in colorectal cancer using combinatorial algorithm-driven analysis.
Not available
S-EPMC8977276 | biostudies-literature
UnknownPatient reported outcome measures for cardiac ablation procedures: a multicentre pilot to develop a new questionnaire.
Not available
S-EPMC4209127 | biostudies-literature
TranscriptomicsTranscription profiling of human skin biopsies from individuals with a diagnosis of systemic sclerosis with diffuse scleroderma vs biopsies from normal individiduals
We used DNA microarrays to characterize gene expression patterns in skin biopsies from individuals with a diagnosis of systemic sclerosis with diffuse scleroderma and compared those to the patterns of gene expression seen in biopsies from normal, unaffected individuals.
ORGANISM(S): Homo sapiens 
2013-01-30 | E-MEXP-32 | biostudies-arrayexpress
UnknownFeature tracking CMR reveals abnormal strain in preclinical arrhythmogenic right ventricular dysplasia/ cardiomyopathy: a multisoftware feasibility and clinical implementation study.
Not available
S-EPMC5581480 | biostudies-literature
UnknownAssociation of Antipsychotic Treatment With Risk of Unexpected Death Among Children and Youths.
Not available
S-EPMC6440238 | biostudies-literature
UnknownDiagnosing arrhythmogenic right ventricular cardiomyopathy by 2010 Task Force Criteria: clinical performance and simplified practical implementation.
Not available
S-EPMC7203633 | biostudies-literature
UnknownOutcome after surgery alone or with restricted use of chemotherapy for patients with low-risk neuroblastoma: results of Children's Oncology Group study P9641.
Not available
S-EPMC3383182 | biostudies-literature
GenomicsGenome wide association study of Coeliac Disease
We performed a second-generation genome-wide association study of 4,533 individuals with celiac disease (cases) and 10,750 control subjects. We genotyped 113 selected SNPs with P(GWAS) < 10(-4) and 18 SNPs from 14 known loci in a further 4,918 cases and 5,684 controls. Variants from 13 new regions r...
EGAS00000000057 | EGA
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