mRNA expression data from human adenocarcinomas of the stomach43adenocarcinomascancerdisease3703FalseE-GEOD-22377humanmrna-expression-data-from-human-adenocarcinomas-of1Mucosal biopsies from groups Normal (NOR) and patients who underwent curative large bowel resection for colorectal cancer (M-CRC)17cancercolorectal cancerdiseasegenomemucosa2209FalseE-GEOD-23194humanmucosal-biopsies-from-groups-normal-nor-and-patien1Multiple Salivary Biomarkers for Early Detection of Pancreatic Cancer24cancerdiseasegenomehepatitishiv infectionpancreatic cancerpancreatitissaliva3127FalseE-GEOD-14245humanmultiple-salivary-biomarkers-for-early-detection-o0New insights into key genes and pathways involved in the pathogenesis of HLA-B27-associated acute anterior uveitis6anterioranterior uveitischoleradiseaselipopolysaccharideperipheralproteinuveitis4474FalseE-GEOD-37588humannew-insights-into-key-genes-and-pathways-involved1NOD2 and desease associated variant NOD2-L1007fsinsC dependent genomewide transcriptional regulation in stable Flp-In HEK cells27asthmaatopic eczemacellcrohn diseasediseasegenome3725FalseE-GEOD-22611humannod2-and-desease-associated-variant-nod2-l1007fsin2Nonlesional atopic dermatitis skin is characterized by broad terminal differentiation defects and variable immune abnormalities33atopic dermatitisdermatitisdiseaseskinskin disease4264FalseE-GEOD-32924humannonlesional-atopic-dermatitis-skin-is-characterize3NOTCH3 knockdown in non-transformed human esophageal cells12cancercarcinomacelldiseasefingernotchsquamoussquamous cellsquamous cell carcinomastem cell3972FalseE-GEOD-27424humannotch3-knockdown-in-non-transformed-human-esophage2Notch is active in Langerhans Cell Histiocytosis and confers pathognomonic features on dendritic cells.17celldendriticdiseasehistiocytosislangerhans cellperipheralskin4395FalseE-GEOD-35340humannotch-is-active-in-langerhans-cell-histiocytosis-a3Novel mutations target distinct subgroups of medulloblastoma.76braincellchromatindiseaselipmedulloblastomapediatric medulloblastoma4469FalseE-GEOD-37418humannovel-mutations-target-distinct-subgroups-of-medul5OXPHOS complex I deficiency leads to transcriptional changes of the Nrf2-Keap1 pathway and selenoproteins.20diseasegenomelactic acidosisleigh syndromemembranemyopathyskinstrokesyndrome3952FalseE-GEOD-27041humanoxphos-complex-i-deficiency-leads-to-transcription4