TOP TEN perturbations for 40062_s_at (Homo sapiens)
Organism: Homo sapiens
Gene: 40062_s_at
Selected probe(set): 210395_x_at
Platform: Affymetrix Human Genome U133 Plus 2.0 Array
Expression of 40062_s_at (210395_x_at) across 6674 perturbations tested by GENEVESTIGATOR:
systemic onset JIA study 4 / juvenile enthesitis related arthritis study 2 (ERA)
Relative Expression (log2-ratio):5.039178Number of Samples:3 / 3
Experimental | systemic onset JIA study 4 |
Peripheral blood mononuclear cell (PBMC) samples from children with systemic onset of juvenile rheumatoid arthritis (JIA). | |
Control | juvenile enthesitis related arthritis study 2 (ERA) |
Peripheral blood mononuclear cell (PBMC) samples from children with enthesitis related arthritis (ERA). |
systemic onset JIA study 5 / oligoarticular JIA study 2
Relative Expression (log2-ratio):4.8316946Number of Samples:3 / 12
Experimental | systemic onset JIA study 5 |
Peripheral blood mononuclear cell (PBMC) samples from children with recent onset and systemic onset of juvenile rheumatoid arthritis (SoJIA). All patients were free of disease modifying antirheumatic drugs or biologics. Subjects were classified according to ILAR criteria. Patients were enrolled in the study very early in the disease course, hence difference between disease onset and age at sampling is small (<4-8 month). | |
Control | oligoarticular JIA study 2 |
Peripheral blood mononuclear cell (PBMC) samples from children with recent onset of persistent oligoarticular juvenile idiopathic arthritis (JIA). All patients were free of disease modifying antirheumatic drugs or biologics. Subjects were classified according to ILAR criteria. Patients were enrolled in the study very early in the disease course, hence difference between disease onset and age at sampling is small (<4-8 month). |
myotonic dystrophy study 4 (deltoid muscle; DM-like) / normal skeletal muscle tisuue (fetal)
Relative Expression (log2-ratio):-4.6418123Number of Samples:3 / 3
Experimental | myotonic dystrophy study 4 (deltoid muscle; DM-like) |
Deltoid muscle biopsies obtained from patients with myotonic-like dystrophy (DMx; DM-like; no DMPK or ZNF9 expansion). | |
Control | normal skeletal muscle tisuue (fetal) |
Commercially purchased normal fetal skeletal muscle tissue samples. |
systemic onset JIA study 5 / normal PBMC sample
Relative Expression (log2-ratio):4.530195Number of Samples:3 / 27
Experimental | systemic onset JIA study 5 |
Peripheral blood mononuclear cell (PBMC) samples from children with recent onset and systemic onset of juvenile rheumatoid arthritis (SoJIA). All patients were free of disease modifying antirheumatic drugs or biologics. Subjects were classified according to ILAR criteria. Patients were enrolled in the study very early in the disease course, hence difference between disease onset and age at sampling is small (<4-8 month). | |
Control | normal PBMC sample |
Peripheral blood mononuclear cell (PBMC) samples from healthy children. |
systemic onset JIA study 4 / normal PBMC sample
Relative Expression (log2-ratio):4.505066Number of Samples:3 / 27
Experimental | systemic onset JIA study 4 |
Peripheral blood mononuclear cell (PBMC) samples from children with systemic onset of juvenile rheumatoid arthritis (JIA). | |
Control | normal PBMC sample |
Peripheral blood mononuclear cell (PBMC) samples from healthy children. |
systemic onset JIA study 4 / oligoarticular JIA study 3
Relative Expression (log2-ratio):4.4818907Number of Samples:3 / 12
Experimental | systemic onset JIA study 4 |
Peripheral blood mononuclear cell (PBMC) samples from children with systemic onset of juvenile rheumatoid arthritis (JIA). | |
Control | oligoarticular JIA study 3 |
Peripheral blood mononuclear cell (PBMC) samples from children with persistent oligoarthritis (oligoarticular JIA). |
myotonic dystrophy study 4 (biceps brachii; DM-like) / normal skeletal muscle tisuue (fetal)
Relative Expression (log2-ratio):-4.3467903Number of Samples:9 / 3
Experimental | myotonic dystrophy study 4 (biceps brachii; DM-like) |
Biceps brachii biopsies obtained from patients with myotonic-like dystrophy (DMx; DM-like; no DMPK or ZNF9 expansion). | |
Control | normal skeletal muscle tisuue (fetal) |
Commercially purchased normal fetal skeletal muscle tissue samples. |
myotonic dystrophy study 4 (skeletal muscle; DM1) / normal skeletal muscle tisuue (fetal)
Relative Expression (log2-ratio):-4.2683945Number of Samples:5 / 3
Experimental | myotonic dystrophy study 4 (skeletal muscle; DM1) |
Unspecified skeletal muscle biopsies obtained from patients with myotonic dystrophy type 1 (DM1). | |
Control | normal skeletal muscle tisuue (fetal) |
Commercially purchased normal fetal skeletal muscle tissue samples. |
myotonic dystrophy study 4 (biceps brachii; DM1) / normal skeletal muscle tisuue (fetal)
Relative Expression (log2-ratio):-4.2325296Number of Samples:3 / 3
Experimental | myotonic dystrophy study 4 (biceps brachii; DM1) |
Biceps brachii biopsies obtained from patients with myotonic dystrophy type 1 (DM1). | |
Control | normal skeletal muscle tisuue (fetal) |
Commercially purchased normal fetal skeletal muscle tissue samples. |
myotonic dystrophy study 4 (biceps brachii; DM2) / normal skeletal muscle tisuue (fetal)
Relative Expression (log2-ratio):-4.2208652Number of Samples:3 / 3
Experimental | myotonic dystrophy study 4 (biceps brachii; DM2) |
Biceps brachii biopsies obtained from patients with myotonic dystrophy type 2 (DM2). | |
Control | normal skeletal muscle tisuue (fetal) |
Commercially purchased normal fetal skeletal muscle tissue samples. |