Pages that link to "Q24312136"
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The following pages link to Human immune disorder arising from mutation of the alpha chain of the interleukin-2 receptor (Q24312136):
Displaying 50 items.
- CD25 deficiency (Q5009803) (← links)
- Interleukin 2 receptor subunit alpha (Q21113423) (← links)
- Identification of STAT5A and STAT5B target genes in human T cells (Q21132341) (← links)
- The Genetic Association of Variants in CD6, TNFRSF1A and IRF8 to Multiple Sclerosis: A Multicenter Case-Control Study (Q21560832) (← links)
- Human IL2RA null mutation mediates immunodeficiency with lymphoproliferation and autoimmunity (Q24317691) (← links)
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Q24550675) (← links)
- Opposing regulation of the locus encoding IL-17 through direct, reciprocal actions of STAT3 and STAT5 (Q24635387) (← links)
- Therapeutic targeting of Janus kinases (Q24658483) (← links)
- The quantal theory of how the immune system discriminates between "self and non-self" (Q24803143) (← links)
- Janus kinases and signal transducers and activators of transcription: their roles in cytokine signaling, development and immunoregulation (Q24806655) (← links)
- Inborn errors of the development of human natural killer cells (Q26827686) (← links)
- Homeostasis and function of regulatory T cells (Tregs) in vivo: lessons from TCR-transgenic Tregs (Q26853599) (← links)
- T-regulatory cells in primary immune deficiencies (Q26862699) (← links)
- Daclizumab therapy for multiple sclerosis (Q27022517) (← links)
- Practice parameter for the diagnosis and management of primary immunodeficiency (Q29042159) (← links)
- Contrasting genetic association of IL2RA with SLE and ANCA-associated vasculitis (Q33415374) (← links)
- Malignant catarrhal fever of cattle is associated with low abundance of IL-2 transcript and a predominantly latent profile of ovine herpesvirus 2 gene expression (Q33482148) (← links)
- Impaired up-regulation of CD25 on CD4 T cells in IFN-gamma knockout mice is associated with progression of myocarditis to heart failure (Q33716103) (← links)
- Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases. (Q33718865) (← links)
- AIRE deficiency in thymus of 2 patients with Omenn syndrome (Q33778516) (← links)
- Primary immunodeficiencies underlying fungal infections (Q33902831) (← links)
- Interleukin-2 gene variation impairs regulatory T cell function and causes autoimmunity (Q33918375) (← links)
- The role of Stat5a and Stat5b in signaling by IL-2 family cytokines (Q33941389) (← links)
- Localization of a type 1 diabetes locus in the IL2RA/CD25 region by use of tag single-nucleotide polymorphisms (Q33942274) (← links)
- Binding of HMG-I(Y) imparts architectural specificity to a positioned nucleosome on the promoter of the human interleukin-2 receptor alpha gene (Q33964298) (← links)
- CD4 CD25 T regulatory cells, immunotherapy of cancer, and interleukin-2. (Q34063120) (← links)
- The basis for TCR-mediated regulation of the IL-2 receptor alpha chain gene: role of widely separated regulatory elements (Q34089393) (← links)
- Severe combined immunodeficiency--molecular pathogenesis and diagnosis (Q34131863) (← links)
- Signaling via the IL-2 and IL-7 receptors from the membrane to the nucleus (Q34170866) (← links)
- Signal-transduction defects in T cells (Q34195514) (← links)
- Primary T-lymphocyte immunodeficiencies (Q34195521) (← links)
- Association of the IL2RA/CD25 gene with juvenile idiopathic arthritis (Q34235185) (← links)
- Defining a functionally distinct subset of human memory CD4 T cells that are CD25POS and FOXP3NEG. (Q34274920) (← links)
- Genetic susceptibility to Candida infections (Q34341908) (← links)
- Guidelines for genetic studies in single patients: lessons from primary immunodeficiencies (Q34375180) (← links)
- Jak3, severe combined immunodeficiency, and a new class of immunosuppressive drugs. (Q34386311) (← links)
- Identification of therapeutic targets for quiescent, chemotherapy-resistant human leukemia stem cells (Q34421127) (← links)
- Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease (Q34429745) (← links)
- Clues to immune tolerance: the monogenic autoimmune syndromes (Q34440616) (← links)
- Cytokines and immunodeficiency diseases (Q34572193) (← links)
- Altered responses to homeostatic cytokines in patients with idiopathic CD4 lymphocytopenia (Q34576725) (← links)
- Molecular aspects of primary immunodeficiencies: lessons from cytokine and other signaling pathways. (Q34647002) (← links)
- Interleukin-2-dependent mechanisms of tolerance and immunity in vivo (Q34655265) (← links)
- Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBA. (Q34892704) (← links)
- Beyond regulatory T cells: the potential role for IL-2 to deplete T-follicular helper cells and treat autoimmune diseases. (Q34901832) (← links)
- Modulation by IL-2 of CD70 and CD27 expression on CD8 T cells: importance for the therapeutic effectiveness of cell transfer immunotherapy (Q34936175) (← links)
- A role for interleukin-2 trans-presentation in dendritic cell-mediated T cell activation in humans, as revealed by daclizumab therapy (Q34949098) (← links)
- Role of inherited defects decreasing Fas function in autoimmunity. (Q35107838) (← links)
- What does it take to make a natural killer? (Q35136013) (← links)
- Daclizumab reverses intrathecal immune cell abnormalities in multiple sclerosis (Q35619174) (← links)