Pages that link to "Q33360497"
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The following pages link to Dermatologic and immunologic findings in the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (Q33360497):
Displaying 34 items.
- FOXP3: genetic and epigenetic implications for autoimmunity (Q27003398) (← links)
- Trachyonychia and Twenty-Nail Dystrophy: A Comprehensive Review and Discussion of Diagnostic Accuracy (Q28074166) (← links)
- A remarkable depletion of both naïve CD4 and CD8 with high proportion of memory T cells in an IPEX infant with a FOXP3 mutation in the forkhead domain. (Q33379659) (← links)
- Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases. (Q33718865) (← links)
- Immunologic features of Cornelia de Lange syndrome (Q33819813) (← links)
- Foxp3 regulates megakaryopoiesis and platelet function (Q34474690) (← links)
- From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation (Q34515848) (← links)
- IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity. (Q34583514) (← links)
- Gene/cell therapy approaches for Immune Dysregulation Polyendocrinopathy Enteropathy X-linked syndrome. (Q35646681) (← links)
- FOXP3 acts as a rheostat of the immune response (Q36015032) (← links)
- Immune dysregulation, polyendocrinopathy, enteropathy, x-linked syndrome: a paradigm of immunodeficiency with autoimmunity (Q36282394) (← links)
- Immunodeficiencies with autoimmune consequences. (Q36472057) (← links)
- Regulatory T cells in human autoimmune diseases (Q36562855) (← links)
- Plasmid-based gene therapy of diabetes mellitus (Q36704473) (← links)
- Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED. (Q37081019) (← links)
- Is FOXP3 a bona fide marker for human regulatory T cells? (Q37131913) (← links)
- Regulatory T cells are reduced during anti-CD25 antibody treatment of multiple sclerosis. (Q37159538) (← links)
- Dendritic cells as controllers of antigen-specific Foxp3 regulatory T cells (Q37414951) (← links)
- Recognizing Gastrointestinal and Hepatic Manifestations of Primary Immunodeficiency Diseases (Q37792762) (← links)
- Inflammatory bowel disease: is it a primary immunodeficiency? (Q37945495) (← links)
- IL-10 and IL-10 receptor defects in humans. (Q37974986) (← links)
- Forkhead box P3: the peacekeeper of the immune system. (Q38172563) (← links)
- Laboratory diagnosis of primary immunodeficiencies (Q38191164) (← links)
- Atopic Dermatitis and Allergic Urticaria: Cutaneous Manifestations of Immunodeficiency (Q39019860) (← links)
- Late-onset of immunodysregulation, polyendocrinopathy, enteropathy, x-linked syndrome (IPEX) with intractable diarrhea. (Q40348808) (← links)
- Forkhead-Box-P3 Gene Transfer in Human CD4 T Conventional Cells for the Generation of Stable and Efficient Regulatory T Cells, Suitable for Immune Modulatory Therapy (Q42655696) (← links)
- Diagnostic value of the skin lesions in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (Q46801249) (← links)
- Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome associated with neonatal epidermolysis bullosa acquisita. (Q52957672) (← links)
- Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound. (Q55078805) (← links)
- Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome (Q59137718) (← links)
- Neonatal diabetes mellitus (Q81152665) (← links)
- Successful Salvage Haploidentical Alpha-Beta T Cell-Depleted Stem Cell Transplantation After Busulfan-Based Myeloablation in a Patient With IPEX Syndrome: A Case Report (Q90700436) (← links)
- Treg-Cell Control of a CXCL5-IL-17 Inflammatory Axis Promotes Hair-Follicle-Stem-Cell Differentiation During Skin-Barrier Repair (Q92505568) (← links)
- Immune modulation of hair follicle regeneration (Q94923835) (← links)