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Find link is a tool written by Edward Betts .
searching for Autoimmune lymphoproliferative syndrome 10 found (37 total)
alternate case: autoimmune lymphoproliferative syndrome
Caspase 10
(1,469 words)
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are associated with apoptosis defects seen in type II autoimmune lymphoproliferative syndrome . Three alternatively spliced transcript variants encoding
CHAI disease
(277 words)
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the role of CTLA-4 in cell signaling. CHAI stands for “Autoimmune lymphoproliferative syndrome due to CTLA4 haplo-insufficiency.” The disease is characterized
HLA-B44
(283 words)
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Protective effects: HLA-B44 appears to be protective against autoimmune lymphoproliferative syndrome in patients with C95 defect (ALPS type Ia). B44 may be
Decoy receptor 3
(1,243 words)
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PMC 1618528. PMID 15215185. GeneReviews/NCBI/NIH/UW entry on Autoimmune Lymphoproliferative Syndrome This article incorporates text from the United States National
Fas receptor
(2,675 words)
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van den Berg A (March 2004). "Development of lymphoma in Autoimmune Lymphoproliferative Syndrome (ALPS) and its relationship to Fas gene mutations". Leukemia
Autoinflammatory diseases
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patients present with Behçet-like characteristics or an autoimmune lymphoproliferative syndrome (ALPS)-like phenotype. In addition to antivirus and antitumor
Adenosine deaminase 2 deficiency
(3,965 words)
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Alfadhel M (April 2018). "Deficiency of ADA2 mimicking autoimmune lymphoproliferative syndrome in the absence of livedo reticularis and vasculitis". Pediatric
Computational immunology
(4,344 words)
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Database Description ALPSbase Autoimmune lymphoproliferative syndrome database AntigenDB Sequence, structure, and other data on pathogen antigens. AntiJen
List of OMIM disorder codes
(18,877 words)
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ITCH Autoimmune lymphoproliferative syndrome , type IA; 601859; TNFRSF6 Autoimmune lymphoproliferative syndrome , type II; 603909; CASP10 Autoimmune lymphoproliferative
Autoimmune enteropathy
(5,487 words)
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with symptoms associated with autoimmune enteropathy and autoimmune lymphoproliferative syndrome . "IPEX-like disorders" can also be caused by mutations