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Background: Staphylococcus aureus (SA) remains a global health threat due to its increasing drug resistance and intracellular persistence, which compromise the efficacy of conventional antibiotics. Host-directed therapy (HDT) has emerged as a promising alternative by modulating host...

2026-02-25 | MTBLS13930 | MetaboLights
The pediatric immune deficiency X-linked proliferative disease-2 (XLP-2) is a unique disease, with patients presenting with either hemophagocytic lymphohistiocytosis (HLH) or intestinal bowel disease (IBD). Interestingly, XLP-2 patients display high levels of IL-18 in the serum even while in stable ...
ORGANISM(S): Mus musculus 
X-linked inhibitor of apoptosis protein (XIAP), a member of the IAP family, is overexpressed in a variety of tumors and plays an important role in tumor progression. Increasing evidence suggests that XIAP promotes metastasis of bladder cancer but the underlying mechanism is not very clear. The RNA N...
ORGANISM(S): Homo sapiens (Human) 
2025-05-07 | PXD055868 | Pride
X-linked inhibitor of apoptosis (XIAP) is the most potent endogenous caspase inhibitor preventing cell death via caspase-9, -7 and -3 (initiator and executioner caspase pathways). Using short hairpin RNA (shRNA) against XIAP, stably expressed in a parent HCT116 human colon cancer cell line, a series...
ORGANISM(S): Homo sapiens 
2008-12-01 | GSE11618 | GEO
Raw KGG ubiquitination MS data files for two biological replicate studies of Nod2 receptor activation +/- XIAP inhibition.
ORGANISM(S): Homo Sapiens (ncbitaxon:9606) 
2018-01-03 | MSV000081881 | MassIVE
Expression profile of cells overexpressing genetic variants encoding XIAP with distinct subcellular localization.
XIAP (X chromosome-linked inhibitor of apoptosis; ILP, BIRC4) is involved not only in apoptosis, but also in signal tranduction in the NF-kappaB, TGF-beta, bone morphogenic protein, and JNK signalling pathways. We have analyzed whether XIAP deletion leads to changes in gene expression, particularly ...
ORGANISM(S): Mus musculus 
2008-11-12 | GSE3700 | GEO
Epstein Barr virus-mediated transformation of B cells from XIAP-deficient patients leads to increased expression of the tumor suppressor CADM1
Epstein Barr virus mediated transformation of B cells from XIAP-deficient patients leads to increased expression of the tumor suppressor CADM1
RNAseq of pedriatic IBD and XIAP-deficient biopsy samples
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