P07 | DISRUPTED GUT-VASCULAR BARRIER AND INFLAMMATORY REMODELING IN MNGIE: A SPATIAL TRANSCRIPTOMIC AND HISTOLOGICAL STUDY
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE) is a rare genetic disorder caused by loss-of-function mutations in the enzyme thymidine phosphorylase (TP). TP deficiency disrupts nucleoside metabolism, leading to progressive and fatal mitochondrial dysfunction. Although liver transpla...
Saved in:
| Format: | Article |
|---|---|
| Language: | English |
| Published: |
PAGEPress Publications
2025-08-01
|
| Series: | European Journal of Histochemistry |
| Subjects: | |
| Online Access: | https://www.ejh.it/ejh/article/view/4327 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
P11 | DOMINO TRANSPLANTATION IN MNGIE: IS THE LIVER A SUITABLE GRAFT?
Published: (2025-08-01) -
P086: Sensorineural hearing loss in a child with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) treated with cochlear implantation
by: Michael Finkel, et al.
Published: (2025-01-01) -
Disrupted mucosal vascular barrier in eosinophilic esophagitis
by: Marco Vincenzo Lenti, et al.
Published: (2025-07-01) -
A new mutation in the TYMP-gene: clinical and morphological characteristics of a patient with MNGIE syndrome
by: S. N. Bardakov, et al.
Published: (2022-12-01) -
Intestinal Microbiota Dysbiosis Disrupts the Mucosal Barrier, Triggering Inflammatory Responses in Gut-Kidney Interaction and Exacerbating Diarrhea
by: Shen J, et al.
Published: (2025-07-01)