Results 161 to 170 of about 162,948 (264)
In human oral keratinocytes, OTUD6A promoted cell migration by deubiquitinating and stabilizing PRDX1. Conversely, OTUD6A deficiency reduced PRDX1 stability, triggering mitochondrial dysfunction and aggravating OU progression. ABSTRACT Oral ulcers (OU), as the most highly prevalent and recurrent oral mucosal lesion, have an unclear pathogenesis that ...
Xiaoyu Sun +15 more
wiley +1 more source
Author Correction: Trib1 deficiency causes brown adipose respiratory chain depletion and mitochondrial disorder. [PDF]
Zhang X, Zhang B, Zhang C, Sun G, Sun X.
europepmc +1 more source
Defining the nuclear genetic architecture of a common maternally inherited mitochondrial disorder
Boggan RM +29 more
europepmc +1 more source
POLG1-related Mitochondrial Disorder with MNGIE- and Leigh-like Features. [PDF]
Finsterer J.
europepmc +1 more source
In this study, MPDA NPs were engineered to encapsulate CTT. To further increase renal accumulation of CTT, L‐serine was conjugated to the surface of the MPDA nanoparticles (CTT/MPDA@L‐Ser NPs). CTT/MPDA@L‐Ser NPs inhibit DPEP1 activity, thereby restoring ferroptosis defense mechanisms through upregulation of GPX4 and SLC7A11 expression, ultimately ...
Wanbing Qin +12 more
wiley +1 more source
Biallelic NSUN3 Variants Cause Diverse Phenotypic Spectrum Disease: From Isolated Optic Atrophy to Severe Early-Onset Mitochondrial Disorder. [PDF]
Jurkute N +30 more
europepmc +1 more source
Polystyrene nanoplastics disrupt pancreatic immune–endocrine homeostasis by promoting MHC‐I‐associated dendritic cell activation and inflammatory crosstalk with β cells. This immune remodeling drives β‐cell dedifferentiation, impairs insulin secretion, and aggravates metabolic dysfunction, revealing a previously unrecognized immunometabolic mechanism ...
Conghui Qiao +10 more
wiley +1 more source
Reconsidering critical illness as an uncharacterised acquired mitochondrial disorder. [PDF]
McKenna HT, Murray AJ.
europepmc +1 more source
Androgenetic alopecia (AGA) is a common form of hair loss with limited treatment options. Silencing of WNT5A signaling, which is widely known as the trigger of the ncWNT signaling pathway, happens in hair follicle stem cells from balding areas. It leads to downregulation of ATF3 and its target FOSB.
Ruiyu Luo +10 more
wiley +1 more source
Auditory Brainstem Response in a Child with Mitochondrial Disorder-Leigh Syndrome. [PDF]
Pooja PS, Greeshma R, Joy EK, Swamy SP.
europepmc +1 more source

