Back to search

Article

The <i>SAMM50</i> rs3761472 causes mitochondrial dysfunction and metabolic dysfunction-associated steatotic liver disease

2025-06-07

Abstract excerpt

Genome-wide association studies (GWAS) have identified the SAMM50 rs3761472 single nucleotide polymorphism (SNP) as a risk factor for metabolic dysfunction-associated steatotic liver disease (MASLD), although its in vivo functions remain unclear. SAMM50 encodes a mitochondrial outer membrane protein critical for maintaining mitochondrial structure. To investigate the biological effects of rs3761472, we generated...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
729e295d-e65e-54f3-b96e-32af64315148
DOI
10.1101/2025.06.04.657815
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
The <i>SAMM50</i> rs3761472 causes mitochondrial dysfunction and metabolic dysfunction-associated steatotic liver diseaseDOI 10.1101/2025.06.04.657815
Select a neighboring publication to make it the new centre.