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Plos One|September 26, 2025
Genetic drivers of liver cirrhosis: The role of SERPINA1 and PNPLA3 variants in disease onset and progressionMikolas Holinka, Sona Frankova, Svetlana Adamcova Selcanova, et al.
Biomaterials|May 15, 2026
KEAP1-mediated mitochondrial remodeling on stiffness-graded collagen substrates drives hepatocellular carcinoma adaptationPetra Elblová, Alicia Calé, Hana Andělová, et al.
The Journal of Pathology|October 15, 2016
Hepcidin knockout mice spontaneously develop chronic pancreatitis owing to cytoplasmic iron overload in acinar cellsMariia Lunova, Peggy Schwarz, Renwar Nuraldeen, et al.
Nano Convergence|May 20, 2020
Progressive lysosomal membrane permeabilization induced by iron oxide nanoparticles drives hepatic cell autophagy and apoptosisKateryna Levada, Stanislav Pshenichnikov, Alexander Omelyanchik, et al.
Orphanet Journal of Rare Diseases|April 7, 2020
Transcript, protein, metabolite and cellular studies in skin fibroblasts demonstrate variable pathogenic impacts of NPC1 mutationsDita Musalkova, Filip Majer, Ladislav Kuchar, et al.
Gastroenterology|November 13, 2012
Troy, a tumor necrosis factor receptor family member, interacts with lgr5 to inhibit wnt signaling in intestinal stem cellsBohumil Fafilek, Michaela Krausova, Martina Vojtechova, et al.
The Journal of Clinical Investigation|January 11, 2012
Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liverEvita van de Steeg, Viktor Stránecký, Hana Hartmannová, et al.
Kidney International|September 24, 2021
A mutation in the SAA1 promoter causes hereditary amyloid A amyloidosisJakub Sikora, Tereza Kmochová, Dita Mušálková, et al.
Plos One|July 20, 2023
Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver diseaseMagdaléna Neřoldová, Elżbieta Ciara, Janka Slatinská, et al.
Cancers|January 8, 2023
Low Frequency of Cancer-Predisposition Gene Mutations in Liver Transplant Candidates with Hepatocellular CarcinomaKlara Horackova, Sona Frankova, Petra Zemankova, et al.
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