Literature for peptidase S01.531: protein FAM111B

(Topics flags: K Knockout, V Review. To select only the references relevant to a single topic, click the link above. See explanation.)

2025
1. He,Q., Li,H., Cong,Y., Chen,K., Cheng,L., Lv,F., Zhang,P., Ju,Y., Yu,Z., Chen,J., Wang,C., Song,Y., Li,X., Chen,L. and Xing,Y.
   FAM111B enhances glycolysis and promotes metastasis of prostate cancer by upregulating LDHA
   Neoplasia (2025) 69, 101227-101227. PubMed  Europe PubMed DOI  PMC  EPMC
2024
2. Naicker,D., Rhoda,C., Sunda,F. and Arowolo,A.
   Unravelling the Intricate Roles of FAM111A and FAM111B: From Protease-Mediated Cellular Processes to Disease Implications
   Int J Mol Sci (2024) 25 PubMed  Europe PubMed DOI  PMC  EPMC  V
2023
3. Huang,N., Peng,L., Yang,J., Li,J., Zhang,S. and Sun,M.
   FAM111B Acts as an Oncogene in Bladder Cancer
   Cancers (Basel) (2023) 15 PubMed  Europe PubMed DOI  PMC  EPMC  K
4. Kliszczak,M., Moralli,D., Jankowska,J.D., Bryjka,P., Subha Meem,L., Goncalves,T., Hester,S.S., Fischer,R., Clynes,D. and Green,C.M.
   Loss of FAM111B protease mutated in hereditary fibrosing poikiloderma negatively regulates telomere length
   Front Cell Dev Biol (2023) 11, 1175069-1175069. PubMed  Europe PubMed DOI  PMC  EPMC
5. Ryabets-Lienhard,A., Panjawatanan,P., Vogt,K., Ji,J., Georgia,S. and Pitukcheewanont,P.
   A Novel De Novo Frameshift Pathogenic Variant in the FAM111B Resulting in Progressive Osseous Heteroplasia Phenotype
   Calcif Tissue Int (2023) 112, 518-523. PubMed  Europe PubMed DOI
6. Wu,H. and Liang,C.
   Pan-Cancer Analysis of the Tumorigenic Effect and Prognostic Diagnostic Value of FAM111B in Human Carcinomas
   Int J Gen Med (2023) 16, 1845-1865. PubMed  Europe PubMed DOI  PMC  EPMC  K
2022
7. Arowolo,A., Rhoda,C. and Khumalo,N.
   Mutations within the putative protease domain of the human FAM111B gene may predict disease severity and poor prognosis: A review of POIKTMP cases
   Exp Dermatol (2022) 31, 648-654. PubMed  Europe PubMed DOI
8. Welter,A.L. and Machida,Y.J.
   Functions and evolution of FAM111 serine proteases
   Front Mol Biosci (2022) 9, 1081166-1081166. PubMed  Europe PubMed DOI  PMC  EPMC  V
2021
9. Ip,W.H., Wilkens,B., Solomatina,A., Martin,J., Melling,M., Hidalgo,P., Bertzbach,L.D., Speiseder,T. and Dobner,T.
   Differential Regulation of Cellular FAM111B by Human Adenovirus C Type 5 E1 Oncogenes
   Viruses (2021) 13 PubMed  Europe PubMed DOI  PMC  EPMC  K
2020
10. Hoffmann,S., Pentakota,S., Mund,A., Haahr,P., Coscia,F., Gallo,M., Mann,M., Taylor,N.M. and Mailand,N.
    FAM111 protease activity undermines cellular fitness and is amplified by gain-of-function mutations in human disease
    EMBO Rep (2020) , e50662-e50662. PubMed  Europe PubMed DOI
2013
11. Mercier,S., Küry,S., Shaboodien,G., Houniet,D.T., Khumalo,N.P., Bou-Hanna,C., Bodak,N., Cormier-Daire,V., David,A., Faivre,L., Figarella-Branger,D., Gherardi,R.K., Glen,E., Hamel,A., Laboisse,C., Le,C.a., Lindenbaum,P., Magot,A., Munnich,A., Mussini,J.M., Pillay,K., Rahman,T., Redon,R., Salort-Campana,E., Santibanez-Koref,M., Thauvin,C., Barbarot,S., Keavney,B., Bézieau,S. and Mayosi,B.M.
    Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis
    Am J Hum Genet (2013) 93, 1100-1107. DOI  PMC  EPMC