206 related articles for article (PubMed ID: 33369867)
1. FAM111A induces nuclear dysfunction in disease and viral restriction.
Nie M; Oravcová M; Jami-Alahmadi Y; Wohlschlegel JA; Lazzerini-Denchi E; Boddy MN
EMBO Rep; 2021 Feb; 22(2):e50803. PubMed ID: 33369867
[TBL] [Abstract][Full Text] [Related]
2. Report of a novel variant in the FAM111A gene in a fetus with multiple anomalies including gracile bones, hypoplastic spleen, and hypomineralized skull.
Müller R; Steffensen T; Krstić N; Cain MA
Am J Med Genet A; 2021 Jun; 185(6):1903-1907. PubMed ID: 33750016
[TBL] [Abstract][Full Text] [Related]
3. FAM111A mutations result in hypoparathyroidism and impaired skeletal development.
Unger S; Górna MW; Le Béchec A; Do Vale-Pereira S; Bedeschi MF; Geiberger S; Grigelioniene G; Horemuzova E; Lalatta F; Lausch E; Magnani C; Nampoothiri S; Nishimura G; Petrella D; Rojas-Ringeling F; Utsunomiya A; Zabel B; Pradervand S; Harshman K; Campos-Xavier B; Bonafé L; Superti-Furga G; Stevenson B; Superti-Furga A
Am J Hum Genet; 2013 Jun; 92(6):990-5. PubMed ID: 23684011
[TBL] [Abstract][Full Text] [Related]
4. Contribution of DNA Replication to the FAM111A-Mediated Simian Virus 40 Host Range Phenotype.
Tarnita RM; Wilkie AR; DeCaprio JA
J Virol; 2019 Jan; 93(1):. PubMed ID: 30333173
[TBL] [Abstract][Full Text] [Related]
5. Case report: Late middle-aged features of
Ohmachi Y; Urai S; Bando H; Yokoi J; Yamamoto M; Kanie K; Motomura Y; Tsujimoto Y; Sasaki Y; Oi Y; Yamamoto N; Suzuki M; Shichi H; Iguchi G; Uehara N; Fukuoka H; Ogawa W
Front Endocrinol (Lausanne); 2022; 13():1073173. PubMed ID: 36686468
[TBL] [Abstract][Full Text] [Related]
6. FAM111 protease activity undermines cellular fitness and is amplified by gain-of-function mutations in human disease.
Hoffmann S; Pentakota S; Mund A; Haahr P; Coscia F; Gallo M; Mann M; Taylor NM; Mailand N
EMBO Rep; 2020 Oct; 21(10):e50662. PubMed ID: 32776417
[TBL] [Abstract][Full Text] [Related]
7. A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2.
Isojima T; Doi K; Mitsui J; Oda Y; Tokuhiro E; Yasoda A; Yorifuji T; Horikawa R; Yoshimura J; Ishiura H; Morishita S; Tsuji S; Kitanaka S
J Bone Miner Res; 2014 Apr; 29(4):992-8. PubMed ID: 23996431
[TBL] [Abstract][Full Text] [Related]
8. Compound Heterozygous Variants in
Eren E; Tezcan Ünlü H; Ceylaner S; Tarım Ö
J Clin Res Pediatr Endocrinol; 2023 Feb; 15(1):97-102. PubMed ID: 34382758
[TBL] [Abstract][Full Text] [Related]
9. Further delineation of phenotype and genotype of Kenny-Caffey syndrome type 2 (phenotype and genotype of KCS type 2).
Chen X; Zou C
Mol Genet Genomic Med; 2024 Apr; 12(4):e2433. PubMed ID: 38591167
[TBL] [Abstract][Full Text] [Related]
10. Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features.
Rosato S; Unger S; Campos-Xavier B; Caraffi SG; Beltrami L; Pollazzon M; Ivanovski I; Castori M; Bonasoni MP; Comitini G; Nikkels PGJ; Lindstrom K; Umandap C; Superti-Furga A; Garavelli L
Genes (Basel); 2022 Jan; 13(2):. PubMed ID: 35205306
[TBL] [Abstract][Full Text] [Related]
11. Human FAM111A inhibits vaccinia virus replication by degrading viral protein I3 and is antagonized by poxvirus host range factor SPI-1.
Zhu J; Gao X; Li Y; Zhang Z; Xie S; Ren S; Li Y; Li H; Niu K; Fu S; Deng Y; Li Y; Moss B; Wu W; Peng C
Proc Natl Acad Sci U S A; 2023 Aug; 120(35):e2304242120. PubMed ID: 37607234
[TBL] [Abstract][Full Text] [Related]
12. Expanding the Phenotypic Spectrum of Kenny-Caffey Syndrome.
Schigt H; Bald M; van der Eerden BCJ; Gal L; Ilenwabor BP; Konrad M; Levine MA; Li D; Mache CJ; Mackin S; Perry C; Rios FJ; Schlingmann KP; Storey B; Trapp CM; Verkerk AJMH; Zillikens MC; Touyz RM; Hoorn EJ; Hoenderop JGJ; de Baaij JHF
J Clin Endocrinol Metab; 2023 Aug; 108(9):e754-e768. PubMed ID: 36916904
[TBL] [Abstract][Full Text] [Related]
13. Overlapping phenotype comprising Kenny-Caffey type 2 and Sanjad-Sakati syndromes: The first case report.
Cavole TR; Perrone E; de Faria Soares MF; Dias da Silva MR; Maeda SS; Lazaretti-Castro M; Alvarez Perez AB
Am J Med Genet A; 2020 Dec; 182(12):3029-3034. PubMed ID: 33010201
[TBL] [Abstract][Full Text] [Related]
14. Functions and evolution of FAM111 serine proteases.
Welter AL; Machida YJ
Front Mol Biosci; 2022; 9():1081166. PubMed ID: 36589246
[TBL] [Abstract][Full Text] [Related]
15. FAM111A is dispensable for electrolyte homeostasis in mice.
Ilenwabor BP; Schigt H; Kompatscher A; Bos C; Zuidscherwoude M; van der Eerden BCJ; Hoenderop JGJ; de Baaij JHF
Sci Rep; 2022 Jun; 12(1):10211. PubMed ID: 35715480
[TBL] [Abstract][Full Text] [Related]
16. Unravelling the Intricate Roles of FAM111A and FAM111B: From Protease-Mediated Cellular Processes to Disease Implications.
Naicker D; Rhoda C; Sunda F; Arowolo A
Int J Mol Sci; 2024 Feb; 25(5):. PubMed ID: 38474092
[TBL] [Abstract][Full Text] [Related]
17. FAM111A regulates replication origin activation and cell fitness.
Rios-Szwed DO; Alvarez V; Sanchez-Pulido L; Garcia-Wilson E; Jiang H; Bandau S; Lamond A; Alabert C
Life Sci Alliance; 2023 Dec; 6(12):. PubMed ID: 37793778
[TBL] [Abstract][Full Text] [Related]
18. [Kenny-Caffey syndrome and its related syndromes].
Isojima T; Kitanaka S
Nihon Rinsho; 2015 Nov; 73(11):1959-64. PubMed ID: 26619675
[TBL] [Abstract][Full Text] [Related]
19. Identification of FAM111A as an SV40 host range restriction and adenovirus helper factor.
Fine DA; Rozenblatt-Rosen O; Padi M; Korkhin A; James RL; Adelmant G; Yoon R; Guo L; Berrios C; Zhang Y; Calderwood MA; Velmurgan S; Cheng J; Marto JA; Hill DE; Cusick ME; Vidal M; Florens L; Washburn MP; Litovchick L; DeCaprio JA
PLoS Pathog; 2012; 8(10):e1002949. PubMed ID: 23093934
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]