173 related articles for article (PubMed ID: 32420600)
21. Fanconi anemia and ubiquitination.
Zhang Y; Zhou X; Huang P
J Genet Genomics; 2007 Jul; 34(7):573-80. PubMed ID: 17643942
[TBL] [Abstract][Full Text] [Related]
22. Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition.
García MJ; Fernández V; Osorio A; Barroso A; Fernández F; Urioste M; Benítez J
Carcinogenesis; 2009 Nov; 30(11):1898-902. PubMed ID: 19737859
[TBL] [Abstract][Full Text] [Related]
23. Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
Ali AM; Kirby M; Jansen M; Lach FP; Schulte J; Singh TR; Batish SD; Auerbach AD; Williams DA; Meetei AR
Hum Mutat; 2009 Jul; 30(7):E761-70. PubMed ID: 19405097
[TBL] [Abstract][Full Text] [Related]
24. RAD18-mediated ubiquitination of PCNA activates the Fanconi anemia DNA repair network.
Geng L; Huntoon CJ; Karnitz LM
J Cell Biol; 2010 Oct; 191(2):249-57. PubMed ID: 20937699
[TBL] [Abstract][Full Text] [Related]
25. Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia.
Hira A; Yoshida K; Sato K; Okuno Y; Shiraishi Y; Chiba K; Tanaka H; Miyano S; Shimamoto A; Tahara H; Ito E; Kojima S; Kurumizaka H; Ogawa S; Takata M; Yabe H; Yabe M
Am J Hum Genet; 2015 Jun; 96(6):1001-7. PubMed ID: 26046368
[TBL] [Abstract][Full Text] [Related]
26. The ubiquitination machinery of the Fanconi Anemia DNA repair pathway.
Tan W; Deans AJ
Prog Biophys Mol Biol; 2021 Aug; 163():5-13. PubMed ID: 33058944
[TBL] [Abstract][Full Text] [Related]
27. Coordinate nuclear targeting of the FANCD2 and FANCI proteins via a FANCD2 nuclear localization signal.
Boisvert RA; Rego MA; Azzinaro PA; Mauro M; Howlett NG
PLoS One; 2013; 8(11):e81387. PubMed ID: 24278431
[TBL] [Abstract][Full Text] [Related]
28. Novel homozygous FANCL mutation and somatic heterozygous SETBP1 mutation in a Chinese girl with Fanconi Anemia.
Wu W; Liu Y; Zhou Q; Wang Q; Luo F; Xu Z; Geng Q; Li P; Zhang HZ; Xie J
Eur J Med Genet; 2017 Jul; 60(7):369-373. PubMed ID: 28419882
[TBL] [Abstract][Full Text] [Related]
29. FANCD2 monoubiquitination provides a link between the HHR6 and FA-BRCA pathways.
Zhang J; Zhao D; Wang H; Lin CJ; Fei P
Cell Cycle; 2008 Feb; 7(3):407-13. PubMed ID: 18277096
[TBL] [Abstract][Full Text] [Related]
30. AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.
Virts EL; Jankowska A; Mackay C; Glaas MF; Wiek C; Kelich SL; Lottmann N; Kennedy FM; Marchal C; Lehnert E; Scharf RE; Dufour C; Lanciotti M; Farruggia P; Santoro A; Savasan S; Scheckenbach K; Schipper J; Wagenmann M; Lewis T; Leffak M; Farlow JL; Foroud TM; Honisch E; Niederacher D; Chakraborty SC; Vance GH; Pruss D; Timms KM; Lanchbury JS; Alpi AF; Hanenberg H
Hum Mol Genet; 2015 Sep; 24(18):5093-108. PubMed ID: 26085575
[TBL] [Abstract][Full Text] [Related]
31. [Functions of FANCL in primordial germ cell formation and Fanconi anemia].
Zhao QG; Lu BS; Huang PT
Yi Chuan Xue Bao; 2005 Sep; 32(9):993-1000. PubMed ID: 16201245
[TBL] [Abstract][Full Text] [Related]
32. DNA robustly stimulates FANCD2 monoubiquitylation in the complex with FANCI.
Sato K; Toda K; Ishiai M; Takata M; Kurumizaka H
Nucleic Acids Res; 2012 May; 40(10):4553-61. PubMed ID: 22287633
[TBL] [Abstract][Full Text] [Related]
33. FANCI binds branched DNA and is monoubiquitinated by UBE2T-FANCL.
Longerich S; San Filippo J; Liu D; Sung P
J Biol Chem; 2009 Aug; 284(35):23182-6. PubMed ID: 19589784
[TBL] [Abstract][Full Text] [Related]
34. Ubiquitylation and the Fanconi anemia pathway.
Garner E; Smogorzewska A
FEBS Lett; 2011 Sep; 585(18):2853-60. PubMed ID: 21605559
[TBL] [Abstract][Full Text] [Related]
35. Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair.
Smogorzewska A; Matsuoka S; Vinciguerra P; McDonald ER; Hurov KE; Luo J; Ballif BA; Gygi SP; Hofmann K; D'Andrea AD; Elledge SJ
Cell; 2007 Apr; 129(2):289-301. PubMed ID: 17412408
[TBL] [Abstract][Full Text] [Related]
36. Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
Chandrasekharappa SC; Lach FP; Kimble DC; Kamat A; Teer JK; Donovan FX; Flynn E; Sen SK; Thongthip S; Sanborn E; Smogorzewska A; Auerbach AD; Ostrander EA;
Blood; 2013 May; 121(22):e138-48. PubMed ID: 23613520
[TBL] [Abstract][Full Text] [Related]
37. A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
Donovan FX; Solanki A; Mori M; Chavan N; George M; C SK; Okuno Y; Muramastsu H; Yoshida K; Shimamoto A; Takaori-Kondo A; Yabe H; Ogawa S; Kojima S; Yabe M; Ramanagoudr-Bhojappa R; Smogorzewska A; Mohan S; Rajendran A; Auerbach AD; Takata M; Chandrasekharappa SC; Vundinti BR
Hum Mutat; 2020 Jan; 41(1):122-128. PubMed ID: 31513304
[TBL] [Abstract][Full Text] [Related]
38. FAVL impairment of the Fanconi anemia pathway promotes the development of human bladder cancer.
Panneerselvam J; Park HK; Zhang J; Dudimah FD; Zhang P; Wang H; Fei P
Cell Cycle; 2012 Aug; 11(15):2947-55. PubMed ID: 22828653
[TBL] [Abstract][Full Text] [Related]
39. FANCC, FANCE, and FANCD2 form a ternary complex essential to the integrity of the Fanconi anemia DNA damage response pathway.
Gordon SM; Alon N; Buchwald M
J Biol Chem; 2005 Oct; 280(43):36118-25. PubMed ID: 16127171
[TBL] [Abstract][Full Text] [Related]
40. The FA Core Complex Contains a Homo-dimeric Catalytic Module for the Symmetric Mono-ubiquitination of FANCI-FANCD2.
Swuec P; Renault L; Borg A; Shah F; Murphy VJ; van Twest S; Snijders AP; Deans AJ; Costa A
Cell Rep; 2017 Jan; 18(3):611-623. PubMed ID: 27986592
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]