169 related articles for article (PubMed ID: 35644338)
1. FANCL supports Parkin-mediated mitophagy in a ubiquitin ligase-independent manner.
Beesetti S; Sirasanagandla S; Sakurada SM; Pruett-Miller SM; Sumpter R; Levine B; Potts MB
Biochim Biophys Acta Mol Basis Dis; 2022 Sep; 1868(9):166453. PubMed ID: 35644338
[TBL] [Abstract][Full Text] [Related]
2. The Fanconi Anemia DNA Repair Pathway Is Regulated by an Interaction between Ubiquitin and the E2-like Fold Domain of FANCL.
Miles JA; Frost MG; Carroll E; Rowe ML; Howard MJ; Sidhu A; Chaugule VK; Alpi AF; Walden H
J Biol Chem; 2015 Aug; 290(34):20995-21006. PubMed ID: 26149689
[TBL] [Abstract][Full Text] [Related]
3. Evidence for subcomplexes in the Fanconi anemia pathway.
Medhurst AL; Laghmani el H; Steltenpool J; Ferrer M; Fontaine C; de Groot J; Rooimans MA; Scheper RJ; Meetei AR; Wang W; Joenje H; de Winter JP
Blood; 2006 Sep; 108(6):2072-80. PubMed ID: 16720839
[TBL] [Abstract][Full Text] [Related]
4. Fanconi Anemia Proteins Function in Mitophagy and Immunity.
Sumpter R; Sirasanagandla S; Fernández ÁF; Wei Y; Dong X; Franco L; Zou Z; Marchal C; Lee MY; Clapp DW; Hanenberg H; Levine B
Cell; 2016 May; 165(4):867-81. PubMed ID: 27133164
[TBL] [Abstract][Full Text] [Related]
5. Mechanism of Ubiquitination and Deubiquitination in the Fanconi Anemia Pathway.
van Twest S; Murphy VJ; Hodson C; Tan W; Swuec P; O'Rourke JJ; Heierhorst J; Crismani W; Deans AJ
Mol Cell; 2017 Jan; 65(2):247-259. PubMed ID: 27986371
[TBL] [Abstract][Full Text] [Related]
6. Modularized functions of the Fanconi anemia core complex.
Huang Y; Leung JW; Lowery M; Matsushita N; Wang Y; Shen X; Huong D; Takata M; Chen J; Li L
Cell Rep; 2014 Jun; 7(6):1849-57. PubMed ID: 24910428
[TBL] [Abstract][Full Text] [Related]
7. The WD40 repeats of FANCL are required for Fanconi anemia core complex assembly.
Gurtan AM; Stuckert P; D'Andrea AD
J Biol Chem; 2006 Apr; 281(16):10896-905. PubMed ID: 16474167
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. A requirement of FancL and FancD2 monoubiquitination in DNA repair.
Seki S; Ohzeki M; Uchida A; Hirano S; Matsushita N; Kitao H; Oda T; Yamashita T; Kashihara N; Tsubahara A; Takata M; Ishiai M
Genes Cells; 2007 Mar; 12(3):299-310. PubMed ID: 17352736
[TBL] [Abstract][Full Text] [Related]
10. Structural analysis of human FANCL, the E3 ligase in the Fanconi anemia pathway.
Hodson C; Cole AR; Lewis LP; Miles JA; Purkiss A; Walden H
J Biol Chem; 2011 Sep; 286(37):32628-37. PubMed ID: 21775430
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. A novel ubiquitin ligase is deficient in Fanconi anemia.
Meetei AR; de Winter JP; Medhurst AL; Wallisch M; Waisfisz Q; van de Vrugt HJ; Oostra AB; Yan Z; Ling C; Bishop CE; Hoatlin ME; Joenje H; Wang W
Nat Genet; 2003 Oct; 35(2):165-70. PubMed ID: 12973351
[TBL] [Abstract][Full Text] [Related]
13. Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia.
Rickman KA; Lach FP; Abhyankar A; Donovan FX; Sanborn EM; Kennedy JA; Sougnez C; Gabriel SB; Elemento O; Chandrasekharappa SC; Schindler D; Auerbach AD; Smogorzewska A
Cell Rep; 2015 Jul; 12(1):35-41. PubMed ID: 26119737
[TBL] [Abstract][Full Text] [Related]
14. The carboxyl terminus of FANCE recruits FANCD2 to the Fanconi Anemia (FA) E3 ligase complex to promote the FA DNA repair pathway.
Polito D; Cukras S; Wang X; Spence P; Moreau L; D'Andrea AD; Kee Y
J Biol Chem; 2014 Mar; 289(10):7003-7010. PubMed ID: 24451376
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. The genetic and biochemical basis of FANCD2 monoubiquitination.
Rajendra E; Oestergaard VH; Langevin F; Wang M; Dornan GL; Patel KJ; Passmore LA
Mol Cell; 2014 Jun; 54(5):858-69. PubMed ID: 24905007
[TBL] [Abstract][Full Text] [Related]
17. Physical and functional crosstalk between Fanconi anemia core components and the GINS replication complex.
Tumini E; Plevani P; Muzi-Falconi M; Marini F
DNA Repair (Amst); 2011 Feb; 10(2):149-58. PubMed ID: 21109493
[TBL] [Abstract][Full Text] [Related]
18. Characterization of FANCL variants observed in patient cancer cells.
Frost MG; Mazloumi Aboukheili AM; Toth R; Walden H
Biosci Rep; 2020 Jun; 40(6):. PubMed ID: 32420600
[TBL] [Abstract][Full Text] [Related]
19. A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network.
Yan Z; Guo R; Paramasivam M; Shen W; Ling C; Fox D; Wang Y; Oostra AB; Kuehl J; Lee DY; Takata M; Hoatlin ME; Schindler D; Joenje H; de Winter JP; Li L; Seidman MM; Wang W
Mol Cell; 2012 Jul; 47(1):61-75. PubMed ID: 22705371
[TBL] [Abstract][Full Text] [Related]
20. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.
Levran O; Attwooll C; Henry RT; Milton KL; Neveling K; Rio P; Batish SD; Kalb R; Velleuer E; Barral S; Ott J; Petrini J; Schindler D; Hanenberg H; Auerbach AD
Nat Genet; 2005 Sep; 37(9):931-3. PubMed ID: 16116424
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
