205 related articles for article (PubMed ID: 32542039)
21. FANCJ is a structure-specific DNA helicase associated with the maintenance of genomic G/C tracts.
London TB; Barber LJ; Mosedale G; Kelly GP; Balasubramanian S; Hickson ID; Boulton SJ; Hiom K
J Biol Chem; 2008 Dec; 283(52):36132-9. PubMed ID: 18978354
[TBL] [Abstract][Full Text] [Related]
22. DOG-1 is the Caenorhabditis elegans BRIP1/FANCJ homologue and functions in interstrand cross-link repair.
Youds JL; Barber LJ; Ward JD; Collis SJ; O'Neil NJ; Boulton SJ; Rose AM
Mol Cell Biol; 2008 Mar; 28(5):1470-9. PubMed ID: 18086896
[TBL] [Abstract][Full Text] [Related]
23. The FANCJ/MutLalpha interaction is required for correction of the cross-link response in FA-J cells.
Peng M; Litman R; Xie J; Sharma S; Brosh RM; Cantor SB
EMBO J; 2007 Jul; 26(13):3238-49. PubMed ID: 17581638
[TBL] [Abstract][Full Text] [Related]
24. The Q motif of Fanconi anemia group J protein (FANCJ) DNA helicase regulates its dimerization, DNA binding, and DNA repair function.
Wu Y; Sommers JA; Loiland JA; Kitao H; Kuper J; Kisker C; Brosh RM
J Biol Chem; 2012 Jun; 287(26):21699-716. PubMed ID: 22582397
[TBL] [Abstract][Full Text] [Related]
25. FANCJ coordinates two pathways that maintain epigenetic stability at G-quadruplex DNA.
Sarkies P; Murat P; Phillips LG; Patel KJ; Balasubramanian S; Sale JE
Nucleic Acids Res; 2012 Feb; 40(4):1485-98. PubMed ID: 22021381
[TBL] [Abstract][Full Text] [Related]
26. FANCJ/BRIP1 recruitment and regulation of FANCD2 in DNA damage responses.
Zhang F; Fan Q; Ren K; Auerbach AD; Andreassen PR
Chromosoma; 2010 Dec; 119(6):637-49. PubMed ID: 20676667
[TBL] [Abstract][Full Text] [Related]
27. Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion.
van Schie JJM; Faramarz A; Balk JA; Stewart GS; Cantelli E; Oostra AB; Rooimans MA; Parish JL; de Almeida Estéves C; Dumic K; Barisic I; Diderich KEM; van Slegtenhorst MA; Mahtab M; Pisani FM; Te Riele H; Ameziane N; Wolthuis RMF; de Lange J
Nat Commun; 2020 Aug; 11(1):4287. PubMed ID: 32855419
[TBL] [Abstract][Full Text] [Related]
28. FANCJ (BACH1) helicase forms DNA damage inducible foci with replication protein A and interacts physically and functionally with the single-stranded DNA-binding protein.
Gupta R; Sharma S; Sommers JA; Kenny MK; Cantor SB; Brosh RM
Blood; 2007 Oct; 110(7):2390-8. PubMed ID: 17596542
[TBL] [Abstract][Full Text] [Related]
29. FancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in mice.
Sun X; Brieño-Enríquez MA; Cornelius A; Modzelewski AJ; Maley TT; Campbell-Peterson KM; Holloway JK; Cohen PE
Chromosoma; 2016 Jun; 125(2):237-52. PubMed ID: 26490168
[TBL] [Abstract][Full Text] [Related]
30. FANCJ DNA helicase is recruited to the replisome by AND-1 to ensure genome stability.
Boavida A; Napolitano LM; Santos D; Cortone G; Jegadesan NK; Onesti S; Branzei D; Pisani FM
EMBO Rep; 2024 Feb; 25(2):876-901. PubMed ID: 38177925
[TBL] [Abstract][Full Text] [Related]
31. Fanconi anemia group J helicase and MRE11 nuclease interact to facilitate the DNA damage response.
Suhasini AN; Sommers JA; Muniandy PA; Coulombe Y; Cantor SB; Masson JY; Seidman MM; Brosh RM
Mol Cell Biol; 2013 Jun; 33(11):2212-27. PubMed ID: 23530059
[TBL] [Abstract][Full Text] [Related]
32. FANCJ suppresses microsatellite instability and lymphomagenesis independent of the Fanconi anemia pathway.
Matsuzaki K; Borel V; Adelman CA; Schindler D; Boulton SJ
Genes Dev; 2015 Dec; 29(24):2532-46. PubMed ID: 26637282
[TBL] [Abstract][Full Text] [Related]
33. The DNA repair helicases XPD and FancJ have essential iron-sulfur domains.
Rudolf J; Makrantoni V; Ingledew WJ; Stark MJ; White MF
Mol Cell; 2006 Sep; 23(6):801-8. PubMed ID: 16973432
[TBL] [Abstract][Full Text] [Related]
34. Visualising G-quadruplex DNA dynamics in live cells by fluorescence lifetime imaging microscopy.
Summers PA; Lewis BW; Gonzalez-Garcia J; Porreca RM; Lim AHM; Cadinu P; Martin-Pintado N; Mann DJ; Edel JB; Vannier JB; Kuimova MK; Vilar R
Nat Commun; 2021 Jan; 12(1):162. PubMed ID: 33420085
[TBL] [Abstract][Full Text] [Related]
35. Multistep mechanism of G-quadruplex resolution during DNA replication.
Sato K; Martin-Pintado N; Post H; Altelaar M; Knipscheer P
Sci Adv; 2021 Sep; 7(39):eabf8653. PubMed ID: 34559566
[TBL] [Abstract][Full Text] [Related]
36. Helicases FANCJ, RTEL1 and BLM Act on Guanine Quadruplex DNA
Lansdorp P; van Wietmarschen N
Genes (Basel); 2019 Oct; 10(11):. PubMed ID: 31683575
[TBL] [Abstract][Full Text] [Related]
37. Landscape of BRIP1 molecular lesions in gastrointestinal cancers from published genomic studies.
Voutsadakis IA
World J Gastroenterol; 2020 Mar; 26(11):1197-1207. PubMed ID: 32231423
[TBL] [Abstract][Full Text] [Related]
38. FANCJ uses its motor ATPase to destabilize protein-DNA complexes, unwind triplexes, and inhibit RAD51 strand exchange.
Sommers JA; Rawtani N; Gupta R; Bugreev DV; Mazin AV; Cantor SB; Brosh RM
J Biol Chem; 2009 Mar; 284(12):7505-17. PubMed ID: 19150983
[TBL] [Abstract][Full Text] [Related]
39. Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome.
Suhasini AN; Rawtani NA; Wu Y; Sommers JA; Sharma S; Mosedale G; North PS; Cantor SB; Hickson ID; Brosh RM
EMBO J; 2011 Feb; 30(4):692-705. PubMed ID: 21240188
[TBL] [Abstract][Full Text] [Related]
40. Biochemical characterization of Warsaw breakage syndrome helicase.
Wu Y; Sommers JA; Khan I; de Winter JP; Brosh RM
J Biol Chem; 2012 Jan; 287(2):1007-21. PubMed ID: 22102414
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
