287 related articles for article (PubMed ID: 18086896)
1. 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]
2. C. elegans FANCD2 responds to replication stress and functions in interstrand cross-link repair.
Collis SJ; Barber LJ; Ward JD; Martin JS; Boulton SJ
DNA Repair (Amst); 2006 Nov; 5(11):1398-406. PubMed ID: 16914393
[TBL] [Abstract][Full Text] [Related]
3. FANCJ helicase defective in Fanconia anemia and breast cancer unwinds G-quadruplex DNA to defend genomic stability.
Wu Y; Shin-ya K; Brosh RM
Mol Cell Biol; 2008 Jun; 28(12):4116-28. PubMed ID: 18426915
[TBL] [Abstract][Full Text] [Related]
4. C. elegans: a model of Fanconi anemia and ICL repair.
Youds JL; Barber LJ; Boulton SJ
Mutat Res; 2009 Jul; 668(1-2):103-16. PubMed ID: 19059419
[TBL] [Abstract][Full Text] [Related]
5. FANCJ helicase operates in the Fanconi Anemia DNA repair pathway and the response to replicational stress.
Wu Y; Brosh RM
Curr Mol Med; 2009 May; 9(4):470-82. PubMed ID: 19519404
[TBL] [Abstract][Full Text] [Related]
6. Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes.
Wu Y; Sommers JA; Suhasini AN; Leonard T; Deakyne JS; Mazin AV; Shin-Ya K; Kitao H; Brosh RM
Blood; 2010 Nov; 116(19):3780-91. PubMed ID: 20639400
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. A minimal threshold of FANCJ helicase activity is required for its response to replication stress or double-strand break repair.
Bharti SK; Sommers JA; Awate S; Bellani MA; Khan I; Bradley L; King GA; Seol Y; Vidhyasagar V; Wu Y; Abe T; Kobayashi K; Shin-Ya K; Kitao H; Wold MS; Branzei D; Neuman KC; Brosh RM
Nucleic Acids Res; 2018 Jul; 46(12):6238-6256. PubMed ID: 29788478
[TBL] [Abstract][Full Text] [Related]
9. FANCD2, FANCJ and BRCA2 cooperate to promote replication fork recovery independently of the Fanconi Anemia core complex.
Raghunandan M; Chaudhury I; Kelich SL; Hanenberg H; Sobeck A
Cell Cycle; 2015; 14(3):342-53. PubMed ID: 25659033
[TBL] [Abstract][Full Text] [Related]
10. Mutational analysis of the breast cancer susceptibility gene BRIP1 /BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families.
Guénard F; Labrie Y; Ouellette G; Joly Beauparlant C; Simard J; ; Durocher F
J Hum Genet; 2008; 53(7):579. PubMed ID: 18414782
[TBL] [Abstract][Full Text] [Related]
11. FANCM-FAAP24 and FANCJ: FA proteins that metabolize DNA.
Ali AM; Singh TR; Meetei AR
Mutat Res; 2009 Jul; 668(1-2):20-6. PubMed ID: 19379763
[TBL] [Abstract][Full Text] [Related]
12. The involvement of FANCM, FANCI, and checkpoint proteins in the interstrand DNA crosslink repair pathway is conserved in C. elegans.
Lee KY; Chung KY; Koo HS
DNA Repair (Amst); 2010 Apr; 9(4):374-82. PubMed ID: 20075016
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Mutagenic capacity of endogenous G4 DNA underlies genome instability in FANCJ-defective C. elegans.
Kruisselbrink E; Guryev V; Brouwer K; Pontier DB; Cuppen E; Tijsterman M
Curr Biol; 2008 Jun; 18(12):900-5. PubMed ID: 18538569
[TBL] [Abstract][Full Text] [Related]
15. Comprehensive Mutational Analysis of the BRCA1-Associated DNA Helicase and Tumor-Suppressor FANCJ/BACH1/BRIP1.
Calvo JA; Fritchman B; Hernandez D; Persky NS; Johannessen CM; Piccioni F; Kelch BA; Cantor SB
Mol Cancer Res; 2021 Jun; 19(6):1015-1025. PubMed ID: 33619228
[TBL] [Abstract][Full Text] [Related]
16. Genomic stability: FANCJ-dependent G4 DNA repair.
Maizels N
Curr Biol; 2008 Jul; 18(14):R613-4. PubMed ID: 18644339
[TBL] [Abstract][Full Text] [Related]
17. Crosstalk between BRCA-Fanconi anemia and mismatch repair pathways prevents MSH2-dependent aberrant DNA damage responses.
Peng M; Xie J; Ucher A; Stavnezer J; Cantor SB
EMBO J; 2014 Aug; 33(15):1698-712. PubMed ID: 24966277
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. The Fanconi anemia proteins FANCD2 and FANCJ interact and regulate each other's chromatin localization.
Chen X; Wilson JB; McChesney P; Williams SA; Kwon Y; Longerich S; Marriott AS; Sung P; Jones NJ; Kupfer GM
J Biol Chem; 2014 Sep; 289(37):25774-82. PubMed ID: 25070891
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
