162 related articles for article (PubMed ID: 27107905)
1. Mutational analysis of FANCJ helicase.
Guo M; Vidhyasagar V; Talwar T; Kariem A; Wu Y
Methods; 2016 Oct; 108():118-29. PubMed ID: 27107905
[TBL] [Abstract][Full Text] [Related]
2. Insight into the roles of helicase motif Ia by characterizing Fanconi anemia group J protein (FANCJ) patient mutations.
Guo M; Vidhyasagar V; Ding H; Wu Y
J Biol Chem; 2014 Apr; 289(15):10551-10565. PubMed ID: 24573678
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Specialization among iron-sulfur cluster helicases to resolve G-quadruplex DNA structures that threaten genomic stability.
Bharti SK; Sommers JA; George F; Kuper J; Hamon F; Shin-ya K; Teulade-Fichou MP; Kisker C; Brosh RM
J Biol Chem; 2013 Sep; 288(39):28217-29. PubMed ID: 23935105
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Welcome the family of FANCJ-like helicases to the block of genome stability maintenance proteins.
Wu Y; Suhasini AN; Brosh RM
Cell Mol Life Sci; 2009 Apr; 66(7):1209-22. PubMed ID: 19099189
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Loss of Mitochondrial Localization of Human FANCG Causes Defective FANCJ Helicase.
K JCB; Kapoor BS; Mandal K; Ghosh S; Mokhamatam RB; Manna SK; Mukhopadhyay SS
Mol Cell Biol; 2020 Nov; 40(23):. PubMed ID: 32989015
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Disease-causing missense mutations in human DNA helicase disorders.
Suhasini AN; Brosh RM
Mutat Res; 2013; 752(2):138-152. PubMed ID: 23276657
[TBL] [Abstract][Full Text] [Related]
13. FANCJ helicase uniquely senses oxidative base damage in either strand of duplex DNA and is stimulated by replication protein A to unwind the damaged DNA substrate in a strand-specific manner.
Suhasini AN; Sommers JA; Mason AC; Voloshin ON; Camerini-Otero RD; Wold MS; Brosh RM
J Biol Chem; 2009 Jul; 284(27):18458-70. PubMed ID: 19419957
[TBL] [Abstract][Full Text] [Related]
14. Fanconi anemia and Bloom's syndrome crosstalk through FANCJ-BLM helicase interaction.
Suhasini AN; Brosh RM
Trends Genet; 2012 Jan; 28(1):7-13. PubMed ID: 22024395
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. An Arabidopsis FANCJ helicase homologue is required for DNA crosslink repair and rDNA repeat stability.
Dorn A; Feller L; Castri D; Röhrig S; Enderle J; Herrmann NJ; Block-Schmidt A; Trapp O; Köhler L; Puchta H
PLoS Genet; 2019 May; 15(5):e1008174. PubMed ID: 31120885
[TBL] [Abstract][Full Text] [Related]
17. Rare
Moyer CL; Ivanovich J; Gillespie JL; Doberstein R; Radke MR; Richardson ME; Kaufmann SH; Swisher EM; Goodfellow PJ
Cancer Res; 2020 Feb; 80(4):857-867. PubMed ID: 31822495
[TBL] [Abstract][Full Text] [Related]
18. FANCJ helicase promotes DNA end resection by facilitating CtIP recruitment to DNA double-strand breaks.
Nath S; Nagaraju G
PLoS Genet; 2020 Apr; 16(4):e1008701. PubMed ID: 32251466
[TBL] [Abstract][Full Text] [Related]
19. Cancer-associated mutations in the iron-sulfur domain of FANCJ affect G-quadruplex metabolism.
Odermatt DC; Lee WTC; Wild S; Jozwiakowski SK; Rothenberg E; Gari K
PLoS Genet; 2020 Jun; 16(6):e1008740. PubMed ID: 32542039
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
