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Hereditary breast cancer and the BRCA1-associated FANCJ/BACH1/BRIP1.

Cantor SB, Guillemette S.

Future Oncol. 2011 Feb;7(2):253-61. doi: 10.2217/fon.10.191. Review.


Assessing the link between BACH1/FANCJ and MLH1 in DNA crosslink repair.

Cantor SB, Xie J.

Environ Mol Mutagen. 2010 Jul;51(6):500-7. doi: 10.1002/em.20568. Review.


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 Jr, Cantor SB.

EMBO J. 2007 Jul 11;26(13):3238-49. Epub 2007 Jun 21.


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; INHERIT BRCAs.

J Hum Genet. 2008;53(7):579-91. doi: 10.1007/s10038-008-0285-z. Epub 2008 Apr 15.


BRCA1-mediated repression of mutagenic end-joining of DNA double-strand breaks requires complex formation with BACH1.

Dohrn L, Salles D, Siehler SY, Kaufmann J, Wiesmüller L.

Biochem J. 2012 Feb 1;441(3):919-26. doi: 10.1042/BJ20110314.


Activation of BRCA1/BRCA2-associated helicase BACH1 is required for timely progression through S phase.

Kumaraswamy E, Shiekhattar R.

Mol Cell Biol. 2007 Oct;27(19):6733-41. Epub 2007 Jul 30.


Assessing the link between BACH1 and BRCA1 in the FA pathway.

Cantor SB, Andreassen PR.

Cell Cycle. 2006 Jan;5(2):164-7. Epub 2006 Jan 16. Review.


FANCJ localization by mismatch repair is vital to maintain genomic integrity after UV irradiation.

Guillemette S, Branagan A, Peng M, Dhruva A, Schärer OD, Cantor SB.

Cancer Res. 2014 Feb 1;74(3):932-44. doi: 10.1158/0008-5472.CAN-13-2474. Epub 2013 Dec 18.


FANCJ/BACH1 acetylation at lysine 1249 regulates the DNA damage response.

Xie J, Peng M, Guillemette S, Quan S, Maniatis S, Wu Y, Venkatesh A, Shaffer SA, Brosh RM Jr, Cantor SB.

PLoS Genet. 2012 Jul;8(7):e1002786. doi: 10.1371/journal.pgen.1002786. Epub 2012 Jul 5.


Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication.

Shen X, Do H, Li Y, Chung WH, Tomasz M, de Winter JP, Xia B, Elledge SJ, Wang W, Li L.

Mol Cell. 2009 Sep 11;35(5):716-23. doi: 10.1016/j.molcel.2009.06.034.


HP1 regulates the localization of FANCJ at sites of DNA double-strand breaks.

Wu W, Togashi Y, Johmura Y, Miyoshi Y, Nobuoka S, Nakanishi M, Ohta T.

Cancer Sci. 2016 Oct;107(10):1406-1415. doi: 10.1111/cas.13008. Epub 2016 Sep 1.


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. doi: 10.1007/s00412-015-0549-2. Epub 2015 Oct 21.


Targeting the FANCJ-BRCA1 interaction promotes a switch from recombination to poleta-dependent bypass.

Xie J, Litman R, Wang S, Peng M, Guillemette S, Rooney T, Cantor SB.

Oncogene. 2010 Apr 29;29(17):2499-508. doi: 10.1038/onc.2010.18. Epub 2010 Feb 22.


Mutation analysis of BRIP1/BACH1 in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives.

Cao AY, Huang J, Hu Z, Li WF, Ma ZL, Tang LL, Zhang B, Su FX, Zhou J, Di GH, Shen KW, Wu J, Lu JS, Luo JM, Yuan WT, Shen ZZ, Huang W, Shao ZM.

Breast Cancer Res Treat. 2009 May;115(1):51-5. doi: 10.1007/s10549-008-0052-z. Epub 2008 May 16.


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 12;289(37):25774-82. doi: 10.1074/jbc.M114.552570. Epub 2014 Jul 28.


FANCJ protein is important for the stability of FANCD2/FANCI proteins and protects them from proteasome and caspase-3 dependent degradation.

Clark DW, Tripathi K, Dorsman JC, Palle K.

Oncotarget. 2015 Oct 6;6(30):28816-32. doi: 10.18632/oncotarget.5006.


BRCA1 and FancJ cooperatively promote interstrand crosslinker induced centrosome amplification through the activation of polo-like kinase 1.

Zou J, Zhang D, Qin G, Chen X, Wang H, Zhang D.

Cell Cycle. 2014;13(23):3685-97. doi: 10.4161/15384101.2014.964973.


FANCJ helicase defective in Fanconia anemia and breast cancer unwinds G-quadruplex DNA to defend genomic stability.

Wu Y, Shin-ya K, Brosh RM Jr.

Mol Cell Biol. 2008 Jun;28(12):4116-28. doi: 10.1128/MCB.02210-07. Epub 2008 Apr 21.

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