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Items: 1 to 20 of 92

1.

The HARP domain dictates the annealing helicase activity of HARP/SMARCAL1.

Ghosal G, Yuan J, Chen J.

EMBO Rep. 2011 Jun;12(6):574-80. doi: 10.1038/embor.2011.74. Epub 2011 Apr 28.

2.

The annealing helicase HARP protects stalled replication forks.

Yuan J, Ghosal G, Chen J.

Genes Dev. 2009 Oct 15;23(20):2394-9. doi: 10.1101/gad.1836409. Epub 2009 Sep 30.

3.

HARP is an ATP-driven annealing helicase.

Yusufzai T, Kadonaga JT.

Science. 2008 Oct 31;322(5902):748-50. doi: 10.1126/science.1161233.

4.

The annealing helicase SMARCAL1 maintains genome integrity at stalled replication forks.

Bansbach CE, Bétous R, Lovejoy CA, Glick GG, Cortez D.

Genes Dev. 2009 Oct 15;23(20):2405-14. doi: 10.1101/gad.1839909. Epub 2009 Sep 30.

5.

The annealing helicase and branch migration activities of Drosophila HARP.

Kassavetis GA, Kadonaga JT.

PLoS One. 2014 May 27;9(5):e98173. doi: 10.1371/journal.pone.0098173. eCollection 2014.

6.

The annealing helicase HARP is recruited to DNA repair sites via an interaction with RPA.

Yusufzai T, Kong X, Yokomori K, Kadonaga JT.

Genes Dev. 2009 Oct 15;23(20):2400-4. doi: 10.1101/gad.1831509. Epub 2009 Sep 30.

7.

A structure-specific nucleic acid-binding domain conserved among DNA repair proteins.

Mason AC, Rambo RP, Greer B, Pritchett M, Tainer JA, Cortez D, Eichman BF.

Proc Natl Acad Sci U S A. 2014 May 27;111(21):7618-23. doi: 10.1073/pnas.1324143111. Epub 2014 May 12.

8.

HARP preferentially co-purifies with RPA bound to DNA-PK and blocks RPA phosphorylation.

Quan J, Yusufzai T.

Epigenetics. 2014 May;9(5):693-7. doi: 10.4161/epi.28310. Epub 2014 Feb 24.

9.

The role of SMARCAL1 in replication fork stability and telomere maintenance.

Lugli N, Sotiriou SK, Halazonetis TD.

DNA Repair (Amst). 2017 Aug;56:129-134. doi: 10.1016/j.dnarep.2017.06.015. Epub 2017 Jun 10. Review.

PMID:
28623093
10.

Annealing helicase 2 (AH2), a DNA-rewinding motor with an HNH motif.

Yusufzai T, Kadonaga JT.

Proc Natl Acad Sci U S A. 2010 Dec 7;107(49):20970-3. doi: 10.1073/pnas.1011196107. Epub 2010 Nov 15.

11.

SMARCAL1 and replication stress: an explanation for SIOD?

Bansbach CE, Boerkoel CF, Cortez D.

Nucleus. 2010 May-Jun;1(3):245-8. doi: 10.4161/nucl.1.3.11739. Epub 2010 Feb 16.

12.
13.

The HARP-like domain-containing protein AH2/ZRANB3 binds to PCNA and participates in cellular response to replication stress.

Yuan J, Ghosal G, Chen J.

Mol Cell. 2012 Aug 10;47(3):410-21. doi: 10.1016/j.molcel.2012.05.025. Epub 2012 Jun 14.

14.

Ligand-induced conformation changes drive ATP hydrolysis and function in SMARCAL1.

Gupta M, Mazumder M, Dhatchinamoorthy K, Nongkhlaw M, Haokip DT, Gourinath S, Komath SS, Muthuswami R.

FEBS J. 2015 Oct;282(19):3841-59. doi: 10.1111/febs.13382. Epub 2015 Aug 26.

15.

Schimke Immunoosseous Dysplasia associated with undifferentiated carcinoma and a novel SMARCAL1 mutation in a child.

Carroll C, Badu-Nkansah A, Hunley T, Baradaran-Heravi A, Cortez D, Frangoul H.

Pediatr Blood Cancer. 2013 Sep;60(9):E88-90. doi: 10.1002/pbc.24542. Epub 2013 Apr 29.

16.

SMARCAL1 catalyzes fork regression and Holliday junction migration to maintain genome stability during DNA replication.

Bétous R, Mason AC, Rambo RP, Bansbach CE, Badu-Nkansah A, Sirbu BM, Eichman BF, Cortez D.

Genes Dev. 2012 Jan 15;26(2):151-62. doi: 10.1101/gad.178459.111.

17.

A novel splice site mutation in SMARCAL1 results in aberrant exon definition in a child with Schimke immunoosseous dysplasia.

Carroll C, Hunley TE, Guo Y, Cortez D.

Am J Med Genet A. 2015 Oct;167A(10):2260-4. doi: 10.1002/ajmg.a.37146. Epub 2015 May 5.

18.

Identification of SMARCAL1 as a component of the DNA damage response.

Postow L, Woo EM, Chait BT, Funabiki H.

J Biol Chem. 2009 Dec 18;284(51):35951-61. doi: 10.1074/jbc.M109.048330.

19.

Annealing helicase HARP closes RPA-stabilized DNA bubbles non-processively.

Burnham DR, Nijholt B, De Vlaminck I, Quan J, Yusufzai T, Dekker C.

Nucleic Acids Res. 2017 May 5;45(8):4687-4695. doi: 10.1093/nar/gkx147.

20.

Schimke immuno-osseous dysplasia: SMARCAL1 loss-of-function and phenotypic correlation.

Elizondo LI, Cho KS, Zhang W, Yan J, Huang C, Huang Y, Choi K, Sloan EA, Deguchi K, Lou S, Baradaran-Heravi A, Takashima H, Lücke T, Quiocho FA, Boerkoel CF.

J Med Genet. 2009 Jan;46(1):49-59. doi: 10.1136/jmg.2008.060095. Epub 2008 Sep 19.

PMID:
18805831

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