Paper · 17545145

Interactions of human rad54 protein with branched DNA molecules.

Mazina OM and 3 others. J Biol Chem, 2007. Cited by 33 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Interactions of human rad54 protein with branched DNA molecules. Papers, record 17545145. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/17545145

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Interactions of human rad54 protein with branched DNA molecules.; PubMed
Journal: J Biol Chem; PubMed
Year: 2007; PubMed
Publication types: Journal Article, Research Support, N.I.H., Extramural; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/17545145/; PubMed
DOI: https://doi.org/10.1074/jbc.m701992200; PubMed
The journal: https://conductscience.org/library/journal-index/2985121R; PubMed
Citations, by iCite: 33; iCite
Relative citation ratio, by iCite: 0.55; iCite
Revised in PubMed: 2024-10-11; PubMed

Authors4

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename
1	Mazina OM	Olga M
2	Rossi MJ	Matthew J
3	Thomaä NH	Nicolas H
4	Mazin AV	Alexander V

Source PubMed

Topics17

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
DNA	Major topic
Nuclear Proteins	Major topic
Adenosine Triphosphatases
Adenosine Triphosphate
Cross-Linking Reagents
DNA Helicases
DNA, Cruciform
DNA-Binding Proteins
Glutathione Transferase
Humans
Hydrolysis
Ions
Kinetics
Magnesium
Nucleic Acid Conformation
Protein Binding
Protein Structure, Tertiary

Source PubMed

Grants2

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes it	Agency	Country	NIH project	Stated by	Source
CA100839	NCI NIH HHS	United States	R01CA100839	PubMed and NIH	NIH RePORTER
			R56CA100839	NIH	NIH RePORTER

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References0

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

None in this release.

Cited by27

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 33 citations.

PMID	Title	Journal	Year	In Papers	Source
42,239,417	FBH1 and RAD54L directly interact and cooperate to drive replication fork reversal.	bioRxiv	2026	https://conductscience.org/library/papers/42239417	PubMed
39,315,725	Disparate requirements for RAD54L in replication fork reversal.	Nucleic Acids Res	2024	https://conductscience.org/library/papers/39315725	PubMed
39,189,453	Mechanism of structure-specific DNA binding by the FANCM branchpoint translocase.	Nucleic Acids Res	2024	https://conductscience.org/library/papers/39189453	PubMed
35,409,332	Cruciform DNA Structures Act as Legible Templates for Accelerating Homologous Recombination in Transgenic Animals.	Int J Mol Sci	2022	https://conductscience.org/library/papers/35409332	PubMed
32,840,778	Branch Migration Activity of Rad54 Protein.	Methods Mol Biol	2021	https://conductscience.org/library/papers/32840778	PubMed
32,337,843	RAD54 promotes alternative lengthening of telomeres by mediating branch migration.	EMBO Rep	2020	https://conductscience.org/library/papers/32337843	PubMed
31,492,866	In vitro role of Rad54 in Rad51-ssDNA filament-dependent homology search and synaptic complexes formation.	Nat Commun	2019	https://conductscience.org/library/papers/31492866	PubMed
29,575,713	Functional transcriptomic annotation and protein-protein interaction analysis identify EZH2 and UBE2C as key upregulated proteins in ovarian cancer.	Cancer Med	2018	https://conductscience.org/library/papers/29575713	PubMed
29,295,984	RAD54 N-terminal domain is a DNA sensor that couples ATP hydrolysis with branch migration of Holliday junctions.	Nat Commun	2018	https://conductscience.org/library/papers/29295984	PubMed
24,744,239	The Mus81-Mms4 structure-selective endonuclease requires nicked DNA junctions to undergo conformational changes and bend its DNA substrates for cleavage.	Nucleic Acids Res	2014	https://conductscience.org/library/papers/24744239	PubMed

1 to 10 of 27

See all 27 cited by

Genes4

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Gene	NCBI Gene ID	Linked by	In Genes	Source
ATP8A2	51,761	PubTator's text mining	https://conductscience.org/library/genes/51761	NCBI Gene
DNAH8	1,769	PubTator's text mining	https://conductscience.org/library/genes/1769	NCBI Gene
RAD54L	8,438	PubTator's text mining	https://conductscience.org/library/genes/8438	NCBI Gene
SMARCA4	6,597	PubTator's text mining	https://conductscience.org/library/genes/6597	NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

Sources 11

ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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