MHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCM (Q24305020)

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29 January 2020

title

MHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCM (English)

1 reference

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29 January 2020

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FA complementation group M

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FA core complex associated protein 24

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Centromere protein S

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3

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29 January 2020

Amom Ruhikanta Meetei

12

object named as

Amom Ruhikanta Meetei

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29 January 2020

author name string

Thiyam Ramsing Singh

1

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29 January 2020

Dorina Saro

2

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29 January 2020

Xiao-Feng Zheng

4

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29 January 2020

Chang-hu Du

5

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29 January 2020

Michael W Killen

6

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29 January 2020

Aristidis Sachpatzidis

7

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29 January 2020

Kebola Wahengbam

8

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29 January 2020

Andrew J Pierce

9

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29 January 2020

Yong Xiong

10

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29 January 2020

Patrick Sung

11

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29 January 2020

language of work or name

English

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publication date

1 March 2010

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29 January 2020

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29 January 2020

volume

37

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29 January 2020

issue

6

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29 January 2020

page(s)

879-886

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BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome

29 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

19 March 2017

1 reference

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Yeast Mph1 helicase dissociates Rad51-made D-loops: implications for crossover control in mitotic recombination.

19 March 2017

1 reference

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Cellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insights

19 March 2017

1 reference

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The human CENP-A centromeric nucleosome-associated complex

19 March 2017

1 reference

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The CENP-S complex is essential for the stable assembly of outer kinetochore structure

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

The Walker B motif in avian FANCM is required to limit sister chromatid exchanges but is dispensable for DNA crosslink repair

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

FANCM-FAAP24 and FANCJ: FA proteins that metabolize DNA.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

The genetic and molecular basis of Fanconi anemia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

FANCM and FAAP24 function in ATR-mediated checkpoint signaling independently of the Fanconi anemia core complex

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

Remodeling of DNA replication structures by the branch point translocase FANCM

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

The Fanconi anemia protein FANCM can promote branch migration of Holliday junctions and replication forks

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

A novel 1p36.2 located gene, APITD1, with tumour-suppressive properties and a putative p53-binding domain, shows low expression in neuroblastoma tumours.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

The histone fold: a ubiquitous architectural motif utilized in DNA compaction and protein dimerization

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

The FANCM ortholog Fml1 promotes recombination at stalled replication forks and limits crossing over during DNA double-strand break repair

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

Regulated interaction of the Fanconi anemia protein, FANCD2, with chromatin

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848122

10.1016/J.MOLCEL.2010.01.036

29 November 2018

Identifiers

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29 January 2020

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29 January 2020

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