Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway (Q28203777)

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5 November 2019

title

Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway (English)

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5 November 2019

1 reference

2

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5 November 2019

James Hejna

6

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5 November 2019

Markus Grompe

7

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5 November 2019

author name string

I Garcia-Higuera

1

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5 November 2019

S Ganesan

3

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5 November 2019

M S Meyn

4

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5 November 2019

C Timmers

5

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5 November 2019

A D D'Andrea

8

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5 November 2019

publication date

1 February 2001

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5 November 2019

language of work or name

0 references

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5 November 2019

volume

7

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5 November 2019

issue

2

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5 November 2019

page(s)

249-262

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Fanconi's anemia and malignancies

5 November 2019

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Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia

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The ubiquitin-proteasome proteolytic pathway

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Requirement of ATM-dependent phosphorylation of brca1 in the DNA damage response to double-strand breaks

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The Fanconi anaemia group G gene FANCG is identical with XRCC9

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Isolation of a cDNA representing the Fanconi anemia complementation group E gene

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The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM

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The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG

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Abnormal response to DNA crosslinking agents of Fanconi anemia fibroblasts can be corrected by transfection with normal human DNA.

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Irreversible repression of DNA synthesis in Fanconi anemia cells is alleviated by the product of a novel cyclin-related gene

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Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining

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Positional cloning of the Fanconi anaemia group A gene

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7 January 2021

Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex

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Radiosensitivity in Fanconi anaemia: application to the conditioning regimen for bone marrow transplantation

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Evidence for at Least Eight Fanconi Anemia Genes

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Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment

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Regulation of transcription by ubiquitination without proteolysis: Cdc34/SCF(Met30)-mediated inactivation of the transcription factor Met4.

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The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomes.

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7 January 2021

The Fanconi anaemia proteins, FAA and FAC interact to form a nuclear complex

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7 January 2021

hCds1-mediated phosphorylation of BRCA1 regulates the DNA damage response

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7 January 2021

Accelerated telomere shortening and telomerase activation in Fanconi's anaemia

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Functional link of BRCA1 and ataxia telangiectasia gene product in DNA damage response

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7 January 2021

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Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p

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7 January 2021

Independence of R/M/N focus formation and the presence of intact BRCA1.

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7 January 2021

The Fanconi anemia polypeptide FACC is localized to the cytoplasm

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7 January 2021

The Fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation

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7 January 2021

Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response

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7 January 2021

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7 January 2021

10.1016/S1097-2765(01)00173-3

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Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239454%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017