Back to search

Article

Role of Fanconi anaemia proteins FANCG, FANCA and FANCD2 in the maintenance of chromosomal stability

2011-01-01

Abstract excerpt

Fanconi anaemia (FA) is a hereditary, heterogeneous disease that is characterized by chromosomal instability, hypersensitivity to DNA cross-linking agents and cancer. Fifteen FA genes are identified, mutations in any of which are known to cause FA: FANCA, B, C, DI, D2, E, F, G, I, J, L, M, N, 0, and P. Cell lines defective for any FA gene show cellular and cytogenetic hypersensitivity to DNA inter-strand cross-lin...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
281029bb-36b9-5315-a0f0-9151813b0d56
DOI
10.17638/03062780
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Role of Fanconi anaemia proteins FANCG, FANCA and FANCD2 in the maintenance of chromosomal stabilityDOI 10.17638/03062780
Select a neighboring publication to make it the new centre.