FAQ

FANCA gene

Known as: FAA, Fanconi anemia complementation group A, Fanconi Anemia, Complementation Group A Gene 
This gene may be involved in the mediation of DNA repair.

Topic mentions per year

Topic mentions per year

1977-2018
051019772018

Related topics

Related topics

8 relations
Cell Cycle ControlDNA RepairDNA stabilityFANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
(More)

Broader (1)

DNA Repair Gene

Narrower (1)

FANCA wt Allele

Related mentions per year

Related mentions per year

1940-2018
19401960198020002020
FANCA gene
DNA Repair
Fanconi Anemia
Cell Cycle Control
DNA stability
FANCA wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Common variants in immune and DNA repair genes and risk for human papillomavirus persistence and progression to cervical cancer.
BACKGROUND We examined host genetic factors to identify those more common in individuals whose human papillomavirus (HPV… (More)
  • table 1
  • table 1
  • table 2
  • table 3
  • table 4
Is this relevant?
2007
2007
Messenger RNA as a source of transposase for sleeping beauty transposon-mediated correction of hereditary tyrosinemia type I.
The Sleeping Beauty (SB) transposon system mediates chromosomal integration and stable gene expression when an engineered SB… (More)
Is this relevant?
2005
2005
Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
Fanconi anemia (FA) is an autosomal recessive disorder that is defined by cellular hypersensitivity to DNA cross-linking agents… (More)
Is this relevant?
2005
2005
A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain.
Fanconi anemia (FA) is a genetic disease characterized by bone marrow failure and cancer predisposition. Here we have identified… (More)
  • figure 1
  • table 1
Is this relevant?
2004
2004
Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia
Fanconi anemia (FA) is an autosomal recessive chromosomal instability disorder caused by mutations in one of seven known genes… (More)
  • figure 1
  • table 1
  • table 2
  • figure 2
Is this relevant?
2003
2003
Nonerythroid alphaII spectrin is required for recruitment of FANCA and XPF to nuclear foci induced by DNA interstrand cross-links.
The events responsible for repair of DNA interstrand cross-links in mammalian cells, the proteins involved and their interactions… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2002
2002
In vivo correction of murine tyrosinemia type I by DNA-mediated transposition.
Gene therapy applications of naked DNA constructs for genetic disorders have been limited because of lack of permanent transgene… (More)
  • table 1
  • figure 1
  • table 2
  • table 3
  • figure 2
Is this relevant?
2001
2001
Fanconi anemia proteins localize to chromatin and the nuclear matrix in a DNA damage- and cell cycle-regulated manner.
Fanconi anemia (FA) is a genetic disease characterized by congenital defects, bone marrow failure, and cancer susceptibility… (More)
Is this relevant?
2000
2000
Adrenal hyperandrogenism in adolescent girls with a history of low birthweight and precocious pubarche.
OBJECTIVE Girls with precocious pubarche (PP) are at increased risk for ovarian dysfunction, hyperinsulinism and dyslipidaemia in… (More)
Is this relevant?
1999
1999
The FANCA gene in Japanese Fanconi anemia: reports of eight novel mutations and analysis of sequence variability.
Fanconi anemia (FA), an autosomal recessive disorder characterized by a progressive pancytopenia associated with congenital… (More)
Is this relevant?