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FRAXF gene

Known as: FAMILY WITH SEQUENCE SIMILARITY 11, MEMBER A, fragile site, folic acid type, rare, fra(X)(q28) F, FRAXF 
National Institutes of Health

Related topics

Related topics

14 relations
BRINP3 geneCALHM1 geneFAM19A4 geneFAM21C gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Low mutation and neoantigen burden and fewer effector tumor infiltrating lymphocytes correlate with breast cancer metastasization to lymph nodes
Lymph node metastasis is of major prognostic significance for breast cancer. Lymph node metastasis arises at a very early stage… 
2009
2009
duplication. FRAXF in a patient with chromosome 8
2002
2002
A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutation
The cytogenetic expression of the FRAXF fragile site is due to an expanded, hypermethylated and unstable CGG repeat in Xq28… 
1999
1999
A simple multiplex FRAXA, FRAXE, and FRAXF PCR assay convenient for wide screening programs
FRAXA, FRAXE, and FRAXF are folate‐sensitive fragile sites originally discovered in patients with X‐linked mental retardation… 
1996
1996
Trinucleotide repeats at the FRAXF locus: frequency and distribution in the general population.
FRAXF, the third X-chromosomal fragile site to be cloned, has been shown to harbour a polymorphic compound triplet array: (GCCGTC… 
1996
1996
FRAXF in a patient with chromosome 8 duplication.
We report on a folate sensitive fragile site at Xq27-28 in a girl with a multiple congenital anomalies and mental retardation… 
Review
1996
Review
1996
Dynamic mutations in human genes: A review of trinucleotide repeat diseases
Dynamic mutations in human genes result from unstable trinucleotide repeats embedded within the transcribed region. The… 
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