Title : Homozygous deletion but not mutation of exons 5 and 8 of the fragile histidine triad (FHIT) gene is associated with features of differentiated thyroid carcinoma.

Pub. Date : 2010 Summer

PMID : 20689140






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Homozygous deletion but not mutation of exons 5 and 8 of the fragile histidine triad (FHIT) gene is associated with features of differentiated thyroid carcinoma. Histidine fragile histidine triad diadenosine triphosphatase Homo sapiens
2 The fragile histidine triad (FHIT) gene encompasses the most common human fragile site, FRA3B at 3p14.2, a region that is involved in homozygous deletions in a variety of human tumors. Histidine fragile histidine triad diadenosine triphosphatase Homo sapiens
3 The fragile histidine triad (FHIT) gene encompasses the most common human fragile site, FRA3B at 3p14.2, a region that is involved in homozygous deletions in a variety of human tumors. Histidine fragile histidine triad diadenosine triphosphatase Homo sapiens