Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Childhood T Acute Lymphoblastic Leukemia
0.060 GeneticVariation disease BEFREE The most common recurrent cytogenetic abnormalities in T-lymphoblastic leukemia (T-acute lymphoblastic leukemia [T-ALL]) involve T-cell receptor (TCR) loci and a variety of partner genes, including HOX11, HOX11L2, MYC, and TAL1. 22563559 2012
Childhood T Acute Lymphoblastic Leukemia
0.060 GeneticVariation disease BEFREE Thirty-one/131 childhood T-ALL cases (24%) enrolled into four population-based Austrian ALL-BFM therapy studies were TLX3+. 19821827 2010
Childhood T Acute Lymphoblastic Leukemia
0.060 AlteredExpression disease BEFREE TLX3 gene expression is an independent risk factor predicting poor survival in childhood T-cell acute lymphoblastic leukemia. 18835836 2008
Childhood T Acute Lymphoblastic Leukemia
0.060 Biomarker disease BEFREE Our data indicate that the basis of the specific association between t(5;14) and T-ALL lies on the juxtaposition of TLX3 to long-range cis-activating regions active during T-cell differentiation. 16926283 2006
Childhood T Acute Lymphoblastic Leukemia
0.060 AlteredExpression disease BEFREE Hence, Hox11L2 expression seems to be the most frequent abnormality in childhood T-ALL to date, comparable to the t(12;21) in child B-ALL. 12454747 2002
Childhood T Acute Lymphoblastic Leukemia
0.060 GeneticVariation disease BEFREE A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia. 11587205 2001