Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Childhood Acute Lymphoblastic Leukemia
0.080 PosttranslationalModification disease BEFREE On the contrary, methylation of the p15 promoter is identified in some 50% of the patients with AML and MDS, but is less frequent in ALL. 27401303 2017
Childhood Acute Lymphoblastic Leukemia
0.080 AlteredExpression disease BEFREE Children with ALL have higher levels of p15 CpG island methylation than a control group of children with ITP. 26501552 2016
Childhood Acute Lymphoblastic Leukemia
0.080 Biomarker disease BEFREE Methylation of both p15 and SHP1 genes occurred more frequently in T-ALL than in precursor B-ALL (p=0.02 and p=0.01, respectively). 21592569 2011
Childhood Acute Lymphoblastic Leukemia
0.080 PosttranslationalModification disease BEFREE The methylation-specific polymerase chain reaction (MS-PCR) was used to analyze p15 and p16 gene methylation in 49 cases of acute lymphoblastic leukemia (ALL) and 29 cases of acute myelogenous leukemia (AML). 11413509 2001
Childhood Acute Lymphoblastic Leukemia
0.080 PosttranslationalModification disease BEFREE We also demonstrated for the first time concomitant p16 and p15 methylation in 22% (8/37) of adults with AML or ALL, exclusively in those with M2, M4, or L2 subtypes. 10706859 2000
Childhood Acute Lymphoblastic Leukemia
0.080 GeneticVariation disease BEFREE To determine whether alterations in these genes play a role in disease progression, we analyzed a panel of 18 matched specimen pairs collected from children with ALL at the time of initial diagnosis and first bone marrow relapse for homozygous p16 and/or p15 deletions or p15 promoter hypermethylation. 10090949 1999
Childhood Acute Lymphoblastic Leukemia
0.080 GeneticVariation disease BEFREE We analyzed 60 B precursor acute lymphoblastic leukemia (ALL) primary samples and 15 cell lines for homozygous deletions of p16 and p15 genes and mutations of p16 gene. 8683987 1996
Childhood Acute Lymphoblastic Leukemia
0.080 GeneticVariation disease BEFREE Homozygous deletions of the p15 gene were also very frequent in T-ALLs (9/22; 41%), and it occurred in 5 of 81 (6%) precursor-B ALL samples. 7606004 1995