The 309T>G polymorphism in the promoter region of the MDM2gene, known as SNP309, has recently been suggested as an unfavorable prognostic marker in chronic lymphocytic leukemia (CLL) although this has been questioned. To investigate this further, we analyzed the MDM2 SNP309 genotypes in 418 CLL patients and correlated the results with established CLL prognostic factors, time to treatment and overall survival. In this Swedish cohort, no association existed between any particular MDM2 SNP309 genotype, overall survival and time to treatment. Furthermore, no correlation was shown between the MDM2 SNP309 genotypes and Binet stage, IGHV mutational status and recurrent genomic aberrations. In summary, this study argues against the use of the MD...
The present thesis is focused on the prognostic value of genetic variations and alterations in the i...
<div><p>Chronic lymphocytic leukemia (CLL) is the most common leukemia in the Western world and is c...
The present thesis is focused on the prognostic value of genetic variations and alterations in the i...
The 309T>G polymorphism in the promoter region of the MDM2 gene, known as SNP309, has recently been ...
A number of single nucleotide polymorphisms have been associated with disease predisposition in chro...
A number of single nucleotide polymorphisms have been associated with disease predisposition in chro...
A number of single nucleotide polymorphisms have been associated with disease predisposition in chro...
The (-938C > A) polymorphism in the promoter region of the BCL-2 gene was recently associated with i...
Background: Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults. The MDM2 and p...
The p53 pathway plays a critical role in chronic lymphocytic leukemia (CLL). The association between...
Introduction The murine double minute 2 (MDM2) gene encodes a regulatory protein of the p53 pathway...
The clinical course of chronic lymphocytic leukemia (CLL) is highly heterogeneous, which has prompte...
Chronic lymphocytic leukemia (CLL) is a clinically heterogeneous disease with no known single predis...
The presence of TP53 mutations has been associated with inferior outcome in diffuse large B-cell lym...
Since the identification of a well-characterized func-tional polymorphism named SNP309 in MDM2, abun...
The present thesis is focused on the prognostic value of genetic variations and alterations in the i...
<div><p>Chronic lymphocytic leukemia (CLL) is the most common leukemia in the Western world and is c...
The present thesis is focused on the prognostic value of genetic variations and alterations in the i...
The 309T>G polymorphism in the promoter region of the MDM2 gene, known as SNP309, has recently been ...
A number of single nucleotide polymorphisms have been associated with disease predisposition in chro...
A number of single nucleotide polymorphisms have been associated with disease predisposition in chro...
A number of single nucleotide polymorphisms have been associated with disease predisposition in chro...
The (-938C > A) polymorphism in the promoter region of the BCL-2 gene was recently associated with i...
Background: Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults. The MDM2 and p...
The p53 pathway plays a critical role in chronic lymphocytic leukemia (CLL). The association between...
Introduction The murine double minute 2 (MDM2) gene encodes a regulatory protein of the p53 pathway...
The clinical course of chronic lymphocytic leukemia (CLL) is highly heterogeneous, which has prompte...
Chronic lymphocytic leukemia (CLL) is a clinically heterogeneous disease with no known single predis...
The presence of TP53 mutations has been associated with inferior outcome in diffuse large B-cell lym...
Since the identification of a well-characterized func-tional polymorphism named SNP309 in MDM2, abun...
The present thesis is focused on the prognostic value of genetic variations and alterations in the i...
<div><p>Chronic lymphocytic leukemia (CLL) is the most common leukemia in the Western world and is c...
The present thesis is focused on the prognostic value of genetic variations and alterations in the i...