International audienceThe chromosome 8p is associated with a large number of allelic imbalances in epithelial tumors including hepatocellular carcinoma (HCC). However, no tumor suppressor gene has been identified so far in this particular region of the genome. To further clarify the pattern of allelic deletions on chromosome 8p in HCC, we have undertaken high-density polymorphic marker analysis of 109 paired normal and primary tumor samples using 40 microsatellites positioned every 2 cm in average throughout 8p. We found that 60% of the tumors exhibited loss of heterozygosity (LOH) at one or more loci at 8p with three distinct minimal deleted areas: a 13 cm region in the distal part of 8p21, a 9 cm area in the more proximal portion of 8p22 ...
Loss of heterozygosity (LOH) at several chromosomal loci is a common feature of the malignant progre...
Purpose: Allelic loss is the most frequently genetic alteration found in hepatocellular carcinoma (H...
[[abstract]]A novel 1-cM (1.8 Mb) homozygous deletion (HD) on 13q12.11 was identified in a human hep...
International audienceThe chromosome 8p is associated with a large number of allelic imbalances in e...
To define the commonly deleted region on chromosome 8p for further positional cloning of the putativ...
BACKGROUND. Allelic deletions are frequent genetic alterations in patients with hepatocellular carci...
Human chromosome 8p23 is known as a region that is associated with loss of heterozygosity (LOH), whi...
International audienceHepatocellular carcinoma (HCC) is one of the most common cancers in many parts...
To understand the genetic mechanisms underlying the progression of hepatocellular carcinoma (HCC) me...
Systematic scan and statistical analysis of loss of heterozygosity (LOH) been widely used to define ...
Loss of heterozygosity (LOH) on chromosome 13q is one of the most common genetic alterations in hepa...
[[abstract]]Systematic scan and statistical analysis of loss of heterozygosity (LOH) been widely use...
Hepatocellular carcinoma (HCC) frequently shows a loss of heterozygosity (LOH) on chromosome 4q. In ...
Hepatocellular carcinoma (HCC) frequently shows an allelic imbalance (AI) on chromosome 16q. In orde...
A novel 1-cM (1.8 Mb) homozygous deletion (HD) on 13q12.11 was identified in a human hepatocellular ...
Loss of heterozygosity (LOH) at several chromosomal loci is a common feature of the malignant progre...
Purpose: Allelic loss is the most frequently genetic alteration found in hepatocellular carcinoma (H...
[[abstract]]A novel 1-cM (1.8 Mb) homozygous deletion (HD) on 13q12.11 was identified in a human hep...
International audienceThe chromosome 8p is associated with a large number of allelic imbalances in e...
To define the commonly deleted region on chromosome 8p for further positional cloning of the putativ...
BACKGROUND. Allelic deletions are frequent genetic alterations in patients with hepatocellular carci...
Human chromosome 8p23 is known as a region that is associated with loss of heterozygosity (LOH), whi...
International audienceHepatocellular carcinoma (HCC) is one of the most common cancers in many parts...
To understand the genetic mechanisms underlying the progression of hepatocellular carcinoma (HCC) me...
Systematic scan and statistical analysis of loss of heterozygosity (LOH) been widely used to define ...
Loss of heterozygosity (LOH) on chromosome 13q is one of the most common genetic alterations in hepa...
[[abstract]]Systematic scan and statistical analysis of loss of heterozygosity (LOH) been widely use...
Hepatocellular carcinoma (HCC) frequently shows a loss of heterozygosity (LOH) on chromosome 4q. In ...
Hepatocellular carcinoma (HCC) frequently shows an allelic imbalance (AI) on chromosome 16q. In orde...
A novel 1-cM (1.8 Mb) homozygous deletion (HD) on 13q12.11 was identified in a human hepatocellular ...
Loss of heterozygosity (LOH) at several chromosomal loci is a common feature of the malignant progre...
Purpose: Allelic loss is the most frequently genetic alteration found in hepatocellular carcinoma (H...
[[abstract]]A novel 1-cM (1.8 Mb) homozygous deletion (HD) on 13q12.11 was identified in a human hep...