DLEC1 (deleted in lung and oesophageal cancer), located on 3p22.3, is a candidate tumour suppressor gene in lung, esophageal, and renal cancer. The aim of this study was determine whether the mRNA expression levels of DLEC1 were consistent with a tumour suppressive function. MATERIALS AND METHODS: A total of 153 samples were analysed. The levels of transcription of DLEC1 were determined using quantitative PCR and normalised against (CK19). Transcript levels within breast cancer specimens were compared to normal background tissues. RESULTS: Levels of transcription were lower [corrected] in tumour samples compared to adjacent non cancerous tissue (ANCT) samples but this was not statistically significant (median 0.167 vs. 0.03; p=0.138). D...
Abstract. DLC1 (deleted in liver cancer-1) is a new candidate tumor suppressor gene, which is inacti...
The critical 8p22 tumor suppressor deleted in liver cancer 1 (DLC1) is frequently inactivated by abe...
Different types of genetic and epigenetic changes are associated with HNSCC. The molecular mechanism...
DLEC1 (deleted in lung and oesophageal cancer), located on 3p22.3, is a candidate tumour suppressor ...
Suppression of ovarian tumor growth by chromosome 3p was demonstrated in a previous study. Deleted i...
AbstractSuppression of ovarian tumor growth by chromosome 3p was demonstrated in a previous study. D...
Background/Aims: The chromosome locus 3p21.3 is a "hot-spot" for chromosomal aberrations and loss of...
Background: Inactivaion of tumor suppressor genes (TSGs) by promoter CpG methylation frequently occu...
Purpose: Identifying tumor suppressor genes silenced by promoter CpG methylation uncovers mechanisms...
Deleted in Liver Cancer-1 (DLC1), a member of the RhoGAP family of proteins, functions as a tumor su...
Deleted in Liver Cancer-1 (DLC1), a member of the RhoGAP family of proteins, functions as a tumor su...
Background: Deleted in liver cancer (DLC) is a family of tumour suppressors that plays a critical ro...
suppressor is haploinsufficient for mammary gland development and epithelial cell polarity Pratima B...
Abstract Background Inactivaion of tumor suppressor genes (TSGs) by promoter CpG methylation frequen...
Identification of tumor suppressor genes (TSG) silenced by methylation uncovers mechanisms of tumori...
Abstract. DLC1 (deleted in liver cancer-1) is a new candidate tumor suppressor gene, which is inacti...
The critical 8p22 tumor suppressor deleted in liver cancer 1 (DLC1) is frequently inactivated by abe...
Different types of genetic and epigenetic changes are associated with HNSCC. The molecular mechanism...
DLEC1 (deleted in lung and oesophageal cancer), located on 3p22.3, is a candidate tumour suppressor ...
Suppression of ovarian tumor growth by chromosome 3p was demonstrated in a previous study. Deleted i...
AbstractSuppression of ovarian tumor growth by chromosome 3p was demonstrated in a previous study. D...
Background/Aims: The chromosome locus 3p21.3 is a "hot-spot" for chromosomal aberrations and loss of...
Background: Inactivaion of tumor suppressor genes (TSGs) by promoter CpG methylation frequently occu...
Purpose: Identifying tumor suppressor genes silenced by promoter CpG methylation uncovers mechanisms...
Deleted in Liver Cancer-1 (DLC1), a member of the RhoGAP family of proteins, functions as a tumor su...
Deleted in Liver Cancer-1 (DLC1), a member of the RhoGAP family of proteins, functions as a tumor su...
Background: Deleted in liver cancer (DLC) is a family of tumour suppressors that plays a critical ro...
suppressor is haploinsufficient for mammary gland development and epithelial cell polarity Pratima B...
Abstract Background Inactivaion of tumor suppressor genes (TSGs) by promoter CpG methylation frequen...
Identification of tumor suppressor genes (TSG) silenced by methylation uncovers mechanisms of tumori...
Abstract. DLC1 (deleted in liver cancer-1) is a new candidate tumor suppressor gene, which is inacti...
The critical 8p22 tumor suppressor deleted in liver cancer 1 (DLC1) is frequently inactivated by abe...
Different types of genetic and epigenetic changes are associated with HNSCC. The molecular mechanism...