Deletions of the 3p21.3 region are a frequent and early event in the formation of lung, breast, kidney and other cancers. Intense investigation of allelic losses and the discovery of overlapping homozygous deletions in lung and breast tumour-cell lines have defined a minimal critical 120 kb deletion region containing eight genes and likely to harbor one or more tumour-suppressor genes (TSGs). The candidate genes are HYAL2, FUS1, Ras-associated factor 1 (RASSF1), BLU/ZMYND10, NPR2L, 101F6, PL6 and CACNA2D2. Recent research indicates that several of these genes can suppress the growth of lung and other tumour cells. Furthermore, some genes (RASSF1A and BLU/ZMYND10) are very frequently inactivated by non-classical mechanisms such as promoter h...
Abstract Background The short arm of human chromosome 3 is involved in the development of many cance...
Deletion on the short arm of chromosome 3 is one of the most important genetic abnormalities in the ...
Homozygous deletions or loss of heterozygosity (LOH) at human chromosome band 3p12 are consistent fe...
Deletions of the 3p21.3 region are a frequent and early event in the formation of lung, breast, kidn...
We have performed a comprehensive deletion survey of 3p on more than 400 lung, renal, breast, cervic...
We used overlapping and nested homozygous deletions, contig building, genomic sequencing, and physic...
Background: The recently identified RASSF1 locus is located within a 120-kilobase region of chromoso...
Clear cell-type renal cell carcinomas (clear RCC) are characterized almost universally by loss of he...
Deletion on the short arm of chromosome 3 is one of the most important genetic abnormalities in the ...
In the search for a tumour suppressor gene in the 3P21.3 region we isolated two genes, RBM5 and RBM6...
Nasopharyngeal carcinoma (NPC) is among the most common malignancies in southern China. Deletion of ...
We recently commented on the burgeoning evidence that epigenetically mediated gene silencing can sel...
Epigenetic mechanisms are frequently deregulated in cancer cells and can lead to the silencing of ge...
High frequencies of allelic loss on the short arm of chromosome 3 in small cell lung cancer (SCLC) a...
Loss of DNA copy number at the short arm of chromosome 3 is one of the most common genetic changes i...
Abstract Background The short arm of human chromosome 3 is involved in the development of many cance...
Deletion on the short arm of chromosome 3 is one of the most important genetic abnormalities in the ...
Homozygous deletions or loss of heterozygosity (LOH) at human chromosome band 3p12 are consistent fe...
Deletions of the 3p21.3 region are a frequent and early event in the formation of lung, breast, kidn...
We have performed a comprehensive deletion survey of 3p on more than 400 lung, renal, breast, cervic...
We used overlapping and nested homozygous deletions, contig building, genomic sequencing, and physic...
Background: The recently identified RASSF1 locus is located within a 120-kilobase region of chromoso...
Clear cell-type renal cell carcinomas (clear RCC) are characterized almost universally by loss of he...
Deletion on the short arm of chromosome 3 is one of the most important genetic abnormalities in the ...
In the search for a tumour suppressor gene in the 3P21.3 region we isolated two genes, RBM5 and RBM6...
Nasopharyngeal carcinoma (NPC) is among the most common malignancies in southern China. Deletion of ...
We recently commented on the burgeoning evidence that epigenetically mediated gene silencing can sel...
Epigenetic mechanisms are frequently deregulated in cancer cells and can lead to the silencing of ge...
High frequencies of allelic loss on the short arm of chromosome 3 in small cell lung cancer (SCLC) a...
Loss of DNA copy number at the short arm of chromosome 3 is one of the most common genetic changes i...
Abstract Background The short arm of human chromosome 3 is involved in the development of many cance...
Deletion on the short arm of chromosome 3 is one of the most important genetic abnormalities in the ...
Homozygous deletions or loss of heterozygosity (LOH) at human chromosome band 3p12 are consistent fe...