[[abstract]]Tumor suppressor gene mutations in TSG101, FHIT, and PTEN/MMAC1 were found in many types of cancer and the defects in these genes are responsible for the tumor development. Since aberrant transcripts of these genes were also identified in normal tissues, the significance of these mutations in carcinogenesis has become a controversy. To determine large deletions or other alterations in these genes, we analyzed the integrity of their transcripts in both cancerous tissues and the matched normal tissues. More than 400 transcripts derived from at least eight different types of tissue were analyzed using nested RT-PCR and direct sequencing. High frequency of abnormal transcripts of all three genes occurred in both cancerous and the no...
Hotspot mutations in splicing factor genes have been recently reported at high frequency in hematolo...
Mutations in the splicing factor SF3B1 are found in several cancer types and have been as-sociated w...
Over 450 distinct BRCA1 missense mutations have been found in patients with a family history of brea...
[[abstract]]Aberrant transcripts of FHIT and TSG101 using nested RT-PCR were reported in many human ...
[[abstract]]The 10q23.3 gene PTEN (phosphatase and Tensin homologue deleted on chromosome 10) or MMA...
Summary: Hotspot mutations in splicing factor genes have been recently reported at high frequency in...
scription-polymerase chain reaction; nt, nucleotide(s) Aberrant transcripts of FHIT (fragile histidi...
The FHIT gene is a putative tumour suppressor gene. In this study, we analysed a set of 50 gastric t...
TIGS-599; No of Pages 3critical impact on all major aspects of cell biology, including cell cycle co...
Summary: For the past decade, cancer genomic studies have focused on mutations leading to splice-sit...
[[abstract]]The gene forms the basic heredity material of life, and cancer commonly occurs because o...
Substitutions that disrupt pre-mRNA splicing are a common cause of genetic disease. On average, 13.4...
Inactivation of tumor suppressor genes is one way in which cancer cells circumvent normal growth con...
In addition to eugenetic changes, cancerous cells exhibit extensive modifications in the expression ...
AbstractIn addition to eugenetic changes, cancerous cells exhibit extensive modifications in the exp...
Hotspot mutations in splicing factor genes have been recently reported at high frequency in hematolo...
Mutations in the splicing factor SF3B1 are found in several cancer types and have been as-sociated w...
Over 450 distinct BRCA1 missense mutations have been found in patients with a family history of brea...
[[abstract]]Aberrant transcripts of FHIT and TSG101 using nested RT-PCR were reported in many human ...
[[abstract]]The 10q23.3 gene PTEN (phosphatase and Tensin homologue deleted on chromosome 10) or MMA...
Summary: Hotspot mutations in splicing factor genes have been recently reported at high frequency in...
scription-polymerase chain reaction; nt, nucleotide(s) Aberrant transcripts of FHIT (fragile histidi...
The FHIT gene is a putative tumour suppressor gene. In this study, we analysed a set of 50 gastric t...
TIGS-599; No of Pages 3critical impact on all major aspects of cell biology, including cell cycle co...
Summary: For the past decade, cancer genomic studies have focused on mutations leading to splice-sit...
[[abstract]]The gene forms the basic heredity material of life, and cancer commonly occurs because o...
Substitutions that disrupt pre-mRNA splicing are a common cause of genetic disease. On average, 13.4...
Inactivation of tumor suppressor genes is one way in which cancer cells circumvent normal growth con...
In addition to eugenetic changes, cancerous cells exhibit extensive modifications in the expression ...
AbstractIn addition to eugenetic changes, cancerous cells exhibit extensive modifications in the exp...
Hotspot mutations in splicing factor genes have been recently reported at high frequency in hematolo...
Mutations in the splicing factor SF3B1 are found in several cancer types and have been as-sociated w...
Over 450 distinct BRCA1 missense mutations have been found in patients with a family history of brea...