The DNA probes met and pJ3.11 are derived from loci on chromosome seven that are closely linked to, and probably flanking, the gene mutation causing cystic fibrosis (CF). We have shown that mitotic chromosomes from the cell line MNNGHOS, which contains an activated met oncogene, can induce morphological transformation of mouse NIH-3T3 cells. Southern analysis of isolated transfectant cell lines with cloned dispersed repetitive human DNA sequences as probes demonstrated that several lines of transformed NIH 3T3 cells had stabley incorporated large segments of chromosome seven DNA. Southern blot analysis also demonstrated the presence of met, pJ3.11 and several other single copy sequences that had been previously localised to chromosome 7 wit...
An understanding of the basic defect in the inherited disorder cystic fibrosis requires cloning of t...
A polymorphic DNA marker has been found genetically linked, in a set of 39 human families, to an aut...
We have conducted, in 64 affected families, a study of linkage between the anonymous DNA segment pB7...
The MET oncogene, present in the MNNG-HOS chemically transformed human cell line, is activated by a ...
Five DNA probes known to originate from the region 7q22-q31 were sublocalized by in situ hybridizati...
The identification of the cystic fibrosis locus (CF) provides a model for the study of single gene d...
We have used a panel of eight human/mouse somatic-cell hybrids, each containing various portions of ...
To facilitate mapping of the cystic fibrosis locus (CF) and to isolate the corresponding gene, we ha...
In contrast o the abundance of studies conducted on chemically transformed rodent cells, there are o...
The mutation causing cystic fibrosis (CF) has been localized to the DNA sequence of 700 kb bounded b...
The mutation causing cystic fibrosis (CF) has been localized to the DNA sequence of 700 kb bounded b...
Our previous linkage analysis suggested that the DNA segment D7S122 is located between MET and D7S8,...
Genetic linkage has been analyzed between cystic fibrosis (CF) and a number of markers on the long a...
Although cystic fibrosis (CF) is among the most common inherited diseases in Caucasian populations, ...
The met proto-oncogene was mapped in the mouse and cat genomes with the use of mouse × hamster and c...
An understanding of the basic defect in the inherited disorder cystic fibrosis requires cloning of t...
A polymorphic DNA marker has been found genetically linked, in a set of 39 human families, to an aut...
We have conducted, in 64 affected families, a study of linkage between the anonymous DNA segment pB7...
The MET oncogene, present in the MNNG-HOS chemically transformed human cell line, is activated by a ...
Five DNA probes known to originate from the region 7q22-q31 were sublocalized by in situ hybridizati...
The identification of the cystic fibrosis locus (CF) provides a model for the study of single gene d...
We have used a panel of eight human/mouse somatic-cell hybrids, each containing various portions of ...
To facilitate mapping of the cystic fibrosis locus (CF) and to isolate the corresponding gene, we ha...
In contrast o the abundance of studies conducted on chemically transformed rodent cells, there are o...
The mutation causing cystic fibrosis (CF) has been localized to the DNA sequence of 700 kb bounded b...
The mutation causing cystic fibrosis (CF) has been localized to the DNA sequence of 700 kb bounded b...
Our previous linkage analysis suggested that the DNA segment D7S122 is located between MET and D7S8,...
Genetic linkage has been analyzed between cystic fibrosis (CF) and a number of markers on the long a...
Although cystic fibrosis (CF) is among the most common inherited diseases in Caucasian populations, ...
The met proto-oncogene was mapped in the mouse and cat genomes with the use of mouse × hamster and c...
An understanding of the basic defect in the inherited disorder cystic fibrosis requires cloning of t...
A polymorphic DNA marker has been found genetically linked, in a set of 39 human families, to an aut...
We have conducted, in 64 affected families, a study of linkage between the anonymous DNA segment pB7...