In summary, a general approach is presented to purify and sequence DNA fragments of a specific gene starting with a heterogeneous mixture of mRNAs. The methodology has been applied to the determination of the DNA sequence of a portion of the gene for human chorionic somatomammotropin. Most of the possible translation codons of the genetic code were found to be used. Some selectivity in the codon choices was found, and this may be important for RNA or gene regulation or structure. The stop codon UAG was found and a second stop codon in the same reading frame was found nine bases farther down. Finally, a palindrome sequence was detected in the 3 noncoding region
An important problem often faced in the molecular characterization of genes is the precise mapping o...
For the rapid identification of noble genes in a specific tissue by computer analysis from the cDNA ...
The human pro-opiomelanocortin (POMC) gene has been characterized by molecular cloning and DNA seque...
In summary, a general approach is presented to purify and sequence DNA fragments of a specific gene ...
A novel purification procedure for DNA complementary to individual mRNA species has been developed b...
DNA complementary to mRNA coding for the human polypeptide hormone, chorionic somatomammotropin, has...
A 2.6-kilobase (kb) EcoRI restriction endonuclease fragment containing human growth hormone (hGH; so...
A DNA fragment of 219 bp was obtained by polymerase chain reaction (PCR) on human genomic DNA using ...
The nucleotide sequences of three nonallelic human genomic DNA fragments which each contain one memb...
Molecular analysis of development frequently implies the isolation and characterization of genes wit...
A list is presented of published reports of DNA polymorphisms found in the human genome by restricti...
As an essential step towards an exhaustive analysis of the coding potential of large regions of the ...
We have identified and mapped 61 novel and previ-ously described chromosome 17 and X genes, using a ...
<p>(A) We compared the expression levels of the Chit1 and AMCase genes. To evaluate the chitinase le...
Using a set of synthetic oligonucleotides homologous to broadly conserved sequences in-vitro amplifi...
An important problem often faced in the molecular characterization of genes is the precise mapping o...
For the rapid identification of noble genes in a specific tissue by computer analysis from the cDNA ...
The human pro-opiomelanocortin (POMC) gene has been characterized by molecular cloning and DNA seque...
In summary, a general approach is presented to purify and sequence DNA fragments of a specific gene ...
A novel purification procedure for DNA complementary to individual mRNA species has been developed b...
DNA complementary to mRNA coding for the human polypeptide hormone, chorionic somatomammotropin, has...
A 2.6-kilobase (kb) EcoRI restriction endonuclease fragment containing human growth hormone (hGH; so...
A DNA fragment of 219 bp was obtained by polymerase chain reaction (PCR) on human genomic DNA using ...
The nucleotide sequences of three nonallelic human genomic DNA fragments which each contain one memb...
Molecular analysis of development frequently implies the isolation and characterization of genes wit...
A list is presented of published reports of DNA polymorphisms found in the human genome by restricti...
As an essential step towards an exhaustive analysis of the coding potential of large regions of the ...
We have identified and mapped 61 novel and previ-ously described chromosome 17 and X genes, using a ...
<p>(A) We compared the expression levels of the Chit1 and AMCase genes. To evaluate the chitinase le...
Using a set of synthetic oligonucleotides homologous to broadly conserved sequences in-vitro amplifi...
An important problem often faced in the molecular characterization of genes is the precise mapping o...
For the rapid identification of noble genes in a specific tissue by computer analysis from the cDNA ...
The human pro-opiomelanocortin (POMC) gene has been characterized by molecular cloning and DNA seque...