AbstractIn the present study, we isolated clones of human argininosuccinate lyase (ASL) cDNA from a liver cDNA library using a clone of rat ASL cDNA and analyzed human ASL cDNA nucleotide sequence. The results reveal that the sequence of human ASL cDNA published by O'Brien et al. in 1986 [Proc. Natl. Acad. Sci USA 83, 7211–7215] had one-base deletions at three independent positions in the coding regions near the COOH-terminus, which caused frame-shift variations in the amino acid sequence. Amino acid sequencing of peptides prepared from purified human liver ASL showed our predicted amino acid sequence to be correct
AbstractWe determined the DNA sequence of the adenylosuccinate lyase (ASL) gene from a 13 year-old f...
BACKGROUND: The urea cycle defect argininosuccinate lyase (ASL) deficiency has a large spectrum of p...
The structure of the 5 ' end region of the human argininosuccinate synthetase (AS) gene was ana...
AbstractIn the present study, we isolated clones of human argininosuccinate lyase (ASL) cDNA from a ...
Pathogenic variants in the argininosuccinate lyase (ASL) gene have been shown to cause argininosucci...
Argininosuccinate lyase deficiency (ASLD) is caused by a defect of the urea cycle enzyme argininosuc...
ObjectiveArgininosuccinate lyase (ASL) gene mutations account for argininosuccinic aciduria (ASA). T...
Argininosuccinic aciduria (ASA) is an autosomal recessive urea cycle disorder caused by deficiency o...
A λgt11 human testicular cDNA library was screened with degenerate oligonucleotide probe mixtures ba...
The pathway for de novo purine nucleotide biosynthesis is conserved among all organisms that have be...
grantor: University of TorontoThe enzyme argininosuccinic acid lyase (ASL) catalyzes the r...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
ObjectiveArgininosuccinate lyase (ASL) gene mutations account for argininosuccinic aciduria (ASA). T...
AbstractWe have isolated a full-length cDNA (HPAsn.6) for human placenta glycosylasparaginase using ...
AbstractWe determined the DNA sequence of the adenylosuccinate lyase (ASL) gene from a 13 year-old f...
BACKGROUND: The urea cycle defect argininosuccinate lyase (ASL) deficiency has a large spectrum of p...
The structure of the 5 ' end region of the human argininosuccinate synthetase (AS) gene was ana...
AbstractIn the present study, we isolated clones of human argininosuccinate lyase (ASL) cDNA from a ...
Pathogenic variants in the argininosuccinate lyase (ASL) gene have been shown to cause argininosucci...
Argininosuccinate lyase deficiency (ASLD) is caused by a defect of the urea cycle enzyme argininosuc...
ObjectiveArgininosuccinate lyase (ASL) gene mutations account for argininosuccinic aciduria (ASA). T...
Argininosuccinic aciduria (ASA) is an autosomal recessive urea cycle disorder caused by deficiency o...
A λgt11 human testicular cDNA library was screened with degenerate oligonucleotide probe mixtures ba...
The pathway for de novo purine nucleotide biosynthesis is conserved among all organisms that have be...
grantor: University of TorontoThe enzyme argininosuccinic acid lyase (ASL) catalyzes the r...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
ObjectiveArgininosuccinate lyase (ASL) gene mutations account for argininosuccinic aciduria (ASA). T...
AbstractWe have isolated a full-length cDNA (HPAsn.6) for human placenta glycosylasparaginase using ...
AbstractWe determined the DNA sequence of the adenylosuccinate lyase (ASL) gene from a 13 year-old f...
BACKGROUND: The urea cycle defect argininosuccinate lyase (ASL) deficiency has a large spectrum of p...
The structure of the 5 ' end region of the human argininosuccinate synthetase (AS) gene was ana...