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
The structure of the 5 ' end region of the human argininosuccinate synthetase (AS) gene was ana...
ObjectiveArgininosuccinate lyase (ASL) gene mutations account for argininosuccinic aciduria (ASA). T...
AbstractPartial cDNAs coding for human protein S were isolated from a pUC9 human liver cDNA library....
AbstractIn the present study, we isolated clones of human argininosuccinate lyase (ASL) cDNA from a ...
Argininosuccinate lyase [EC 4.3.2.1] is an enzyme of the urea cycle in the liver of ureotelic animal...
Argininosuccinic aciduria (ASA) is an autosomal recessive urea cycle disorder caused by deficiency o...
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...
Pathogenic variants in the argininosuccinate lyase (ASL) gene have been shown to cause argininosucci...
The pathway for de novo purine nucleotide biosynthesis is conserved among all organisms that have be...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
A full-length aryl sulfotransferase cDNA was isolated from a human liver cDNA library. It was 1155 b...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
AbstractWe have isolated and sequenced the l-arginine:glycine amidinotransferase of pig kidney mitoc...
A 1,179 bp and a 1,424 bp full-length aryl sulfotransferase cDNAs were isolated from a human brain c...
The structure of the 5 ' end region of the human argininosuccinate synthetase (AS) gene was ana...
ObjectiveArgininosuccinate lyase (ASL) gene mutations account for argininosuccinic aciduria (ASA). T...
AbstractPartial cDNAs coding for human protein S were isolated from a pUC9 human liver cDNA library....
AbstractIn the present study, we isolated clones of human argininosuccinate lyase (ASL) cDNA from a ...
Argininosuccinate lyase [EC 4.3.2.1] is an enzyme of the urea cycle in the liver of ureotelic animal...
Argininosuccinic aciduria (ASA) is an autosomal recessive urea cycle disorder caused by deficiency o...
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...
Pathogenic variants in the argininosuccinate lyase (ASL) gene have been shown to cause argininosucci...
The pathway for de novo purine nucleotide biosynthesis is conserved among all organisms that have be...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
A full-length aryl sulfotransferase cDNA was isolated from a human liver cDNA library. It was 1155 b...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
AbstractWe have isolated and sequenced the l-arginine:glycine amidinotransferase of pig kidney mitoc...
A 1,179 bp and a 1,424 bp full-length aryl sulfotransferase cDNAs were isolated from a human brain c...
The structure of the 5 ' end region of the human argininosuccinate synthetase (AS) gene was ana...
ObjectiveArgininosuccinate lyase (ASL) gene mutations account for argininosuccinic aciduria (ASA). T...
AbstractPartial cDNAs coding for human protein S were isolated from a pUC9 human liver cDNA library....