Construction of a cDNA to the hamster CAD gene and its application toward defining the domain for aspartate transcarbamylase.
about
The evolutionary history of the first three enzymes in pyrimidine biosynthesisMYC abrogates p53-mediated cell cycle arrest in N-(phosphonacetyl)-L-aspartate-treated cells, permitting CAD gene amplification.p53-dependent growth arrest of REF52 cells containing newly amplified DNA.Suppression of endo B cytokeratin by its antisense RNA inhibits the normal coexpression of endo A cytokeratin.Aspartate transcarbamoylase genes of Pseudomonas putida: requirement for an inactive dihydroorotase for assembly into the dodecameric holoenzyme.Cloning and expression of the aspartate carbamoyltransferase gene from Treponema denticola.Multiple mechanisms of N-phosphonacetyl-L-aspartate resistance in human cell lines: carbamyl-P synthetase/aspartate transcarbamylase/dihydro-orotase gene amplification is frequent only when chromosome 2 is rearranged.Human chromosome 3 mediates growth arrest and suppression of apoptosis in microcell hybrids.Evolution and stability of chromosomal DNA coamplified with the CAD geneUnstable and stable CAD gene amplification: importance of flanking sequences and nuclear environment in gene amplification.Simian virus 40 large tumor antigen alone or two cooperating oncogenes convert REF52 cells to a state permissive for gene amplification.Role of a carboxyl-terminal helix in the assembly, interchain interactions, and stability of aspartate transcarbamoylase.Trapping an activated conformation of mammalian carbamyl-phosphate synthetase.Proteolytic cleavage of the multienzyme polypeptide CAD to release the mammalian aspartate transcarbamoylase. Biochemical comparison with the homologous Escherichia coli catalytic subunit.Structure of DNA formed in the first step of CAD gene amplification.Phenotypic resistance to methotrexate and N-phosphonacetyl L-aspartate is induced by treatment with 12-O-tetradecanoylphorbol-13-acetate (TPA).Overexpression of the 18 kDa and 22/24 kDa FGF-2 isoforms results in differential drug resistance and amplification potential.Aspartate-90 and arginine-269 of hamster aspartate transcarbamylase affect the oligomeric state of a chimaeric protein with an Escherichia coli maltose-binding domain.Gradient expression of Cdx along the rat intestine throughout postnatal development.Molecular evolution of enzyme structure: construction of a hybrid hamster/Escherichia coli aspartate transcarbamoylase.Substructure of the amidotransferase domain of mammalian carbamyl phosphate synthetase.
P2860
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P2860
Construction of a cDNA to the hamster CAD gene and its application toward defining the domain for aspartate transcarbamylase.
description
1985 nî lūn-bûn
@nan
1985 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1985 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
name
Construction of a cDNA to the ...... or aspartate transcarbamylase.
@ast
Construction of a cDNA to the ...... or aspartate transcarbamylase.
@en
type
label
Construction of a cDNA to the ...... or aspartate transcarbamylase.
@ast
Construction of a cDNA to the ...... or aspartate transcarbamylase.
@en
prefLabel
Construction of a cDNA to the ...... or aspartate transcarbamylase.
@ast
Construction of a cDNA to the ...... or aspartate transcarbamylase.
@en
P2093
P2860
P356
P1476
Construction of a cDNA to the ...... or aspartate transcarbamylase.
@en
P2093
J N Davidson
K Shigesada
L A Niswander
P2860
P304
P356
10.1128/MCB.5.7.1735
P407
P577
1985-07-01T00:00:00Z