durapatite has been researched along with Chromosome Deletion in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Clarke, B; Foote, T; Money, T; Moore, G; Stancombe, P | 1 |
| Coon, MJ; Larson, JR; Porter, TD | 1 |
| Brandazza, A; Cauet, G; Lansen, J; Molinari, A; Orsini, G; Sarmientos, P | 1 |
| Pollard, TD; Rimm, DL; Sinard, JH | 1 |
4 other study(ies) available for durapatite and Chromosome Deletion
| Article | Year |
|---|---|
Targeting deletion (homoeologous chromosome pairing locus) or addition line single copy sequences from cereal genomes.
Topics: Chromosome Deletion; Cloning, Molecular; DNA; Durapatite; Genome; Hydroxyapatites; Mutation; Polyploidy; Triticum | 1992 |
Purification and properties of a shortened form of cytochrome P-450 2E1: deletion of the NH2-terminal membrane-insertion signal peptide does not alter the catalytic activities.
Topics: Amino Acid Sequence; Chromatography; Chromatography, Ion Exchange; Chromosome Deletion; Cytochrome P-450 CYP2E1; Cytochrome P-450 Enzyme System; Durapatite; Hydroxyapatites; Kinetics; Molecular Sequence Data; NADPH-Ferrihemoprotein Reductase; Oxidoreductases, N-Demethylating; Protein Sorting Signals; Recombinant Proteins; Substrate Specificity | 1991 |
Efficient renaturation and fibrinolytic properties of prourokinase and a deletion mutant expressed in Escherichia coli as inclusion bodies.
Topics: Amino Acid Sequence; Base Sequence; Chromatography; Chromatography, Gel; Chromosome Deletion; Durapatite; Escherichia coli; Fibrinolytic Agents; Humans; Hydroxyapatites; Inclusion Bodies; Kinetics; Molecular Sequence Data; Oligonucleotide Probes; Plasmids; Plasminogen Activators; Protein Conformation; Protein Denaturation; Recombinant Proteins; Restriction Mapping; Urokinase-Type Plasminogen Activator | 1991 |
Identification of functional regions on the tail of Acanthamoeba myosin-II using recombinant fusion proteins. II. Assembly properties of tails with NH2- and COOH-terminal deletions.
Topics: Acanthamoeba; Animals; Base Sequence; Binding Sites; Chromatography; Chromatography, DEAE-Cellulose; Chromatography, Gel; Chromosome Deletion; Cloning, Molecular; Durapatite; Electrophoresis, Polyacrylamide Gel; Escherichia coli; Hydroxyapatites; Kinetics; Macromolecular Substances; Magnesium; Microscopy, Electron; Molecular Sequence Data; Molecular Weight; Myosins; Potassium Chloride; Recombinant Fusion Proteins; Scattering, Radiation | 1990 |