aspartic acid has been researched along with Chromosome Deletion in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (27.27) | 18.7374 |
| 1990's | 5 (45.45) | 18.2507 |
| 2000's | 1 (9.09) | 29.6817 |
| 2010's | 2 (18.18) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bourdillon, P; Cotton, F; Ducray, F; Guillotton, L; Guyotat, J; Hlaihel, C; Honnorat, J | 1 |
| Tada, H; Takanashi, J | 1 |
| Anhuf, D; Häusler, M; Möller-Hartmann, W; Ramaekers, VT; Schüler, H; Thron, A; Zerres, K | 1 |
| Dozy, AM; Kan, YW; Lie-Injo, LE; Lopes, M; Todd, D | 1 |
| Jacks, T; Livanos, E; Livingstone, LR; Sprouse, J; Tlsty, TD; White, A | 1 |
| Bischoff, FZ; Strong, LC; Tainsky, MA; Wahl, GM; Yin, Y | 1 |
| Davidson, K; Forseth, B; Scott, J; Von Hoff, DD; Waddelow, T; Wahl, G | 1 |
| Hederstedt, L; Saraste, M; van der Oost, J; von Wachenfeld, C | 1 |
| Bardet, J; de Blois, MC; Kamoun, P; Lejeune, J; Parvy, P; Peeters, M; Rabier, D; Rethoré, MO | 1 |
| Bamforth, FJ; Graham, A; Kalsheker, NA; Markham, AF; Newton, CR; Powell, SJ | 1 |
| Crechet, JB; De Vendittis, E; Fasano, O; Feger, G; Parmeggiani, A; Vitelli, A; Zahn, R | 1 |
11 other study(ies) available for aspartic acid and Chromosome Deletion
| Article | Year |
|---|---|
Prediction of anaplastic transformation in low-grade oligodendrogliomas based on magnetic resonance spectroscopy and 1p/19q codeletion status.
Topics: Adult; Aged; Aspartic Acid; Brain Neoplasms; Choline; Chromosome Deletion; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 19; Creatine; Female; Humans; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Middle Aged; Oligodendroglioma | 2015 |
MR spectroscopy in 18q(-) syndrome suggesting other than hypomyelination.
Topics: Aspartic Acid; Brain; Child, Preschool; Choline; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 18; Creatine; Humans; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Nerve Fibers, Myelinated | 2014 |
White-matter disease in 18q deletion (18q-) syndrome: magnetic resonance spectroscopy indicates demyelination or increased myelin turnover rather than dysmyelination.
Topics: Aspartic Acid; Brain Diseases; Choline; Chromosome Deletion; Chromosomes, Human, Pair 18; Demyelinating Diseases; Female; Follow-Up Studies; Glutamic Acid; Humans; Infant; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Myelin Sheath | 2005 |
The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia.
Topics: Aspartic Acid; Chemical Phenomena; Chemistry; Chromosome Deletion; DNA; Genetic Carrier Screening; Globins; Glutamates; Glutamine; Hemoglobin H; Hemoglobins, Abnormal; Histidine; Humans; Hybridization, Genetic; Peptides; Thalassemia | 1979 |
Altered cell cycle arrest and gene amplification potential accompany loss of wild-type p53.
Topics: Animals; Aspartate Carbamoyltransferase; Aspartic Acid; Base Sequence; Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing); Cell Cycle; Cells, Cultured; Chromosome Deletion; Cytogenetics; Dihydroorotase; Embryo, Mammalian; Fibroblasts; Gene Amplification; Genes, p53; Germ Cells; Heterozygote; Humans; Li-Fraumeni Syndrome; Mice; Mice, Transgenic; Molecular Sequence Data; Multienzyme Complexes; Mutation; Phosphonoacetic Acid; Tumor Cells, Cultured | 1992 |
Wild-type p53 restores cell cycle control and inhibits gene amplification in cells with mutant p53 alleles.
Topics: Aspartic Acid; Base Sequence; Cell Cycle; Chromosome Deletion; Fibroblasts; G1 Phase; Gene Amplification; Genes, p53; Humans; Li-Fraumeni Syndrome; Molecular Sequence Data; Mutation; Phosphonoacetic Acid; S Phase; Suppression, Genetic; Tumor Cells, Cultured | 1992 |
Hydroxyurea accelerates loss of extrachromosomally amplified genes from tumor cells.
Topics: Aspartate Carbamoyltransferase; Aspartic Acid; Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing); Carcinoma, Squamous Cell; Cell Division; Chromosome Deletion; Dihydroorotase; DNA Replication; Drug Resistance; Gene Amplification; Humans; Hydroxyurea; Methotrexate; Multienzyme Complexes; Phosphonoacetic Acid; Plasmids; Tumor Cells, Cultured; Vinblastine | 1991 |
Bacillus subtilis cytochrome oxidase mutants: biochemical analysis and genetic evidence for two aa3-type oxidases.
Topics: Aspartic Acid; Bacillus subtilis; Blotting, Southern; Chromosome Deletion; Cytochrome c Group; Cytochrome d Group; Cytochromes; Drug Resistance, Microbial; Electron Transport Complex IV; Escherichia coli; Glucose; Glutamates; Glutamic Acid; Mutation; Phleomycins; Plasmids; Spectrophotometry; Tetramethylphenylenediamine | 1991 |
[Cri-du-chat disease: plasma and urinary amino acids].
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Asparagine; Aspartic Acid; Child; Child, Preschool; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosome Mapping; Chromosomes, Human, Pair 5; Cri-du-Chat Syndrome; Female; Histidine; Humans; Intellectual Disability; Male; Models, Biological; Purine-Pyrimidine Metabolism, Inborn Errors | 1990 |
Molecular characterisation of three alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) nullcardiff (Asp256----Val); PiMmalton (Phe51----deletion) and PiI (Arg39----Cys).
Topics: alpha 1-Antitrypsin; alpha 1-Antitrypsin Deficiency; Amino Acid Sequence; Arginine; Aspartic Acid; Base Sequence; Chromosome Deletion; Cysteine; Genes; Genetic Variation; Humans; Molecular Sequence Data; Oligonucleotide Probes; Phenylalanine; Valine | 1989 |
Yeast mutants temperature-sensitive for growth after random mutagenesis of the chromosomal RAS2 gene and deletion of the RAS1 gene.
Topics: Adenylyl Cyclases; Amino Acid Sequence; Arginine; Asparagine; Aspartic Acid; Base Sequence; Carbon; Chromosome Deletion; Cloning, Molecular; Culture Media; DNA, Fungal; Fungal Proteins; Galactose; Genes, ras; Glucose; Glycine; Immunoblotting; Molecular Sequence Data; Mutation; Phenotype; ras Proteins; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Serine; Temperature; Transformation, Genetic | 1988 |