galactose has been researched along with Abnormalities, Autosome in 18 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 17 (94.44) | 18.7374 |
| 1990's | 1 (5.56) | 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 |
|---|---|
| Ahmed, A; Fiandt, M; Szybalski, W | 1 |
| Ahmed, A; Johansen, E | 1 |
| Dahlqvist, A; Hall, B | 1 |
| Dahlqvist, A; Hall, B; Källén, B | 1 |
| Adelberg, EA; Bergquist, P | 1 |
| Ellis, JH; Rotman, B | 1 |
| Saedler, H; Starlinger, P | 2 |
| Bergmann, D; Hamlaoui, M; Hirsch, HJ; Pfeifer, D | 1 |
| Oellermann, R; Pfeifer, D | 1 |
| Pfeifer, D; Rosypal, S | 1 |
| Adhya, SL; Shapiro, JA | 1 |
| Chemke, J; Robinson, A | 1 |
| Elsas, LJ | 1 |
| Handmaker, S; Kampine, JP; Kanfer, JN; Richards, R; Yankee, RA | 1 |
| Miller, DA; Miller, OJ | 1 |
| Frankos, VH; Kruger, CL; Whittaker, MH | 1 |
| Calne, DB; King, RH; Thomas, PK | 1 |
1 review(s) available for galactose and Abnormalities, Autosome
| Article | Year |
|---|---|
Chromosomes and cancer in the mouse: studies in tumors, established cell lines, and cell hybrids.
Topics: AKR murine leukemia virus; Aneuploidy; Animals; Cell Fusion; Cell Transformation, Neoplastic; Cell Transformation, Viral; Cells, Cultured; Chromosome Aberrations; Chromosomes; Gammaretrovirus; Genes; Hexoses; Humans; Hybrid Cells; Leukemia, Experimental; Mice; Neoplasm Transplantation; Neoplasms, Experimental; Plasmacytoma; Simian virus 40; Transformation, Genetic | 1983 |
17 other study(ies) available for galactose and Abnormalities, Autosome
| Article | Year |
|---|---|
Identification of the gal3 insertion in Escherichia coli AS IS2.
Topics: Chromosome Aberrations; Coliphages; Escherichia coli; Galactose; Mutation; Nucleic Acid Hybridization; Operon; Transduction, Genetic | 1977 |
Reversion of the gal3 mutation of Escherichia coli: partial deletion of the insertion sequence.
Topics: Base Sequence; Chromosome Aberrations; Chromosome Deletion; Chromosomes, Bacterial; Coliphages; DNA, Bacterial; DNA, Viral; Escherichia coli; Galactose; Mutation; Nucleic Acid Conformation; Operon; Phenotype | 1976 |
Enzyme activity in D trisomies.
Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Chromosomes, Human, 16-18; Galactose; Humans; Nucleotidyltransferases; Phosphates; Trisomy; Uracil Nucleotides | 1971 |
Blood cell galactose-1-phosphate uridyl transferase activity in dysplastic patients, with and without chromosomal aberrations.
Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Congenital Abnormalities; Cri-du-Chat Syndrome; Down Syndrome; Female; Galactose; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Middle Aged; Nucleotidyltransferases; Trisomy; Uracil Nucleotides | 1969 |
The stabilization of episomal integration by genetic inversion: a general hypothesis.
Topics: Chromosome Aberrations; Chromosomes, Bacterial; Coliphages; Conjugation, Genetic; Crossing Over, Genetic; Escherichia coli; Extrachromosomal Inheritance; Fucose; Galactose; Glucose; Isomerases; Lysogeny; Models, Biological; Radiation Effects; Recombination, Genetic; Ultraviolet Rays | 1972 |
Antibody-mediated modification of the binding properties of a protein related to galactose transport.
Topics: Animals; Antibodies; Antibody Specificity; Bacterial Proteins; Biological Transport, Active; Chromosome Aberrations; Escherichia coli; Galactose; Immune Sera; Immunoglobulins; Kinetics; Membrane Transport Proteins; Mutation; Protein Binding; Rabbits; Tritium | 1972 |
Insertion mutations in microorganisms.
Topics: Bacteriophages; Base Sequence; Chromosome Aberrations; Chromosomes, Bacterial; DNA, Bacterial; Escherichia coli; Galactose; Genetics, Microbial; Microscopy, Electron; Mutation; Nucleic Acid Hybridization; Operon; Transcription, Genetic; Transduction, Genetic | 1972 |
Non-random distribution of deletion endpoints in the gal operon of E. coli.
Topics: Chromosome Aberrations; Chromosome Mapping; Coliphages; DNA, Bacterial; Escherichia coli; Galactose; Genetics, Microbial; Lysogeny; Microscopy, Electron; Mutation; Operon | 1974 |
0 degree mutations in the galactose operon in E. coli. I. Genetic characterization.
Topics: Chromosome Aberrations; Chromosome Mapping; Escherichia coli; Galactose; Genetic Complementation Test; Genetics, Microbial; Molecular Biology; Mutagens; Mutation; Recombination, Genetic; Transduction, Genetic | 1967 |
Mapping of gal minus-mutants by transducing lambda dg carrying deletions of the gal-region.
Topics: Chromosome Aberrations; Chromosome Mapping; Chromosomes, Bacterial; Coliphages; DNA, Bacterial; Escherichia coli; Galactose; Phosphotransferases; Transduction, Genetic; Transferases | 1967 |
Deletion mapping of galactose mutants with transducing lambda phages.
Topics: Chromosome Aberrations; Chromosome Mapping; Chromosomes, Bacterial; Coliphages; Escherichia coli; Galactose; Operon; Recombination, Genetic; Transduction, Genetic | 1969 |
The galactose operon of E. coli K-12. II. A deletion analysis of operon structure and polarity.
Topics: Chromosome Aberrations; Chromosome Mapping; Chromosomes, Bacterial; Coliphages; Crosses, Genetic; Escherichia coli; Galactose; Isomerases; Molecular Biology; Mutation; Operon; Phosphotransferases; Transferases | 1969 |
The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+).
Topics: Adolescent; Adult; Aged; Blood Group Antigens; Child; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, 16-18; Dermatoglyphics; Erythrocytes; Female; Fibroblasts; Galactose; Genetic Linkage; Haptoglobins; Humans; Immunoglobulin A; Immunoglobulin G; Infant; Karyotyping; Lymphocytes; Male; Middle Aged; Nucleotidyltransferases; Pedigree; Phenylthiourea; Phosphotransferases; Uracil Nucleotides | 1971 |
Glucose reabsorption in familial renal glycosuria and glucose-galactose malabsorption.
Topics: Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Female; Galactose; Genes, Recessive; Glucose; Glycosuria, Renal; Humans; Jejunum; Kidney; Kidney Concentrating Ability; Kidney Tubules; Malabsorption Syndromes; Male | 1970 |
Alteration of e sphingolipid content in leucocytes from patients with Chediak-Higashi syndrome.
Topics: Amides; Chromatography, Thin Layer; Chromosome Aberrations; Chromosome Disorders; Hexoses; Humans; Leukocytes; Lipids; Phosphates; Sphingomyelins | 1967 |
Genotoxicity tests on D-tagatose.
Topics: Animals; CHO Cells; Chromosome Aberrations; Cricetinae; Escherichia coli; Female; Hexoses; Male; Mice; Micronucleus Tests; Mutagenicity Tests; Mutation; Salmonella typhimurium; Sweetening Agents; Tumor Cells, Cultured | 1999 |
Autosomal dominant forms of hereditary hypertrophic neuropathy.
Topics: Age Factors; Ceramides; Chromosome Aberrations; Chromosome Disorders; Genes, Dominant; Hexoses; Humans; Hypertrophy; Metabolism, Inborn Errors; Muscular Atrophy; Neuritis; Syndrome | 1972 |