ethylnitrosourea has been researched along with Apolipoprotein B-100, Familial Defective in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ahituv, N; Durgin, RS; Foreman, O; Magnani, PA; Paigen, B; Peters, LL; Savage, H; Svenson, KL | 1 |
| Amato, J; Babij, P; Baker, DM; Bass, MB; Carlson, GA; Chhoa, M; Damore, MA; Ebeling, C; Gyuris, T; Helmering, J; Juan, T; Li, CM; Lloyd, DJ; Véniant, MM | 1 |
2 other study(ies) available for ethylnitrosourea and Apolipoprotein B-100, Familial Defective
| Article | Year |
|---|---|
A new mouse mutant for the LDL receptor identified using ENU mutagenesis.
Topics: Amino Acid Sequence; Animals; Base Sequence; Disease Models, Animal; Ethylnitrosourea; Female; Hyperlipoproteinemia Type II; Male; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Knockout; Molecular Sequence Data; Mutagenesis; Mutagens; Mutation, Missense; Receptors, LDL | 2008 |
Identification of three loci affecting HDL-cholesterol levels in a screen for chemically induced recessive mutations in mice.
Topics: Animals; ATP Binding Cassette Transporter 1; ATP-Binding Cassette Transporters; Base Sequence; CCAAT-Enhancer-Binding Protein-alpha; Cholesterol; Cholesterol, HDL; Chromosome Mapping; DNA; Ethylnitrosourea; Female; Genes, Recessive; Genetic Testing; Hyperlipoproteinemia Type II; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mutagenesis; Mutagens; Mutation; Mutation, Missense; Phenotype; Polymorphism, Single Nucleotide | 2009 |