bromodeoxyuridine has been researched along with Abnormalities, Congenital in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ashery-Padan, R; Davidoff, MS; Molnár, Z; Piñon, MC; Radyushkin, K; Stoykova, A; Tonchev, AB; Tuoc, TC | 1 |
| Day, DW; Garcia-Heras, J; Martin, JA; Scacheri, P; Witchel, SF | 1 |
2 other study(ies) available for bromodeoxyuridine and Abnormalities, Congenital
| Article | Year |
|---|---|
Selective cortical layering abnormalities and behavioral deficits in cortex-specific Pax6 knock-out mice.
Topics: Analysis of Variance; Animals; Animals, Newborn; Behavior, Animal; Bromodeoxyuridine; Cell Adhesion Molecules, Neuronal; Cell Cycle; Cell Differentiation; Cell Movement; Cerebral Cortex; Conditioning, Classical; Congenital Abnormalities; DNA-Binding Proteins; Embryo, Mammalian; Extracellular Matrix Proteins; Eye Proteins; Fear; Gene Expression Regulation, Developmental; Green Fluorescent Proteins; Homeodomain Proteins; Indoles; Ki-67 Antigen; Memory Disorders; Mental Disorders; Mice; Mice, Inbred C57BL; Mice, Knockout; Motor Activity; Nerve Tissue Proteins; Neurogenesis; Neurons; Pain Threshold; Paired Box Transcription Factors; PAX6 Transcription Factor; Psychomotor Performance; Reaction Time; Reelin Protein; Repressor Proteins; Serine Endopeptidases; Transcription Factors | 2009 |
"De novo" duplication Xq23-->Xq26 of paternal origin in a girl with a mildly affected phenotype.
Topics: Alleles; Bromodeoxyuridine; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Congenital Abnormalities; Dosage Compensation, Genetic; Fathers; Female; Growth Disorders; Humans; Multigene Family; Phenotype; Receptors, Androgen; X Chromosome | 1997 |