bromodeoxyuridine has been researched along with 22q11.2 Deletion Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Baldini, A; Bruneau, BG; Lindsay, EA; Morishima, M; Schwartz, RJ; Wylie, JN; Xu, H | 1 |
1 other study(ies) available for bromodeoxyuridine and 22q11.2 Deletion Syndrome
Article | Year |
---|---|
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
Topics: Alleles; Animals; Bromodeoxyuridine; Cell Differentiation; Cell Division; Coloring Agents; DiGeorge Syndrome; DNA Mutational Analysis; Endothelial Cells; Fibroblast Growth Factor 10; Fibroblast Growth Factors; Gene Deletion; Gene Expression Regulation, Developmental; Heart; Homeobox Protein Nkx-2.5; Homeodomain Proteins; Immunohistochemistry; In Situ Hybridization; Luciferases; Mesoderm; Mice; Mice, Inbred C57BL; Mice, Transgenic; Models, Biological; Models, Genetic; Mutation; Myocardium; Myocytes, Cardiac; Reverse Transcriptase Polymerase Chain Reaction; T-Box Domain Proteins; Transcription Factors | 2004 |