Page last updated: 2024-08-17

bromodeoxyuridine and 22q11.2 Deletion Syndrome

bromodeoxyuridine has been researched along with 22q11.2 Deletion Syndrome in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baldini, A; Bruneau, BG; Lindsay, EA; Morishima, M; Schwartz, RJ; Wylie, JN; Xu, H1

Other Studies

1 other study(ies) available for bromodeoxyuridine and 22q11.2 Deletion Syndrome

ArticleYear
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
    Development (Cambridge, England), 2004, Volume: 131, Issue:13

    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