Page last updated: 2024-08-17

bromodeoxyuridine and Chromosomal Triplication

bromodeoxyuridine has been researched along with Chromosomal Triplication in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19906 (66.67)18.7374
1990's1 (11.11)18.2507
2000's1 (11.11)29.6817
2010's1 (11.11)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Adayev, T; Flory, M; Frackowiak, J; Golabek, A; Hwang, YW; Kaczmarski, W; Kida, E; Marchi, E; Mazur-Kolecka, B; Rabe, A; Wegiel, J1
Bartesaghi, R; Bonapace, L; Bonasoni, P; Ceccarelli, C; Ciani, E; Contestabile, A; Fila, T; Santini, D1
Breg, WR; Willard, HF1
Garcia-Heras, J; Martin, JA; Scacheri, P; Witchel, SF1
Dutrillaux, B; Fosse, AM1
Ayraud, N; Letourneau, J; Llyod, M; Martinon, J; Noel, B1
Gould, SL; Martin-DeLeon, PA1
Kida, M; Uehara, M1
Palmer, CG1

Other Studies

9 other study(ies) available for bromodeoxyuridine and Chromosomal Triplication

ArticleYear
Effect of DYRK1A activity inhibition on development of neuronal progenitors isolated from Ts65Dn mice.
    Journal of neuroscience research, 2012, Volume: 90, Issue:5

    Topics: Animals; Animals, Newborn; Bromodeoxyuridine; Cell Differentiation; Cell Movement; Cells, Cultured; Chromosomes, Human, Pair 16; Disease Models, Animal; Down Syndrome; Dyrk Kinases; Gene Expression Regulation, Developmental; Glial Fibrillary Acidic Protein; Glutamate Decarboxylase; Harmine; Mice; Mice, Transgenic; Monoamine Oxidase Inhibitors; Mosaicism; Neural Stem Cells; Protein Serine-Threonine Kinases; Protein-Tyrosine Kinases; Time Factors; Trisomy

2012
Cell cycle alteration and decreased cell proliferation in the hippocampal dentate gyrus and in the neocortical germinal matrix of fetuses with Down syndrome and in Ts65Dn mice.
    Hippocampus, 2007, Volume: 17, Issue:8

    Topics: Animals; Bromodeoxyuridine; Cell Cycle; Cell Proliferation; Chromosomes, Human, Pair 21; Cyclin A; Dentate Gyrus; Disease Models, Animal; Down Syndrome; Female; Fetus; Histones; Humans; In Situ Nick-End Labeling; Ki-67 Antigen; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Neocortex; Nerve Tissue Proteins; Neurons; Trisomy

2007
Human X chromosomes: synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomes.
    Somatic cell genetics, 1980, Volume: 6, Issue:2

    Topics: Aneuploidy; Azure Stains; Bisbenzimidazole; Bromodeoxyuridine; Cell Cycle; Cells, Cultured; Chromosome Banding; DNA Replication; Female; Fibroblasts; Genetic Markers; Glucosephosphate Dehydrogenase; Humans; Infant, Newborn; Male; Sex Chromosomes; Time Factors; Trisomy; X Chromosome

1980
De novo der(X)t(X;10)(q26;q21) with features of distal trisomy 10q: case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR).
    Journal of medical genetics, 1997, Volume: 34, Issue:3

    Topics: Abnormalities, Multiple; Bromodeoxyuridine; Child; Chromosome Deletion; Chromosomes, Human, Pair 10; Developmental Disabilities; DNA Replication; Dosage Compensation, Genetic; Female; Humans; Receptors, Androgen; Translocation, Genetic; Trisomy; X Chromosome

1997
[Use of BrdU in the study of cell cycle in normal and abnormal subjects].
    Annales de genetique, 1976, Volume: 19, Issue:2

    Topics: Bromodeoxyuridine; Cell Division; Down Syndrome; Fanconi Anemia; Humans; Mosaicism; Trisomy

1976
[A small supernumerary metacentric chromosome: interprétation test (author's transl)].
    Journal de genetique humaine, 1976, Volume: 24, Issue:2

    Topics: Acridines; Azure Stains; Bromodeoxyuridine; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 16-18; Chromosomes, Human, 19-20; Female; Humans; Hypertelorism; Infant; Infant, Newborn; Karyotyping; Microcephaly; Micrognathism; Phenotype; Psychomotor Disorders; Trisomy

1976
BrDU-Giemsa labeling studies of satellite associations in parents of children with trisomy 21 or 13.
    American journal of medical genetics, 1987, Volume: 26, Issue:4

    Topics: Age Factors; Bromodeoxyuridine; Cells, Cultured; Chromosome Banding; Chromosomes, Human, Pair 13; Chromosomes, Human, Pair 21; Humans; Nondisjunction, Genetic; Polymorphism, Genetic; Sex Factors; Staining and Labeling; Trisomy

1987
A complex mosaic with tdic(13;18) (p11;p11), +13p-, +18p-, r(13) etc. in a male infant. II. Increased dissociation of dicentric chromosome by mitomycin C.
    Jinrui idengaku zasshi. The Japanese journal of human genetics, 1986, Volume: 31, Issue:1

    Topics: Abnormalities, Multiple; Bromodeoxyuridine; Cells, Cultured; Centromere; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Chromosomes, Human, 16-18; Ethidium; Female; Humans; Lymphocytes; Male; Mitomycin; Mitomycins; Mosaicism; Translocation, Genetic; Trisomy

1986
5-bromodeoxyuridine-induced constrictions in human chromosomes.
    Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie, 1970, Volume: 12, Issue:4

    Topics: Autoradiography; Bromodeoxyuridine; Chromosome Aberrations; Chromosomes; Chromosomes, Human, 13-15; Chromosomes, Human, 21-22 and Y; Chromosomes, Human, 4-5; Culture Techniques; Female; Humans; Leukocytes; Male; Sex Chromosome Aberrations; Sex Chromosomes; Trisomy

1970