bromodeoxyuridine has been researched along with Adult Premature Aging Syndrome in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Poot, M; Rabinovitch, PS; Silber, JR | 1 |
| Brown, WT; Darlington, GJ; Dutkowski, R | 1 |
| Edelman, JR; Lin, YJ | 1 |
| Chebotarev, AN; Kuleshov, NP; Kuzina, NIu; Stobetskiĭ, VI | 1 |
| Bartram, CR; Koske-Westphal, T; Passarge, E | 1 |
5 other study(ies) available for bromodeoxyuridine and Adult Premature Aging Syndrome
| Article | Year |
|---|---|
A novel flow cytometric technique for drug cytotoxicity gives results comparable to colony-forming assays.
Topics: 4-Nitroquinoline-1-oxide; Antimetabolites; Antineoplastic Agents, Phytogenic; Benzimidazoles; Bromodeoxyuridine; Camptothecin; Carcinogens; Cell Division; Cell Line; Cell Survival; Fibroblasts; Flow Cytometry; Fluorescent Dyes; Humans; Lymphocytes; Stem Cells; Werner Syndrome | 2002 |
Sister chromatid exchange frequencies in Progeria and Werner syndrome patients.
Topics: Adult; Bromodeoxyuridine; Crossing Over, Genetic; Female; Humans; Male; Metaphase; Mitomycins; Progeria; Sister Chromatid Exchange; Werner Syndrome | 1981 |
Translocation of unstable heterochromatin as the mechanism of sister chromatid exchange formation: a proposed hypothesis.
Topics: Animals; Azure Stains; Bromodeoxyuridine; Cell Division; Cells, Cultured; Cricetinae; Gerbillinae; Hematopoietic Stem Cells; Heterochromatin; Humans; Interphase; Lymphocytes; Male; Models, Biological; Rats; Rats, Sprague-Dawley; Sister Chromatid Exchange; Translocation, Genetic; Werner Syndrome | 2001 |
[Chromosomal abnormalities in lymphocytes from a patient with Werner's syndrome in intact culture and after treatment with halogenated analogs of thymidine].
Topics: Adult; Bromodeoxyuridine; Chromosome Aberrations; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 15; Deoxyuridine; Humans; Idoxuridine; Lymphocytes; Male; Nucleic Acid Synthesis Inhibitors; Werner Syndrome | 2002 |
Chromatid exchanges in ataxia telangiectasia, Bloom syndrome, Werner syndrome, and xeroderma pigmentosum.
Topics: Abnormalities, Multiple; Adolescent; Adult; Aged; Ataxia Telangiectasia; Bromodeoxyuridine; Cells, Cultured; Child; Chromatids; Facial Dermatoses; Female; Humans; Infant, Newborn; Lectins; Lymphocytes; Male; Middle Aged; Radiation Effects; Syndrome; Telangiectasis; Ultraviolet Rays; Werner Syndrome; Xeroderma Pigmentosum | 1976 |