cetylpyridinium chloride anhydrous has been researched along with Chromosomal Breakage in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bakhoum, SF; Birmann, BM; Finucane, HK; Genovese, G; Handsaker, RE; Loh, PR; McCarroll, SA; Palamara, PF; Price, AL; Reshef, YA; Talkowski, ME | 1 |
Mohseni Meybodi, A; Mozdarani, H | 1 |
Brown, J; Drabkin, HA; Emanuel, BS; Gemmill, RM; Gimelli, G; Gimelli, S; Hacker, AM; Haldeman-Englert, C; Jalali, GR; Kato, T; Klaes, R; Kurahashi, H; Milunsky, JM; Shaikh, TH; Sheridan, MB; Tomkins, D; Zackai, EH; Zou, Y | 1 |
Lowe, X; Moore II, DH; Nath, J; Sloter, ED; Wyrobek, AJ | 1 |
4 other study(ies) available for cetylpyridinium chloride anhydrous and Chromosomal Breakage
Article | Year |
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Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations.
Topics: Adult; Aged; Alleles; Biological Specimen Banks; Chromosome Aberrations; Chromosome Breakage; Chromosome Fragile Sites; Chromosomes, Human, Pair 10; Clone Cells; Female; Health; Hematologic Neoplasms; Hematopoiesis; Humans; Male; Middle Aged; Mosaicism; Penetrance; United Kingdom | 2018 |
DNA damage in leukocytes from Fanconi anemia (FA) patients and heterozygotes induced by mitomycin C and ionizing radiation as assessed by the comet and comet-FISH assay.
Topics: Adolescent; Adult; Case-Control Studies; Child; Child, Preschool; Chromosome Breakage; Chromosomes, Human; Comet Assay; DNA Damage; Fanconi Anemia; Health; Heterozygote; Humans; In Situ Hybridization, Fluorescence; Leukocytes; Mitomycin; Radiation Tolerance; Radiation, Ionizing | 2009 |
A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
Topics: Adolescent; Adult; AT Rich Sequence; Base Sequence; Child; Child, Preschool; Chromosome Breakage; Chromosomes, Human, Pair 22; Chromosomes, Human, Pair 8; Female; Gene Dosage; Genotype; Health; Humans; Inverted Repeat Sequences; Male; Meiosis; Molecular Sequence Data; Nondisjunction, Genetic; Phenotype; Sequence Analysis, DNA; Spermatogenesis; Spermatozoa; Translocation, Genetic | 2010 |
Multicolor FISH analysis of chromosomal breaks, duplications, deletions, and numerical abnormalities in the sperm of healthy men.
Topics: Animals; Centromere; Chromosome Aberrations; Chromosome Breakage; Chromosome Deletion; Chromosomes, Human, Pair 1; Cricetinae; DNA Mutational Analysis; Female; Gene Frequency; Genes, Duplicate; Genetic Variation; Genome; Health; Humans; In Situ Hybridization, Fluorescence; Male; Mutation; Ovum; Ploidies; Reproducibility of Results; Spermatozoa | 2000 |