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cetylpyridinium chloride anhydrous and Chromosomal Breakage

cetylpyridinium chloride anhydrous has been researched along with Chromosomal Breakage in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bakhoum, SF; Birmann, BM; Finucane, HK; Genovese, G; Handsaker, RE; Loh, PR; McCarroll, SA; Palamara, PF; Price, AL; Reshef, YA; Talkowski, ME1
Mohseni Meybodi, A; Mozdarani, H1
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, Y1
Lowe, X; Moore II, DH; Nath, J; Sloter, ED; Wyrobek, AJ1

Other Studies

4 other study(ies) available for cetylpyridinium chloride anhydrous and Chromosomal Breakage

ArticleYear
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations.
    Nature, 2018, Volume: 559, Issue:7714

    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.
    Iranian biomedical journal, 2009, Volume: 13, Issue:1

    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).
    American journal of human genetics, 2010, Aug-13, Volume: 87, Issue:2

    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.
    American journal of human genetics, 2000, Volume: 67, Issue:4

    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