Extensive loss of heterozygosity is suppressed during homologous repair of chromosomal breaks

Molecular and Cellular Biology

Volumn 23, Issue 2, 2003, Pages 733-743

  Stark, Jeremy M ^a   Jasin, Maria ^a  

^a Weill Cornell Graduate School of Biomedical Sciences   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

RECOMBINANT PROTEIN;

ALLELE; ANIMAL CELL; ARTICLE; BINDING SITE; CELL LINE; CHROMOSOME; DNA REPAIR; DNA STRAND BREAKAGE; EMBRYO CELL; GENE REPRESSION; HETEROZYGOSITY LOSS; MAMMAL CELL; NONHUMAN; PATERNITY; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SISTER CHROMATID; STEM CELL;

ALLELES; ANIMALS; CELL LINE; CHROMATIDS; CHROMOSOMES; CROSSING OVER, GENETIC; DNA DAMAGE; DNA REPAIR; GENETIC MARKERS; GENOTYPE; HETEROZYGOTE; HUMANS; KARYOTYPING; LOSS OF HETEROZYGOSITY; MICE; MICE, INBRED BALB C; MITOSIS; MODELS, GENETIC; PHENOTYPE; POLYMORPHISM, GENETIC; RECOMBINATION, GENETIC;

ANIMALIA; MAMMALIA;

EID: 0037221249     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.23.2.733-743.2003     Document Type: Article

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