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Sister chromatid exchange

Index Sister chromatid exchange

Sister chromatid exchange (SCE) is the exchange of genetic material between two identical sister chromatids. [1]

20 relations: Anaphase, Behçet's disease, Bloom syndrome, Bromodeoxyuridine, Chromatid, Deletion (genetics), DNA repair, G1 phase, G2 phase, Genome, Giemsa stain, HLA-B51, Holliday junction, Homologous recombination, Insertion (genetics), Meiosis, Mitosis, Mutagen, Neoplasm, Sister chromatids.

Anaphase

Anaphase (from the Greek ἀνά, "up" and φάσις, "stage"), is the stage of mitosis after the metaphase when replicated chromosomes are split and the daughter chromatids are moved to opposite poles of the cell.

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Behçet's disease

Behçet's disease (BD) is a type of inflammatory disorder which affects multiple parts of the body.

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Bloom syndrome

Bloom syndrome (often abbreviated as BS in literature), also known as Bloom-Torre-Machacek syndrome, is a rare autosomal recessive disorder characterized by short stature, predisposition to the development of cancer and genomic instability.

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Bromodeoxyuridine

Bromodeoxyuridine (5-bromo-2'-deoxyuridine, BrdU, BUdR, BrdUrd, broxuridine) is a synthetic nucleoside that is an analog of thymidine.

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Chromatid

A chromatid (Greek khrōmat- 'color' + -id) is one copy of a newly copied chromosome which is still joined to the original chromosome by a single centromere.

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Deletion (genetics)

In genetics, a deletion (also called gene deletion, deficiency, or deletion mutation) (sign: Δ) is a mutation (a genetic aberration) in which a part of a chromosome or a sequence of DNA is lost during DNA replication.

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DNA repair

DNA repair is a collection of processes by which a cell identifies and corrects damage to the DNA molecules that encode its genome.

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G1 phase

The g1 phase, or Gap 1 phase, is the first of four phases of the cell cycle that takes place in eukaryotic cell division.

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G2 phase

G2 phase, or Gap 2 phase, is the second subphase of Interphase in the cell cycle directly preceding mitosis.

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Genome

In the fields of molecular biology and genetics, a genome is the genetic material of an organism.

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Giemsa stain

Giemsa stain, named after German chemist and bacteriologist Gustav Giemsa, is used in cytogenetics and for the histopathological diagnosis of malaria and other parasites.

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HLA-B51

HLA-B51 (B51) is an HLA-B serotype.

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Holliday junction

A Holliday junction is a branched nucleic acid structure that contains four double-stranded arms joined together.

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Homologous recombination

Homologous recombination is a type of genetic recombination in which nucleotide sequences are exchanged between two similar or identical molecules of DNA.

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Insertion (genetics)

In genetics, an insertion (also called an insertion mutation) is the addition of one or more nucleotide base pairs into a DNA sequence.

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Meiosis

Meiosis (from Greek μείωσις, meiosis, which means lessening) is a specialized type of cell division that reduces the chromosome number by half, creating four haploid cells, each genetically distinct from the parent cell that gave rise to them.

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Mitosis

In cell biology, mitosis is a part of the cell cycle when replicated chromosomes are separated into two new nuclei.

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Mutagen

In genetics, a mutagen is a physical or chemical agent that changes the genetic material, usually DNA, of an organism and thus increases the frequency of mutations above the natural background level.

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Neoplasm

Neoplasia is a type of abnormal and excessive growth of tissue.

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Sister chromatids

A sister chromatid refers to the identical copies (chromatids) formed by the replication of a chromosome, with both copies joined together by a common centromere.

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Redirects here:

Sister Chromatid Exchange, Sister-chromatid exchange.

References

[1] https://en.wikipedia.org/wiki/Sister_chromatid_exchange

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