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What does BER stand for?

Base Excision Repair (biology)


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This definition appears very rarely and is found in the following Acronym Finder categories:

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Bulletin d'Exploitation Quotidien (French: Daily Operating Bulletin; Transport Canada)
Bury St. Edmunds Honington (airport code; Royal Air Force station; England, UK)
Business Ethics Quarterly (journal)
Bank of England Quarterly Bulletin (UK)
Branch on Equal Likely
Bank of England Quarterly Model
Biological Effects Quality Assurance in Monitoring Programmes (est. 1998)
Branch on Equal to Zero
Back End Ratio
Back End Rebate (retail marketing)
Basic Electrical Rhythm
Basic Encoding Rules (ASN.1)
Basic Error Rate
Bassin d'Emploi a Redynamiser (French: Labor Pool Revitalization)
Berlin, Germany - Schoenefeld (Airport Code)
Beryllium Electrorefining
Beyond Economical Repair
Bilateral Economic Relations
Biological and Environmental Research
Biomedical and Environmental Research



Samples in periodicals archive:
DNA damage checkpoint, HR, nonhomologous end-joining, interstrand DNA cross-link repair, translesion DNA synthesis, nucleotide excision repair, and base excision repair [see Supplemental Material, Table 1, available online (doi:10.
Additionally, SWI/ SNF has been shown to stimulate both NER and base excision repair in reconstituted positioned nucleosomes (Hara and Sancar 2002; Menoni et al.
The base excision repair pathway repairs small isolated foci of DNA damage including reduced or oxidized single bases or fragments and small, nonbulky adducts.
The three main excision repair pathways are nucleotide excision repair (NER), base excision repair (BER), and mismatch repair (MMR).
OGG1 encodes 8-oxoguanine DNA glycosylase, which is involved in base excision repair of 8-oxoguanine caused by the effects of ROS on DNA (Memisoglu and Samson 2000).
Mammalian polynucleotide kinase (PNK) is a key component of both the base excision repair (BER) and nonhomologous end-joining (NHEJ) DNA repair pathways.
Molecular mechanism of PCNA-dependent base excision repair.
The 633 amino acid protein encoded by the human XRCC1 gene is required for maintenance of genome stability (2) and efficient repair of oxidative DNA base damage and DNA single-strand breaks by the base excision repair (BER)1 and single-strand break repair (SSBR) pathways, respectively (3, 4).

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