Evidence map›Paper›PMID 35975606›Full record

ReviewActa biochimica et biophysica Sinica2022

AID function in somatic hypermutation and class switch recombination.

Kefei Yu

Open access · diamondAbstract readReview
In one paragraph

Review in Acta biochimica et biophysica Sinica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  4. Importance of B cells (Review).International journal of molecular medicine · 2026
    Review
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  6. Explore antibody repertoire in the era of AI.Acta biochimica et biophysica Sinica · 2025
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Kefei Yu

Funding

DNA Structure Directed AID Deamination During Immunoglobulin Isotype SwitchingR01AI139039 · NIAID · MICHIGAN STATE UNIVERSITY · PI YU, KEFEI · 2018 to 2022
$1.5M
Footprint analyses of AID cytosine deaminationR21AI126359 · NIAID · MICHIGAN STATE UNIVERSITY · PI YU, KEFEI · 2016 to 2017
$416k
NIAID NIH HHS R01 AI139039NIAID NIH HHS R21 AI126359
6 · The paper itself

Abstract

Activation-induced cytidine deaminase (AID) initiates somatic hypermutation of immunoglobulin (Ig) gene variable regions and class switch recombination (CSR) of Ig heavy chain constant regions. Two decades of intensive research has greatly expanded our knowledge of how AID functions in peripheral B cells to optimize antibody responses against infections, while maintaining tight regulation of AID to restrain its activity to protect B cell genomic integrity. The many exciting recent advances in the field include: 1) the first description of AID's molecular structure, 2) remarkable advances in high throughput approaches that precisely track AID targeting genome-wide, and 3) the discovery that the cohesion-mediate loop extrusion mechanism [initially discovered in V(D)J recombination studies] also governs AID-medicated CSR. These advances have significantly advanced our understanding of AID's biochemical properties

Indexed as

Cytidine DeaminaseSomatic Hypermutation, ImmunoglobulinB-LymphocytesImmunoglobulin Class SwitchingCytidine DeaminaseAIDbase excision repairclass switch recombinationerror prone DNA repairmismatch repairsomatic hypermutation

Identifiers

PMID35975606
PMCPMC9827813
OpenAlexW4286681044

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.