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Base Excision Repair Pathway

Overview of attention for book
Cover of 'Base Excision Repair Pathway'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Simultaneous Short- and Long-Patch Base Excision Repair (BER) Assay in Live Mammalian Cells
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    Chapter 2 In Vitro Assay to Measure APE1 Enzymatic Activity on Ribose Monophosphate Abasic Site
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    Chapter 3 Highly Sensitive Radioactivity-Based DNA 3′-Phosphatase Activity Assay for Polynucleotide Kinase 3′-Phosphatase
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    Chapter 4 Generation of Recombinant Nucleosomes Containing Site-Specific DNA Damage
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    Chapter 5 A DNA Cleavage Assay Using Synthetic Oligonucleotide Containing a Single Site-Directed Lesion for In Vitro Base Excision Repair Study
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    Chapter 6 In Vitro Reconstitutive Base Excision Repair (BER) Assay
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    Chapter 7 Detection of Oxidatively Modified Base Lesion(s) in Defined DNA Sequences by FLARE Quantitative PCR
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    Chapter 8 Isolation and Immunodetection of Enzymatic DNA–Protein Crosslinks by RADAR Assay
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    Chapter 9 Slot Blot Assay for Detection of R Loops
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    Chapter 10 Assays with Patient-Derived Organoids to Evaluate the Impact of Microbial Infection on Base Excision Repair (BER) Enzymes
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    Chapter 11 Characterizing the Repair of DNA Double-Strand Breaks: A Review of Surrogate Plasmid-Based Reporter Methods
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    Chapter 12 Interactome Profiling of DNA Damage Response (DDR) Mediators with Immunoprecipitation-Mass Spectrometry
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    Chapter 13 Using Affinity Pulldown Assays to Study Protein–Protein Interactions of Human NEIL1 Glycosylase and the Checkpoint Protein RAD9–RAD1–HUS1 (9-1-1) Complex
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    Chapter 14 Tandem Affinity Purification and Mass-Spectrometric Analysis of FACT and Associated Proteins
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    Chapter 15 Analysis of Copy Number Variation of DNA Repair/Damage Response Genes in Tumor Tissues
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    Chapter 16 Genome-Wide Binding Analysis of DNA Repair Protein APE1 in Tumor Cells by ChIP-Seq
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    Chapter 17 Tumorsphere Formation Assay: A Cancer Stem-Like Cell Characterization in Pediatric Brain Cancer Medulloblastoma
Attention for Chapter 4: Generation of Recombinant Nucleosomes Containing Site-Specific DNA Damage
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About this Attention Score

  • Good Attention Score compared to outputs of the same age (74th percentile)
  • High Attention Score compared to outputs of the same age and source (92nd percentile)

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Chapter title
Generation of Recombinant Nucleosomes Containing Site-Specific DNA Damage
Chapter number 4
Book title
Base Excision Repair Pathway
Published in
Methods in molecular biology, January 2023
DOI 10.1007/978-1-0716-3373-1_4
Pubmed ID
Book ISBNs
978-1-07-163372-4, 978-1-07-163373-1
Authors

Ryan, Benjamin J., Weaver, Tyler M., Spencer, Jonah J., Freudenthal, Bret D.

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Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 6. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 30 August 2023.
All research outputs
#6,708,976
of 25,870,142 outputs
Outputs from Methods in molecular biology
#1,890
of 14,394 outputs
Outputs of similar age
#122,138
of 480,998 outputs
Outputs of similar age from Methods in molecular biology
#50
of 714 outputs
Altmetric has tracked 25,870,142 research outputs across all sources so far. This one has received more attention than most of these and is in the 74th percentile.
So far Altmetric has tracked 14,394 research outputs from this source. They receive a mean Attention Score of 3.4. This one has done well, scoring higher than 86% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 480,998 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 74% of its contemporaries.
We're also able to compare this research output to 714 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 92% of its contemporaries.