Evidence map›Paper›PMID 26443211›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2016

The Development of TALE Nucleases for Biotechnology.

David G Ousterout, Charles A Gersbach

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. International journal of molecular sciences · 2023
    Article
  6. Review
  7. A new era in functional genomics screens.Nature reviews. Genetics · 2022
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Applications of Alternative Nucleases in the Age of CRISPR/Cas9.International journal of molecular sciences · 2017
    Review
  18. TALEN-Mediated FLAG-Tagging of Endogenous Histone Methyltransferase DOT1L.Advances in bioscience and biotechnology (Print) · 2017
    Article
  19. Novel AIDS therapies based on gene editing.Cellular and molecular life sciences : CMLS · 2017
    Review
  20. Review
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

2 authors.

David G OusteroutDepartment of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.
Charles A GersbachDepartment of Biomedical Engineering, Duke University, Room 136 Hudson Hall, Box 90281, Durham, NC, 27708-0281, USA. charles.gersbach@duke.edu.

Funding

Interaction of Subchondral Bone and Articular Cartilage System with Skeletal MuscleUH3TR000505 · NCATS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2014 to 2016
$3.6M
Engineering Targeted Epigenetic Modifiers for Precise Control of Gene RegulationR01DA036865 · NIDA · DUKE UNIVERSITY · PI CRAWFORD, GREGORY E, GERSBACH, CHARLES A. · 2013 to 2017
$2.6M
Engineering Morphogenetic Factors for Enhanced Genetic ReprogrammingDP2OD008586 · OD · DUKE UNIVERSITY · PI GERSBACH, CHARLES A. · 2011 to 2011
$2.4M
Tissue Procurement and Analysis CoreP30AR066527 · NIAMS · DUKE UNIVERSITY · PI HALL, RUSSELL P. · 2014 to 2015
$1.3M
Genome Editing of Stem Cells for Analysis of Osteoarthritis Causal VariantsR21AR065956 · NIAMS · DUKE UNIVERSITY · PI GERSBACH, CHARLES A., GUILAK, FARSHID · 2014 to 2015
$382k
NCATS NIH HHS UH3 TR000505NCATS NIH HHS UH3TR000505NIAMS NIH HHS P30 AR066527NIAMS NIH HHS P30AR066527NIAMS NIH HHS R21 AR065956NIAMS NIH HHS R21AR065956NIDA NIH HHS R01 DA036865NIDA NIH HHS R01DA036865NIH HHS DP2 OD008586NIH HHS DP2OD008586
6 · The paper itself

Abstract

The development of a facile genome engineering technology based on transcription activator-like effector nucleases (TALENs) has led to significant advances in diverse areas of science and medicine. In this review, we provide a broad overview of the development of TALENs and the use of this technology in basic science, biotechnology, and biomedical applications. This includes the discovery of DNA recognition by TALEs, engineering new TALE proteins to diverse targets, general advances in nuclease-based editing strategies, and challenges that are specific to various applications of the TALEN technology. We review examples of applying TALENs for studying gene function and regulation, generating disease models, and developing gene therapies. The current status of genome editing and future directions for other uses of these technologies are also discussed.

Indexed as

AnimalsDeoxyribonucleasesGene TargetingGenetic TherapyHomeodomain ProteinsHumansMiceRepressor ProteinsRNA EditingDeoxyribonucleasesHomeodomain ProteinsRepressor ProteinsTgif1 protein, mouseGene editingGene targetingGene therapyGenome engineering

Identifiers

PMID26443211
PMCPMC5316914

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Registered trials

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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.