Evidence map›Paper›PMID 34741732›Full record

SynthesisMolecular biotechnology2022

CRISPR/Cas-Based Modifications for Therapeutic Applications: A Review.

Nagaraj Bharathkumar, Abraham Sunil, Prabhakar Meera, Sam Aksah, Muthu Kannan, Konda Mani Saravanan, Thirunavukarasou Anand

Open access · bronzeAbstract readSystematic Review
In one paragraph

Synthesis in Molecular biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 67 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Nagaraj Bharathkumar *B Aatral Biosciences Private Limited, Bangalore, Karnataka, India.
Abraham Sunil *Department of Animal Behavior and Physiology, Madurai Kamaraj University, Madurai, Tamil Nadu, India.
Prabhakar MeeraB Aatral Biosciences Private Limited, Bangalore, Karnataka, India.
Sam AksahB Aatral Biosciences Private Limited, Bangalore, Karnataka, India.
Muthu KannanB Aatral Biosciences Private Limited, Bangalore, Karnataka, India.
Konda Mani SaravananB Aatral Biosciences Private Limited, Bangalore, Karnataka, India.
Thirunavukarasou AnandB Aatral Biosciences Private Limited, Bangalore, Karnataka, India. anand.t@baatral.com.
Anthem Biosciences (India) · INMadurai Kamaraj University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CRISPR-Cas genome editing system is an intrinsic property of a bacteria-based immune system. This employs a guide RNA to detect and cleave the PAM-associated target DNA or RNA in subsequent infections, by the invasion of a similar bacteriophage. The discovery of Cas systems has paved the way to overcome the limitations of existing genome editing tools. In this review, we focus on Cas proteins that are available for gene modifications among which Cas9, Cas12a, and Cas13 have been widely used in the areas of medicine, research, and diagnostics. Since CRISPR has been already proven for its potential research applications, the next milestone for CRISPR will be proving its efficacy and safety. In this connection, we systematically review recent advances in exploring multiple variants of Cas proteins and their modifications for therapeutic applications.

Indexed as

CRISPR-Cas SystemsGene EditingDNARNARNA, Guide, CRISPR-Cas SystemsDNARNARNA, Guide, CRISPR-Cas SystemsCRISPRCRISPR-associated proteinsHomology-directed repairNon-homologous end joiningNucleic acidsTherapeutic applications

Identifiers

PMID34741732
PMCPMC8571677
OpenAlexW3214336809

What OpenQuestion holds

Textmetadata
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.