Article metadata + abstract

Code snippets

curl "https://api.oanor.com/pubmed-api/v1/article" \
  -H "x-oanor-key: oanor_test_..."

await fetch("https://api.oanor.com/pubmed-api/v1/article", {
  headers: { "x-oanor-key": "oanor_test_..." }
});

$ch = curl_init("https://api.oanor.com/pubmed-api/v1/article");
curl_setopt($ch, CURLOPT_HTTPHEADER, ["x-oanor-key: oanor_test_..."]);
curl_setopt($ch, CURLOPT_RETURNTRANSFER, true);
$out = curl_exec($ch);

import requests
requests.get(
    "https://api.oanor.com/pubmed-api/v1/article",
    headers={"x-oanor-key": "oanor_test_..."}
)

Example response

A real response from this endpoint, captured by the latest health check.

{
    "data": {
        "doi": "10.1016/j.lfs.2019.116636",
        "url": "https://pubmed.ncbi.nlm.nih.gov/31295471/",
        "pmid": "31295471",
        "issue": null,
        "pages": "116636",
        "title": "CRISPR-Cas9 system: A new-fangled dawn in gene editing",
        "volume": "232",
        "authors": [
            "Gupta D",
            "Bhattacharjee O",
            "Mandal D",
            "Sen MK",
            "Dey D",
            "Dasgupta A",
            "Kazi TA",
            "Gupta R",
            "Sinharoy S",
            "Acharya K",
            "Chattopadhyay D",
            "Ravichandiran V",
            "Roy S",
            "Ghosh D"
        ],
        "journal": "Life sciences",
        "abstract": "Till date, only three techniques namely Zinc Finger Nuclease (ZFN), Transcription-Activator Like Effector Nucleases (TALEN) and Clustered Regularly Interspaced Short Palindromic Repeats-CRISPR-Associated 9 (CRISPR-Cas9) are available for targeted genome editing. CRISPR-Cas system is very efficient, fast, easy and cheap technique for achieving knock-out gene in the cell. CRISPR-Cas9 system refurbishes the targeted genome editing approach into a more expedient and competent way, thus facilitating proficient genome editing through embattled double-strand breaks in approximately any organism and cell type. The off-target effects of CRISPR Cas system has been circumnavigated by using paired nickases. Moreover, CRISPR-Cas9 has been used effectively for numerous purposes, like knock-out of a gene, regulation of endogenous gene expression, live-cell labelling of chromosomal loci, edition of single-stranded RNA and high-throughput gene screening. The execution of the CRISPR-Cas9 system has amplified the number of accessible scientific substitutes for studying gene function, thus enabling generation of CRISPR-based disease models. Even though many mechanistic questions are left behind to be answered and the system is not yet fool-proof i.e., a number of challenges are yet to be addressed, the employment of CRISPR-Cas9-based genome engineering technologies will increase our understanding to disease processes and their treatment in the near future. In this review we have discussed the history of CRISPR-Cas9, its mechanism for genome editing and its application in animal, plant and protozoan parasites. Additionally, the pros and cons of CRISPR-Cas9 and its potential in therapeutic application have also been detailed here.",
        "language": "eng",
        "pub_date": "2019 Sep 1",
        "epub_date": "2019 Jul 8",
        "pub_types": [
            "Journal Article",
            "Review"
        ]
    },
    "meta": {
        "timestamp": "2026-05-30T18:16:52.545Z",
        "request_id": "28f3a271-c9bc-43a3-8131-9def61908eda"
    },
    "status": "ok",
    "message": "Article retrieved",
    "success": true
}