Evidence map›Paper›PMID 37485339›Full record

ArticleFrontiers in genetics2023

Functional identification of two novel variants and a hypomorphic variant in

Jing Liu, Zhongjie Wang, Huiming Yan, Yanling Teng, Qingxin Shi, Jing Chen, Wanglan Tang, Wenxian Yu, Ying Peng, Hui Xi and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Visualization of argininosuccinate synthetase byFrontiers in molecular biosciences · 2024
    Article
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

14 authors at 3 institutions in 1 country.

Jing LiuDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, Hunan, China.
Zhongjie WangCenter for Medical Genetics, Hunan Key Laboratory of Medical Genetics, Hunan Key Laboratory of Animal Models for Human Diseases, School of Life Sciences, Central South University, Changsha, China.
Huiming YanDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, Hunan, China.
Yanling TengCenter for Medical Genetics, Hunan Key Laboratory of Medical Genetics, Hunan Key Laboratory of Animal Models for Human Diseases, School of Life Sciences, Central South University, Changsha, China.
Qingxin ShiCenter for Medical Genetics, Hunan Key Laboratory of Medical Genetics, Hunan Key Laboratory of Animal Models for Human Diseases, School of Life Sciences, Central South University, Changsha, China.
Jing ChenDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, Hunan, China.
Wanglan TangDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, Hunan, China.
Wenxian YuDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, Hunan, China.
Ying PengDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, Hunan, China.
Hui XiDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, Hunan, China.
Na MaDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, Hunan, China.
Desheng LiangCenter for Medical Genetics, Hunan Key Laboratory of Medical Genetics, Hunan Key Laboratory of Animal Models for Human Diseases, School of Life Sciences, Central South University, Changsha, China.
Zhuo LiCenter for Medical Genetics, Hunan Key Laboratory of Medical Genetics, Hunan Key Laboratory of Animal Models for Human Diseases, School of Life Sciences, Central South University, Changsha, China.
Lingqian WuCenter for Medical Genetics, Hunan Key Laboratory of Medical Genetics, Hunan Key Laboratory of Animal Models for Human Diseases, School of Life Sciences, Central South University, Changsha, China.
Central South University · CNHunan Provincial Maternal and Child Health Hospital · CNNational Health and Family Planning Commission · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ASS1Citrullinemia type Ienzyme activityhypomorphic varianturea cycle disorder

Identifiers

PMID37485339
PMCPMC10360398
OpenAlexW4383555844

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.