Evidence map›Paper›PMID 30233643›Full record

ArticleFrontiers in genetics2018

The Lysine Demethylase dKDM2 Is Non-essential for Viability, but Regulates Circadian Rhythms in

Yani Zheng, Yongbo Xue, Xingjie Ren, Mengmeng Liu, Xiao Li, Yu Jia, Ye Niu, Jian-Quan Ni, Yong Zhang, Jun-Yuan Ji

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Variant Polycomb complexes inScience advances · 2022
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Targeted Downregulation ofJournal of Korean medical science · 2019
    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

10 authors at 4 institutions in 2 countries.

Yani ZhengDepartment of Molecular and Cellular Medicine, College of Medicine, Texas A&M University Health Science Center, College Station, TX, United States.
Yongbo XueDepartment of Biology, University of Nevada, Reno, Reno, NV, United States.
Xingjie RenGene Regulatory Laboratory, School of Medicine, Tsinghua University, Beijing, China.
Mengmeng LiuDepartment of Molecular and Cellular Medicine, College of Medicine, Texas A&M University Health Science Center, College Station, TX, United States.
Xiao LiDepartment of Molecular and Cellular Medicine, College of Medicine, Texas A&M University Health Science Center, College Station, TX, United States.
Yu JiaGene Regulatory Laboratory, School of Medicine, Tsinghua University, Beijing, China.
Ye NiuDepartment of Biology, University of Nevada, Reno, Reno, NV, United States.
Jian-Quan NiGene Regulatory Laboratory, School of Medicine, Tsinghua University, Beijing, China.
Yong ZhangDepartment of Biology, University of Nevada, Reno, Reno, NV, United States.
Jun-Yuan JiDepartment of Molecular and Cellular Medicine, College of Medicine, Texas A&M University Health Science Center, College Station, TX, United States.
Texas A&M University · USTsinghua University · CNUniversity of Nevada, Reno · USTexas A&M Health Science Center · US

Funding

Context-specific Functions of CDK8R01DK095013 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI JI, JUN-YUAN · 2013 to 2017
$1.5M
NIDDK NIH HHS R01 DK095013
6 · The paper itself

Abstract

Post-translational modification of histones, such as histone methylation controlled by specific methyltransferases and demethylases, play critical roles in modulating chromatin dynamics and transcription in eukaryotes. Misregulation of histone methylation can lead to aberrant gene expression, thereby contributing to abnormal development and diseases such as cancer. As such, the mammalian lysine-specific demethylase 2 (KDM2) homologs, KDM2A and KDM2B, are either oncogenic or tumor suppressive depending on specific pathological contexts. However, the role of KDM2 proteins during development remains poorly understood. Unlike vertebrates,

Indexed as

circadian rhythmsdemethylasedevelopmentDrosophilaKDM2

Identifiers

PMID30233643
PMCPMC6131532
OpenAlexW2953184869

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.