Evidence map›Paper›PMID 39078538›Full record

ArticleCell biochemistry and biophysics2024

CMPK2 Promotes CD4

Ya-Nan Tan, Ge-Ge Jiang, Xiang-Wen Meng, Zhi-Yuan Lu, Yan-Ma, Jin Li, Nan-Xiang, Xiao-Ge Sun, Qian Wang, Xue Wang and 2 more

Abstract read
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In one paragraph

Article in Cell biochemistry and biophysics, 2024. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

12 authors.

Ya-Nan Tan *School of Pharmacy, Anhui University of Chinese Medicine, Hefei, PR China.
Ge-Ge Jiang *School of Pharmacy, Anhui University of Chinese Medicine, Hefei, PR China.
Xiang-Wen MengSchool of Pharmacy, Anhui University of Chinese Medicine, Hefei, PR China.
Zhi-Yuan LuSchool of Pharmacy, Anhui University of Chinese Medicine, Hefei, PR China.
Yan-MaDivision of Life Sciences and Medicine, Department of Rheumatology and Immunology, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, PR China.
Jin LiDivision of Life Sciences and Medicine, Department of Rheumatology and Immunology, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, PR China.
Nan-XiangDivision of Life Sciences and Medicine, Department of Rheumatology and Immunology, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, PR China.
Xiao-Ge SunDivision of Life Sciences and Medicine, Department of Rheumatology and Immunology, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, PR China.
Qian WangDivision of Life Sciences and Medicine, Department of Rheumatology and Immunology, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, PR China.
Xue WangDivision of Life Sciences and Medicine, Department of Rheumatology and Immunology, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, PR China.
Xiao-Yi JiaSchool of Pharmacy, Anhui University of Chinese Medicine, Hefei, PR China.
Min ZhangDivision of Life Sciences and Medicine, Department of Rheumatology and Immunology, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, PR China. doczhangmin@ustc.edu.cn.

Funding

Anhui Province Postdoctoral Research Funding Program Project 2021A480China Postdoctoral Science Foundation Grant 2020M682051National Natural Science Foundation of China 81603362Natural Science Foundation of Anhui Province 1808085MH298
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is a classic autoimmune disease characterized by abnormal autoantibodies, immune complex deposition, and tissue inflammation. Despite extensive research, the exact etiology and progression of SLE remain elusive. Cytidine/uridine monophosphate kinase 2 (CMPK2), a mitochondrial nucleoside monophosphate kinase, has garnered attention for its potential involvement in the development of various diseases, including SLE, where it has been observed to be dysregulated in affected individuals. However, the specific involvement of CMPK2 in the pathogenesis of SLE remains unclear. This study aims to clarify the expression level of CMPK2 in SLE CD4

Indexed as

ApoptosisCD4-Positive T-LymphocytesLupus Erythematosus, SystemicMitochondriaReactive Oxygen SpeciesAdultFemaleHumansLymphocyte ActivationMaleMembrane Potential, MitochondrialMiddle AgedNucleoside-Phosphate KinaseRNA InterferenceNucleoside-Phosphate KinaseReactive Oxygen SpeciesApoptosisCD4+ T cellCD4+ T cell activationCMPK2Mitochondrial dysfunctionSystemic lupus erythematosus

Identifiers

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.