Evidence map›Paper›PMID 31721013›Full record

ArticleCellular and molecular neurobiology2020

PKC and Ras are Involved in M1 Muscarinic Receptor-Mediated Modulation of AMPA Receptor GluA1 Subunit.

Mu-Wen Chen, Han Zhu, Cai-Hong Xiong, Jia-Bing Li, Lan-Xue Zhao, Hong-Zhuan Chen, Yu Qiu

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2020. 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
0.5field-weighted citation impact, top 35% 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, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Molecular Mechanisms of AMPA Receptor Trafficking in the Nervous System.International journal of molecular sciences · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. 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

7 authors at 2 institutions in 1 country.

Mu-Wen ChenDepartment of Pharmacology and Chemical Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai, 200025, China.
Han ZhuDepartment of Pharmacology and Chemical Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai, 200025, China.
Cai-Hong XiongDepartment of Pharmacology and Chemical Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai, 200025, China.
Jia-Bing LiDepartment of Pharmacology and Chemical Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai, 200025, China.
Lan-Xue ZhaoDepartment of Pharmacology and Chemical Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai, 200025, China. annzoor@shsmu.edu.cn.
Hong-Zhuan ChenInstitute of Interdisciplinary Integrative Biomedical Research, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai, 201210, China.
Yu QiuDepartment of Pharmacology and Chemical Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai, 200025, China. qiuy@shsmu.edu.cn.ORCID http://orcid.org/0000-0002-1236-1941
Shanghai Jiao Tong University · CNShanghai University of Traditional Chinese Medicine · CN

Funding

Major Research Plan 81473217Major Research Plan 81573415Major Research Plan 81872840Shanghai Jiao Tong University Medical-Science Cross Fund YG2017ZD14Young Scientists Fund 81803499
6 · The paper itself

Abstract

M1 muscarinic acetylcholine receptors (M1 mAChRs) have long been an attractive target for the treatment of Alzheimer's disease (AD), the most common cause of dementia in the elderly. M1 mAChR agonists show desirably preclinical activities; however, most have not gone further into late clinical trials due to ineffectiveness or side effects. Thus, to understand the signaling pathways involved in M1 mAChR-mediated memory improvement may be important for design of biased agonists with on-target therapeutic effects. M1 mAChRs are classically coupled to Gα

Indexed as

AnimalsAnimals, NewbornCells, CulturedMaleMice, Inbred C57BLModels, BiologicalPhosphatidylinositol 3-KinasesPhosphorylationPhosphoserineProtein Kinase CProto-Oncogene Proteins c-aktras ProteinsRats, Sprague-DawleyReceptor, Muscarinic M1Receptors, AMPASignal TransductionPhosphatidylinositol 3-KinasesPhosphoserineProtein Kinase CProto-Oncogene Proteins c-aktras ProteinsReceptor, Muscarinic M1Receptors, AMPAGluA1M1 mAChRsPKCRas

Identifiers

PMID31721013
PMCPMC11448767
OpenAlexW2984887946

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.