Evidence map›Paper›PMID 38505670›Full record

ArticleBioImpacts : BI2024

Essential role of CD38 in platelet aggregation through the PKC-mediated internalization and activation.

Mazhar Mushtaq, Maira Mahmood, Uzma Jabbar, Uh-Hyun Kim

Open access · diamondAbstract read
In one paragraph

Article in BioImpacts : BI, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Ablation of CD38 Alleviates the Secondary Aggregation of Platelets.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2025
    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

4 authors at 4 institutions in 3 countries.

Mazhar MushtaqBasic Medical Sciences, Sulaiman Al Rajhi University, Al-Qaseem, Kingdom of Saudi Arabia.ORCID https://orcid.org/0000-0002-2126-924X
Maira MahmoodDepartment of Biochemistry, FMH College of Medicine and Dentistry, Lahore, Pakistan ‎.ORCID https://orcid.org/0000-0002-0459-2598
Uzma JabbarDepartment of Biochemistry, Gujranwala Medical College, Gujranwala, Pakistan.ORCID https://orcid.org/0000-0003-4078-2636
Uh-Hyun KimDepartment of Biochemistry, Chonbuk National University, Chonbuk, South Korea.ORCID https://orcid.org/0000-0003-3304-7190
CMH Lahore Medical College and Institute of Dentistry · PKGIFT University · PKJeonbuk National University · KRSulaiman Al Rajhi Colleges · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: CD38 is a multifunctional enzyme with a potent Ca Methods: Mouse platelets were used in this study. Thrombin, an agonist of platelet function, provoked a prompt and long-lasting increase in intracellular Ca Results: We observed a sequential formation of cADPR and NAADP through CD38 activation by PKC of non-muscle myosin heavy chain IIA (MHCIIA), resulting in phospholipase C (PLC) activation in the thrombin-stimulated platelets. These findings reveal that PKC is fundamental in activating CD38 and elicits a physiological response in the murine platelets. Conclusion: PKC is involved in many signaling pathways. Specifically, PKC is involved in the internalization of CD38 via MHCIIA in CD38

Indexed as

cADPRCalciumCD38NAADPPKCPlatelets

Identifiers

PMID38505670
PMCPMC10945299
OpenAlexW4387435151

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.