Evidence map›Paper›PMID 41055736›Full record

ArticleAnnals of hematology2025

Microvesicles secreted by CoCl

Shalmali Pendse, Vaijayanti Kale, Anuradha Vaidya

Abstract read
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

3 authors.

Shalmali PendseSymbiosis School of Biological Sciences, Symbiosis International (Deemed University), Pune, 412115, India.
Vaijayanti KaleSymbiosis Centre for Stem Cell Research, Symbiosis International (Deemed University), Pune, 412115, India.
Anuradha VaidyaSymbiosis School of Biological Sciences, Symbiosis International (Deemed University), Pune, 412115, India. anuradha.vaidya@ssbs.edu.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rapid hematopoietic regeneration post-hematopoietic stem cell transplantation (HSCT) is vital for prompt immune recovery, infection prevention, and averting complications such as anemia and thrombocytopenia. The hematopoietic stem cells (HSCs) produce mature blood cells through a process known as hematopoiesis that is tightly regulated by the hypoxic bone marrow microenvironment. However, the limited number of HSCs present in the bone marrow is one of the major challenges for successful HSCT. Hence, developing novel ex vivo expansion strategies that address the clinical limitations of the current HSCT becomes imperative. Our prior work demonstrated that priming of mesenchymal stromal cells (MSCs) with a hypoxia-mimetic compound, cobalt chloride (CoCl

Indexed as

Cell-Derived MicroparticlesCobaltHematopoietic Stem CellsMesenchymal Stem CellsAnimalsCell HypoxiaCells, CulturedCoculture TechniquesExosomesHumansMiceCobaltcobaltous chlorideExtracellular vesiclesHematopoietic stem and progenitor cellsHypoxiaMesenchymal stromal cellsNotch signaling pathwayPriming

Identifiers

PMID41055736
PMCPMC12619781

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.