ArticleJournal of cellular and molecular medicine2019
Cytochrome P450 26A1 modulates uterine dendritic cells in mice early pregnancy.
Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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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.
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Who cites it
7 citing papers in PubMed, 10 citations in OpenAlex.
- Genomic signatures and evolutionary history of the endangered blue-crowned laughingthrush and other Garrulax species.BMC biology · 2022Article
- Cytochrome P450 26A1 regulates the clusters and killing activity of NK cells during the peri-implantation period.Journal of cellular and molecular medicine · 2022Article
- Dietary protein source contributes to the risk of developing maternal syndrome in the Dahl salt-sensitive rat.Pregnancy hypertension · 2021Article
- A novel Cytochrome P450 26A1 expressing NK cell subset at the mouse maternal-foetal interface.Journal of cellular and molecular medicine · 2021Article
- Seminal Plasma and Seminal Plasma Exosomes of Aged Male Mice Affect Early Embryo ImplantationFrontiers in immunology · 2021Article
- Cytochrome P450 26A1 Modulates the Polarization of Uterine Macrophages During the Peri-Implantation Period.Frontiers in immunology · 2021Article
- Cytochrome P450 26A1 modulates uterine dendritic cells in mice early pregnancy.Journal of cellular and molecular medicine · 2019Article
Corrections and comments
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Authors and funding
8 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cytochrome P450 26A1 (CYP26A1) plays important roles in the mice peri-implantation period. Inhibiting its expression or function leads to pregnancy failure. However, little is known about the underlying mechanisms involved, especially the relationship between CYP26A1 and immune cells. In this study, using Cyp26a1-specific antisense morpholigos (Cyp26a1-MO) knockdown mice model and pCR3.1-Cyp26a1 vaccine mice model, we found that the number of uterine CD45
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Registered trials
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