Evidence map›Paper›PMID 31087243›Full record

ArticleMolecular biology reports2019

Expression and localization of transient receptor potential channels in the bovine uterus epithelium throughout the estrous cycle.

Maryam Ghavideldarestani, Alexandra E Butler, Sadegh Shirian, Stephen L Atkin

Abstract read
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Article in Molecular biology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 54% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

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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 3 institutions in 3 countries.

Maryam GhavideldarestaniHull York Medical School, Cottingham Road, Hull, HU67RX, UK.
Alexandra E ButlerDiabetes Research Center, Biomedical Research Institute, Doha, Qatar.
Sadegh ShirianDepartment of Pathology, School of Veterinary Medicine, Shahrekord University, Shahrekord, Iran.
Stephen L AtkinWeill Cornell Medical College Qatar, Qatar Foundation, Education City, PO Box 24144, Doha, Qatar. sla2002@qatar-med.cornell.edu.ORCID http://orcid.org/0000-0002-5887-7257
Hull York Medical School · GBShahrekord University · IRWeill Cornell Medical College in Qatar · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transient receptor potential (TRP) channels are expressed in the endometrium but it is unknown if they are modulated through the estrous cycle (EC). This study was undertaken to identify the modulation of the TRPC gene and protein isoforms in bovine uterine epithelium, as a model for human, throughout the EC. Changes in the expression of TRPC genes in bovine uterine epithelium throughout the EC were measured using Real-Time PCR, while immunohistochemistry and immunocytochemistry were used to determine the localization of these channels. Out of the 7 members of the TRPC family, TRPC1, 2, 3, 4 and 6 genes were expressed in bovine uterine epithelial tissue and TRPC 5 and 7 were not. Gene expression levels of all TRPC isoforms underwent cyclical changes throughout the EC. Moreover, cyclical changes were detected in the protein levels of TRPC1 and TRPC6 throughout the EC. These findings show that TRPC channels are modulated through the EC and therefore may have a role in reproductive events.

Indexed as

AnimalsCattleEndometriumEpitheliumEstrous CycleFemaleProtein IsoformsTranscriptomeTransient Receptor Potential ChannelsTRPC Cation ChannelsUterusProtein IsoformsTransient Receptor Potential ChannelsTRPC Cation ChannelsCalciumEndometriumSex hormonesTRPC channels

Identifiers

PMID31087243
OpenAlexW2945525535

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.