Evidence map›Paper›PMID 42473675›Full record

ArticleFrontiers in genetics2026

Effects of prenatal transportation stress on liver gene expression in male and female Brahman calves.

Sierra R Sebesta, Emilie C Baker, Kubra Z Cilkiz, Rodolfo C Cardoso, Thomas B Hairgrove, Charles R Long, Ronald D Randel, Thomas H Welsh, David G Riley

Abstract read
In one paragraph

Article in Frontiers in genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Sierra R SebestaDepartment of Animal Science, College Station, Texas A&M University, College Station, TX, United States.
Emilie C BakerDepartment of Animal Science, College Station, Texas A&M University, College Station, TX, United States.
Kubra Z CilkizDepartment of Animal Science, College Station, Texas A&M University, College Station, TX, United States.
Rodolfo C CardosoDepartment of Animal Science, College Station, Texas A&M University, College Station, TX, United States.
Thomas B HairgroveDepartment of Animal Science, College Station, Texas A&M University, College Station, TX, United States.
Charles R LongDepartment of Animal Science, College Station, Texas A&M University, College Station, TX, United States.
Ronald D RandelDepartment of Animal Science, College Station, Texas A&M University, College Station, TX, United States.
Thomas H WelshDepartment of Animal Science, College Station, Texas A&M University, College Station, TX, United States.
David G RileyDepartment of Animal Science, College Station, Texas A&M University, College Station, TX, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The liver is a central regulator of metabolic and endocrine functions that support fetal growth and postnatal development. Prenatal stress can reprogram hepatic development in the offspring, potentially causing long-term changes in metabolism and production efficiency. However, the influence of prenatal stress on hepatic molecular function and resulting phenotypes in beef cattle remains poorly understood. Therefore, the objectives of this study were to evaluate phenotypic traits and liver tissue gene expression in Brahman heifer and bull calves from prenatal transportation stress (PNS) and control (Control) treatment groups. One group of pregnant Brahman cows were transported for a 2-h period every 20 (±5) d from 60 to 140 days of gestation. Another group of pregnant Brahman cows served as Control. Thirty-two calves, eight heifer and eight bull calves from the PNS and Control groups, respectively, were utilized. Calves were weighed at approximately 25 (±2) d of age. The following day, calves were euthanized, and liver tissues were harvested. Phenotypic traits evaluated include birth weight, harvest weight, liver weight, pen score, and liver weight:harvest weight. Interaction of sex and treatment did not explain substantial variation for any trait (

Indexed as

BEGAINHSPA6sex differencesstressTAT

Identifiers

PMID42473675
PMCPMC13381019

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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.