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Relevance of the intestinal health-related pathways to broiler residual feed intake revealed by duodenal transcriptome profiling

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s004240050124openalex-snapshot
The regulation of GLUT5 and GLUT2 activity in the adaptation of intestinal brush-border fructose transport in diabetes
inferredcites →https://doi.org/10.1007/s00438-015-1025-7openalex-snapshot
Transcriptomic analysis to elucidate the molecular mechanisms that underlie feed efficiency in meat-type chickens
inferredcites →https://doi.org/10.1016/0016-5085(93)90948-copenalex-snapshot
GLUT2 is the transporter for fructose across the rat intestinal basolateral membrane
inferredcites →https://doi.org/10.1016/j.it.2009.05.007openalex-snapshot
The ubiquitin-editing enzyme A20 (TNFAIP3) is a central regulator of immunopathology
inferredcites →https://doi.org/10.1016/j.molimm.2010.04.020openalex-snapshot
Serine proteases of the human immune system in health and disease
inferredcites →https://doi.org/10.1017/s1751731116000847openalex-snapshot
Pigs that are divergent in feed efficiency, differ in intestinal enzyme and nutrient transporter gene expression, nutrient digestibility and microbial activity
inferredcites →https://doi.org/10.1038/nature07002openalex-snapshot
Dynamic repertoire of a eukaryotic transcriptome surveyed at single-nucleotide resolution
inferredcites →https://doi.org/10.1038/nbt.1621openalex-snapshot
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation
inferredcites →https://doi.org/10.1071/ea02221openalex-snapshot
Biological basis for variation in residual feed intake in beef cattle. 2. Synthesis of results following divergent selection
inferredcites →https://doi.org/10.1074/jbc.272.12.8099openalex-snapshot
A Novel Human Chymotrypsin-like Digestive Enzyme
inferredcites →https://doi.org/10.1089/dna.1993.12.1openalex-snapshot
The P450 Superfamily: Update on New Sequences, Gene Mapping, Accession Numbers, Early Trivial Names of Enzymes, and Nomenclature
inferredcites →https://doi.org/10.1093/molbev/msr127openalex-snapshot
The Origins, Evolution, and Functional Potential of Alternative Splicing in Vertebrates
inferredcites →https://doi.org/10.1093/nar/gkh131openalex-snapshot
UniProt: the Universal Protein knowledgebase
inferredcites →https://doi.org/10.1111/j.1365-2052.2011.02182.xopenalex-snapshot
Global gene expression profiling reveals genes expressed differentially in cattle with high and low residual feed intake
inferredcites →https://doi.org/10.1146/annurev-environ-031113-093503openalex-snapshot
Livestock and the Environment: What Have We Learned in the Past Decade?
inferredcites →https://doi.org/10.1186/gb-2013-14-4-r36openalex-snapshot
TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
inferredcites →https://doi.org/10.1186/s12864-015-1364-0openalex-snapshot
Messenger RNA sequencing and pathway analysis provide novel insights into the biological basis of chickens’ feed efficiency
inferredcites →https://doi.org/10.1186/s12864-015-1464-xopenalex-snapshot
Global liver gene expression differences in Nelore steers with divergent residual feed intake phenotypes
inferredcites →https://doi.org/10.1186/s12864-016-2861-5openalex-snapshot
Combination analysis of genome-wide association and transcriptome sequencing of residual feed intake in quality chickens
inferredcites →https://doi.org/10.1186/s12864-017-4092-9openalex-snapshot
Genome-wide association study reveals putative role of gga-miR-15a in controlling feed conversion ratio in layer chickens
inferredcites →https://doi.org/10.1186/s40104-018-0261-1openalex-snapshot
Feed conversion ratio, residual feed intake and cholecystokinin type A receptor gene polymorphisms are associated with feed intake and average daily gain in a Chinese local chicken population
inferredcites →https://doi.org/10.1371/journal.pone.0023253openalex-snapshot
Transcriptomic Analysis Brings New Insight into the Biological Role of the Prion Protein during Mouse Embryogenesis
inferredcites →https://doi.org/10.1371/journal.pone.0135810openalex-snapshot
RNA-Seq Analysis of Abdominal Fat Reveals Differences between Modern Commercial Broiler Chickens with High and Low Feed Efficiencies
inferredcites →https://doi.org/10.1371/journal.pone.0136765openalex-snapshot
In-Depth Duodenal Transcriptome Survey in Chickens with Divergent Feed Efficiency Using RNA-Seq
inferredcites →https://doi.org/10.2527/2006.841145xopenalex-snapshot
Relationships of feedlot feed efficiency, performance, and feeding behavior with metabolic rate, methane production, and energy partitioning in beef cattle1
inferredcites →https://doi.org/10.2527/jas.2008-1345openalex-snapshot
Physiological basis for residual feed intake1
inferredcites →https://doi.org/10.2527/jas1963.222486xopenalex-snapshot
Efficiency of Feed Use in Beef Cattle
inferredcites →https://doi.org/10.3168/jds.2016-11079openalex-snapshot
Relationship between residual feed intake and digestibility for lactating Holstein cows fed high and low starch diets
inferredcites →https://doi.org/10.3168/jds.2017-14278openalex-snapshot
Methane production, rumen fermentation, and diet digestibility of Holstein and Jersey dairy cows being divergent in residual feed intake and fed at 2 forage-to-concentrate ratios
inferredcites →https://doi.org/10.3382/ps/pex262openalex-snapshot
Differential mRNA expression of nutrient transporters in male and female chickens
inferredcites →https://doi.org/10.3390/genes9020057openalex-snapshot
Exploring Genomic Variants Related to Residual Feed Intake in Local and Commercial Chickens by Whole Genomic Resequencing
inferredcites →https://doi.org/10.3748/wjg.v16.i17.2080openalex-snapshot
Connection between inflammation and carcinogenesis in gastrointestinal tract: Focus on TGF-β signaling
inferredcites →https://doi.org/10.3920/978-90-8686-756-1_12openalex-snapshot
Physiology of feed efficiency in the pig: emphasis on the gastrointestinal tract and specific dietary examples
inferredcites →https://doi.org/10.3920/978-90-8686-756-1_7openalex-snapshot
The genetic and biological basis of residual feed intake as a measure of feed efficiency

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4765151openalex-extracted
Genes Involved in the Cholecystokinin Receptor Signaling Map Were Differentially Expressed in the Jejunum of Steers with Variation in Residual Feed Intake
inferred← citeshttps://doi.org/10.1007/s11250-020-02519-9openalex-snapshot
Differential gene expression in duodenum of colored broiler chicken divergently selected for residual feed intake
inferred← citeshttps://doi.org/10.1007/s11250-021-02844-7openalex-snapshot
Differential gene expression in liver of colored broiler chicken divergently selected for residual feed intake
inferred← citeshttps://doi.org/10.1016/j.animal.2025.101521openalex-snapshot
Transcriptome analysis reveals key genes and signalling pathways related to residual feed intake in meat-type ducks
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2022.737915openalex-snapshot
Proteomic investigation of brain, liver and intestine in high feed intake and low feed intake Chinook salmon (Oncorhynchus tshawytscha)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2022.738845openalex-snapshot
An integrated proteomics and metabolomics investigation of feed efficiency in seawater reared Chinook salmon (Oncorhynchus tshawytscha)
inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.152846openalex-snapshot
Tannic acid decreased the synthesis and secretion of sIgA in the small intestine of Brandt's voles (Lasiopodomys brandtii) by modifying gut microbiota
inferred← citeshttps://doi.org/10.1016/j.cellsig.2024.111275openalex-snapshot
The role of α7nAchR and PD-L1 in neuroimmune regulation of keloid treatment
inferred← citeshttps://doi.org/10.1016/j.gene.2023.147944openalex-snapshot
RNA-seq transcriptome analysis provides new insights into the negative effects of tannic acid on the intestinal function of Brandt’s voles (Lasiopodomys brandtii)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.139938openalex-snapshot
A comprehensive study of liver-gut microbiota and antioxidant enzyme activity mediated regulation of late-laying hens by high and low residual feed intake
inferred← citeshttps://doi.org/10.1016/j.psj.2022.101990openalex-snapshot
Effects of residual feed intake divergence on growth performance, carcass traits, meat quality, and blood biochemical parameters in small-sized meat ducks
inferred← citeshttps://doi.org/10.1016/j.psj.2023.102703openalex-snapshot
Trade-off between feed efficiency and immunity in specialized high-performing chickens
inferred← citeshttps://doi.org/10.1016/j.psj.2024.103726openalex-snapshot
Integrated transcriptome and microbiome analyses of residual feed intake in ducks during high production period
inferred← citeshttps://doi.org/10.1016/j.psj.2024.103879openalex-snapshot
Effects of residual feed intake on the economic traits of fast-growing meat ducks
inferred← citeshttps://doi.org/10.1016/j.psj.2024.104050openalex-snapshot
A multitissue transcriptomic analysis reveals a potential mechanism whereby Brevibacillus laterosporus S62-9 promotes broiler growth
inferred← citeshttps://doi.org/10.1016/j.psj.2025.104903openalex-snapshot
Mechanisms of the effects of turpiniae folium extract on growth performance, immunity, antioxidant activity and intestinal barrier function in LPS-challenged broilers
inferred← citeshttps://doi.org/10.1016/j.psj.2025.105058openalex-snapshot
Identification of key genes associated with residual feed intake in small-sized meat ducks through integrated analysis of mRNA and miRNA transcriptomes
inferred← citeshttps://doi.org/10.1016/j.psj.2025.105481openalex-snapshot
Changes in gene and protein expression related to feed intake and thermoregulation in broilers challenged with different doses of mixed Eimeria spp
inferred← citeshttps://doi.org/10.1016/j.psj.2025.105669openalex-snapshot
Mitochondrial genes and antioxidant mechanisms in the duodenum relate to feed efficiency in slow-growing chickens
inferred← citeshttps://doi.org/10.1016/j.psj.2025.105816openalex-snapshot
Understanding the impact of glycolysis and oxidative stress on residual feed intake in slow-growing chicken
inferred← citeshttps://doi.org/10.1016/j.psj.2026.106687openalex-snapshot
Identification of central regulators related to residual feed intake in Huainan chickens based on weighted gene co-expression network analysis
inferred← citeshttps://doi.org/10.1016/j.vas.2024.100357openalex-snapshot
Genes involved in the cholecystokinin receptor signaling map were differentially expressed in the jejunum of steers with variation in residual feed intake
inferred← citeshttps://doi.org/10.1080/00071668.2026.2632914openalex-snapshot
Multi-omics reveals associations between feed efficiency, physiological traits and meat quality in slow-growing chickens
inferred← citeshttps://doi.org/10.1080/1828051x.2025.2596846openalex-snapshot
Transcriptome profiling of the pituitary gland reveals candidate genes for divergent feed efficiency in slow-growing chickens
inferred← citeshttps://doi.org/10.1101/2024.03.20.585923openalex-snapshot
In-depth investigation of the mechanisms of high and low residual feed intake regulating hens during the late laying period via liver and gut microbiota
inferred← citeshttps://doi.org/10.1186/s12864-019-6320-yopenalex-snapshot
Transcriptome analysis reveals mechanism underlying the differential intestinal functionality of laying hens in the late phase and peak phase of production
inferred← citeshttps://doi.org/10.1186/s12864-023-09317-1openalex-snapshot
Combined transcriptome and metabolome analysis reveal key regulatory genes and pathways of feed conversion efficiency of oriental river prawn Macrobrachium nipponense
inferred← citeshttps://doi.org/10.1186/s12864-026-12865-xopenalex-snapshot
Intestinal microbiota-host crosstalk reveals mechanisms regulating residual feed intake in egg-type ducks
inferred← citeshttps://doi.org/10.1186/s12917-026-05562-0openalex-snapshot
Differences in meat and wool quality and gastrointestinal/hypothalamic functions in Dexin fine-wool meat sheep with divergent residual feed intake
inferred← citeshttps://doi.org/10.1186/s13567-023-01144-2openalex-snapshot
Temporal transcriptome profiling of floating apical out chicken enteroids suggest stability and reproducibility
inferred← citeshttps://doi.org/10.1186/s40104-022-00775-3openalex-snapshot
Identification of biomarkers associated with the feed efficiency by metabolomics profiling: results from the broiler lines divergent for high or low abdominal fat content
inferred← citeshttps://doi.org/10.1186/s40168-023-01627-6openalex-snapshot
Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.1262/jrd.2018-105openalex-snapshot
Studying the variations in differently expressed serum proteins of Hainan black goat during the breeding cycle using isobaric tags for relative and absolute quantitation (iTRAQ) technology
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002961openalex-snapshot
VANGL2 alleviates inflammatory bowel disease by recruiting the ubiquitin ligase MARCH8 to limit NLRP3 inflammasome activation through OPTN-mediated selective autophagy
inferred← citeshttps://doi.org/10.1371/journal.pone.0286051openalex-snapshot
Impact of divergence of residual feed intake on triglyceride metabolism-related gene expression in meat-type ducks
inferred← citeshttps://doi.org/10.17582/journal.aavs/2023/11.1.1.10openalex-snapshot
Growth Traits and Carcass Characteristics of Kalosi Chicken Selected Based on Residual Feed Intake (RFI) Phenotype
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1561000/v1openalex-snapshot
Combined effect of microbially-derived caecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.3168/jds.2019-17304openalex-snapshot
Symposium review: Decomposing efficiency of milk production and maximizing profit
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1244004openalex-snapshot
Heat stress exposure cause alterations in intestinal microbiota, transcriptome, and metabolome of broilers
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1362487openalex-snapshot
Bacillus amyloliquefaciens attenuates the intestinal permeability, oxidative stress and endoplasmic reticulum stress: transcriptome and microbiome analyses in weaned piglets
inferred← citeshttps://doi.org/10.3389/fvets.2025.1594749openalex-snapshot
Integrating metabolomics for precision nutrition in poultry: optimizing growth, feed efficiency, and health
inferred← citeshttps://doi.org/10.3390/ani11102977openalex-snapshot
Revealing Pathways Associated with Feed Efficiency and Meat Quality Traits in Slow-Growing Chickens
inferred← citeshttps://doi.org/10.3390/ani14223335openalex-snapshot
Lactiplantibacillus plantarum Ameliorated Morphological Damage and Barrier Dysfunction and Reduced Apoptosis and Ferroptosis in the Jejunum of Oxidatively Stressed Piglets
inferred← citeshttps://doi.org/10.5713/ab.20.0736openalex-snapshot
The significant influence of residual feed intake on flavor precursors and biomolecules in slow-growing Korat chicken meat
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603621openalex-snapshot
Additional file 1 of Temporal transcriptome profiling of floating apical out chicken enteroids suggest stability and reproducibility
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603624openalex-snapshot
Additional file 2 of Temporal transcriptome profiling of floating apical out chicken enteroids suggest stability and reproducibility
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603627openalex-snapshot
Additional file 3 of Temporal transcriptome profiling of floating apical out chicken enteroids suggest stability and reproducibility
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603633openalex-snapshot
Additional file 5 of Temporal transcriptome profiling of floating apical out chicken enteroids suggest stability and reproducibility
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603639openalex-snapshot
Additional file 7 of Temporal transcriptome profiling of floating apical out chicken enteroids suggest stability and reproducibility
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603642openalex-snapshot
Additional file 8 of Temporal transcriptome profiling of floating apical out chicken enteroids suggest stability and reproducibility
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603651openalex-snapshot
Additional file 10 of Temporal transcriptome profiling of floating apical out chicken enteroids suggest stability and reproducibility
inferred← citeshttps://doi.org/10.6084/m9.figshare.22978045openalex-snapshot
Additional file 1 of Combined transcriptome and metabolome analysis reveal key regulatory genes and pathways of feed conversion efficiency of oriental river prawn Macrobrachium nipponense
inferred← citeshttps://doi.org/10.6084/m9.figshare.22978048openalex-snapshot
Additional file 2 of Combined transcriptome and metabolome analysis reveal key regulatory genes and pathways of feed conversion efficiency of oriental river prawn Macrobrachium nipponense
inferred← citeshttps://doi.org/10.6084/m9.figshare.22978051openalex-snapshot
Additional file 3 of Combined transcriptome and metabolome analysis reveal key regulatory genes and pathways of feed conversion efficiency of oriental river prawn Macrobrachium nipponense
inferred← citeshttps://doi.org/10.6084/m9.figshare.22978054openalex-snapshot
Additional file 4 of Combined transcriptome and metabolome analysis reveal key regulatory genes and pathways of feed conversion efficiency of oriental river prawn Macrobrachium nipponense
inferred← citeshttps://doi.org/10.6084/m9.figshare.22978057openalex-snapshot
Additional file 5 of Combined transcriptome and metabolome analysis reveal key regulatory genes and pathways of feed conversion efficiency of oriental river prawn Macrobrachium nipponense
inferred← citeshttps://doi.org/10.6084/m9.figshare.22978060openalex-snapshot
Additional file 6 of Combined transcriptome and metabolome analysis reveal key regulatory genes and pathways of feed conversion efficiency of oriental river prawn Macrobrachium nipponense
inferred← citeshttps://doi.org/10.6084/m9.figshare.22978063openalex-snapshot
Additional file 7 of Combined transcriptome and metabolome analysis reveal key regulatory genes and pathways of feed conversion efficiency of oriental river prawn Macrobrachium nipponense
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070281openalex-snapshot
Additional file 1 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070284openalex-snapshot
Additional file 2 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070287openalex-snapshot
Additional file 3 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070290openalex-snapshot
Additional file 4 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070293openalex-snapshot
Additional file 5 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070296openalex-snapshot
Additional file 6 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070299openalex-snapshot
Additional file 7 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070302openalex-snapshot
Additional file 8 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070305openalex-snapshot
Additional file 9 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070308openalex-snapshot
Additional file 10 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070314openalex-snapshot
Additional file 11 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070317openalex-snapshot
Additional file 12 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070320openalex-snapshot
Additional file 13 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070323openalex-snapshot
Additional file 14 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
inferred← citeshttps://doi.org/10.6084/m9.figshare.24070326openalex-snapshot
Additional file 15 of Combined effect of microbially derived cecal SCFA and host genetics on feed efficiency in broiler chickens
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