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PPARs and Microbiota in Skeletal Muscle Health and Wasting
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/dvdy.10457openalex-snapshot
Embryonic myogenesis pathways in muscle regeneration
inferredcites →https://doi.org/10.1002/ijc.11447openalex-snapshot
15‐hydroxy‐eicosatetraenoic acid arrests growth of colorectal cancer cells via a peroxisome proliferator‐activated receptor gamma‐dependent pathway
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05072.xopenalex-snapshot
The mouse peroxisome proliferator activated receptor recognizes a response element in the 5′ flanking sequence of the rat acyl CoA oxidase gene.
inferredcites →https://doi.org/10.1002/mnfr.201900603openalex-snapshot
Lactobacillus and Bifidobacterium Improves Physiological Function and Cognitive Ability in Aged Mice by the Regulation of Gut Microbiota
inferredcites →https://doi.org/10.1002/mus.880060807openalex-snapshot
Age‐related differences in absolute numbers of skeletal muscle satellite cells
inferredcites →https://doi.org/10.1002/wsbm.11openalex-snapshot
Transcriptional networks that regulate muscle stem cell function
inferredcites →https://doi.org/10.1006/bbrc.1996.0832openalex-snapshot
Expression of the Peroxisome Proliferator-Activated Receptor (PPAR) in the Mouse Colonic Mucosa
inferredcites →https://doi.org/10.1006/bbrc.2000.2793openalex-snapshot
PPAR-γ Is Selectively Upregulated in Caco-2 Cells by Butyrate
inferredcites →https://doi.org/10.1007/bf00220299openalex-snapshot
The effects of aging on satellite cells in skeletal muscles of mice and rats
inferredcites →https://doi.org/10.1007/s00125-014-3331-8openalex-snapshot
PPARβ/δ prevents endoplasmic reticulum stress-associated inflammation and insulin resistance in skeletal muscle cells through an AMPK-dependent mechanism
inferredcites →https://doi.org/10.1007/s001250051642openalex-snapshot
Peroxisome Proliferator-Activated Receptor (PPAR) γ and Retinoid X Receptor (RXR) agonists have complementary effects on glucose and lipid metabolism in human skeletal muscle
inferredcites →https://doi.org/10.1007/s00223-017-0345-5openalex-snapshot
Gut Microbiota Contribute to Age-Related Changes in Skeletal Muscle Size, Composition, and Function: Biological Basis for a Gut-Muscle Axis
inferredcites →https://doi.org/10.1007/s00424-009-0676-9openalex-snapshot
Peroxisome proliferator-activated receptor β activation promotes myonuclear accretion in skeletal muscle of adult and aged mice
inferredcites →https://doi.org/10.1007/s004410051281openalex-snapshot
Genetic and epigenetic control of muscle development in vertebrates
inferredcites →https://doi.org/10.1007/s10620-006-9644-9openalex-snapshot
PPARβ/δ Protects Against Experimental Colitis Through a Ligand-Independent Mechanism
inferredcites →https://doi.org/10.1007/s11882-019-0851-9openalex-snapshot
Birth Mode, Breastfeeding, Pet Exposure, and Antibiotic Use: Associations With the Gut Microbiome and Sensitization in Children
inferredcites →https://doi.org/10.1007/s13539-014-0135-0openalex-snapshot
Muscle wasting disease: a proposal for a new disease classification
inferredcites →https://doi.org/10.1016/0092-8674(92)90031-7openalex-snapshot
Control of the peroxisomal β-oxidation pathway by a novel family of nuclear hormone receptors
inferredcites →https://doi.org/10.1016/0960-0760(93)90058-5openalex-snapshot
Xenopus peroxisome proliferator activated receptors: Genomic organization, response element recognition, heterodimer formation with retinoid X receptor and activation by fatty acids
inferredcites →https://doi.org/10.1016/b978-0-12-391498-9.00007-3openalex-snapshot
Skeletal Muscle Degeneration and Regeneration in Mice and Flies
inferredcites →https://doi.org/10.1016/j.bbadis.2004.11.011openalex-snapshot
Roles of PPAR delta in lipid absorption and metabolism: a new target for the treatment of type 2 diabetes
inferredcites →https://doi.org/10.1016/j.bbalip.2016.09.020openalex-snapshot
Lysophosphatidylcholines activate PPARδ and protect human skeletal muscle cells from lipotoxicity
inferredcites →https://doi.org/10.1016/j.bbrc.2008.04.086openalex-snapshot
Quantitative expression patterns of peroxisome proliferator-activated receptor-β/δ (PPARβ/δ) protein in mice
inferredcites →https://doi.org/10.1016/j.bbrc.2020.09.144openalex-snapshot
Rosiglitazone ameliorates skeletal muscle insulin resistance by decreasing free fatty acids release from adipocytes
inferredcites →https://doi.org/10.1016/j.biochi.2004.09.024openalex-snapshot
Roles of peroxisome proliferator-activated receptor delta (PPARδ) in the control of fatty acid catabolism. A new target for the treatment of metabolic syndrome
inferredcites →https://doi.org/10.1016/j.biochi.2013.11.011openalex-snapshot
Peroxisome proliferator-activated receptor-α activation and excess energy burning in hepatocarcinogenesis
inferredcites →https://doi.org/10.1016/j.biochi.2016.11.010openalex-snapshot
Roles of Peroxisome Proliferator-Activated Receptor β/δ in skeletal muscle physiology
inferredcites →https://doi.org/10.1016/j.cell.2005.05.010openalex-snapshot
Stem Cell Function, Self-Renewal, and Behavioral Heterogeneity of Cells from the Adult Muscle Satellite Cell Niche
inferredcites →https://doi.org/10.1016/j.cell.2006.06.050openalex-snapshot
Nuclear Receptor Expression Links the Circadian Clock to Metabolism
inferredcites →https://doi.org/10.1016/j.cell.2013.04.020openalex-snapshot
Homeostasis in Intestinal Epithelium Is Orchestrated by the Circadian Clock and Microbiota Cues Transduced by TLRs
inferredcites →https://doi.org/10.1016/j.celrep.2016.09.010openalex-snapshot
MyoD Regulates Skeletal Muscle Oxidative Metabolism Cooperatively with Alternative NF-κB
inferredcites →https://doi.org/10.1016/j.clnu.2005.12.008openalex-snapshot
CLA and n-3 PUFA differentially modulate clinical activity and colonic PPAR-responsive gene expression in a pig model of experimental IBD
inferredcites →https://doi.org/10.1016/j.cmet.2005.01.006openalex-snapshot
A potential link between muscle peroxisome proliferator- activated receptor-α signaling and obesity-related diabetes
inferredcites →https://doi.org/10.1016/j.cmet.2006.10.003openalex-snapshot
PGC1α expression is controlled in skeletal muscles by PPARβ, whose ablation results in fiber-type switching, obesity, and type 2 diabetes
inferredcites →https://doi.org/10.1016/j.cmet.2006.12.003openalex-snapshot
The Transcriptional Coactivator PGC-1β Drives the Formation of Oxidative Type IIX Fibers in Skeletal Muscle
inferredcites →https://doi.org/10.1016/j.cmet.2008.02.005openalex-snapshot
PPARγ: Ally and Foe in Bone Metabolism
inferredcites →https://doi.org/10.1016/j.cmet.2017.04.029openalex-snapshot
PPARβ Is Essential for Maintaining Normal Levels of PGC-1α and Mitochondria and for the Increase in Muscle Mitochondria Induced by Exercise
inferredcites →https://doi.org/10.1016/j.exger.2019.110722openalex-snapshot
Muscle strength is increased in mice that are colonized with microbiota from high-functioning older adults
inferredcites →https://doi.org/10.1016/j.gde.2008.07.018openalex-snapshot
PGC-1 coactivators and skeletal muscle adaptations in health and disease
inferredcites →https://doi.org/10.1016/j.molimm.2007.04.010openalex-snapshot
Involvement of different nuclear hormone receptors in butyrate-mediated inhibition of inducible NFκB signalling
inferredcites →https://doi.org/10.1016/j.numecd.2012.02.002openalex-snapshot
Role of satellite cells in muscle growth and maintenance of muscle mass
inferredcites →https://doi.org/10.1016/j.plefa.2011.04.016openalex-snapshot
New insights into the role of PPARs
inferredcites →https://doi.org/10.1016/j.plipres.2005.12.002openalex-snapshot
From molecular action to physiological outputs: Peroxisome proliferator-activated receptors are nuclear receptors at the crossroads of key cellular functions
inferredcites →https://doi.org/10.1016/j.plipres.2016.09.001openalex-snapshot
Transcriptional control of physiological and pathological processes by the nuclear receptor PPARβ/δ
inferredcites →https://doi.org/10.1016/j.semcdb.2010.09.003openalex-snapshot
Heterogeneity in the muscle satellite cell population
inferredcites →https://doi.org/10.1016/j.tcb.2005.10.007openalex-snapshot
Stem cells in postnatal myogenesis: molecular mechanisms of satellite cell quiescence, activation and replenishment
inferredcites →https://doi.org/10.1016/j.ydbio.2004.08.015openalex-snapshot
Pax-7 up-regulation inhibits myogenesis and cell cycle progression in satellite cells: a potential mechanism for self-renewal
inferredcites →https://doi.org/10.1016/j.ydbio.2010.01.006openalex-snapshot
The depletion of skeletal muscle satellite cells with age is concomitant with reduced capacity of single progenitors to produce reserve progeny
inferredcites →https://doi.org/10.1016/s0021-9258(19)74184-2openalex-snapshot
Cloning of a new member of the peroxisome proliferator-activated receptor gene family from mouse liver.
inferredcites →https://doi.org/10.1016/s0024-3205(02)01510-2openalex-snapshot
Apoptosis induced by activation of peroxisome-proliferator activated receptor-gamma is associated with Bcl-2 and Nf-kB in human colon cancer
inferredcites →https://doi.org/10.1016/s0070-2153(05)71004-8openalex-snapshot
Muscle Stem Cells and Regenerative Myogenesis
inferredcites →https://doi.org/10.1016/s0092-8674(00)00066-0openalex-snapshot
Pax7 Is Required for the Specification of Myogenic Satellite Cells
inferredcites →https://doi.org/10.1016/s0092-8674(03)00269-1openalex-snapshot
Peroxisome-Proliferator-Activated Receptor δ Activates Fat Metabolism to Prevent Obesity
inferredcites →https://doi.org/10.1038/25931openalex-snapshot
Ligand binding and co-activator assembly of the peroxisome proliferator-activated receptor-γ
inferredcites →https://doi.org/10.1038/347645a0openalex-snapshot
Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators
inferredcites →https://doi.org/10.1038/35013000openalex-snapshot
Roles of PPARs in health and disease
inferredcites →https://doi.org/10.1038/384266a0openalex-snapshot
Muscle progenitor cells failing to respond to positional cues adopt non-myogenic fates in myf-5 null mice
inferredcites →https://doi.org/10.1038/labinvest.3700185openalex-snapshot
Role of endogenous and exogenous ligands for the peroxisome proliferators activated receptors alpha (PPAR-α) in the development of inflammatory bowel disease in mice
inferredcites →https://doi.org/10.1038/nature00904openalex-snapshot
Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres
inferredcites →https://doi.org/10.1038/nature03572openalex-snapshot
A common somitic origin for embryonic muscle progenitors and satellite cells
inferredcites →https://doi.org/10.1038/nature03594openalex-snapshot
A Pax3/Pax7-dependent population of skeletal muscle progenitor cells
inferredcites →https://doi.org/10.1038/nature11053openalex-snapshot
Human gut microbiome viewed across age and geography
inferredcites →https://doi.org/10.1038/ncomms8486openalex-snapshot
Metabolic and metagenomic outcomes from early-life pulsed antibiotic treatment
inferredcites →https://doi.org/10.1038/nm1672openalex-snapshot
PPAR-γ regulates osteoclastogenesis in mice
inferredcites →https://doi.org/10.1038/nm956openalex-snapshot
Muscle-specific Pparg deletion causes insulin resistance
inferredcites →https://doi.org/10.1038/s41591-019-0485-4openalex-snapshot
Meta-omics analysis of elite athletes identifies a performance-enhancing microbe that functions via lactate metabolism
inferredcites →https://doi.org/10.1038/sj.emboj.7600209openalex-snapshot
In vivo activation of PPAR target genes by RXR homodimers
inferredcites →https://doi.org/10.1038/srep09884openalex-snapshot
A metabolomic study of the PPARδ agonist GW501516 for enhancing running endurance in Kunming mice
inferredcites →https://doi.org/10.1038/srep31786openalex-snapshot
Gut microbiota can transfer fiber characteristics and lipid metabolic profiles of skeletal muscle from pigs to germ-free mice
inferredcites →https://doi.org/10.1038/srep36937openalex-snapshot
Intestinal PPARγ signalling is required for sympathetic nervous system activation in response to caloric restriction
inferredcites →https://doi.org/10.1038/srep43199openalex-snapshot
Commensal gut bacteria modulate phosphorylation-dependent PPARγ transcriptional activity in human intestinal epithelial cells
inferredcites →https://doi.org/10.1042/bj20041150openalex-snapshot
CLOCK is involved in the circadian transactivation of peroxisome-proliferator-activated receptor α (PPARα) in mice
inferredcites →https://doi.org/10.1042/cs20080022openalex-snapshot
Role of peroxisome-proliferator-activated receptor β/δ (PPARβ/δ) in gastrointestinal tract function and disease
inferredcites →https://doi.org/10.1046/j.1469-7580.2003.00139.xopenalex-snapshot
The formation of skeletal muscle: from somite to limb
inferredcites →https://doi.org/10.1053/j.gastro.2006.05.004openalex-snapshot
PPARβ/δ Regulates Paneth Cell Differentiation Via Controlling the Hedgehog Signaling Pathway
inferredcites →https://doi.org/10.1053/j.gastro.2007.12.012openalex-snapshot
Rosiglitazone for Active Ulcerative Colitis: A Randomized Placebo-Controlled Trial
inferredcites →https://doi.org/10.1053/j.gastro.2008.07.007openalex-snapshot
Lactobacillus crispatus M247-Derived H2O2 Acts as a Signal Transducing Molecule Activating Peroxisome Proliferator Activated Receptor-γ in the Intestinal Mucosa
inferredcites →https://doi.org/10.1053/j.gastro.2011.01.045openalex-snapshot
PPARβ/δ Activation Induces Enteroendocrine L Cell GLP-1 Production
inferredcites →https://doi.org/10.1056/nejm199001253220403openalex-snapshot
Quantitation of Muscle Glycogen Synthesis in Normal Subjects and Subjects with Non-Insulin-Dependent Diabetes by13C Nuclear Magnetic Resonance Spectroscopy
inferredcites →https://doi.org/10.1073/pnas.0407076101openalex-snapshot
The gut microbiota as an environmental factor that regulates fat storage
inferredcites →https://doi.org/10.1073/pnas.0711734105openalex-snapshot
Enterococcus faecalis from newborn babies regulate endogenous PPARγ activity and IL-10 levels in colonic epithelial cells
inferredcites →https://doi.org/10.1073/pnas.0905745107openalex-snapshot
Peroxisome proliferator-activated receptor gamma activation is required for maintenance of innate antimicrobial immunity in the colon
inferredcites →https://doi.org/10.1073/pnas.0932671100openalex-snapshot
Expression of utrophin A mRNA correlates with the oxidative capacity of skeletal muscle fiber types and is regulated by calcineurin/NFAT signaling
inferredcites →https://doi.org/10.1073/pnas.1232352100openalex-snapshot
An autoregulatory loop controls peroxisome proliferator-activated receptor γ coactivator 1α expression in muscle
inferredcites →https://doi.org/10.1073/pnas.1307680110openalex-snapshot
Pax7 is critical for the normal function of satellite cells in adult skeletal muscle
inferredcites →https://doi.org/10.1073/pnas.1714703115openalex-snapshot
Fenofibrate prevents skeletal muscle loss in mice with lung cancer
inferredcites →https://doi.org/10.1073/pnas.2536828100openalex-snapshot
Adipose-specific peroxisome proliferator-activated receptor γ knockout causes insulin resistance in fat and liver but not in muscle
inferredcites →https://doi.org/10.1073/pnas.90.4.1440openalex-snapshot
Interaction of the peroxisome-proliferator-activated receptor and retinoid X receptor.
inferredcites →https://doi.org/10.1073/pnas.91.15.7355openalex-snapshot
Differential expression and activation of a family of murine peroxisome proliferator-activated receptors.
inferredcites →https://doi.org/10.1073/pnas.92.17.7921openalex-snapshot
Structural organization of mouse peroxisome proliferator-activated receptor gamma (mPPAR gamma) gene: alternative promoter use and different splicing yield two mPPAR gamma isoforms.
inferredcites →https://doi.org/10.1074/jbc.272.32.20108openalex-snapshot
Polarity and Specific Sequence Requirements of Peroxisome Proliferator-activated Receptor (PPAR)/Retinoid X Receptor Heterodimer Binding to DNA
inferredcites →https://doi.org/10.1074/jbc.m109.008797openalex-snapshot
PPARδ Agonism Activates Fatty Acid Oxidation via PGC-1α but Does Not Increase Mitochondrial Gene Expression and Function
inferredcites →https://doi.org/10.1074/jbc.m203997200openalex-snapshot
Fatty Acid Homeostasis and Induction of Lipid Regulatory Genes in Skeletal Muscles of Peroxisome Proliferator-activated Receptor (PPAR) α Knock-out Mice
inferredcites →https://doi.org/10.1074/jbc.m706478200openalex-snapshot
CD36-dependent Regulation of Muscle FoxO1 and PDK4 in the PPARδ/β-mediated Adaptation to Metabolic Stress
inferredcites →https://doi.org/10.1080/13543776.2020.1703952openalex-snapshot
Peroxisome proliferator-activated receptor agonists and antagonists: a patent review (2014-present)
inferredcites →https://doi.org/10.1080/14653240701508437openalex-snapshot
Activated β-catenin induces myogenesis and inhibits adipogenesis in BM-derived mesenchymal stromal cells
inferredcites →https://doi.org/10.1083/jcb.200508001openalex-snapshot
Distinct roles for Pax7 and Pax3 in adult regenerative myogenesis
inferredcites →https://doi.org/10.1083/jcb.9.2.493openalex-snapshot
SATELLITE CELL OF SKELETAL MUSCLE FIBERS
inferredcites →https://doi.org/10.1089/scd.2007.0058openalex-snapshot
Skeletal Muscle Development and Regeneration
inferredcites →https://doi.org/10.1093/cvr/cvp106openalex-snapshot
Peroxisome proliferator-activated receptor β stimulation induces rapid cardiac growth and angiogenesis via direct activation of calcineurin
inferredcites →https://doi.org/10.1093/hmg/ddi303openalex-snapshot
Bezafibrate increases very-long-chain acyl-CoA dehydrogenase protein and mRNA expression in deficient fibroblasts and is a potential therapy for fatty acid oxidation disorders
inferredcites →https://doi.org/10.1093/hmg/ddp431openalex-snapshot
Pharmacological activation of PPAR / stimulates utrophin A expression in skeletal muscle fibers and restores sarcolemmal integrity in mature mdx mice
inferredcites →https://doi.org/10.1096/fj.03-0269fjeopenalex-snapshot
Peroxisome proliferator‐activated receptor δ controls muscle development and oxydative capability
inferredcites →https://doi.org/10.1096/fj.11-194019openalex-snapshot
Sustained activation of PPARα by endogenous ligands increases hepatic fatty acid oxidation and prevents obesity in ob/ob mice
inferredcites →https://doi.org/10.1096/fj.201801209ropenalex-snapshot
Gut microbiome catabolites as novel modulators of muscle cell glucose metabolism
inferredcites →https://doi.org/10.1096/fj.201802681rropenalex-snapshot
The PPAR–microbiota–metabolic organ trilogy to fine‐tune physiology
inferredcites →https://doi.org/10.1097/mco.0b013e328336ea98openalex-snapshot
Muscle stem cells in developmental and regenerative myogenesis
inferredcites →https://doi.org/10.1097/shk.0b013e318033eb29openalex-snapshot
ABSENCE OF FUNCTIONAL PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-α ENHANCED ILEUM PERMEABILITY DURING EXPERIMENTAL COLITIS
inferredcites →https://doi.org/10.1097/shk.0b013e31818339e7openalex-snapshot
PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-α MODULATES THE ANTI-INFLAMMATORY EFFECT OF GLUCOCORTICOIDS IN A MODEL OF INFLAMMATORY BOWEL DISEASE IN MICE
inferredcites →https://doi.org/10.1101/gad.1419406openalex-snapshot
Muscle stem cells in development, regeneration, and disease
inferredcites →https://doi.org/10.1101/gad.8.10.1224openalex-snapshot
mPPAR gamma 2: tissue-specific regulator of an adipocyte enhancer.
inferredcites →https://doi.org/10.1101/sqb.2008.73.064openalex-snapshot
The Molecular Regulation of Muscle Stem Cell Function
inferredcites →https://doi.org/10.1111/j.1365-2796.2009.02158.xopenalex-snapshot
Skeletal muscle stem cells in developmental versus regenerative myogenesis
inferredcites →https://doi.org/10.1124/mol.53.1.14openalex-snapshot
Peroxisome Proliferator Activated Receptor-α Expression in Human Liver
inferredcites →https://doi.org/10.1124/pr.112.006833openalex-snapshot
Nuclear Receptors and Their Selective Pharmacologic Modulators
inferredcites →https://doi.org/10.1126/science.294.5548.1866openalex-snapshot
Nuclear Receptors and Lipid Physiology: Opening the X-Files
inferredcites →https://doi.org/10.1126/science.aam9949openalex-snapshot
Microbiota-activated PPAR-γ signaling inhibits dysbiotic Enterobacteriaceae expansion
inferredcites →https://doi.org/10.1126/scitranslmed.aan5662openalex-snapshot
The gut microbiota influences skeletal muscle mass and function in mice
inferredcites →https://doi.org/10.1128/mbio.01438-14openalex-snapshot
Differential Modulation by Akkermansia muciniphila and Faecalibacterium prausnitzii of Host Peripheral Lipid Metabolism and Histone Acetylation in Mouse Gut Organoids
inferredcites →https://doi.org/10.1128/mcb.18.6.3483openalex-snapshot
Transactivation by Retinoid X Receptor–Peroxisome Proliferator-Activated Receptor γ (PPARγ) Heterodimers: Intermolecular Synergy Requires Only the PPARγ Hormone-Dependent Activation Function
inferredcites →https://doi.org/10.1136/gutjnl-2016-312297openalex-snapshot
Antibiotics as deep modulators of gut microbiota: between good and evil
inferredcites →https://doi.org/10.1152/ajpendo.00446.2009openalex-snapshot
Selective activation of PPARγ in skeletal muscle induces endogenous production of adiponectin and protects mice from diet-induced insulin resistance
inferredcites →https://doi.org/10.1152/ajpendo.00510.2018openalex-snapshot
Microbiome potentiates endurance exercise through intestinal acetate production
inferredcites →https://doi.org/10.1152/ajpendo.00521.2018openalex-snapshot
Gut bacteria are critical for optimal muscle function: a potential link with glucose homeostasis
inferredcites →https://doi.org/10.1152/ajpendo.00581.2007openalex-snapshot
Pharmacological activation of PPARβ promotes rapid and calcineurin-dependent fiber remodeling and angiogenesis in mouse skeletal muscle
inferredcites →https://doi.org/10.1152/ajpendo.00586.2014openalex-snapshot
Inactivation of PPARβ/δ adversely affects satellite cells and reduces postnatal myogenesis
inferredcites →https://doi.org/10.1152/ajpregu.2001.280.3.r661openalex-snapshot
Muscle fiber type comparison of PDH kinase activity and isoform expression in fed and fasted rats
inferredcites →https://doi.org/10.1152/jappl.2000.89.2.465openalex-snapshot
Estimation of skeletal muscle mass by bioelectrical impedance analysis
inferredcites →https://doi.org/10.1152/japplphysiol.01318.2003openalex-snapshot
Pyruvate dehydrogenase activation and kinase expression in human skeletal muscle during fasting
inferredcites →https://doi.org/10.1152/physrev.00025.2005openalex-snapshot
Transcriptional Regulation of Metabolism
inferredcites →https://doi.org/10.1152/physrev.00027.2013openalex-snapshot
Physiological Functions of Peroxisome Proliferator-Activated Receptor β
inferredcites →https://doi.org/10.1152/physrev.00031.2010openalex-snapshot
Fiber Types in Mammalian Skeletal Muscles
inferredcites →https://doi.org/10.1155/2007/93416openalex-snapshot
Involvement of PPARs in Cell Proliferation and Apoptosis in Human Colon Cancer Specimens and in Normal and Cancer Cell Lines
inferredcites →https://doi.org/10.1155/2010/917312openalex-snapshot
PPAR- α Contributes to the Anti-Inflammatory Activity of Verbascoside in a Model of Inflammatory Bowel Disease in Mice
inferredcites →https://doi.org/10.1155/2012/620839openalex-snapshot
PPARγin Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1155/2018/7026198openalex-snapshot
Gut Dysbiosis and Muscle Aging: Searching for Novel Targets against Sarcopenia
inferredcites →https://doi.org/10.1159/000447628openalex-snapshot
PPAR Agonists Promote the Differentiation of Porcine Bone Marrow Mesenchymal Stem Cells into the Adipogenic and Myogenic Lineages
inferredcites →https://doi.org/10.1172/jci17305openalex-snapshot
Muscle-specific PPARγ-deficient mice develop increased adiposity and insulin resistance but respond to thiazolidinediones
inferredcites →https://doi.org/10.1172/jci7145openalex-snapshot
A novel therapy for colitis utilizing PPAR-γ ligands to inhibit the epithelial inflammatory response
inferredcites →https://doi.org/10.1177/002215540405200205openalex-snapshot
Frequency of M-Cadherin-stained Satellite Cells Declines in Human Muscles During Aging
inferredcites →https://doi.org/10.1177/1535370217749494openalex-snapshot
Myogenic regulatory factors: The orchestrators of myogenesis after 30 years of discovery
inferredcites →https://doi.org/10.1186/2044-5040-1-33openalex-snapshot
PPARδ regulates satellite cell proliferation and skeletal muscle regeneration
inferredcites →https://doi.org/10.1203/01.pdr.0000083001.91588.bbopenalex-snapshot
Correction of Fatty Acid Oxidation in Carnitine Palmitoyl Transferase 2–Deficient Cultured Skin Fibroblasts by Bezafibrate
inferredcites →https://doi.org/10.1210/edrv.20.5.0380openalex-snapshot
Peroxisome Proliferator-Activated Receptors: Nuclear Control of Metabolism
inferredcites →https://doi.org/10.1210/endo.137.1.8536636openalex-snapshot
Differential expression of peroxisome proliferator-activated receptors (PPARs): tissue distribution of PPAR-alpha, -beta, and -gamma in the adult rat
inferredcites →https://doi.org/10.1210/endo.139.6.6049openalex-snapshot
Differential Expression of Peroxisome Proliferator-Activated Receptor- , - , and - during Rat Embryonic Development
inferredcites →https://doi.org/10.1210/me.2003-0151openalex-snapshot
The Peroxisome Proliferator-Activated Receptor β/δ Agonist, GW501516, Regulates the Expression of Genes Involved in Lipid Catabolism and Energy Uncoupling in Skeletal Muscle Cells
inferredcites →https://doi.org/10.1210/me.2006-0052openalex-snapshot
Reciprocal Regulation of Brain and Muscle Arnt-Like Protein 1 and Peroxisome Proliferator-Activated Receptor α Defines a Novel Positive Feedback Loop in the Rodent Liver Circadian Clock
inferredcites →https://doi.org/10.1242/dev.120.3.603openalex-snapshot
Pax-3 is required for the development of limb muscles: a possible role for the migration of dermomyotomal muscle progenitor cells
inferredcites →https://doi.org/10.1242/dev.124.8.1601openalex-snapshot
Location and growth of epaxial myotome precursor cells
inferredcites →https://doi.org/10.1242/dev.125.21.4259openalex-snapshot
The cellular mechanism by which the dermomyotome contributes to the second wave of myotome development
inferredcites →https://doi.org/10.1242/dev.151035openalex-snapshot
Making muscle: skeletal myogenesis in vivo and in vitro
inferredcites →https://doi.org/10.1242/dev.167197openalex-snapshot
Prepubertal skeletal muscle growth requires Pax7-expressing satellite cell-derived myonuclear contribution
inferredcites →https://doi.org/10.1242/jcs.114.2.303openalex-snapshot
A calcineurin- and NFAT-dependent pathway regulates Myf5 gene expression in skeletal muscle reserve cells
inferredcites →https://doi.org/10.1249/00005768-198004001-00180openalex-snapshot
SATELLITE CELL AND GROWTH FACTOR INVOLVEMENT IN SKELETAL MUSCLE GROWTH.
inferredcites →https://doi.org/10.1249/00005768-198910001-00007openalex-snapshot
Satellite cell and growth factor involvement in skeletal muscle growth
inferredcites →https://doi.org/10.1371/journal.pbio.0020294openalex-snapshot
Regulation of Muscle Fiber Type and Running Endurance by PPARδ
inferredcites →https://doi.org/10.1371/journal.pmed.0020161openalex-snapshot
Derivation of Multipotent Mesenchymal Precursors from Human Embryonic Stem Cells
inferredcites →https://doi.org/10.1371/journal.pone.0011307openalex-snapshot
Postnatal PPARδ Activation and Myostatin Inhibition Exert Distinct yet Complimentary Effects on the Metabolic Profile of Obese Insulin-Resistant Mice
inferredcites →https://doi.org/10.1371/journal.pone.0080628openalex-snapshot
Mechanisms Regulating GLUT4 Transcription in Skeletal Muscle Cells Are Highly Conserved across Vertebrates
inferredcites →https://doi.org/10.1371/journal.pone.0125371openalex-snapshot
Commensal Streptococcus salivarius Modulates PPARγ Transcriptional Activity in Human Intestinal Epithelial Cells
inferredcites →https://doi.org/10.1371/journal.ppat.1003887openalex-snapshot
Absence of Intestinal PPARγ Aggravates Acute Infectious Colitis in Mice through a Lipocalin-2–Dependent Pathway
inferredcites →https://doi.org/10.14814/phy2.12625openalex-snapshot
Combined pharmacological activation of AMPK and PPARδpotentiates the effects of exercise in trained mice
inferredcites →https://doi.org/10.1515/hmbci.2010.076openalex-snapshot
Peroxisome proliferator-activated receptor β/δ: a master regulator of metabolic pathways in skeletal muscle
inferredcites →https://doi.org/10.1621/nrs.08002openalex-snapshot
PPARα: Energy Combustion, Hypolipidemia, Inflammation and Cancer
inferredcites →https://doi.org/10.22029/eir.2019.1723openalex-snapshot
Exercise and immune system as modulators of intestinal microbiome: implications for the gut-muscle axis hypothesis
inferredcites →https://doi.org/10.2337/db08-1637openalex-snapshot
Butyrate Improves Insulin Sensitivity and Increases Energy Expenditure in Mice
inferredcites →https://doi.org/10.2337/db15-1670openalex-snapshot
Bezafibrate Improves Insulin Sensitivity and Metabolic Flexibility in STZ-Induced Diabetic Mice
inferredcites →https://doi.org/10.2337/diab.30.12.1000openalex-snapshot
The Effect of Insulin on the Disposal of Intravenous Glucose: Results from Indirect Calorimetry and Hepatic and Femoral Venous Catheterization
inferredcites →https://doi.org/10.2337/diabetes.52.12.2874openalex-snapshot
Endurance Training in Humans Leads to Fiber Type-Specific Increases in Levels of Peroxisome Proliferator-Activated Receptor-γ Coactivator-1 and Peroxisome Proliferator-Activated Receptor-α in Skeletal Muscle
inferredcites →https://doi.org/10.23736/s1121-421x.18.02511-4openalex-snapshot
Skeletal muscle-gut axis: emerging mechanisms of sarcopenia for intestinal and extra intestinal diseases
inferredcites →https://doi.org/10.3181/00379727-181-42296openalex-snapshot
Cell-Mediated Immune Responses to Chlamydia trachomatis in Mothers and Infants
inferredcites →https://doi.org/10.3389/fendo.2019.00255openalex-snapshot
Osteoporosis and Sarcopenia Increase Frailty Syndrome in the Elderly
inferredcites →https://doi.org/10.3389/fmicb.2017.01162openalex-snapshot
Geography, Ethnicity or Subsistence-Specific Variations in Human Microbiome Composition and Diversity
inferredcites →https://doi.org/10.3389/fmicb.2019.01906openalex-snapshot
Investigation of the Effects of Microbiota on Exercise Physiological Adaption, Performance, and Energy Utilization Using a Gnotobiotic Animal Model
inferredcites →https://doi.org/10.3389/fphys.2018.00112openalex-snapshot
Obesity, Metabolic Syndrome, and Musculoskeletal Disease: Common Inflammatory Pathways Suggest a Central Role for Loss of Muscle Integrity
inferredcites →https://doi.org/10.3389/fphys.2019.01435openalex-snapshot
The Role of the Gut Microbiome on Skeletal Muscle Mass and Physical Function: 2019 Update
inferredcites →https://doi.org/10.3390/cells9020352openalex-snapshot
PPAR-Mediated Toxicology and Applied Pharmacology
inferredcites →https://doi.org/10.3390/cells9051133openalex-snapshot
PPAR Beta/Delta and the Hallmarks of Cancer
inferredcites →https://doi.org/10.3390/cells9071638openalex-snapshot
Peroxisome Proliferator-Activated Receptors and Their Novel Ligands as Candidates for the Treatment of Non-Alcoholic Fatty Liver Disease
inferredcites →https://doi.org/10.3390/ijms19051425openalex-snapshot
An aPPARent Functional Consequence in Skeletal Muscle Physiology via Peroxisome Proliferator-Activated Receptors
inferredcites →https://doi.org/10.3390/ijms19082210openalex-snapshot
Enteric Microbiota–Gut–Brain Axis from the Perspective of Nuclear Receptors
inferredcites →https://doi.org/10.3390/ijms19082418openalex-snapshot
Metronidazole Causes Skeletal Muscle Atrophy and Modulates Muscle Chronometabolism
inferredcites →https://doi.org/10.3390/ijms20205055openalex-snapshot
Exploration and Development of PPAR Modulators in Health and Disease: An Update of Clinical Evidence
inferredcites →https://doi.org/10.3390/ijms21051830openalex-snapshot
Stem Cell Aging in Skeletal Muscle Regeneration and Disease
inferredcites →https://doi.org/10.3390/ijms21072277openalex-snapshot
At the Crossroads of the Adipocyte and Osteoclast Differentiation Programs: Future Therapeutic Perspectives
inferredcites →https://doi.org/10.3390/ijms21165723openalex-snapshot
PPARs and Angiogenesis—Implications in Pathology
inferredcites →https://doi.org/10.3390/nu10070929openalex-snapshot
Dietary Protein and Muscle in Aging People: The Potential Role of the Gut Microbiome
inferredcites →https://doi.org/10.3390/nu11071633openalex-snapshot
Gut Microbiota, Muscle Mass and Function in Aging: A Focus on Physical Frailty and Sarcopenia
inferredcites →https://doi.org/10.3390/nu9121303openalex-snapshot
Aging Gut Microbiota at the Cross-Road between Nutrition, Physical Frailty, and Sarcopenia: Is There a Gut–Muscle Axis?
inferredcites →https://doi.org/10.4049/jimmunol.1501489openalex-snapshot
Homeostatic PPARα Signaling Limits Inflammatory Responses to Commensal Microbiota in the Intestine
inferredcites →https://doi.org/10.5604/20831862.1180170openalex-snapshot
Sports genetics: the PPARA gene and athletes' high ability in endurance sports. A systematic review and meta-analysis.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Exposure to per- and polyfluoroalkyl substances and body composition in US adolescents aged 12-18 years: an analysis of data from the National Health and Nutrition Examination Surveys 2011-2018
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Hyperacmotone A alleviates Non-alcoholic Steatohepatitis via regulating PPARα signaling
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Metabolic, neurotoxic and immunotoxic effects of PFAAs and their mixtures on the proteome of the head kidney and plasma from rainbow trout (Oncorhynchus mykiss)
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Effects of high-/low-temperature and high-altitude hypoxic environments on gut microbiota of sports people: A retrospective analysis
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Single-Nucleus RNA Sequencing Reveals Cellular Heterogeneity and Trajectories of Lineage Differentiation during Chicken Skeletal Muscle Development
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Computational Screening and Experimental Validation of Natural Compounds that Enhance Butyrate Production in Gut Bacteria and Promote Muscle Cell Mass
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Cannabigerol Enhances Muscle Strength and Performance in Dexamethasone-Treated Mice
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Cellular senescence in musculoskeletal homeostasis, diseases, and regeneration
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Skeletal muscle gene expression dysregulation in long-term spaceflights and aging is clock-dependent
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Gut microbiota and its metabolites: Bridge of dietary nutrients and obesity-related diseases
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Kcnma1 is involved in mitochondrial homeostasis in diabetes‐related skeletal muscle atrophy
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Intermittent fasting—the future treatment in NASH patients?
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Time‐dependent reduction in oxidative capacity among cultured myotubes from spinal cord injured individuals
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Potential Therapeutic Effects of Short-Chain Fatty Acids on Chronic Pain
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Axis “microbiota - muscle”
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Sarcopenia and non-alcoholic fatty liver disease
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Sarcopenia in patients with non-alcoholic fatty liver disease: pathogenesis, diagnosis and treatment (expert opinion)
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PPARγ: a key orchestrator of epidermal barrier, immune responses, and lipid metabolism in atopic dermatitis pathogenesis and therapy
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Targeting nuclear receptors in muscular dystrophies and regenerative myogenesis
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The role of PPARγ in cancer cachexia: friend or foe?
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Multi-omics integration reveals the role of PFOS in sarcopenia via ESRRG and RBP4: from computational prediction to experimental validation
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Untargeted Metabolomic Characteristics of Skeletal Muscle Dysfunction in Rabbits Induced by a High Fat Diet
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Identification of miRNA–mRNA Networks Associated with Pigeon Skeletal Muscle Development and Growth
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Long-Term Tetrabromobisphenol A Exposure Induces Gut Microbiota Imbalance and Metabolic Disorders via the Peroxisome Proliferator-Activated Receptor Signaling Pathway in the Regenerated Gut of Apostichopus japonicus
inferred← citeshttps://doi.org/10.3390/biom12020191openalex-snapshot
miR-27b-3p Attenuates Muscle Atrophy by Targeting Cbl-b in Skeletal Muscles
inferred← citeshttps://doi.org/10.3390/biom14020207openalex-snapshot
Inspiring Tactics with the Improvement of Mitophagy and Redox Balance for the Development of Innovative Treatment against Polycystic Kidney Disease
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Molecular Mechanisms and Current Treatment Options for Cancer Cachexia
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Palmitoylethanolamide: A Natural Compound for Health Management
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inferred← citeshttps://doi.org/10.3390/livers4040035openalex-snapshot
Sarcopenia and Metabolic Dysfunction-Associated Steatotic Liver Disease: A Narrative Review
inferred← citeshttps://doi.org/10.3390/metabo15070472openalex-snapshot
Aerobic Exercise Delays Age-Related Sarcopenia in Mice via Alleviating Imbalance in Mitochondrial Quality Control
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A Narrative Review on the Impact of Probiotic Supplementation on Muscle Development, Metabolic Regulation, and Fiber Traits Related to Meat Quality in Broiler Chickens
inferred← citeshttps://doi.org/10.3390/nu12113476openalex-snapshot
Peroxisome Proliferator-Activated Receptors as Molecular Links between Caloric Restriction and Circadian Rhythm
inferred← citeshttps://doi.org/10.3390/nu15143224openalex-snapshot
The Influence of the Mediterranean Dietary Pattern on Osteoporosis and Sarcopenia
inferred← citeshttps://doi.org/10.4081/ejtm.2022.10695openalex-snapshot
Immodulin peptides influence musculoskeletal homeostasis by linking extracellular cues to macrophage and myoblast nuclear receptors
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Catalpa bignonioides extract improves exercise performance through regulation of growth and metabolism in skeletal muscles
inferred← citeshttps://doi.org/10.4236/abc.2025.153005openalex-snapshot
Piceatannol Enhances Intracellular Energy Metabolism via SIRT1 in C2C12 Cells
inferred← citeshttps://doi.org/10.4236/ojas.2022.123033openalex-snapshot
Transcriptional Features of Cattle Visceral and Subcutaneous Adipose Tissues: A Study of RNA-seq
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767519openalex-snapshot
Additional file 1 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767522openalex-snapshot
Additional file 2 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767525openalex-snapshot
Additional file 3 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767528openalex-snapshot
Additional file 4 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767531openalex-snapshot
Additional file 5 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767534openalex-snapshot
Additional file 6 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767537openalex-snapshot
Additional file 7 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767540openalex-snapshot
Additional file 8 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767543openalex-snapshot
Additional file 9 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767546openalex-snapshot
Additional file 10 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767549openalex-snapshot
Additional file 11 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767552openalex-snapshot
Additional file 12 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.22767555openalex-snapshot
Additional file 13 of Transcriptome-wide analysis of RNA m6A methylation regulation of muscle development in Queshan Black pigs
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