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Impaired exercise tolerance, mitochondrial biogenesis, and muscle fiber maintenance in miR‐133a–deficient mice

https://doi.org/10.1096/fj.201600529r

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1 of the 60 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1096/fj.05-3993fje (notice 2009-07-29).

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What this work says

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

inferredcites →https://doi.org/10.1002/jcp.20696openalex-snapshot

Regulation of phosphatidylinositol 3‐kinase (PI3K)/Akt and nuclear factor‐kappa B signaling pathways in dystrophin‐deficient skeletal muscle in response to mechanical stretch

inferredcites →https://doi.org/10.1007/s00421-010-1545-0openalex-snapshot

The muscle fiber type–fiber size paradox: hypertrophy or oxidative metabolism?

inferredcites →https://doi.org/10.1007/s00424-014-1517-zopenalex-snapshot

MicroRNA-23a has minimal effect on endurance exercise-induced adaptation of mouse skeletal muscle

inferredcites →https://doi.org/10.1016/0034-5687(94)90122-8openalex-snapshot

Metabolic and antioxidant enzyme activities in the diaphragm: effects of acute exercise

inferredcites →https://doi.org/10.1016/bs.pmbts.2015.07.016openalex-snapshot

Endurance Exercise and the Regulation of Skeletal Muscle Metabolism

inferredcites →https://doi.org/10.1016/j.abb.2014.08.013openalex-snapshot

Insulin inhibits AMPK activity and phosphorylates AMPK Ser485/491 through Akt in hepatocytes, myotubes and incubated rat skeletal muscle

inferredcites →https://doi.org/10.1016/j.bbagrm.2008.03.001openalex-snapshot

MicroRNA-206: The skeletal muscle-specific myomiR

inferredcites →https://doi.org/10.1016/j.cell.2010.02.026openalex-snapshot

Mitochondrial Fusion Is Required for mtDNA Stability in Skeletal Muscle and Tolerance of mtDNA Mutations

inferredcites →https://doi.org/10.1016/j.cmet.2013.01.004openalex-snapshot

MicroRNA-133 Controls Brown Adipose Determination in Skeletal Muscle Satellite Cells by Targeting Prdm16

inferredcites →https://doi.org/10.1016/j.devcel.2009.10.013openalex-snapshot

A Family of microRNAs Encoded by Myosin Genes Governs Myosin Expression and Muscle Performance

inferredcites →https://doi.org/10.1016/j.tig.2008.01.007openalex-snapshot

MicroRNAs flex their muscles

inferredcites →https://doi.org/10.1016/s0092-8674(04)00045-5openalex-snapshot

MicroRNAs

inferredcites →https://doi.org/10.1023/a:1006868130002openalex-snapshot

Impaired mitochondrial oxidative phosphorylation in skeletal muscle of the dystrophin-deficient mdx mouse

inferredcites →https://doi.org/10.1038/cdd.2014.150openalex-snapshot

Oxidative stress and autophagy: the clash between damage and metabolic needs

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/nature02871openalex-snapshot

The functions of animal microRNAs

inferredcites →https://doi.org/10.1038/nature03817openalex-snapshot

Serum response factor regulates a muscle-specific microRNA that targets Hand2 during cardiogenesis

inferredcites →https://doi.org/10.1038/nature05861openalex-snapshot

Akt/PKB regulates hepatic metabolism by directly inhibiting PGC-1α transcription coactivator

inferredcites →https://doi.org/10.1038/ng1725openalex-snapshot

The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation

inferredcites →https://doi.org/10.1042/bj20081386openalex-snapshot

How mitochondria produce reactive oxygen species

inferredcites →https://doi.org/10.1042/bse0470069openalex-snapshot

Regulation of mitochondrial biogenesis

inferredcites →https://doi.org/10.1073/pnas.0710558105openalex-snapshot

An intragenic MEF2-dependent enhancer directs muscle-specific expression of microRNAs 1 and 133

inferredcites →https://doi.org/10.1073/pnas.1000300107openalex-snapshot

Regulation of PI3-kinase/Akt signaling by muscle-enriched microRNA-486

inferredcites →https://doi.org/10.1073/pnas.96.13.7421openalex-snapshot

Protein kinase B/Akt-mediated phosphorylation promotes nuclear exclusion of the winged helix transcription factor FKHR1

inferredcites →https://doi.org/10.1073/pnas.96.21.11836openalex-snapshot

Regulation of nuclear translocation of Forkhead transcription factor AFX by protein kinase B

inferredcites →https://doi.org/10.1074/jbc.274.24.17179openalex-snapshot

Phosphorylation of the Transcription Factor Forkhead Family Member FKHR by Protein Kinase B

inferredcites →https://doi.org/10.1074/jbc.m704817200openalex-snapshot

Skeletal Muscle Fiber-type Switching, Exercise Intolerance, and Myopathy in PGC-1α Muscle-specific Knock-out Animals

inferredcites →https://doi.org/10.1083/jcb.200603008openalex-snapshot

Muscle-specific microRNA miR-206 promotes muscle differentiation

inferredcites →https://doi.org/10.1083/jcb.200903131openalex-snapshot

Muscle inactivation of mTOR causes metabolic and dystrophin defects leading to severe myopathy

inferredcites →https://doi.org/10.1083/jcb.201406068openalex-snapshot

Thyroid hormone regulates muscle fiber type conversion via miR-133a1

inferredcites →https://doi.org/10.1096/fj.05-3993fjeopenalex-snapshot

PGC‐1α gene expression is down‐regulated by Akt‐mediated phosphorylation and nuclear exclusion of FoxO1 in insulin‐stimulated skeletal muscle

inferredcites →https://doi.org/10.1096/fj.05-4809fjeopenalex-snapshot

Early signaling responses to divergent exercise stimuli in skeletal muscle from well‐trained humans

inferredcites →https://doi.org/10.1096/fj.15-276337openalex-snapshot

Molecular mechanisms for mitochondrial adaptation to exercise training in skeletal muscle

inferredcites →https://doi.org/10.1101/gad.1738708openalex-snapshot

microRNA-133a regulates cardiomyocyte proliferation and suppresses smooth muscle gene expression in the heart

inferredcites →https://doi.org/10.1113/jphysiol.2004.080663openalex-snapshot

Age is no barrier to muscle structural, biochemical and angiogenic adaptations to training up to 24 months in female rats

inferredcites →https://doi.org/10.1113/jphysiol.2008.153916openalex-snapshot

Differential effects of resistance and endurance exercise in the fed state on signalling molecule phosphorylation and protein synthesis in human muscle

inferredcites →https://doi.org/10.1113/jphysiol.2010.189860openalex-snapshot

Muscle specific microRNAs are regulated by endurance exercise in human skeletal muscle

inferredcites →https://doi.org/10.1113/jphysiol.2013.255695openalex-snapshot

Regulation of miRNAs in human skeletal muscle following acute endurance exercise and short‐term endurance training

inferredcites →https://doi.org/10.1126/science.286.5441.950openalex-snapshot

A Species of Small Antisense RNA in Posttranscriptional Gene Silencing in Plants

inferredcites →https://doi.org/10.1139/h02-023openalex-snapshot

The Adaptive Potential of Skeletal Muscle Fibers

inferredcites →https://doi.org/10.1152/ajpcell.00402.2005openalex-snapshot

Type II skeletal myofibers possess unique properties that potentiate mitochondrial H2O2 generation

inferredcites →https://doi.org/10.1152/ajpendo.00076.2009openalex-snapshot

PGC-1α mediates exercise-induced skeletal muscle VEGF expression in mice

inferredcites →https://doi.org/10.1152/ajpendo.00227.2013openalex-snapshot

Mitochondrial and performance adaptations to exercise training in mice lacking skeletal muscle LKB1

inferredcites →https://doi.org/10.1152/ajpendo.00448.2009openalex-snapshot

The microRNA miR-696 regulates PGC-1α in mouse skeletal muscle in response to physical activity

inferredcites →https://doi.org/10.1152/ajpregu.1994.266.2.r375openalex-snapshot

Influence of exercise and fiber type on antioxidant enzyme activity in rat skeletal muscle

inferredcites →https://doi.org/10.1152/japplphysiol.00634.2010openalex-snapshot

A transcriptional map of the impact of endurance exercise training on skeletal muscle phenotype

inferredcites →https://doi.org/10.1152/japplphysiol.00932.2006openalex-snapshot

MicroRNA-1 and microRNA-133a expression are decreased during skeletal muscle hypertrophy

inferredcites →https://doi.org/10.1152/physrev.00015.2007openalex-snapshot

Skeletal Muscle Fatigue: Cellular Mechanisms

inferredcites →https://doi.org/10.1161/hypertensionaha.111.185801openalex-snapshot

Exercise Training Prevents the Microvascular Rarefaction in Hypertension Balancing Angiogenic and Apoptotic Factors

inferredcites →https://doi.org/10.1172/jci118798openalex-snapshot

Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase.

inferredcites →https://doi.org/10.1172/jci46267openalex-snapshot

Mice lacking microRNA 133a develop dynamin 2–dependent centronuclear myopathy

inferredcites →https://doi.org/10.1249/00005768-199310000-00009openalex-snapshot

High intensity training-induced changes in skeletal muscle antioxidant enzyme activity

inferredcites →https://doi.org/10.1371/journal.pgen.1003626openalex-snapshot

miR-133a Regulates Adipocyte Browning In Vivo

inferredcites →https://doi.org/10.1371/journal.pone.0005610openalex-snapshot

miRNA in the Regulation of Skeletal Muscle Adaptation to Acute Endurance Exercise in C57Bl/6J Male Mice

inferredcites →https://doi.org/10.1371/journal.pone.0029173openalex-snapshot

Insulin-Like Growth Factor-1 Receptor Is Regulated by microRNA-133 during Skeletal Myogenesis

inferredcites →https://doi.org/10.21769/bioprotoc.1602openalex-snapshot

Measurement of Resting Energy Metabolism in Mice Using Oxymax Open Circuit Indirect Calorimeter

inferredcites →https://doi.org/10.2337/diabetes.52.3.642openalex-snapshot

Regulation of PGC-1 Promoter Activity by Protein Kinase B and the Forkhead Transcription Factor FKHR

inferredcites →https://doi.org/10.3181/0709-mr-237openalex-snapshot

Muscling Through the microRNA World

inferredcites →https://doi.org/10.4081/bam.2010.3.105openalex-snapshot

The exercised skeletal muscle: a review

inferredcites →https://doi.org/10.4081/jnai.2011.e5openalex-snapshot

Non-coding RNAs and cancer: microRNAs and beyond

What points at this work

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

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A novel brown adipocyte-enriched long non-coding RNA that is required for brown adipocyte differentiation and sufficient to drive thermogenic gene program in white adipocytes

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Unraveling the hnRNPK/miR-133a-3p/UCP2 axis: a novel regulatory circuit governing porcine skeletal muscle satellite cell fate

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Astragalus polysaccharide promotes sheep satellite cell differentiation by regulating miR-133a through the MAPK/ERK signaling pathway

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The therapeutic potential of exercise for neuropsychiatric diseases: A review

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The roles of microRNA in redox metabolism and exercise-mediated adaptation

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Fasudil, a ROCK inhibitor, preserves limb integrity in a mouse model of unilateral critical limb ischemia: Possible interplay of inflammatory and angiogenic signaling pathways

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Blood flow restriction during the resting periods of high-intensity resistance training does not alter performance but decreases MIR-1 and MIR-133A levels in human skeletal muscle

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Effects of Ginsenoside Rg3 on fatigue resistance and SIRT1 in aged rats

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Exosomal microRNAs as Central Regulators of Cancer Cachexia: Multi-Omics Insights into Muscle Wasting and Adipose Browning

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Angiogenin mediates cell-cell fusion as a mitochondrial RNA processing enzyme

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Transforming growth factor (TGF)-β1-induced miR-133a inhibits myofibroblast differentiation and pulmonary fibrosis

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In vivo partial reprogramming of myofibers promotes muscle regeneration by remodeling the stem cell niche

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Loss of microRNA-23–27–24 clusters in skeletal muscle is not influential in skeletal muscle development and exercise-induced muscle adaptation

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Dicer-mediated miRNA processing is not involved in controlling muscle mass during muscle atrophy

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Identification of miRNA, lncRNA and mRNA-associated ceRNA networks and potential biomarker for MELAS with mitochondrial DNA A3243G mutation

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microRNAs in High and Low Responders to Resistance Training in Breast Cancer Survivors

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Sprint Interval Training Decreases Circulating MicroRNAs Important for Muscle Development

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Paternal preconception exercise and sperm epigenetic mechanisms: a systematic review on offspring health

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Lactobacillus Strains Alleviated Aging Symptoms and Aging-Induced Metabolic Disorders in Aged Rats

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miR-30e is negatively regulated by myostatin in skeletal muscle and is functionally related to fiber-type composition

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Purification of mitochondria from skeletal muscle tissue for transcriptomic analyses reveals localization of nuclear‐encoded noncoding RNAs

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HBP ‐A Attenuates Knee Osteoarthritis Progression via MLK3 / P38 / HDAC4 Axis‐Mediated Dual Protection of Articular Cartilage and Quadriceps

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Skeletal muscle‐derived exosomes regulate endothelial cell functions via reactive oxygen species‐activated nuclear factor‐κB signalling

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Remodeling p38 signaling in muscle controls locomotor activity via IL-15

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An inducible knockout of Dicer in adult mice does not affect endurance exercise-induced muscle adaptation

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Interaction of the C2C12 myotube contractions and glucose availability on transcriptome and extracellular vesicle microRNAs

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Micro(RNA)-managing muscle wasting

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Potencial das vesículas extracelulares circulantes de camundongos exercitados no tratamento da obesidade.

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The Effect of MicroRNA-Mediated Exercise on Delaying Sarcopenia in Elderly Individuals

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Transcriptomic and epigenomic landscapes of muscle growth during the postnatal period of broilers

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miR-130a-3p promotes fiber type transition and improves exercise tolerance in mice

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The response of muscle and inflammation-related miRNAs to breast cancer and its treatment

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MicroRNA Regulatory Pathways in the Control of the Actin–Myosin Cytoskeleton

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Acute and Chronic High-Intensity Exercise Differentially Regulate the miRNA Biogenesis Pathway in Human Skeletal Muscle

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MicroRNAs as Potential Biomarkers for Exercise-Based Cancer Rehabilitation in Cancer Survivors

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Detection of miR-133a-5p Using a Molecular Beacon Probe for Investigating Postmortem Intervals

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Functional Role of Extracellular Vesicles in Skeletal Muscle Physiology and Sarcopenia: The Importance of Physical Exercise and Nutrition

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Additional file 1 of Transcriptomic and epigenomic landscapes of muscle growth during the postnatal period of broilers

inferred← citeshttps://doi.org/10.6084/m9.figshare.26734011openalex-snapshot

Additional file 2 of Transcriptomic and epigenomic landscapes of muscle growth during the postnatal period of broilers

inferred← citeshttps://doi.org/10.7554/elife.44876openalex-snapshot

Myonuclear accretion is a determinant of exercise-induced remodeling in skeletal muscle

inferred← citeshttps://doi.org/10.7759/cureus.76212openalex-snapshot

Circulating miR-29c, miR-195, and miR-486 Are Objective Indicators to Determine the Moderate Intensity of Resistance Exercise

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