On the public citation graph
The formation of skeletal muscle myotubes requires functional membrane receptors activated by extracellular ATP
0 signed · 168 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9861(20000605)421:3<289::aid-cne1>3.0.co;2-0openalex-snapshot
Immunohistochemical localization of adenosine 5`-triphosphate-gated ion channel P2X2 receptor subunits in adult and developing rat cochlea
inferredcites →https://doi.org/10.1002/(sici)1097-0177(199902)214:2<152::aid-aja5>3.0.co;2-lopenalex-snapshot
Selective expression of purinoceptor cP2Y1 suggests a role for nucleotide signalling in development of the chick embryo
inferredcites →https://doi.org/10.1002/(sici)1097-0177(199912)216:4/5<442::aid-dvdy12>3.0.co;2-zopenalex-snapshot
Expression of two ATP-gated ion channels, P2X5 and P2X6, in developing chick skeletal muscle
inferredcites →https://doi.org/10.1002/(sici)1520-6408(1997)20:2<133::aid-dvg6>3.0.co;2-8openalex-snapshot
Blocking gap junctional intercellular communication in myoblasts inhibits myogenin and MRF4 expression
inferredcites →https://doi.org/10.1002/1097-0177(200007)218:3<438::aid-dvdy1001>3.0.co;2-6openalex-snapshot
Denervation induces a rapid nuclear accumulation of MRF4 in mature myofibers
inferredcites →https://doi.org/10.1002/ar.1091780206openalex-snapshot
Muscle satellite cells: A validated technique for light microscopic identification and a quantitative study of changes in their population following denervation
inferredcites →https://doi.org/10.1002/ar.1092070407openalex-snapshot
A quantitative ultrastructural analysis of satellite cells in denervated fast and slow muscles of the mouse
inferredcites →https://doi.org/10.1002/bies.950170306openalex-snapshot
The MyoD family of transcription factors and skeletal myogenesis
inferredcites →https://doi.org/10.1002/dvdy.1147openalex-snapshot
Sequential expression of three receptor subtypes for extracellular ATP in developing rat skeletal muscle
inferredcites →https://doi.org/10.1006/bbrc.1995.1027openalex-snapshot
Transcriptional Regulation of Phospholipase C-γ1 Gene during Muscle Differentiation
inferredcites →https://doi.org/10.1006/dbio.1993.1034openalex-snapshot
Expression of Gap Junctions in Cultured Rat L6 Cells during Myogenesis
inferredcites →https://doi.org/10.1006/dbio.1993.1097openalex-snapshot
Formation of Myotubes in Aneural Rat Muscles
inferredcites →https://doi.org/10.1006/dbio.1995.0002openalex-snapshot
Regulation of Muscle Differentiation by the MEF2 Family of MADS Box Transcription Factors
inferredcites →https://doi.org/10.1006/dbio.1995.1305openalex-snapshot
The Inositol 1,4,5-Triphosphate Receptor Expression in Drosophila Suggests a Role for IP3 Signalling in Muscle Development and Adult Chemosensory Functions
inferredcites →https://doi.org/10.1006/dbio.1996.0091openalex-snapshot
Involvement of KCaChannels and Stretch-Activated Channels in Calcium Influx, Triggering Membrane Fusion of Chick Embryonic Myoblasts
inferredcites →https://doi.org/10.1007/978-3-642-28863-0_5openalex-snapshot
Receptors for Purines and Pyrimidines
inferredcites →https://doi.org/10.1007/bf00187825openalex-snapshot
Expression of gap junction genes, connexin40 and connexin43, during fetal mouse development
inferredcites →https://doi.org/10.1007/s00424-001-0757-xopenalex-snapshot
A purinergic signal transduction pathway in mammalian skeletal muscle cells in culture
inferredcites →https://doi.org/10.1007/s00424-001-0758-9openalex-snapshot
Effects of extracellular ATP on freshly isolated mouse skeletal muscle cells during pre-natal and post-natal development
inferredcites →https://doi.org/10.1016/0012-1606(74)90066-9openalex-snapshot
Freeze-cleave demonstration of gap junctions between skeletal myogenic cells in vivo
inferredcites →https://doi.org/10.1016/0012-1606(81)90453-xopenalex-snapshot
Fusion of chick embryo skeletal myoblasts: Role of calcium influx preceding membrane union
inferredcites →https://doi.org/10.1016/0012-1606(82)90056-2openalex-snapshot
Skeletal muscle fibers of newborn rats are coupled by gap junctions
inferredcites →https://doi.org/10.1016/0012-1606(91)90051-4openalex-snapshot
A reevaluation of the role of innervation in primary and secondary myogenesis in developing chick muscle
inferredcites →https://doi.org/10.1016/0014-4827(69)90127-xopenalex-snapshot
Control of myogenesis in vitro by Ca2+ concentration in nutrittonal medium
inferredcites →https://doi.org/10.1016/0014-4827(73)90502-8openalex-snapshot
The effect of calcium ion concentration on myotube formation in vitro
inferredcites →https://doi.org/10.1016/0092-8674(93)90610-3openalex-snapshot
The MyoD family and myogenesis: Redundancy, networks, and thresholds
inferredcites →https://doi.org/10.1016/0092-8674(93)90621-vopenalex-snapshot
MyoD or Myf-5 is required for the formation of skeletal muscle
inferredcites →https://doi.org/10.1016/0092-8674(95)90139-6openalex-snapshot
Cooperative activation of muscle gene expression by MEF2 and myogenic bHLH proteins
inferredcites →https://doi.org/10.1016/0143-4160(94)90052-3openalex-snapshot
Calcium regulation of skeletal myogenesis. II. Extracellular and cell surface effects
inferredcites →https://doi.org/10.1016/s0003-9861(02)00056-5openalex-snapshot
ATP stimulates glucose transport through activation of P2 purinergic receptors in C2C12 skeletal muscle cells
inferredcites →https://doi.org/10.1016/s0006-8993(98)01016-6openalex-snapshot
Arachidonic acid-induced dye uncoupling in rat cortical astrocytes is mediated by arachidonic acid byproducts
inferredcites →https://doi.org/10.1016/s0014-5793(98)00973-9openalex-snapshot
Cloning of a human ether‐a‐go‐go potassium channel expressed in myoblasts at the onset of fusion
inferredcites →https://doi.org/10.1016/s0021-9258(18)53082-9openalex-snapshot
Oxidized ATP. An irreversible inhibitor of the macrophage purinergic P2Z receptor.
inferredcites →https://doi.org/10.1016/s0021-9258(18)66595-0openalex-snapshot
Transforming growth factor-beta. A very potent inhibitor of myoblast differentiation, identical to the differentiation inhibitor secreted by Buffalo rat liver cells.
inferredcites →https://doi.org/10.1016/s0021-9258(18)69028-3openalex-snapshot
Decrease in transforming growth factor-beta binding and action during differentiation in muscle cells.
inferredcites →https://doi.org/10.1016/s0021-9258(19)39275-0openalex-snapshot
Role of myogenin in myoblast differentiation and its regulation by fibroblast growth factor.
inferredcites →https://doi.org/10.1016/s0026-895x(25)10232-0openalex-snapshot
Pharmacological characterization of heterologously expressed ATP-gated cation channels (P2x purinoceptors).
inferredcites →https://doi.org/10.1016/s0031-6997(24)01373-5openalex-snapshot
Receptors for Purines and Pyrimidines
inferredcites →https://doi.org/10.1016/s0074-7696(00)96001-7openalex-snapshot
Involvement of gap junctional communication in myogenesis
inferredcites →https://doi.org/10.1016/s0092-8674(05)80031-5openalex-snapshot
Synaptic structure and development: The neuromuscular junction
inferredcites →https://doi.org/10.1016/s0092-8674(05)80066-2openalex-snapshot
FGF inactivates myogenic helix-loop-helix proteins through phosphorylation of a conserved protein kinase C site in their DNA-binding domains
inferredcites →https://doi.org/10.1016/s0305-0491(96)00244-1openalex-snapshot
Changes in IP3 Metabolism During Skeletal Muscle Development In Vivo and In Vitro
inferredcites →https://doi.org/10.1016/s0896-6273(00)80384-0openalex-snapshot
Xestospongins: Potent Membrane Permeable Blockers of the Inositol 1,4,5-Trisphosphate Receptor
inferredcites →https://doi.org/10.1023/a:1005657607591openalex-snapshot
Analysis for transcript expression of meltrin alpha in normal, regenerating, and denervated rat muscle.
inferredcites →https://doi.org/10.1038/270725a0openalex-snapshot
Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle
inferredcites →https://doi.org/10.1038/303621a0openalex-snapshot
Transmitter-like action of ATP on patched membranes of cultured myoblasts and myotubes
inferredcites →https://doi.org/10.1038/305634a0openalex-snapshot
Spontaneous release of transmitter from growth cones of embryonic neurones
inferredcites →https://doi.org/10.1038/377652a0openalex-snapshot
A metalloprotease-disintegrin participating in myoblast fusion
inferredcites →https://doi.org/10.1038/7225openalex-snapshot
Pore dilation of neuronal P2X receptor channels
inferredcites →https://doi.org/10.1038/sj.bjp.0701341openalex-snapshot
G protein‐independent stimulation of human myocardial phospholipase C by mastoparan
inferredcites →https://doi.org/10.1038/sj.bjp.0705523openalex-snapshot
Extracellular ATP and adenosine induce cell apoptosis of human hepatoma Li‐7A cells via the A3 adenosine receptor
inferredcites →https://doi.org/10.1046/j.0953-816x.2001.01714.xopenalex-snapshot
ATP stimulation of P2X7 receptors activates three different ionic conductances on cultured mouse Schwann cells
inferredcites →https://doi.org/10.1046/j.1365-2184.1996.00996.xopenalex-snapshot
Effects of calcitonin gene-related peptide and interleukin 6 on myoblast differentiation
inferredcites →https://doi.org/10.1046/j.1525-1373.1999.d01-81.xopenalex-snapshot
Changes in Ryanodine Receptor‐Mediated Calcium Release During Skeletal Muscle Differentiation
inferredcites →https://doi.org/10.1054/ceca.2001.0235openalex-snapshot
Lack of effect of cADP-ribose and NAADP on the activity of skeletal muscle and heart ryanodine receptors
inferredcites →https://doi.org/10.1073/pnas.88.4.1349openalex-snapshot
Myogenin and MyoD join a family of skeletal muscle genes regulated by electrical activity.
inferredcites →https://doi.org/10.1073/pnas.97.13.7627openalex-snapshot
T-type α1H Ca 2+ channels are involved in Ca 2+ signaling during terminal differentiation (fusion) of human myoblasts
inferredcites →https://doi.org/10.1074/jbc.272.11.7360openalex-snapshot
Dyspedic Mouse Skeletal Muscle Expresses Major Elements of the Triadic Junction but Lacks Detectable Ryanodine Receptor Protein and Function
inferredcites →https://doi.org/10.1074/jbc.272.29.18418openalex-snapshot
Syndecan-1 Expression Is Down-regulated during Myoblast Terminal Differentiation
inferredcites →https://doi.org/10.1074/jbc.272.32.19808openalex-snapshot
Expression of the Ryanodine Receptor Type 3 Calcium Release Channel during Development and Differentiation of Mammalian Skeletal Muscle Cells
inferredcites →https://doi.org/10.1074/jbc.273.1.157openalex-snapshot
A Novel, Secreted Form of Human ADAM 12 (Meltrin α) Provokes Myogenesis in Vivo
inferredcites →https://doi.org/10.1074/jbc.275.19.14401openalex-snapshot
Molecular Cloning and Characterization of a Novel ATP P2X Receptor Subtype from Embryonic Chick Skeletal Muscle
inferredcites →https://doi.org/10.1074/jbc.m005030200openalex-snapshot
The Insulin-like Growth Factor-Phosphatidylinositol 3-Kinase-Akt Signaling Pathway Regulates Myogenin Expression in Normal Myogenic Cells but Not in Rhabdomyosarcoma-derived RD Cells
inferredcites →https://doi.org/10.1074/jbc.m100091200openalex-snapshot
Critical Proliferation-independent Window for Basic Fibroblast Growth Factor Repression of Myogenesis via the p42/p44 MAPK Signaling Pathway
inferredcites →https://doi.org/10.1074/jbc.m104991200openalex-snapshot
Insulin-like Growth Factor-mediated Muscle Differentiation
inferredcites →https://doi.org/10.1080/cac.10.4-6.451.456openalex-snapshot
Presence and Importance of Connexin43 During Myogenesis
inferredcites →https://doi.org/10.1083/jcb.106.5.1693openalex-snapshot
The control of chick myoblast fusion by ion channels operated by prostaglandins and acetylcholine.
inferredcites →https://doi.org/10.1083/jcb.132.4.657openalex-snapshot
Myogenin expression, cell cycle withdrawal, and phenotypic differentiation are temporally separable events that precede cell fusion upon myogenesis.
inferredcites →https://doi.org/10.1083/jcb.137.5.1057openalex-snapshot
A Natural Hepatocyte Growth Factor/Scatter Factor Autocrine Loop in Myoblast Cells and the Effect of the ConstitutiveMetKinase Activation on Myogenic Differentiation
inferredcites →https://doi.org/10.1083/jcb.149.3.657openalex-snapshot
Calcineurin Activity Is Required for the Initiation of Skeletal Muscle Differentiation
inferredcites →https://doi.org/10.1083/jcb.200202025openalex-snapshot
ATP regulates the differentiation of mammalian skeletal muscle by activation of a P2X5 receptor on satellite cells
inferredcites →https://doi.org/10.1083/jcb.75.3.788openalex-snapshot
Cell-to-cell communication and myogenesis.
inferredcites →https://doi.org/10.1085/jgp.20028671openalex-snapshot
Dihydropyridine Receptors as Voltage Sensors for a Depolarization-evoked, IP3R-mediated, Slow Calcium Signal in Skeletal Muscle Cells
inferredcites →https://doi.org/10.1091/mbc.02-02-0016openalex-snapshot
p38 Mitogen-activated Protein Kinase-, Calcium-Calmodulin–dependent Protein Kinase-, and Calcineurin-mediated Signaling Pathways Transcriptionally Regulate Myogenin Expression
inferredcites →https://doi.org/10.1091/mbc.9.11.3119openalex-snapshot
Direct Involvement of N-Cadherin–mediated Signaling in Muscle Differentiation
inferredcites →https://doi.org/10.1096/fasebj.9.15.8529839openalex-snapshot
Transcription factor families: muscling in on the myogenic program.
inferredcites →https://doi.org/10.1096/fj.00-0031comopenalex-snapshot
The P2 purinergic receptors of human dendritic cells: identification and coupling to cytokine release
inferredcites →https://doi.org/10.1097/00001756-200109170-00048openalex-snapshot
Co-expression of P2X receptor subunits on rat nodose neurons that bind the isolectin GS-I-B4
inferredcites →https://doi.org/10.1111/j.1469-7793.1998.317be.xopenalex-snapshot
An ether ‐à‐go‐go K+ current, Ih‐eag, contributes to the hyperpolarization of human fusion‐competent myoblasts
inferredcites →https://doi.org/10.1111/j.1469-7793.1998.467bk.xopenalex-snapshot
Role of an inward rectifier K+ current and of hyperpolarization in human myoblast fusion
inferredcites →https://doi.org/10.1111/j.1748-1716.1985.tb07734.xopenalex-snapshot
ATP‐induced cation influx in myotubes is additive to cholinergic agonist action
inferredcites →https://doi.org/10.1113/jphysiol.1978.sp012546openalex-snapshot
The development of motor projection patterns in the chick hind limb.
inferredcites →https://doi.org/10.1113/jphysiol.1994.sp020176openalex-snapshot
ATP released together with acetylcholine as the mediator of neuromuscular depression at frog motor nerve endings.
inferredcites →https://doi.org/10.1113/jphysiol.1996.sp021348openalex-snapshot
Synchronous release of ATP and neurotransmitter within milliseconds of a motor nerve impulse in the frog.
inferredcites →https://doi.org/10.1113/jphysiol.1996.sp021369openalex-snapshot
Contribution of a non‐inactivating potassium current to the resting membrane potential of fusion‐competent human myoblasts.
inferredcites →https://doi.org/10.1124/mol.64.1.104openalex-snapshot
Pharmacological Characterization of the Human P2Y13 Receptor
inferredcites →https://doi.org/10.1124/mol.64.4.785openalex-snapshot
Mechanisms of Release of Nucleotides and Integration of Their Action as P2X- and P2Y-Receptor Activating Molecules
inferredcites →https://doi.org/10.1128/mcb.13.10.5943openalex-snapshot
Fibroblast Growth Factor Inhibits MRF4 Activity Independently of the Phosphorylation Status of a Conserved Threonine Residue within the DNA-Binding Domain
inferredcites →https://doi.org/10.1128/mcb.5.3.484openalex-snapshot
Regulation of Creatine Kinase Induction in Differentiating Mouse Myoblasts
inferredcites →https://doi.org/10.1152/ajpcell.00168.2002openalex-snapshot
Differentiation in C2C12 myoblasts depends on the expression of endogenous IGFs and not serum depletion
inferredcites →https://doi.org/10.1152/ajpcell.1986.250.5.c771openalex-snapshot
Biphasic concentration dependency of stimulation of myoblast differentiation by somatomedins
inferredcites →https://doi.org/10.1152/physrev.00015.2002openalex-snapshot
Molecular Physiology of P2X Receptors
inferredcites →https://doi.org/10.1159/000057322openalex-snapshot
The Signaling Pathways Mediated by P2Y Nucleotide Receptors in the Formation and Maintenance of the Skeletal Neuromuscular Junction
inferredcites →https://doi.org/10.1177/002215540104900709openalex-snapshot
Expression and Neural Control of Myogenic Regulatory Factor Genes During Regeneration of Mouse Soleus
inferredcites →https://doi.org/10.1182/blood.v96.3.996openalex-snapshot
Pharmacologic properties of P2Z/P2X7receptor characterized in murine dendritic cells: role on the induction of apoptosis
inferredcites →https://doi.org/10.1210/en.143.2.511openalex-snapshot
Early Stimulation and Late Inhibition of Extracellular Signal-Regulated Kinase 1/2 Phosphorylation by IGF-I: A Potential Mechanism Mediating the Switch in IGF-I Action on Skeletal Muscle Cell Differentiation
inferredcites →https://doi.org/10.1210/endo-120-1-115openalex-snapshot
The Type II Insulin-Like Growth Factor (IGF) Receptor Has Low Affinity for IGF-I Analogs: Pleiotypic Actions of IGFs on Myoblasts Are Apparently Mediated by the Type I Receptor*
inferredcites →https://doi.org/10.1523/jneurosci.23-04-01320.2003openalex-snapshot
P2X 7 Receptor-Mediated Release of Excitatory Amino Acids from Astrocytes
inferredcites →https://doi.org/10.1677/joe.0.1670175openalex-snapshot
Functional inactivation of the IGF-I receptor delays differentiation of skeletal muscle cells
inferredcites →https://doi.org/10.2174/1566524024605707openalex-snapshot
Cyclic ADP-ribose (cADPR) and Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP): Novel Regulators of Ca 2+-Signaling and Cell Function
inferredcites →https://doi.org/10.3109/15419069409014208openalex-snapshot
Is Intercellular Communication Via Gap Junctions Required for Myoblast Fusion?
inferredcites →https://doi.org/10.4049/jimmunol.146.9.2889openalex-snapshot
Signal transduction through the T cell antigen receptor. Activation of phospholipase C through a G protein-independent coupling mechanism
inferredcites →https://doi.org/10.4049/jimmunol.147.9.3122openalex-snapshot
Fc gamma receptor signal transduction in natural killer cells. Coupling to phospholipase C via a G protein-independent, but tyrosine kinase-dependent pathway
inferredcites →https://doi.org/10.4049/jimmunol.156.4.1531openalex-snapshot
Mouse microglial cells express a plasma membrane pore gated by extracellular ATP
inferredcites →https://doi.org/10.4049/jimmunol.170.3.1320openalex-snapshot
TNF-α Plus IFN-γ Induce Connexin43 Expression and Formation of Gap Junctions Between Human Monocytes/Macrophages That Enhance Physiological Responses
inferredcites →https://doi.org/10.4049/jimmunol.172.10.6011openalex-snapshot
The Serotoninergic Receptors of Human Dendritic Cells: Identification and Coupling to Cytokine Release
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/cbin.10962openalex-snapshot
A transcriptomics study of differentiated C2C12 myoblasts identified novel functional responses to 17β‐estradiol
inferred← citeshttps://doi.org/10.1002/jcp.20679openalex-snapshot
Calcium sources used by post‐natal human myoblasts during initial differentiation
inferred← citeshttps://doi.org/10.1002/jcp.20902openalex-snapshot
Differential gene expression in skeletal muscle cells after membrane depolarization
inferred← citeshttps://doi.org/10.1002/mus.23893openalex-snapshot
A differential pattern of gene expression in skeletal muscle of tumor‐bearing rats reveals dysregulation of excitation–contraction coupling together with additional muscle alterations
inferred← citeshttps://doi.org/10.1002/wmts.96openalex-snapshot
P2X receptor signaling in skeletal muscle health and disease
inferred← citeshttps://doi.org/10.1007/5584_2016_53openalex-snapshot
Regulation of Skeletal Muscle Myoblast Differentiation and Proliferation by Pannexins
inferred← citeshttps://doi.org/10.1007/978-3-030-25890-0_5openalex-snapshot
Role of Connexins and Pannexins in Bone and Muscle Mass and Function
inferred← citeshttps://doi.org/10.1007/s00018-015-1968-1openalex-snapshot
Regulation of pannexin and connexin channels and their functional role in skeletal muscles
inferred← citeshttps://doi.org/10.1007/s00018-021-04070-8openalex-snapshot
Contingent intramuscular boosting of P2XR7 axis improves motor function in transgenic ALS mice
inferred← citeshttps://doi.org/10.1007/s00232-012-9485-8openalex-snapshot
Connexin- and Pannexin-Based Channels in Normal Skeletal Muscles and Their Possible Role in Muscle Atrophy
inferred← citeshttps://doi.org/10.1007/s10974-006-9058-5openalex-snapshot
Properties and role of voltage-dependent calcium channels during mouse skeletal muscle differentiation
inferred← citeshttps://doi.org/10.1007/s11010-011-0726-4openalex-snapshot
Extracellular ATP signaling during differentiation of C2C12 skeletal muscle cells: role in proliferation
inferred← citeshttps://doi.org/10.1007/s11302-008-9124-0openalex-snapshot
Amino acid variations resulting in functional and nonfunctional zebrafish P2X1 and P2X5.1 receptors
inferred← citeshttps://doi.org/10.1007/s11302-013-9381-4openalex-snapshot
Purinergic signalling in the musculoskeletal system
inferred← citeshttps://doi.org/10.1007/s11914-017-0374-zopenalex-snapshot
Connexins and Pannexins in Bone and Skeletal Muscle
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2017.10.030openalex-snapshot
Effect of dietary methionine level on muscle growth mechanisms in juvenile rainbow trout ( Oncorhynchus mykiss )
inferred← citeshttps://doi.org/10.1016/j.bbadis.2019.01.002openalex-snapshot
Dystrophic mdx mouse myoblasts exhibit elevated ATP/UTP-evoked metabotropic purinergic responses and alterations in calcium signalling
inferred← citeshttps://doi.org/10.1016/j.bbadva.2024.100135openalex-snapshot
Loss or inhibition of lysosomal acid lipase in vitro leads to cholesteryl ester accumulation without affecting muscle formation or mitochondrial function
inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.153142openalex-snapshot
Extracellular adenosine mediated activation of the A2B adenosine receptor increases human syncytiotrophoblast formation
inferred← citeshttps://doi.org/10.1016/j.bcp.2006.02.003openalex-snapshot
Extracellular ATP activates ERK1/ERK2 via a metabotropic P2Y1 receptor in a Ca2+ independent manner in differentiated human skeletal muscle cells
inferred← citeshttps://doi.org/10.1016/j.bios.2024.116117openalex-snapshot
Merging BioActuation and BioCapacitive properties: A 3D bioprinted devices to self-stimulate using self-stored energy
inferred← citeshttps://doi.org/10.1016/j.cardiores.2005.07.017openalex-snapshot
How much intimacy is compatible with survival for a cardiomyocyte?
inferred← citeshttps://doi.org/10.1016/j.ceca.2014.10.014openalex-snapshot
Inositol 1,4,5 trisphosphate receptor 1 is a key player of human myoblast differentiation
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.08.002openalex-snapshot
Reactive oxygen species contribute to the promotion of the ATP-mediated proliferation of mouse skeletal myoblasts
inferred← citeshttps://doi.org/10.1016/j.matbio.2010.02.002openalex-snapshot
Glycosaminoglycan mimetics trigger IP3-dependent intracellular calcium release in myoblasts
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2013.03.022openalex-snapshot
The ATP required for potentiation of skeletal muscle contraction is released via pannexin hemichannels
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.01.012openalex-snapshot
Myoblast proliferation and syncytial fusion both depend on connexin43 function in transfected skeletal muscle primary cultures
inferred← citeshttps://doi.org/10.1016/j.yexcr.2019.05.012openalex-snapshot
A “noisy” electrical stimulation protocol favors muscle regeneration in vitro through release of endogenous ATP
inferred← citeshttps://doi.org/10.1038/s41389-018-0100-4openalex-snapshot
Pannexin 1 inhibits rhabdomyosarcoma progression through a mechanism independent of its canonical channel function
inferred← citeshttps://doi.org/10.1073/pnas.1312331110openalex-snapshot
De novo expression of connexin hemichannels in denervated fast skeletal muscles leads to atrophy
inferred← citeshttps://doi.org/10.1074/jbc.m109.057315openalex-snapshot
ATP Released by Electrical Stimuli Elicits Calcium Transients and Gene Expression in Skeletal Muscle
inferred← citeshttps://doi.org/10.1074/jbc.m114.572131openalex-snapshot
Pannexin 1 and Pannexin 3 Channels Regulate Skeletal Muscle Myoblast Proliferation and Differentiation
inferred← citeshttps://doi.org/10.1096/fj.05-4022comopenalex-snapshot
Increased susceptibility to ATP via alteration of P2X receptor function in dystrophic mdx mouse muscle cells
inferred← citeshttps://doi.org/10.1111/apha.12473openalex-snapshot
Adenosine enhances acetylcholine receptor channel openings and intracellular calcium ‘spiking’ in mouse skeletal myotubes
inferred← citeshttps://doi.org/10.1111/j.1582-4934.2011.01397.xopenalex-snapshot
P2X7 purinoceptor alterations in dystrophic mdx mouse muscles: relationship to pathology and potential target for treatment
inferred← citeshttps://doi.org/10.1113/jp286173openalex-snapshot
Pathophysiological role of connexin and pannexin hemichannels in neuromuscular disorders
inferred← citeshttps://doi.org/10.1134/s1990747808040107openalex-snapshot
Expression and functional role of the protein Orai-1 in skeletal myoblasts and myotubes
inferred← citeshttps://doi.org/10.1134/s1990747810040082openalex-snapshot
Elevation of the expression of the inositol-1,4,5-trisphosphate receptors and increase of calcium signaling in response to ATP during differentiation of skeletal myoblasts C2C12 into myotubes
inferred← citeshttps://doi.org/10.1146/annurev-physiol-021115-105305openalex-snapshot
Systemic Nutrient and Stress Signaling via Myokines and Myometabolites
inferred← citeshttps://doi.org/10.1152/ajpcell.00200.2009openalex-snapshot
Metabolic inhibition increases activity of connexin-32 hemichannels permeable to Ca2+ in transfected HeLa cells
inferred← citeshttps://doi.org/10.1152/ajpcell.00405.2010openalex-snapshot
The calcium channel α2/δ1 subunit interacts with ATP5b in the plasma membrane of developing muscle cells
inferred← citeshttps://doi.org/10.1159/000110438openalex-snapshot
18α-Glycyrrhetinic Acid Induces Phenotypic Changes of Skeletal Muscle Cells to Enter Adipogenesis
inferred← citeshttps://doi.org/10.1186/1471-2180-11-110openalex-snapshot
Toxoplasma gondiidown modulates cadherin expression in skeletal muscle cells inhibiting myogenesis
inferred← citeshttps://doi.org/10.1186/s12864-018-5209-5openalex-snapshot
Intramuscular preadipocytes impede differentiation and promote lipid deposition of muscle satellite cells in chickens
inferred← citeshttps://doi.org/10.1371/journal.pone.0239428openalex-snapshot
Acetic acid stimulates G-protein-coupled receptor GPR43 and induces intracellular calcium influx in L6 myotube cells
inferred← citeshttps://doi.org/10.20381/ruor-21403openalex-snapshot
Regulation of Pannexin 1 and Pannexin 3 During Skeletal Muscle Development, Regeneration and Dystrophy
inferred← citeshttps://doi.org/10.20381/ruor-2832openalex-snapshot
Characterization and Function of the ~70kDa Immunoreactive Species of Pannexin3 in Rhabdomyosarcomas
inferred← citeshttps://doi.org/10.3389/fcell.2015.00025openalex-snapshot
Pannexin channels mediate the acquisition of myogenic commitment in C2C12 reserve cells promoted by P2 receptor activation
inferred← citeshttps://doi.org/10.3389/fcell.2021.736813openalex-snapshot
Pannexin 1 Regulates Skeletal Muscle Regeneration by Promoting Bleb-Based Myoblast Migration and Fusion Through a Novel Lipid Based Signaling Mechanism
inferred← citeshttps://doi.org/10.3389/fncel.2014.00405openalex-snapshot
Neuronal involvement in muscular atrophy
inferred← citeshttps://doi.org/10.3389/fncel.2019.00340openalex-snapshot
Comparative Embryonic Spatio-Temporal Expression Profile Map of the Xenopus P2X Receptor Family
inferred← citeshttps://doi.org/10.3390/ani14233506openalex-snapshot
Polymorphisms of TXK and PLCE1 Genes and Their Correlation Analysis with Growth Traits in Ashidan Yaks
inferred← citeshttps://doi.org/10.3390/antiox10050633openalex-snapshot
The Impact of H2S on Obesity-Associated Metabolic Disturbances
inferred← citeshttps://doi.org/10.3390/ijms21175963openalex-snapshot
eATP/P2X7R Axis: An Orchestrated Pathway Triggering Inflammasome Activation in Muscle Diseases
inferred← citeshttps://doi.org/10.3390/ijms222413615openalex-snapshot
Ion Channels and Transporters in Muscle Cell Differentiation
inferred← citeshttps://doi.org/10.3390/ijms23169444openalex-snapshot
Mechanical Disturbance of Osteoclasts Induces ATP Release That Leads to Protein Synthesis in Skeletal Muscle through an Akt-mTOR Signaling Pathway
inferred← citeshttps://doi.org/10.3390/ijms24119434openalex-snapshot
The Role of P2X7 Purinoceptors in the Pathogenesis and Treatment of Muscular Dystrophies
inferred← citeshttps://doi.org/10.3858/emm.2008.40.2.220openalex-snapshot
Secretion of adenylate kinase 1 is required for extracellular ATP synthesis in C2C12 myotubes
inferred← citeshttps://doi.org/10.4161/15548627.2014.994402openalex-snapshot
A novel mechanism of autophagic cell death in dystrophic muscle regulated by P2RX7 receptor large-pore formation and HSP90
inferred← citeshttps://doi.org/10.5772/29729openalex-snapshot
Altered Gene Expression Pathways in Duchenne Muscular Dystrophy
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.