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Why are fetal muscles slow?
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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/ar.1090500209openalex-snapshot
An anatomical study of the initiation of movement in rat embryos
inferredcites →https://doi.org/10.1002/ar.1091890410openalex-snapshot
Neonatal muscle: An electron microscopic study
inferredcites →https://doi.org/10.1007/bf00219408openalex-snapshot
Developmental aspects of the innervation of skeletal muscle fibers in the chick embryo
inferredcites →https://doi.org/10.1007/bf00580815openalex-snapshot
Differentiation of myosin in soleus and extensor digitorum longus muscle in different animal species during development
inferredcites →https://doi.org/10.1016/0012-1606(75)90108-6openalex-snapshot
Structural and functional changes of myosin during development
inferredcites →https://doi.org/10.1016/0012-1606(78)90229-4openalex-snapshot
Myogenic and neurogenic contributions to the development of fast and slow twitch muscles in rat
inferredcites →https://doi.org/10.1016/0014-4886(72)90071-4openalex-snapshot
Biphasic development of muscle fibers in the fetal lamb
inferredcites →https://doi.org/10.1016/0014-4886(76)90283-1openalex-snapshot
Free grafting of the extensor digitorum longus muscle in the rat after Marcaine pretreatment
inferredcites →https://doi.org/10.1016/0014-5793(76)80872-1openalex-snapshot
Myosin light chains of developing fast and slow rabbit skeletal muscle
inferredcites →https://doi.org/10.1016/0022-2836(78)90049-9openalex-snapshot
Identification of a novel form of myosin light chain present in embryonic muscle tissue and cultured muscle cells
inferredcites →https://doi.org/10.1016/0022-510x(76)90001-0openalex-snapshot
Adaptive transformation of rat soleus motor units during growth
inferredcites →https://doi.org/10.1016/s0300-9084(79)80160-1openalex-snapshot
Transitions in contractile protein isozymes during muscle cell differentiation
inferredcites →https://doi.org/10.1038/217452a0openalex-snapshot
3-Methyl Histidine and Adult and Foetal Forms of Skeletal Muscle Myosin
inferredcites →https://doi.org/10.1038/263030a0openalex-snapshot
Significance of impulse activity in the transformation of skeletal muscle type
inferredcites →https://doi.org/10.1038/274025a0openalex-snapshot
Fast and slow myosin in developing muscle fibres
inferredcites →https://doi.org/10.1038/280321a0openalex-snapshot
Rabbit skeletal myosin isoenzymes from fetal, fast-twitch and slow-twitch muscles
inferredcites →https://doi.org/10.1038/newbio240260a0openalex-snapshot
Developmental Changes of the Primary Structure and Histidine Methylation in Rabbit Skeletal Muscle Myosin
inferredcites →https://doi.org/10.1073/pnas.74.10.4524openalex-snapshot
Myosin types during the development of embryonic chicken fast and slow muscles.
inferredcites →https://doi.org/10.1073/pnas.76.10.5197openalex-snapshot
Contractile protein isozymes in muscle development: identification of an embryonic form of myosin heavy chain.
inferredcites →https://doi.org/10.1073/pnas.76.9.4331openalex-snapshot
Comparison of adult, embryonic, and dystrophic myosin heavy chains from chicken muscle by sodium dodecyl sulfate/polyacrylamide gel electrophoresis and peptide mapping.
inferredcites →https://doi.org/10.1083/jcb.42.1.135openalex-snapshot
THE HISTOGENESIS OF RAT INTERCOSTAL MUSCLE
inferredcites →https://doi.org/10.1083/jcb.42.1.154openalex-snapshot
THE FINE STRUCTURE OF MOTOR ENDPLATE MORPHOGENESIS
inferredcites →https://doi.org/10.1083/jcb.55.3.586openalex-snapshot
SOME PROPERTIES OF EMBRYONIC MYOSIN
inferredcites →https://doi.org/10.1086/physzool.8.2.30152388openalex-snapshot
The Origin and Early Development of Somatic Behavior in the Albino Rat
inferredcites →https://doi.org/10.1113/jphysiol.1960.sp006394openalex-snapshot
Differentiation of fast and slow muscles in the cat hind limb
inferredcites →https://doi.org/10.1113/jphysiol.1964.sp007444openalex-snapshot
Dynamic properties of fast and slow skeletal muscles of the rat during development
inferredcites →https://doi.org/10.1113/jphysiol.1969.sp008771openalex-snapshot
The influence of activity on some contractile characteristics of mammalian fast and slow muscles
inferredcites →https://doi.org/10.1113/jphysiol.1974.sp010670openalex-snapshot
The formation of synapses in striated muscle during development
inferredcites →https://doi.org/10.1113/jphysiol.1979.sp013051openalex-snapshot
The size of motor units during post‐natal development of rat lumbrical muscle.
inferredcites →https://doi.org/10.1152/jn.1940.3.4.358openalex-snapshot
NATURE OF THE FIRST VISIBLE CONTRACTIONS OF THE FORELIMB MUSCULATURE IN RAT FETUSES
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/(sici)1097-0177(199809)213:1<147::aid-aja15>3.0.co;2-#openalex-snapshot
Primary myotubes preferentially mature into either the fastest or slowest muscle fibers
inferred← citeshttps://doi.org/10.1002/(sici)1097-4687(200006)244:3<203::aid-jmor5>3.0.co;2-vopenalex-snapshot
Precocial development of axial locomotor muscle in bottlenose dolphins (Tursiops truncatus)
inferred← citeshttps://doi.org/10.1002/aja.1001710202openalex-snapshot
The organogenesis of murine striated muscle: A cytoarchitectural study
inferred← citeshttps://doi.org/10.1002/aja.1001970406openalex-snapshot
Localisation of transforming growth factor beta 1 in developing muscles: Implications for connective tissue and fiber type pattern formation
inferred← citeshttps://doi.org/10.1002/cne.902710104openalex-snapshot
Quantitative relationships between motoneuron and muscle development in Xenopus laevis: Implications for motoneuron cell death and motor unit formation
inferred← citeshttps://doi.org/10.1002/cphy.cp100117openalex-snapshot
Emergence of Specialization in Skeletal Muscle
inferred← citeshttps://doi.org/10.1002/dvdy.21223openalex-snapshot
Sox6 is required for normal fiber type differentiation of fetal skeletal muscle in mice
inferred← citeshttps://doi.org/10.1002/j.2040-4603.1983.tb01668.xopenalex-snapshot
Emergence of Specialization in Skeletal Muscle
inferred← citeshttps://doi.org/10.1002/jcb.24938openalex-snapshot
The Effect of Serum Origin on Tissue Engineered Skeletal Muscle Function
inferred← citeshttps://doi.org/10.1002/jcp.24857openalex-snapshot
Glucose Concentration and Streptomycin Alter In Vitro Muscle Function and Metabolism
inferred← citeshttps://doi.org/10.1002/jmor.1052200308openalex-snapshot
Ontogeny of the Pectoralis muscle in the little brown bat, Myotis lucifugus
inferred← citeshttps://doi.org/10.1002/mus.880050902openalex-snapshot
Myofiber differentiation in normal and hypotrophied canine pectineal muscles
inferred← citeshttps://doi.org/10.1002/mus.880100905openalex-snapshot
Characterization of a prostaglandin dysfunction myopathy
inferred← citeshttps://doi.org/10.1006/dbio.2001.0528openalex-snapshot
Sonic Hedgehog Inhibits the Terminal Differentiation of Limb Myoblasts Committed to the Slow Muscle Lineage
inferred← citeshttps://doi.org/10.1007/3540528806_3openalex-snapshot
Cellular and molecular diversities of mammalian skeletal muscle fibers
inferred← citeshttps://doi.org/10.1007/978-1-4613-0939-0_13openalex-snapshot
Accepted and Controversial Neuromotor Therapies for Infants at High Risk for Cerebral Palsy
inferred← citeshttps://doi.org/10.1007/bf00122120openalex-snapshot
Comparison of the foetal development of fibre types in four bovine muscles
inferred← citeshttps://doi.org/10.1007/bf00214640openalex-snapshot
Postnatal growth and differentiation in three hindlimb muscles of the rat
inferred← citeshttps://doi.org/10.1007/bf00240928openalex-snapshot
Spatial and temporal patterns of myosin heavy chain expression in developing rat extraocular muscle
inferred← citeshttps://doi.org/10.1007/bf00261666openalex-snapshot
Contractile responses in rat extensor digitorum longus muscles at different times of postnatal development
inferred← citeshttps://doi.org/10.1007/bf01181536openalex-snapshot
Growth-related alterations in motor endplates of type-identified diaphragm muscle fibres
inferred← citeshttps://doi.org/10.1007/bf01611441openalex-snapshot
The role of innervation in the establishment of the topographical distribution of primary myotube types during development
inferred← citeshttps://doi.org/10.1007/bf01745114openalex-snapshot
Expression of slow and fast myosin heavy chains in overloaded muscles of the developing rat
inferred← citeshttps://doi.org/10.1016/0012-1606(82)90171-3openalex-snapshot
Size of motoneuron pool may be related to number of myotubes in developing muscle
inferred← citeshttps://doi.org/10.1016/0012-1606(83)90080-5openalex-snapshot
The development of the pattern of innervation in chicken hindlimb muscles: Evidence for specification of nerve-muscle connections
inferred← citeshttps://doi.org/10.1016/0012-1606(85)90433-6openalex-snapshot
Specific innervation of muscle fiber types in a developmentally polyinnervated muscle
inferred← citeshttps://doi.org/10.1016/0012-1606(91)90050-dopenalex-snapshot
Relationship of primary and secondary myogenesis to fiber type development in embryonic chick muscle
inferred← citeshttps://doi.org/10.1016/0012-1606(91)90457-eopenalex-snapshot
Coordination of skeletal muscle gene expression occurs late in mammalian development
inferred← citeshttps://doi.org/10.1016/0014-4886(84)90158-4openalex-snapshot
Physiologic and histologic features of muscle development in the hamster
inferred← citeshttps://doi.org/10.1016/0014-5793(81)80088-9openalex-snapshot
Differential distribution of tropomyosin subunits in fast and slow rat muscles and its changes in long‐term denervated hemidiaphragm
inferred← citeshttps://doi.org/10.1016/0014-5793(84)80979-5openalex-snapshot
A developmentally regulated disappearance of slow myosin in fast‐type muscles of the mouse
inferred← citeshttps://doi.org/10.1016/0022-510x(86)90165-6openalex-snapshot
Immunocytochemical analysis of myosin heavy chains in human fetal skeletal muscles
inferred← citeshttps://doi.org/10.1016/0022-510x(87)90181-xopenalex-snapshot
Primary, secondary and tertiary myotubes in developing skeletal muscle: A new approach to the analysis of human myogenesis
inferred← citeshttps://doi.org/10.1016/0045-6039(86)90097-7openalex-snapshot
The development of fibre types in grafts of a slow tonic avian muscle, the dorsocutaneous latissimus dorsi
inferred← citeshttps://doi.org/10.1016/0165-3806(90)90042-wopenalex-snapshot
The development of locomotion in the rat
inferred← citeshttps://doi.org/10.1016/0300-9629(88)90429-xopenalex-snapshot
Fiber type composition of the plantarflexors of giraffes (giraffa camelopardalis) at different postnatal stages of development
inferred← citeshttps://doi.org/10.1016/0301-0082(93)90041-popenalex-snapshot
Activity-dependent interactions between motoneurones and muscles: Their role in the development of the motor unit
inferred← citeshttps://doi.org/10.1016/b978-0-12-800040-3.00002-9openalex-snapshot
Basics of Skeletal Muscle Function and Normal Physiology
inferred← citeshttps://doi.org/10.1016/b978-012492543-4/50022-2openalex-snapshot
The Chemistry of Movement
inferred← citeshttps://doi.org/10.1016/j.acthis.2017.03.005openalex-snapshot
Differential effect of chronic undernutrition on the fiber type composition of fascicles in the extensor digitorum longus muscles of the rat
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.01.019openalex-snapshot
MusTRD can regulate postnatal fiber-specific expression
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.01.016openalex-snapshot
Intrinsic phenotypic diversity of embryonic and fetal myoblasts is revealed by genome-wide gene expression analysis on purified cells
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.06.006openalex-snapshot
Cellular heterogeneity during vertebrate skeletal muscle development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.11.031openalex-snapshot
Six1 and Six4 gene expression is necessary to activate the fast-type muscle gene program in the mouse primary myotome
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.04.014openalex-snapshot
A hypoplastic model of skeletal muscle development displaying reduced foetal myoblast cell numbers, increased oxidative myofibres and improved specific tension capacity
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.08.010openalex-snapshot
Genesis of muscle fiber-type diversity during mouse embryogenesis relies on Six1 and Six4 gene expression
inferred← citeshttps://doi.org/10.1016/j.ydbio.2023.04.002openalex-snapshot
Slow myosin heavy chain 1 is required for slow myofibril and muscle fibre growth but not for myofibril initiation
inferred← citeshttps://doi.org/10.1016/j.ygeno.2022.110409openalex-snapshot
MicroRNA expression signature in the striated and smooth adductor muscles of Yesso scallop Patinopecten yessoensis
inferred← citeshttps://doi.org/10.1016/s0021-9258(18)61421-8openalex-snapshot
Adult forms of the Ca2+ATPase of sarcoplasmic reticulum. Expression in developing skeletal muscle.
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)60625-0openalex-snapshot
Chapter 9 Cell Heterogeneity in The Myogenic Lineage
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)62075-6openalex-snapshot
Immunocytochemical Localization of Proteins in Striated Muscle
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)62349-9openalex-snapshot
Myosin Isoenzyme Transitions in Muscle Development, Maturation, and Disease
inferred← citeshttps://doi.org/10.1016/s0165-5728(84)80014-4openalex-snapshot
Immunocytochemical analysis of fibre type differentiation in developing skeletal muscle
inferred← citeshttps://doi.org/10.1016/s0248-4900(03)00087-xopenalex-snapshot
Myosin heavy chain isoforms in postnatal muscle development of mice
inferred← citeshttps://doi.org/10.1016/s0925-4773(98)00036-7openalex-snapshot
The generation and interpretation of positional information within the vertebrate myotome
inferred← citeshttps://doi.org/10.1038/292805a0openalex-snapshot
Three myosin heavy-chain isozymes appear sequentially in rat muscle development
inferred← citeshttps://doi.org/10.1038/s41467-025-61767-1openalex-snapshot
Early lineage segregation of primary myotubes from secondary myotubes and adult muscle stem cells
inferred← citeshttps://doi.org/10.1083/jcb.104.3.447openalex-snapshot
Slow myosin in developing rat skeletal muscle.
inferred← citeshttps://doi.org/10.1083/jcb.92.2.471openalex-snapshot
Distribution and properties of myosin isozymes in developing avian and mammalian skeletal muscle fibers
inferred← citeshttps://doi.org/10.1088/1748-605x/acf25bopenalex-snapshot
Human adipose-derived mesenchymal stem cells laden in gellan gum spongy-like hydrogels for volumetric muscle loss treatment
inferred← citeshttps://doi.org/10.1089/rej.2010.1065openalex-snapshot
Altered Primary and Secondary Myogenesis in the Myostatin-Null Mouse
inferred← citeshttps://doi.org/10.1101/gad.11.17.2163openalex-snapshot
Notochord induction of zebrafish slow muscle mediated by Sonic hedgehog
inferred← citeshttps://doi.org/10.1101/gad.1769009openalex-snapshot
Embryonic and fetal limb myogenic cells are derived from developmentally distinct progenitors and have different requirements for β-catenin
inferred← citeshttps://doi.org/10.1111/apha.12073openalex-snapshot
Differential developmental programming by early protein restriction of rat skeletal muscle according to its fibre‐type composition
inferred← citeshttps://doi.org/10.1111/j.1432-0436.1984.tb01352.xopenalex-snapshot
Myosin transitions in developing fast and slow muscles of the rat hindlimb
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2004.00738.xopenalex-snapshot
Differentiation of slow and fast fibers in tentacles of Sepia officinalis (Mollusca)
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2012.01338.xopenalex-snapshot
Muscle development and differentiation in the urodele A mbystoma mexicanum
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2006.05079.xopenalex-snapshot
Generality of vertebrate developmental patterns: evidence for a dermomyotome in fish
inferred← citeshttps://doi.org/10.1111/j.1748-1716.1994.tb09694.xopenalex-snapshot
Differences in ultrastructural and metabolic profiles within the same type of fibres in various muscles of young and adult rats
inferred← citeshttps://doi.org/10.1152/jappl.2001.90.3.1158openalex-snapshot
Invited Review: Plasticity and energetic demands of contraction in skeletal and cardiac muscle
inferred← citeshttps://doi.org/10.1186/1471-213x-7-65openalex-snapshot
A role for Insulin-like growth factor 2 in specification of the fast skeletal muscle fibre
inferred← citeshttps://doi.org/10.1186/s12864-018-4770-2openalex-snapshot
Differences between fast and slow muscles in scallops revealed through proteomics and transcriptomics
inferred← citeshttps://doi.org/10.1242/dev.107.4.751openalex-snapshot
Neural control of the sequence of expression of myosin heavy chain isoforms in foetal mammalian muscles
inferred← citeshttps://doi.org/10.1242/dev.117.4.1435openalex-snapshot
Contractile protein gene expression in primary myotubes of embryonic mouse hindlimb muscles
inferred← citeshttps://doi.org/10.1242/jcs.111.16.2397openalex-snapshot
Mouse myoblasts can fuse and form a normal sarcomere in the absence of β1 integrin expression
inferred← citeshttps://doi.org/10.1387/ijdb.10235391openalex-snapshot
Fetal myoblast clones contribute to both fast and slow fibres in developing rat muscle
inferred← citeshttps://doi.org/10.23868/201808014openalex-snapshot
Fusion-phenomenon in normal histogenesis and in pathology: part 1
inferred← citeshttps://doi.org/10.2527/2000.7861485xopenalex-snapshot
Growth- and breed-related changes of muscle fiber characteristics in cattle.
inferred← citeshttps://doi.org/10.3389/fphys.2021.651112openalex-snapshot
Auto-Regulation Method vs. Fixed-Loading Method in Maximum Strength Training for Athletes: A Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.70675/d30bcd75z2b3dz47b1za355zb03cfbe26c48openalex-snapshot
Regulatory roots of cranial muscle diversity : developmental origins of muscular resilience
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