Sexually dimorphic expression of myosin heavy chains in the adult mouse masseter

Three myosin heavy chain isoforms in type 2 skeletal muscle fibres

Schiaffino, S., Gorza, L., Sartore, S., Saggin, L., Ausoni, S., Vianello, M., Gundersen, K., & Lømo, T. (1989) · Journal of Muscle Research and Cell Motility · doi:10.1007/bf01739810 · Cited by 960 · see citing works

Electrophoretic separation of rat skeletal muscle myosin heavy-chain isoforms

Talmadge, R. J., & Roy, R. R. (1993) · Journal of Applied Physiology · doi:10.1152/jappl.1993.75.5.2337 · Cited by 804 · see citing works

Invited review: Neural control of phenotypic expression in mammalian muscle fibers

Pette, D., & Vrbovà, G. (1985) · Muscle & Nerve · doi:10.1002/mus.880080810 · Cited by 731 · see citing works

Myosin isoforms in mammalian skeletal muscle

Schiaffino, S., & Reggiani, C. (1994) · Journal of Applied Physiology · doi:10.1152/jappl.1994.77.2.493 · Cited by 538 · see citing works

Force‐velocity relations and myosin heavy chain isoform compositions of skinned fibres from rat skeletal muscle.

Bottinelli, R., Schiaffino, S., & Reggiani, C. (1991) · The Journal of Physiology · doi:10.1113/jphysiol.1991.sp018617 · Cited by 486 · see citing works

Shortening velocity in single fibers from adult rabbit soleus muscles is correlated with myosin heavy chain composition.

Reiser, P. J., Moss, R. L., Giulian, G. G., & Greaser, M. L. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)39330-4 · Cited by 380 · see citing works

Myosin isozyme transitions occurring during the postnatal development of the rat soleus muscle

Butler-Browne, G. S., & Whalen, R. G. (1984) · Developmental Biology · doi:10.1016/0012-1606(84)90197-0 · Cited by 294 · see citing works

Effect of age and gender on sudomotor and cardiovagal function and blood pressure response to tilt in normal subjects

Low, P. A., Denq, J.-C., Opfer‐Gehrking, T. L., Dyck, P. J., O’Brien, P. C., & Slezak, J. M. (1997) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(199712)20:12 · Cited by 277 · see citing works

Anatomy and innervation patterns of cat lateral gastrocnemius and plantaris muscles

ENGLISH, A. W., & Letbetter, W. D. (1982) · American Journal of Anatomy · doi:10.1002/aja.1001640107 · Cited by 270 · see citing works

Three Slow Myosin Heavy Chains Sequentially Expressed in Developing Mammalian Skeletal Muscle

Hughes, S. M., Cho, M. K., Karsch‐Mizrachi, I., Travis, M. A., Silberstein, L., Leinwand, L. A., & Blau, H. M. (1993) · Developmental Biology · doi:10.1006/dbio.1993.1178 · Cited by 211 · see citing works

Involution and hormone-induced persistence of the M. sphincter (levator) ani in female rats.

Cihák, R., GUTMANN, E., & Hanzlíková, V. (1970) · PubMed · Cited by 206 · see citing works

Compartmentalization of Muscles and Their Motor Nuclei: The Partitioning Hypothesis

ENGLISH, A. W., Wolf, S. L., & Segal, R. L. (1993) · Physical Therapy · doi:10.1093/ptj/73.12.857 · Cited by 198 · see citing works

A one-step biuret assay for protein in the presence of detergent

Watters, C. D. (1978) · Analytical Biochemistry · doi:10.1016/0003-2697(78)90475-x · Cited by 105 · see citing works

Regulation of the Androgen and Glucocorticoid Receptors in Rat and Mouse Skeletal Muscle Cytosol*

Dahlberg, E., Snochowski, M., & Gustafsson, J.-Α. (1981) · Endocrinology · doi:10.1210/endo-108-4-1431 · Cited by 89 · see citing works

Electromyographic Heterogeneity in the Human Temporalis and Masseter Muscles during Dynamic Tasks Guided by Visual Feedback

Blanksma, N. G., van Eijden, T. M. G. J., van Ruijven, L. J., & Weijs, W. A. (1997) · Journal of Dental Research · doi:10.1177/00220345970760010401 · Cited by 78 · see citing works

Testosterone-induced changes in contractile protein isoforms in the sexually dimorphic temporalis muscle of the guinea pig.

Lyons, G. E., Kelly, A. M., & Rubinstein, N. A. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)69301-9 · Cited by 71 · see citing works

Regional differences in fibre type composition in the human temporalis muscle

Korfage, J. A. M., & van Eijden, T. M. G. J. (1999) · Journal of Anatomy · doi:10.1046/j.1469-7580.1999.19430355.x · Cited by 71 · see citing works

Role of dihydrotestosterone in androgen action

Wilson, J. D. (1996) · The Prostate · doi:10.1002/(sici)1097-0045(1996)6+ · Cited by 69 · see citing works

Effects of Gonadectomy and Estrogen Administration on Rat Skeletal Muscle

Kobori, M., & Yamamuro, T. (1989) · Clinical Orthopaedics and Related Research · doi:10.1097/00003086-198906000-00045 · Cited by 66 · see citing works

Effect of androgens on histochemical fibre type: Differentiation in the temporal muscle of the guinea pig

Gutmann, E., Hanzlíková, V., & Lojda, Z. (1970) · Histochemie · doi:10.1007/bf00278213 · Cited by 63 · see citing works

Long-term effects of estrogen on rat skeletal muscle

Suzuki, S., & Yamamuro, T. (1985) · Experimental Neurology · doi:10.1016/0014-4886(85)90219-5 · Cited by 62 · see citing works

Estrogen binding proteins in rat skeletal and perineal muscles: in vitro and in vivo studies.

Dionne, F., Lesage, R., Dubé, J., & Tremblay, R. (1979) · Journal of Steroid Biochemistry · doi:10.1016/0022-4731(79)90156-0 · Cited by 59 · see citing works

Steroid Receptors in Two Types of Rabbit Skeletal Muscle*

Saartok, T. (1984) · International Journal of Sports Medicine · doi:10.1055/s-2008-1025894 · Cited by 59 · see citing works

Trophic Effects of Androgen: Receptor Expression and the Survival of Laryngeal Motor Neurons after Axotomy

Perez, J. D., & Kelley, D. B. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-21-06625.1996 · Cited by 47 · see citing works

Histochemical enzyme profile of the masseter muscle in different mammalian species

Schiaffino, S. (1974) · The Anatomical Record · doi:10.1002/ar.1091800107 · Cited by 41 · see citing works

Effect of hypothyroidism on myosin heavy chain expression in rat pharyngeal dilator muscles

Petrof, B., Kelly, A. M., Rubinstein, N. A., & Pack, A. I. (1992) · Journal of Applied Physiology · doi:10.1152/jappl.1992.73.1.179 · Cited by 35 · see citing works

Anatomical Partitioning and Nerve Branching Patterns in the Adult Rabbit Masseter

Widmer, C. G., Klugman, D., & ENGLISH, A. W. (1997) · Cells Tissues Organs · doi:10.1159/000147988 · Cited by 34 · see citing works

Different phenotypes among slow/beta myosin heavy chain-containing fibres of rabbit masseter muscle: a novel type of diversity in adult muscle.

ENGLISH, A. W., Eason, J. M., Pol‐Rodriguez, M., Schwartz, G., & Shirley, A. (1998) · Journal of Muscle Research and Cell Motility · doi:10.1023/a:1005360526559 · Cited by 27 · see citing works

Opposite regulations by androgenic and thyroid hormones of V1 myosin expression in the two types of rabbit striated muscle: skeletal and cardiac

d’Albis, A., Couteaux, R., Janmot, C., & Mira, J. (1993) · FEBS Letters · doi:10.1016/0014-5793(93)81326-u · Cited by 20 · see citing works

Torques Produced by Different Compartments of the Rabbit Masseter Muscle

ENGLISH, A. W., Carrasco, D. I., & Widmer, C. G. (1999) · Journal of Applied Biomechanics · doi:10.1123/jab.15.4.348 · Cited by 17 · see citing works

Retention of hormonal sensitivity in free grafts of the levator ani muscle

Carlson, B. M., Herbrychová, A., & GUTMANN, E. (1979) · Experimental Neurology · doi:10.1016/0014-4886(79)90187-0 · Cited by 14 · see citing works

Testosterone control of endplate and non-endplate acetylcholinesterase in the rat levator ani muscle

Godinho, R. O., Souccar, C., & Lapa, A. J. (1994) · Neurochemical Research · doi:10.1007/bf00967703 · Cited by 6 · see citing works

SEXUAL DIMORPHISM OF ISOZYME PATTERNS OF LACTATE DEHYDROGENASE AND EFFECTS OF TESTECTOMY AND OVARIECTOMY ON THE ISOZYME DISTRIBUTION IN THE MASSETER MUSCLE AND TONGUE OF MICE

Sekino, K., Suzuki, Y., Miyata, K., Osawa, K., Suemune, S., Hosoi, M., Niida, S., Wakisaka, H., & Maeda, N. (1993) · Biomedical Research · doi:10.2220/biomedres.14.49 · Cited by 5 · see citing works

Fiber Types in Mammalian Skeletal Muscles

Schiaffino, S., & Reggiani, C. (2011) · Physiological Reviews · doi:10.1152/physrev.00031.2010 · Cited by 3,022 · see citing works

Sex-Based Differences in Skeletal Muscle Kinetics and Fiber-Type Composition

Haizlip, K. M., Harrison, B. C., & Leinwand, L. A. (2015) · Physiology · doi:10.1152/physiol.00024.2014 · Cited by 521 · see citing works

Regulation of the Growth of Multinucleated Muscle Cells by an Nfatc2-Dependent Pathway

Horsley, V., Friday, B. B., Matteson, S., Kegley, K. M., Gephart, J., & Pavlath, G. K. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.2.329 · Cited by 257 · see citing works

Morphology, performance and fighting capacity in male lizards, Gallotia galloti

Huyghe, K., Vanhooydonck, B., Scheers, H., Molina–Borja, M., & Damme, R. V. (2005) · Functional Ecology · doi:10.1111/j.1365-2435.2005.01038.x · Cited by 245 · see citing works

Influence of age, sex, and strength training on human muscle gene expression determined by microarray

Roth, S. M., Ferrell, R. E., Peters, D. G., Metter, E. J., Hurley, B. F., & Rogers, M. A. (2002) · Physiological Genomics · doi:10.1152/physiolgenomics.00028.2002 · Cited by 134 · see citing works

Diet-induced obesity alters skeletal muscle fiber types of male but not female mice

DeNies, M. S., Johnson, J., Maliphol, A. B., Bruno, M., Kim, A., Rizvi, A., Rustici, K., & Medler, S. (2014) · Physiological Reports · doi:10.1002/phy2.204 · Cited by 94 · see citing works

Fiber-type Composition of the Human Jaw Muscles—(Part 2) Role of Hybrid Fibers and Factors Responsible for Inter-individual Variation

Korfage, J. A. M., Koolstra, J. H., Langenbach, G. E. J., & van Eijden, T. M. G. J. (2005) · Journal of Dental Research · doi:10.1177/154405910508400902 · Cited by 94 · see citing works

It is all in the head: morphological basis for differences in bite force among colour morphs of the Dalmatian wall lizard

Huyghe, K., Herrel, A., Adriaens, D., Tadić, Z., & Damme, R. V. (2008) · Biological Journal of the Linnean Society · doi:10.1111/j.1095-8312.2008.01103.x · Cited by 89 · see citing works

Functional and molecular outcomes of the human masticatory muscles

Isola, G., Anastasi, G., Matarese, G., Williams, R., Cutroneo, G., Bracco, P., & Piancino, M. (2017) · Oral Diseases · doi:10.1111/odi.12806 · Cited by 86 · see citing works

Relationships between hormones, physiological performance and immunocompetence in a color-polymorphic lizard species, Podarcis melisellensis

Huyghe, K., Husak, J. F., Herrel, A., Tadić, Z., Moore, I. T., Damme, R. V., & Vanhooydonck, B. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.02.005 · Cited by 73 · see citing works

Estradiol modulates myosin regulatory light chain phosphorylation and contractility in skeletal muscle of female mice

Lai, S., Collins, B. C., Colson, B. A., Kararigas, G., & Lowe, D. A. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00439.2015 · Cited by 70 · see citing works

The ontogeny of sexual dimorphism in the facial skeleton of the African apes

Cobb, S. N., & O’Higgins, P. (2007) · Journal of Human Evolution · doi:10.1016/j.jhevol.2007.03.006 · Cited by 69 · see citing works

Slow or fast: Implications of myofibre type and associated differences for manifestation of neuromuscular disorders

Lloyd, E. M., Pinniger, G. J., Murphy, R. M., & Grounds, M. D. (2023) · Acta Physiologica · doi:10.1111/apha.14012 · Cited by 65 · see citing works

MuSK antibody positive myasthenia gravis plasma modifies MURF-1 expression in C2C12 cultures and mouse muscle in vivo

Benvéniste, O., Jacobson, L. W., Farrugia, M. E., Clover, L. M., & Vincent, A. C. (2005) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2005.08.016 · Cited by 60 · see citing works

Developmental and functional considerations of masseter muscle partitioning

Widmer, C. G., ENGLISH, A. W., & Morris-Wiman, J. A. (2006) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2006.09.015 · Cited by 57 · see citing works

The ancient sarcomeric myosins found in specialized muscles

Lee, L. A., Karabina, A., Broadwell, L. J., & Leinwand, L. A. (2019) · Skeletal Muscle · doi:10.1186/s13395-019-0192-3 · Cited by 56 · see citing works

Mouse sarcopenia model reveals sex- and age-specific differences in phenotypic and molecular characteristics

Kerr, H. L., Krumm, K., Anderson, B., Christiani, A. J., Strait‐Bodey, L., Li, T., Irwin, B., Jiang, S., Rybachok, A., Chen, A. L., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci172890 · Cited by 54 · see citing works

Sex as a Biological Variable in Oral Diseases: Evidence and Future Prospects

Sangalli, L., de Souza, L. C., Letra, A., Shaddox, L. M., & Ioannidou, E. (2023) · Journal of Dental Research · doi:10.1177/00220345231197143 · Cited by 45 · see citing works

Sexual Dimorphism in the Musculoskeletal System: Sex Hormones and Beyond

Plotkin, L. I., Bruzzaniti, A., & Pianeta, R. (2024) · Journal of the Endocrine Society · doi:10.1210/jendso/bvae153 · Cited by 42 · see citing works

Uncoupling proteins: gender dependence and their relation to body weight control

Rodríguez, A. M., & Palou, A. (2004) · International Journal of Obesity · doi:10.1038/sj.ijo.0802588 · Cited by 42 · see citing works

Investigation of sexual dimorphism in the rabbit masseter muscle showing different effects of androgen deprivation in adult and young adult animals

Eason, J. M., Schwartz, G., Shirley, K., & ENGLISH, A. W. (2000) · Archives of Oral Biology · doi:10.1016/s0003-9969(00)00030-3 · Cited by 42 · see citing works

Characteristics of Myofibres in the Masseter Muscle of Mice during Postnatal Growth Period

Gojyo, K., Abe, S., & Ide, Y. (2002) · Anatomia Histologia Embryologia · doi:10.1046/j.1439-0264.2002.00368.x · Cited by 39 · see citing works

Intermittent glucocorticoid treatment enhances skeletal muscle performance through sexually dimorphic mechanisms

Salamone, I. M., Quattrocelli, M., Barefield, D. Y., Page, P., Tahtah, I., Hadhazy, M., Tomar, G., & McNally, E. M. (2022) · Journal of Clinical Investigation · doi:10.1172/jci149828 · Cited by 34 · see citing works

Developmental, physiologic and phylogenetic perspectives on the expression and regulation of myosin heavy chains in mammalian skeletal muscles

Hoh, J. F. Y. (2023) · Journal of Comparative Physiology B · doi:10.1007/s00360-023-01499-0 · Cited by 35 · see citing works

Spatial Distribution of Myosin Heavy-chain Isoforms in Mouse Masseter

Widmer, C. G., Morris-Wiman, J. A., & Nekula, C. (2002) · Journal of Dental Research · doi:10.1177/002203450208100108 · Cited by 33 · see citing works

The evolution of androgen receptor expression and behavior in Anolis lizard forelimb muscles

Johnson, M. A., Kircher, B. K., & Castro, D. J. (2017) · Journal of Comparative Physiology A · doi:10.1007/s00359-017-1228-y · Cited by 33 · see citing works

Physiological Adaptations to Progressive Endurance Exercise Training in Adult and Aged Rats: Insights from the Molecular Transducers of Physical Activity Consortium (MoTrPAC)

Schenk, S., Sagendorf, T. J., Many, G. M., Lira, A. K., de Sousa, L. G. O., Bae, D., Cicha, M. Z., Kramer, K. S., Muehlbauer, M. J., Hevener, A. L., et al. (2024) · Function · doi:10.1093/function/zqae014 · Cited by 32 · see citing works

Muscle-fiber characteristics in adult mouse-tongue muscles

Abe, S., Maejima, M., Watanabe, H., Shibahara, T., Agematsu, H., Doi, T., Sakiyama, K., Usami, A., Gojyo, K., Hashimoto, M., et al. (2002) · Anatomical Science International · doi:10.1046/j.0022-7722.2002.00019.x · Cited by 30 · see citing works

Effects of 14 days of microgravity on fast hindlimb and diaphragm muscles of the rat

Schuenke, M. D., Reed, D. W., Kraemer, W. J., Staron, R. S., Volek, J. S., Hymer, W. C., Gordon, S., & Koziris, L. P. (2009) · European Journal of Applied Physiology · doi:10.1007/s00421-009-1091-9 · Cited by 28 · see citing works

Changes in the properties of mouse tongue muscle fibres before and after weaning

Maejima, M., Abe, S., Sakiyama, K., Agematsu, H., Hashimoto, M., Tamatsu, Y., & Ide, Y. (2005) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2005.03.007 · Cited by 28 · see citing works

Androgen dependent seasonal changes in muscle fiber type in the dewlap neuromuscular system of green anoles

Holmes, M. M., Bartrem, C. L., & Wade, J. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.03.022 · Cited by 27 · see citing works

Development of sex differences in the rabbit masseter muscle is not restricted to a critical period

ENGLISH, A. W., & Schwartz, G. (2002) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00953.2001 · Cited by 27 · see citing works

Superficial and deep layer muscle fibre properties of the mouse masseter before and after weaning

Shida, T., Abe, S., Sakiyama, K., Agematsu, H., Mitarashi, S., Tamatsu, Y., & Ide, Y. (2004) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2004.08.005 · Cited by 26 · see citing works

Identification of candidate genes and proteins in aging skeletal muscle (sarcopenia) using gene expression and structural analysis

Shafiee, G., Asgari, Y., Soltani, A., Larijani, B. A., & Heshmat, R. (2018) · PeerJ · doi:10.7717/peerj.5239 · Cited by 25 · see citing works

Positive correlation of skeletal muscle UCP3 mRNA levels with overweight in male, but not in female, rats

Rodríguez, A. M., Roca, P., Bonet, M. L., Picó, C., Oliver, P., & Palou, A. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00698.2002 · Cited by 25 · see citing works

Gestational Exposure to Bisphenol A and Bisphenol S Leads to Fetal Skeletal Muscle Hypertrophy Independent of Sex

Jing, J., Pu, Y., Gingrich, J., & Veiga‐Lopez, A. (2019) · Toxicological Sciences · doi:10.1093/toxsci/kfz198 · Cited by 23 · see citing works

Characteristics of muscle fibers reconstituted in the regeneration process of masseter muscle in an mdx mouse model of muscular dystrophy

Lee, W.-H., Abe, S., Kim, H.-J., Usami, A., Honda, A., Sakiyama, K., & Ide, Y. (2006) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-006-9066-5 · Cited by 23 · see citing works

Sex Differences in Rabbit Masseter Muscle Function

ENGLISH, A. W., & Widmer, C. G. (2003) · Cells Tissues Organs · doi:10.1159/000070577 · Cited by 22 · see citing works

Brief Exposure to Testosterone Is Sufficient to Induce Sex Differences in the Rabbit Masseter Muscle

Reader, M., Schwartz, G., & ENGLISH, A. W. (2001) · Cells Tissues Organs · doi:10.1159/000047884 · Cited by 22 · see citing works

The content of myosin heavy chains in hindlimb muscles of female and male rats.

Drzymała‐Celichowska, H., Karolczak, J., Rędowicz, M. J., & Bukowska, D. (2012) · PubMed · Cited by 22 · see citing works

Masticatory (`superfast') myosin heavy chain and embryonic/atrial myosin light chain 1 in rodent jaw-closing muscles

Reiser, P. J., Bicer, S., Chen, Q., Zhu, L., & Quan, N. (2009) · Journal of Experimental Biology · doi:10.1242/jeb.031369 · Cited by 22 · see citing works

Sexual dimorphisms in skeletal muscle: current concepts and research horizons

Emmert, M. E., Emmert, A. S., Goh, Q., & Cornwall, R. (2024) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00529.2023 · Cited by 22 · see citing works

Changes in Muscle-fiber Properties of the Murine Digastric Muscle Before and After Weaning

Okubo, K., Abe, S., Usami, A., Agematsu, H., Nakamura, H., Hashimoto, M., & Ide, Y. (2006) · ZOOLOGICAL SCIENCE · doi:10.2108/zsj.23.1079 · Cited by 20 · see citing works

Sexual dimorphism of murine masticatory muscle function

Daniels, D. W., Tian, Z., & Barton, E. R. (2008) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2007.09.006 · Cited by 19 · see citing works

Age‐related changes of skeletal muscle metabolic response to contraction are also sex‐dependent

Campbell, M. D., Djukovic, D., Raftery, D., & Marcinek, D. J. (2023) · The Journal of Physiology · doi:10.1113/jp285124 · Cited by 17 · see citing works

Effects of short term forced oral breathing: Physiological changes and structural adaptation of diaphragm and orofacial muscles in rats

Padzys, G. S., Martrette, J., Tankosic, C., Thornton, S. N., & Trabalon, M. (2011) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2011.06.004 · Cited by 19 · see citing works

Masticatory function and properties of masseter muscle fibers in microphthalmic (mi/mi) mice during postnatal development

Doi, T., Abe, S., & Ide, Y. (2003) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/s0940-9602(03)80103-6 · Cited by 19 · see citing works

Fiber Type Composition of the Muscle Responsible for Throat Fan Extension in Green Anole Lizards

Rosen, G. J., O’Bryant, E. L., Swender, D. A., & Wade, J. (2004) · Brain Behavior and Evolution · doi:10.1159/000077541 · Cited by 19 · see citing works

Changes in the Muscle Fibre Properties of the Mouse Temporal Muscle after Weaning

Suzuki, K. P., Abe, S., Kim, H. J., Usami, A., Iwanuma, O., Okubo, H., & Ide, Y. (2006) · Anatomia Histologia Embryologia · doi:10.1111/j.1439-0264.2006.00729.x · Cited by 18 · see citing works

Expression profiling reveals heightened apoptosis and supports fiber size economy in the murine muscles of mastication

Evans, M., Morine, K., Kulkarni, C., & Barton, E. R. (2008) · Physiological Genomics · doi:10.1152/physiolgenomics.00232.2007 · Cited by 17 · see citing works

Limb, respiratory, and masticatory muscle compartmentalization

Widmer, C. G., & Morris-Wiman, J. A. (2010) · Progress in brain research · doi:10.1016/b978-0-444-53613-6.00005-8 · Cited by 16 · see citing works

Significant roles of microtubules in mature striated muscle deduced from the correlation between tubulin and its molecular chaperone αB-crystallin in rat muscles

Jee, H., Sakurai, T., Kawada, S., Ishii, N., & Atomi, Y. (2009) · The Journal of Physiological Sciences · doi:10.1007/s12576-008-0014-6 · Cited by 16 · see citing works

Feeding with powdered diet after weaning affects sex difference in acetylcholine release in the hippocampus in rats

Takase, K., Mitsushima, D., Masuda, J., Mogi, K., Funabashi, T., Endo, Y., & Kimura, F. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.08.012 · Cited by 16 · see citing works

Histological features of masticatory muscles after botulinum toxin A injection into the right masseter muscle of dystrophin deficient (mdx-) mice

Botzenhart, U. U., Gredes, T., Gerlach, R., Zeidler-Rentzsch, I., Gedrange, T., & Keil, C. (2020) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2020.151464 · Cited by 14 · see citing works

Neonatal low-protein diet reduces the masticatory efficiency in rats

Ferraz‐Pereira, K. N., Aragão, R. D. S., Verdier, D., Toscano, A. E., Lacerda, D. C., Manhães‐de‐Castro, R., & Kolta, A. (2015) · British Journal Of Nutrition · doi:10.1017/s0007114515003062 · Cited by 14 · see citing works

Alternative splicing diversifies the skeletal muscle transcriptome during prolonged spaceflight

Henrich, M., Ha, P., Wang, Y., Ting, K., Stodieck, L., Soo, C. B., Adams, J. S., & Chun, R. F. (2022) · Skeletal Muscle · doi:10.1186/s13395-022-00294-9 · Cited by 13 · see citing works

Influence of age and gender on sex steroid receptors in rat masticatory muscles

Galhardo, A. P. M., Mukai, M. K., Mori, M., Carvalho, K. C., Baracat, M. C. P., Simões, M. D. J., Soares, J. M., & Baracat, E. C. (2019) · Scientific Reports · doi:10.1038/s41598-019-54774-y · Cited by 13 · see citing works

Influence of the Lurcher mutation on myosin heavy chain expression in skeletal and cardiac muscles

Hartmann, N., Martrette, J., & Westphal, A. (2001) · Journal of Cellular Biochemistry · doi:10.1002/jcb.1109 · Cited by 13 · see citing works

Muscle Plasticity: Changes in Oral Function of Muscle Fiber Characteristics

Abe, S., Sakiyama, K., & Ide, Y. (2007) · Journal of Oral Biosciences · doi:10.1016/s1349-0079(07)80036-3 · Cited by 12 · see citing works

Relationship between Function of Masticatory Muscle in Mouse and Properties of Muscle Fibers

Abe, S., Hiroki, E., Iwanuma, O., Sakiyama, K., Shirakura, Y., Hirose, D., Shimoo, Y., Suzuki, M., Ikari, Y., Kikuchi, R., et al. (2008) · The Bulletin of Tokyo Dental College · doi:10.2209/tdcpublication.49.53 · Cited by 11 · see citing works

Feeding with powdered diet after weaning increases visuospatial ability in association with increases in the expression of N-methyl-d-aspartate receptors in the hippocampus of female rats

Takase, K., Funabashi, T., Mogi, K., Mitsushima, D., & Kimura, F. (2005) · Neuroscience Research · doi:10.1016/j.neures.2005.06.013 · Cited by 11 · see citing works

Slow- and fast-twitch hindlimb skeletal muscle phenotypes 12 wk after ⅚ nephrectomy in Wistar rats of both sexes

Acevedo, L. M., Peralta-Ramírez, A., López, I., Chamizo, V. E., Pineda, C., Rodríguez-Ortiz, M. E., Rodríguez, M., Aguilera‐Tejero, E., & Rivero, J. L. L. (2015) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00195.2015 · Cited by 11 · see citing works

Uncoupling proteins: gender-dependence and their relation to body weight control

Rodríguez, A. M., & Palou, A. (2004) · International Journal of Obesity · doi:10.1038/sj.ijo.0802579 · Cited by 10 · see citing works

Metabolic Cost of Activation and Mechanical Efficiency of Mouse Soleus Muscle Fiber Bundles During Repetitive Concentric and Eccentric Contractions

Lemaire, K. K., Jaspers, R. T., Kistemaker, D. A., van Soest, A., & van der Laarse, W. J. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00760 · Cited by 9 · see citing works

Age-related histone H3.3 accumulation associates with a repressive chromatin in mouse tibialis anterior muscle

Masuzawa, R., Flete, H. K. R., Shimizu, J., & Kawano, F. (2024) · The Journal of Physiological Sciences · doi:10.1186/s12576-024-00935-2 · Cited by 8 · see citing works

Gravitational Effects on Human Physiology

Atomi, Y. (2015) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-017-9918-8_29 · Cited by 8 · see citing works

Changes in the Myosin Heavy Chain 2a and 2b Isoforms of the Anterior Belly of the Digastric Muscle Before and After Weaning in Mice

Yoshii, M., Sakiyama, K., Abe, S., Agematsu, H., Mitarashi, S., Tamatsu, Y., & Ide, Y. (2007) · Anatomia Histologia Embryologia · doi:10.1111/j.1439-0264.2007.00813.x · Cited by 8 · see citing works

Skeletal Muscle Uncoupling Proteins in Mice Models of Obesity

Bombek, L. K., & Čater, M. (2022) · Metabolites · doi:10.3390/metabo12030259 · Cited by 7 · see citing works

Developmental, Physiological and Phylogenetic Perspectives on the Expression and Regulation of Myosin Heavy Chains in Craniofacial Muscles

Hoh, J. F. Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084546 · Cited by 7 · see citing works

Histochemical study of rabbit medial pterygoid muscle during postnatal development

Saito, K., Morita, T., Takasu, H., Kuroki, K., Fujiwara, T., Hiraba, K., & Goto, S. (2016) · Odontology · doi:10.1007/s10266-016-0262-5 · Cited by 7 · see citing works

Influence of Botulinumtoxin A on the Expression of Adult MyHC Isoforms in the Masticatory Muscles in Dystrophin-Deficient Mice (Mdx-Mice)

Botzenhart, U. U., Constantin, W., Тодоров, Т., & Kunert‐Keil, C. (2016) · BioMed Research International · doi:10.1155/2016/7063093 · Cited by 7 · see citing works

Motor Units and Muscle Receptors

Celichowski, J., & Krutki, P. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814593-7.00004-9 · Cited by 7 · see citing works

Patterns of tropomyosin and troponin-T isoform expression in jaw-closing muscles of mammals and reptiles that express masticatory myosin

Bicer, S., Patel, R. J., Williams, J. B., & Reiser, P. J. (2011) · Journal of Experimental Biology · doi:10.1242/jeb.049213 · Cited by 7 · see citing works

Increased vertical dimension effects on masseter muscle fiber phenotype during maturation

Widmer, C. G., Nguyen, V. D., Chiang, H. K., & Morris-Wiman, J. A. (2012) · The Angle Orthodontist · doi:10.2319/122111-786.1 · Cited by 7 · see citing works

Variability and Plasticity of Motor Unit Properties in Mammalian Skeletal Muscle

Celichowski, J., & Piotr, K. (2012) · Journal of Applied Biomedicine · doi:10.1016/s0208-5216(12)70047-5 · Cited by 7 · see citing works

Jaw‐Muscle Structure and Function in Primates: Insights Into Muscle Performance and Feeding‐System Behaviors

Taylor, A. B., Holmes, M. A., Laird, M. F., & Terhune, C. E. (2025) · Evolutionary Anthropology Issues News and Reviews · doi:10.1002/evan.22053 · Cited by 8 · see citing works

Muscle plasticity is influenced by renal function and caloric intake through the FGF23-vitamin D axis

Acevedo, L. M., Vidal, Á., Aguilera‐Tejero, E., & Rivero, J. L. L. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00306.2022 · Cited by 6 · see citing works

The expression of myogenic regulatory factors and muscle growth factors in the masticatory muscles of dystrophin-deficient (MDX) mice

SPASSOV, A. W., Gredes, T., Gedrange, T., Lucke, S., Pavlović, D., & Kunert‐Keil, C. (2011) · Cellular & Molecular Biology Letters · doi:10.2478/s11658-011-0003-2 · Cited by 6 · see citing works

A study of chewing muscles: Age-related changes in type I collagen and matrix metalloproteinase-2 expression

Cicek, M., Tümer, M. K., & Ünsal, V. (2019) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2019.104583 · Cited by 6 · see citing works

The effects of altering vertical dimension onthe masticatory muscles and temporomandibular joint

Widmer, C. G. (2002) · Seminars in Orthodontics · doi:10.1053/sodo.2002.125435 · Cited by 6 · see citing works

Myosin heavy chain composition of tongue muscle in microphthalmic (mi/mi) mice before and after weaning

Yanagisawa, N., Abe, S., Agematsu, H., Sakiyama, K., Usami, A., Tamatsu, Y., & Ide, Y. (2006) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2006.02.004 · Cited by 6 · see citing works

Androgen action on myogenesis throughout the lifespan; comparison with neurogenesis

Barsky, S. T., & Monks, D. A. (2023) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2023.101101 · Cited by 5 · see citing works

Musculoskeletal mass and shape are correlated with competitive ability in male house mice (Mus musculus)

Cooper, A. N., Cunningham, C. B., Morris, J. S., Ruff, J. S., Potts, W. K., & Carrier, D. R. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.213389 · Cited by 4 · see citing works

The anatomy and histochemistry of flight hindlimb posture in birds. II . The flexed hindlimb posture of perching birds

Walker, A. M., & Meyers, R. A. (2019) · Journal of Anatomy · doi:10.1111/joa.12960 · Cited by 4 · see citing works

Distribution of LYVE-1 and CD31 in postnatal rat masseter muscle

Sato, I., Imura, K., Miwa, Y., Miyado, M., & Sunohara, M. (2008) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2008.03.013 · Cited by 3 · see citing works

Skeletal Fiber Type in Muscle Pain and Dysfunction

Cardia, M. L., Carneiro, B. D., Tavares, I., & Pozza, D. H. (2026) · Biomedicines · doi:10.3390/biomedicines14040794 · Cited by 2 · see citing works

HGF and IGF-1 is Present during the Developmental Process of Murine Masseter Muscle

Abe, S., Nonami, K., Iwanuma, O., Hiroki, E., Yanagisawa, N., Sakiyama, K., & Ide, Y. (2009) · Journal of Hard Tissue Biology · doi:10.2485/jhtb.18.1 · Cited by 2 · see citing works

Effect of aquaporin 1 and 4 on masticatory muscles degeneration as a result of aging

Tümer, M. K., Demır, M., & Cicek, M. (2017) · Bratislavské lekárske listy/Bratislava medical journal · doi:10.4149/bll_2017_127 · Cited by 2 · see citing works

Myofiber Properties of Mouse Mylohyoid Muscle in the Growth Period

Kado, S., Abe, S., Hiroki, E., Iwanuma, O., Sakiyama, K., Kim, H., & Ide, Y. (2008) · ZOOLOGICAL SCIENCE · doi:10.2108/zsj.25.806 · Cited by 1 · see citing works

Effect of triiodothyronine on the maxilla and masseter muscles of the rat stomatognathic system

Mariuba, M. V., Goulart-Silva, F., Bordin, S. A., & Nunes, M. T. (2011) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2011000700013 · Cited by 1 · see citing works

Phenomenon of muscle anti-aging after dental treatment-changes in oral function of muscle fiber characteristics

Abe, S. (2008) · Japanese Dental Science Review · doi:10.1016/j.jdsr.2007.10.002

Masseter muscle gene expression in relation to various craniofacial deformities : a genotype-phenotype study

Moawad, H. A. (2009) · UCL Discovery (University College London)

Age and sex dependent effects of metabolic response to muscle contractionPreprint

Campbell, M. D., Djukovic, D., Raftery, D., & Marcinek, D. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.30.542769

NYERI MUSKULOSKELETAL PADA ANAK SD DI SD KRISTEN HARAPAN USIA 10 HINGGA 12 TAHUN KARENA TAS RANSEL YANG BERAT : STUDI PILOT

Syahirah, A., Muliani, & Yuliana, Y. (2021) · E-Jurnal Medika Udayana · doi:10.24843/mu.2021.v10.i5.p08

Optimizing Confocal Imaging Protocols for Muscle Fiber Typing in the Mouse Masseter Muscle

Matias, C., Yamada, C., Movilă, A., & Brault, J. J. (2025) · BIO-PROTOCOL · doi:10.21769/bioprotoc.5267

Influence of Ovarian Hormones on Skeletal Muscle Contractility

Lowe, D. A., & Greising, S. M. (2013) · Springer eBooks · doi:10.1007/978-1-4614-8630-5_1

Additional file 6 of Alternative splicing diversifies the skeletal muscle transcriptome during prolonged spaceflight

Henrich, M., Ha, P., Wang, Y., Ting, K., Stodieck, L., Soo, C. B., Adams, J. S., & Chun, R. (2022) · Figshare · doi:10.6084/m9.figshare.19947329

Development of sex differences in the rabbit masseter muscle is not restricted to a critical period

ENGLISH, A. W., & Schwartz, G. (2002) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00953.2001 · Cited by 27 · see citing works

Investigation of sexual dimorphism in the rabbit masseter muscle showing different effects of androgen deprivation in adult and young adult animals

Eason, J. M., Schwartz, G., Shirley, K., & ENGLISH, A. W. (2000) · Archives of Oral Biology · doi:10.1016/s0003-9969(00)00030-3 · Cited by 42 · see citing works

Sexual Dimorphism in the Rabbit Masseter Muscle: Myosin Heavy Chain Composition of Neuromuscular Compartments

English, A. W., Eason, J., Schwartz, G., Shirley, A., & Carrasco, D. I. (1999) · Cells Tissues Organs · doi:10.1159/000016658 · Cited by 71 · see citing works

Brief Exposure to Testosterone Is Sufficient to Induce Sex Differences in the Rabbit Masseter Muscle

Reader, M., Schwartz, G., & ENGLISH, A. W. (2001) · Cells Tissues Organs · doi:10.1159/000047884 · Cited by 22 · see citing works

Spatial Distribution of Myosin Heavy-chain Isoforms in Mouse Masseter

Widmer, C. G., Morris-Wiman, J. A., & Nekula, C. (2002) · Journal of Dental Research · doi:10.1177/002203450208100108 · Cited by 33 · see citing works