Cited by 172Hearing, Cochlea, Tinnitus, GeneticsVestibular and auditory disordersHearing Loss and Rehabilitation

The DOI matches its Crossref record; 33 of the 34 references it cites were found in a registry or an index.

Hair cell innervation by spiral ganglion neurons in the mouse

Berglund, A. M., Ryugo, D. K.·1987·Journal of Comparative Neurology

Open this paper in CoChat — free account

Abstract

Horseradish peroxidase (HRP) was injected extracellularly into the auditory nerve of adult mice so that the enzyme could infuse individual spiral ganglion neurons. Forty-two well-stained neurons were reconstructed through serial sections from their cell bodies to peripheral terminations in the organ of Corti with the aid of a light microscope and drawing tube. No neuron was observed to innervate both inner and outer hair cells (IHCs and OHCs). Previous observations from neonatal mammals that reported that IHCs and OHCs were innervated by the same neuron are thus presumed to describe a transient developmental phenomenon. Two populations of spiral ganglion neurons were determined on the basis of the differences in receptor innervation. The type I neurons innervated exclusively IHCs by way of thick (1-2 microns) radial fibers, whereas the type II neurons innervated only OHCs by way of thin (approximately 0.5 micron) outer spiral fibers. Certain features of the peripheral process in the vicinity of the cell body were highly correlated with fiber type. This pattern of separate innervation of IHCs and OHCs by type I and type II neurons, respectively, may represent the general plan of afferent organization for the adult mammalian cochlea.

Integrity signals

Registry

Crossref · 10.1002/cne.902550408

Cites

33 of 33 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Histologie du système nerveux de l'homme & des vertébrés
y Cajal, S. R. (1909) · Maloine eBooks · doi:10.5962/bhl.title.48637 · Cited by 2,393
The Auditory psychobiology of the mouse
Willott, J. F. (1983) · Medical Entomology and Zoology · Cited by 460
The cochlear frequency map for the cat: Labeling auditory-nerve fibers of known characteristic frequency
Liberman, M. C. (1982) · The Journal of the Acoustical Society of America · doi:10.1121/1.388677 · Cited by 445
Exuberant projection into the corpus callosum from the visual cortex of newborn cats
Innocenti, G. M., Fiore, L., & Caminiti, R. (1977) · Neuroscience Letters · doi:10.1016/0304-3940(77)90185-9 · Cited by 341
Hair-Cell Innervation by Spiral Ganglion Cells in Adult Cats
Kiang, N. Y.-S., Rho, J. M., Northrop, C. C., Liberman, M. C., & Ryugo, D. K. (1982) · Science · doi:10.1126/science.7089553 · Cited by 302
Self-citation
Comparative Physiology of Sensory Systems
Land, M. F. (1985) · Trends in Neurosciences · doi:10.1016/0166-2236(85)90133-x · Cited by 277
Morphometry of intracellularly labeled neurons of the auditory nerve: Correlations with functional properties
Liberman, M. C., & Oliver, M. E. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902230203 · Cited by 272
Fiber analysis of the statoacoustic nerve of guinea pig, cat, and monkey
Gacek, R. R., & Rasmussen, G. L. (1961) · The Anatomical Record · doi:10.1002/ar.1091390402 · Cited by 222
The transient corticospinal projection from the occipital cortex during the postnatal development of the rat
Stanfield, B. B., & O’Leary, D. D. M. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902380210 · Cited by 206
A study of cochlear innervation patterns in cats and rats with the Golgi method and Nomarski optics
Perkins, R. E., & Morest, D. K. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901630202 · Cited by 159

Show all 34 references

Research works printed but not linked: 8

Firbas W., 1972, Uber anatomische Anpassungen des Hörorgans an die Aufnahme hoher Frequenzen, Mschr. Ohrhk. Laryngol.‐Rhinol., Vienna, 106, 105
Held H., 1926, Handbuch der normalen and pathologischen Physiologie XI, 467
Kolmer W., 1927, Gehörorgan. In: Handbuch der mikroskopischen Anatomie des Menschen. Band III, 351
Münzer F. T., 1931, Uber markhaltige Ganglienzellen, Z. Mikrosk. Anat. Forsch., 24, 286
Rasmussen A. T., 1943, Outlines of Neuroanatomy
Retzius G., 1892, Die Endigungsweise des Gehörnerven. Biolog. Untersuchungen, Neue Folge, III
Thomsen E., 1966, Ultrastructure of the spiral ganglion in the guinea pig, Acta Otolaryngol. [Suppl.] (Stockh.), 224, 442
Von Ebner B., 1903, Die Endigung des Schneckennerven im Cortischen Organe. Kölliker's Handbuch der Gewebelehre des Menschen, III, 944

Sorted by citations

Complementary roles of BDNF and NT-3 in vestibular and auditory development
Ernfors, P., Water, T. R. V. D., Loring, J. M., & Jaenisch, R. (1995) · Neuron · doi:10.1016/0896-6273(95)90263-5 · Cited by 460
Sensory neuron diversity in the inner ear is shaped by activity
Shrestha, B. R., Chia, C., Wu, L., Kujawa, S. G., Liberman, M. C., & Goodrich, L. V. (2018) · Cell · doi:10.1016/j.cell.2018.07.007 · Cited by 432
Structure of the Mammalian Cochlea
Slepecky, N. B. (1996) · Springer handbook of auditory research · doi:10.1007/978-1-4612-0757-3_2 · Cited by 257
The spiral ganglion: Connecting the peripheral and central auditory systems
Nayagam, B. A., Muniak, M. A., & Ryugo, D. K. (2011) · Hearing Research · doi:10.1016/j.heares.2011.04.003 · Cited by 224
Self-citation
Auditory Neurons Make Stereotyped Wiring Decisions before Maturation of Their Targets
Koundakjian, E. J., Appler, J. M., & Goodrich, L. V. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3765-07.2007 · Cited by 207
SNARE complex at the ribbon synapses of cochlear hair cells: analysis of synaptic vesicle‐ and synaptic membrane‐associated proteins
Safieddine, S., & Wenthold, R. J. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00487.x · Cited by 200
Connecting the ear to the brain: Molecular mechanisms of auditory circuit assembly
Appler, J. M., & Goodrich, L. V. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.01.004 · Cited by 202
Where Is the Spike Generator of the Cochlear Nerve? Voltage-Gated Sodium Channels in the Mouse Cochlea
Hossain, W. A., Antic, S. D., Yang, Y., Rasband, M. N., & Morest, D. K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0123-05.2005 · Cited by 181
Hair cell ribbon synapses
Moser, T., Brandt, A., & Lysakowski, A. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0276-3 · Cited by 174
Delayed Inner Ear Maturation and Neuronal Loss in PostnatalIgf-1-Deficient Mice
Camarero, G., Avendaño, C., Fernández-Moreno, C., Villar, Á., Contreras, J., de Pablo, F., Pichel, J. G., & Varela‐Nieto, I. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-19-07630.2001 · Cited by 170
Central trajectories of type II spiral ganglion neurons
Brown, M. C., Berglund, A. M., Kiang, N. Y.-S., & Ryugo, D. K. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902780409 · Cited by 163
Self-citation
The postsynaptic function of type II cochlear afferents
Weisz, C., Glowatzki, E., & Fuchs, P. (2009) · Nature · doi:10.1038/nature08487 · Cited by 160
Morphology of labeled efferent fibers in the guinea pig cochlea
Brown, M. C. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902600412 · Cited by 141
Morphology of labeled afferent fibers in the guinea pig cochlea
Brown, M. C. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902600411 · Cited by 137
Developmental segregation in the afferent projections to mammalian auditory hair cells.
Echteler, S. M. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.14.6324 · Cited by 131
Primary innervation of the avian and mammalian cochlear nucleus
Ryugo, D. K., & Parks, T. N. (2003) · Brain Research Bulletin · doi:10.1016/s0361-9230(03)00049-2 · Cited by 125
Self-citation
The Auditory Nerve: Peripheral Innervation, Cell Body Morphology, and Central Projections
Ryugo, D. K. (1992) · Springer handbook of auditory research · doi:10.1007/978-1-4612-4416-5_2 · Cited by 121
Self-citation
Molecular organization of a type of peripheral glutamate synapse: the afferent synapses of hair cells in the inner ear
Ottersen, O. P., Takumi, Y., Matsubara, A., Landsend, A. S., Laake, J. H., & Usami, S. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00054-3 · Cited by 118
Two classes of outer hair cells along the tonotopic axis of the cochlea
Engel, J., Braig, C., Rüttiger, L., Kuhn, S. A. C., Zimmermann, U., Blin, N., Sausbier, M., Kalbacher, H., Münkner, S., Rohbock, K., et al. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.08.060 · Cited by 100
Peripherin-like immunoreactivity in type II spiral ganglion cell body and projections
Hafidi, A. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00448-x · Cited by 95
Age-Related Changes of Myelin Basic Protein in Mouse and Human Auditory Nerve
Xing, Y., Samuvel, D. J., Stevens, S. M., Dubno, J. R., Schulte, B. A., & Lang, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034500 · Cited by 97
Synaptic transfer from outer hair cells to type II afferent fibers in the rat cochlea
Weisz, C. J. C., Lehar, M., Hiel, H., Glowatzki, E., & Fuchs, P. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6194-11.2012 · Cited by 92
Neurofilament antibodies and spiral ganglion neurons of the mammalian cochlea
Berglund, A. M., & Ryugo, D. K. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903060304 · Cited by 92
Self-citation
Persistence of Cav1.3 Ca2+ Channels in Mature Outer Hair Cells Supports Outer Hair Cell Afferent Signaling
Knirsch, M., Brandt, N., Braig, C., Kuhn, S. A. C., Hirt, B., Münkner, S., Knipper, M., & Engel, J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5364-06.2007 · Cited by 85
Auditory primary afferents in the starling: Correlation of function and morphology
Gleich, O. (1989) · Hearing Research · doi:10.1016/0378-5955(89)90026-9 · Cited by 85
Type II spiral ganglion afferent neurons drive medial olivocochlear reflex suppression of the cochlear amplifier
Froud, K. E., Wong, A. C. Y., Cederholm, J. M. E., Klugmann, M., Sandow, S. L., Julien, J., Ryan, A. F., & Housley, G. D. (2015) · Nature Communications · doi:10.1038/ncomms8115 · Cited by 82
Membrane properties of type II spiral ganglion neurones identified in a neonatal rat cochlear slice
Jagger, D. J., & Housley, G. D. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00525.x · Cited by 79
Transient expression of NMDA receptors during rearrangement of AMPA-receptor-expressing fibers in the developing inner ear
Knipper, M., Köpschall, I., Rohbock, K., Köpke, A. K. E., Bonk, I., Zimmermann, U., & Zenner, H. P. (1996) · Cell and Tissue Research · doi:10.1007/s004410050729 · Cited by 78
Endogenous Firing Patterns of Murine Spiral Ganglion Neurons
Mo, Z., & Davis, R. L. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.3.1294 · Cited by 77
Afferent innervation of outer hair cells in adult cats: I. Light microscopic analysis of fibers labeled with horseradish peroxidase
Simmons, D. D., & Liberman, M. C. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902700111 · Cited by 77
Firing Patterns of Type II Spiral Ganglion Neurons In Vitro
Reid, M. A., Flores‐Otero, J., & Davis, R. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3923-03.2004 · Cited by 75
Neural Circuit Development in the Mammalian Cochlea
Bulankina, A. V., & Moser, T. (2012) · Physiology · doi:10.1152/physiol.00036.2011 · Cited by 70
Reinnervation of hair cells by auditory neurons after selective removal of spiral ganglion neurons
Martinez‐Monedero, R., Corrales, C. E., Cuajungco, M. P., Heller, S., & Edge, A. S. B. (2006) · Journal of Neurobiology · doi:10.1002/neu.20232 · Cited by 71
Three-dimensional imaging of the intact mouse cochlea by fluorescent laser scanning confocal microscopy
MacDonald, G. H., & Rubel, E. W. (2008) · Hearing Research · doi:10.1016/j.heares.2008.05.009 · Cited by 70
Central trajectories of type II spiral ganglion cells from various cochlear regions in mice
Berglund, A. M., & Brown, M. C. (1994) · Hearing Research · doi:10.1016/0378-5955(94)90063-9 · Cited by 66
Self-citation
The Glutamate Receptor Subunit δ1 Is Highly Expressed in Hair Cells of the Auditory and Vestibular Systems
Safieddine, S., & Wenthold, R. J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-19-07523.1997 · Cited by 65
Recent advances in the development and function of type II spiral ganglion neurons in the mammalian inner ear
Zhang, K. D., & Coate, T. M. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.09.017 · Cited by 66
Spiral ganglion neurones: an overview of morphology, firing behaviour, ionic channels and function
Rusznák, Z., & Szűcs, G. (2008) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-008-0586-2 · Cited by 62
P2X receptor signaling inhibits BDNF-mediated spiral ganglion neuron development in the neonatal rat cochlea
Greenwood, D., Jagger, D. J., Huang, L.-C., Hoya, N., Thorne, P. R., Wildman, S. S. P., King, B. F., Pak, K. K., Ryan, A. F., & Housley, G. D. (2007) · Development · doi:10.1242/dev.002279 · Cited by 60
Correlation Between the Length of Outer Hair Cells and the Frequency Coding of the Cochlea
Pujol, R., Lenoir, M., Ladrech, S., Tribillac, F., & Rebillard, G. (1992) · Elsevier eBooks · doi:10.1016/b978-0-08-041847-6.50011-3 · Cited by 59
Chemical neuroprotection in the cochlea: The modulation of dopamine release from lateral olivocochlear efferents
Lendvai, B., Halmos, G. B., Polony, G., Kapocsi, J., Horváth, T., Aller, M., Vizi, E. S., & Zelles, T. (2011) · Neurochemistry International · doi:10.1016/j.neuint.2011.05.015 · Cited by 57
Current concepts in cochlear ribbon synapse formation
Coate, T. M., Scott, M. K., & Gurjar, M. (2018) · Synapse · doi:10.1002/syn.22087 · Cited by 58
Synaptophysin and Gap-43 proteins in efferent fibers of the inner ear during postnatal development
Knipper, M., Zimmermann, U., Rohbock, K., Köpschall, I., & Zenner, H. (1995) · Developmental Brain Research · doi:10.1016/0165-3806(95)00113-r · Cited by 54
Developmental regulation of neuron‐specific P2X3 receptor expression in the rat cochlea
Huang, L.-C., Greenwood, D., Thorne, P. R., & Housley, G. D. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20442 · Cited by 53
Ontogenesis of type II spiral ganglion neurons during development: Peripherin immunohistochemistry
Hafidi, A., Desprès, G., & Romand, R. (1993) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(93)90024-8 · Cited by 52
GluA2-containing AMPA receptors distinguish ribbon-associated from Ribbonless afferent contacts on rat Cochlear hair cells
Martinez-Monedero, R., Liu, C., Weisz, C., Vyas, P., Fuchs, P. A., & Glowatzki, E. (2016) · eNeuro · doi:10.1523/eneuro.0078-16.2016 · Cited by 47
Electrically evoked compound action potentials are different depending on the site of cochlear stimulation
de Heyning, P. V., Arauz, S. L., Atlas, M. D., Baumgartner, W., Caversaccio, M. D., Chester-Browne, R., Estienne, P., Gavilán, J., Godey, B., Gstöttner, W., et al. (2016) · Cochlear Implants International · doi:10.1080/14670100.2016.1240427 · Cited by 47
The innervation of the organ of Corti in the rat
Dannhof, B. J., & Bruns, V. (1993) · Hearing Research · doi:10.1016/0378-5955(93)90255-y · Cited by 47
Expression of neurotrophin receptor trkB in rat cochlear hair cells at time of rearrangement of innervation
Knipper, M., Zimmermann, U., Rohbock, K., Köpschall, I., & Zenner, H. (1996) · Cell and Tissue Research · doi:10.1007/s004410050545 · Cited by 45
Hair Cell Afferent Synapses: Function and DysfunctionPreprint
Johnson, S. L., Safieddine, S., Mustapha, M., & Marcotti, W. (2019) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a033175 · Cited by 51
Neurotrophic Factors in the Auditory Periphery
QUN, L. X., Pirvola, U., Saarma, M., & Ylikoski, J. S. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb08649.x · Cited by 46
Auditory receptor of the red‐eared turtle: II. Afferent and efferent synapses and innervation patterns
Sneary, M. G. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902760411 · Cited by 46
Untitled work
(1998) · doi:10.1002/(sici)1096-9861(19981207)402:1
Outer Hair Cell Glutamate Signaling through Type II Spiral Ganglion Afferents Activates Neurons in the Cochlear Nucleus in Response to Nondamaging Sounds
Weisz, C. J. C., Williams, S. G., Eckard, C. S., Divito, C. B., Ferreira, D. W., Fantetti, K. N., Dettwyler, S. A., Cai, H.-M., Rubio, M. E., Kandler, K., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0619-20.2021 · Cited by 44
Visualization of synaptic markers in the optic neuropils ofDrosophila using a new constrained deconvolution method
Hiesinger, P. R., Scholz, M., Meinertzhagen, I. A., Fischbach, K., & Obermayer, K. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20000108)429:2 · Cited by 35
Unmyelinated axons of the auditory nerve in cats
Ryugo, D. K., Dodds, L. W., Benson, T. E., & Kiang, N. Y.-S. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903080208 · Cited by 43
Self-citation
Kainate and NMDA toxicity for cultured developing and adult rat spiral ganglion neurons: further evidence for a glutamatergic excitatory neurotransmission at the inner hair cell synapse
Lefebvre, P. P., Weber, T., Leprince, P., Rigo, J., Delrée, P., Rogister, B., & Moonen, G. (1991) · Brain Research · doi:10.1016/0006-8993(91)90862-p · Cited by 42
Synaptic transmission at the endbulb of Held deteriorates during age‐related hearing loss
Xie, R., & Manis, P. B. (2016) · The Journal of Physiology · doi:10.1113/jp272683 · Cited by 41
Sequential Retraction Segregates SGN Processes during Target Selection in the Cochlea
Druckenbrod, N. R., & Goodrich, L. V. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2236-15.2015 · Cited by 39
Semaphorin-5B Controls Spiral Ganglion Neuron Branch Refinement during Development
Jung, J. S., Zhang, K. D., Wang, Z., McMurray, M., Tkaczuk, A. T., Ogawa, Y., Hertzano, R. P., & Coate, T. M. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0113-19.2019 · Cited by 40
Neurotoxicity of kainic acid in the rat cochlea during early developmental stages
Gil-Loyzaga, P. E., & Pujol, R. (1990) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/bf00634780 · Cited by 40
Cochlear afferent innervation development
Delacroix, L., & Malgrange, B. (2015) · Hearing Research · doi:10.1016/j.heares.2015.07.015 · Cited by 40
Developmental Changes in Peripherin-eGFP Expression in Spiral Ganglion Neurons
Elliott, K. L., Kersigo, J., Lee, J. H., Jahan, I., Pavlínková, G., Fritzsch, B., & Yamoah, E. N. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.678113 · Cited by 35
Structure and development of cochlear afferent innervation in mammals
Defourny, J., Lallemend, F., & Malgrange, B. (2011) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00516.2010 · Cited by 33
Afferent innervation of outer hair cells in adult cats: II. Electron microscopic analysis of fibers labeled with horseradish peroxidase
Simmons, D. D., & Liberman, M. C. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902700112 · Cited by 33
Distribution of frequenin in the mouse inner ear during development, comparison with other calcium-binding proteins and synaptophysin
Sage, C., Ventéo, S., Jeromin, A., Roder, J., & Dechesne, C. J. (2000) · Hearing Research · doi:10.1016/s0378-5955(00)00183-0 · Cited by 33
Postnatal maturation of spiral ganglion neurons: A horseradish peroxidase study
Simmons, D. D., Manson-Gieseke, L., Hendrix, T. W., Morris, K. A., & Williams, S. J. (1991) · Hearing Research · doi:10.1016/0378-5955(91)90094-p · Cited by 32
Characterization of spiral ganglion neurons cultured on silicon micro-pillar substrates for new auditory neuro-electronic interfaces
Mattotti, M., Micholt, L., Braeken, D., & Kovačić, D. (2015) · Journal of Neural Engineering · doi:10.1088/1741-2560/12/2/026001 · Cited by 30
Tyrosine Hydroxylase Expression in Type II Cochlear Afferents in Mice
Vyas, P., Wu, S. J., Zimmerman, A., Fuchs, P. A., & Glowatzki, E. (2016) · Journal of the Association for Research in Otolaryngology · doi:10.1007/s10162-016-0591-7 · Cited by 30
Untitled work
Fashena, D. (1999) · doi:10.1002/(sici)1096-9861(19990412)406:3
Voltage-gated sodium channel expression in rat spiral ganglion neurons
Fryatt, A. G., Vial, C., Mulheran, M., Gunthorpe, M. J., & Grubb, B. D. (2009) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2009.09.001 · Cited by 29
TSLIM imaging and a morphometric analysis of the mouse spiral ganglion
Johnson, S. B., Schmitz, H. M., & Santi, P. A. (2011) · Hearing Research · doi:10.1016/j.heares.2011.02.008 · Cited by 29
A non-autonomous function of the core PCP protein VANGL2 directs peripheral axon turning in the developing cochlea
Ghimire, S. R., Ratzan, E. M., & Deans, M. R. (2018) · Development · doi:10.1242/dev.159012 · Cited by 29
Patterns of neurofilament stain in the spiral ganglion of the developing and adult mouse
Romand, R., Sobkowicz, H. M., Emmerling, M. R., Whitlon, D. S., & Dahl, D. R. (1990) · Hearing Research · doi:10.1016/0378-5955(90)90099-b · Cited by 29
Neuronal expression of peripherin, a type III intermediate filament protein, in the mouse hindbrain
Barclay, M., Noakes, P. G., Ryan, A. F., Julien, J., & Housley, G. D. (2007) · Histochemistry and Cell Biology · doi:10.1007/s00418-007-0340-4 · Cited by 28
NCAM in the organ of Corti of the developing mouse
Whitlon, D. S., & Rutishauser, U. S. (1990) · Journal of Neurocytology · doi:10.1007/bf01186824 · Cited by 27
Characterization of transgenic mouse lines for labeling type I and type II afferent neurons in the cochlea
Vyas, P., Wu, J. S., Jimenez, A., Glowatzki, E., & Fuchs, P. A. (2019) · Scientific Reports · doi:10.1038/s41598-019-41770-5 · Cited by 26
Kanamycin‐Furosemide Ototoxicity in the Mouse Cochlea: A 3‐Dimensional Analysis
Schmitz, H. M., Johnson, S. B., & Santi, P. A. (2014) · Otolaryngology · doi:10.1177/0194599813519071 · Cited by 26
Immunocytochemical localization of neurofilament subunits in the spiral ganglion of normal and neomycin-treated guinea pigs
DAU, J., & Wenthold, R. J. (1989) · Hearing Research · doi:10.1016/0378-5955(89)90149-4 · Cited by 26
Anatomical evidence of synaptic plasticity in the cochlear nuclei of white-deaf cats
Larsen, S. A., & Kirchhoff, T. M. (1992) · Experimental Neurology · doi:10.1016/0014-4886(92)90240-q · Cited by 26
Single-Cell RNA Analysis of Type I Spiral Ganglion Neurons Reveals a Lmx1a Population in the Cochlea
Grandi, F. C., Tomasi, L. D., & Mustapha, M. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00083 · Cited by 25
Spatiotemporal patterns of neuronal programmed cell death during postnatal development of the gerbil cochlea
Echteler, S. M., Magardino, T. M., & Rontal, M. L. (2005) · Developmental Brain Research · doi:10.1016/j.devbrainres.2005.04.004 · Cited by 23
Temporal pattern of innervation in the developing mouse inner ear: An immunocytochemical study of a 66‐kD subunit of mammalian neurofilaments
Galinović-Schwartz, V., Peng, D., Chiu, F., & Water, T. R. V. D. (1991) · Journal of Neuroscience Research · doi:10.1002/jnr.490300114 · Cited by 23
Synaptic studies inform the functional diversity of cochlear afferents
Fuchs, P. A., & Glowatzki, E. (2015) · Hearing Research · doi:10.1016/j.heares.2015.09.007 · Cited by 24
Acoustic trauma increases ribbon number and size in outer hair cells of the mouse cochlea
Wood, M. B., Nowak, N., Mull, K., Goldring, A., Lehar, M., & Fuchs, P. A. (2021) · Journal of the Association for Research in Otolaryngology · doi:10.1007/s10162-020-00777-w · Cited by 21
Expression of peripherin in human cochlea
Liu, W., Kinnefors, A., Boström, M., & Rask‐Andersen, H. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-1081-6 · Cited by 21
Hyperpolarization-activated, cyclic nucleotide-gated, cation non-selective channel subunit expression pattern of guinea-pig spiral ganglion cells
Bakondi, G., Pór, Á., Kovács, I., Szűcs, G., & Rusznák, Z. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.10.056 · Cited by 20
Anatomie et physiologie de la cochlée
Pujol, R. (1989) · Archives Internationales de Physiologie et de Biochimie · doi:10.3109/13813458909105536 · Cited by 20
Intracellular injection of Ca2+ chelator does not affect spike repolarization of cat spinal motoneurons
Zhang, L., & Krnjević, K. (1988) · Brain Research · doi:10.1016/0006-8993(88)90602-6 · Cited by 20
Central Projections of Spiral Ganglion Neurons
Muniak, M. A., Connelly, C. J., Suthakar, K., Milinkeviciute, G., Ayeni, F. E., & Ryugo, D. K. (2015) · Springer handbook of auditory research · doi:10.1007/978-1-4939-3031-9_6 · Cited by 19
Self-citation
Voltage-gated K+ channel (Kv) subunit expression of the guinea pig spiral ganglion cells studied in a newly developed cochlear free-floating preparation
Bakondi, G., Pór, Á., Kovács, I., Szűcs, G., & Rusznák, Z. (2008) · Brain Research · doi:10.1016/j.brainres.2008.02.072 · Cited by 19
Synaptic arrangements between inner hair cells and tunnel fibers in the mouse cochlea
Sobkowicz, H. M., August, B. K., & Slapnick, S. M. (2004) · Synapse · doi:10.1002/syn.20026 · Cited by 18
C1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient
Biswas, J., Pijewski, R. S., Makol, R., Miramontes, T. G., Thompson, B. L., Kresic, L. C., Burghard, A. L., Oliver, D. L., & Martinelli, D. C. (2021) · PLoS ONE · doi:10.1371/journal.pone.0251412 · Cited by 17
Response profiles of murine spiral ganglion neurons on multi-electrode arrays
Hahnewald, S., Tscherter, A., Marconi, E., Streit, J., Widmer, H. R., Garnham, C., Benav, H., Mueller, M., Löwenheim, H., Roccio, M., et al. (2015) · Journal of Neural Engineering · doi:10.1088/1741-2560/13/1/016011 · Cited by 17
Auditory System
Malmierca, M. S., & Ryugo, D. K. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-369497-3.10024-x · Cited by 17
Self-citation
Pharmacological Approaches to Hearing Loss
Cederroth, C. R., Dyhrfjeld‐Johnsen, J., & Canlon, B. (2024) · Pharmacological Reviews · doi:10.1124/pharmrev.124.001195 · Cited by 18
Differential Expression of Ca2+-buffering Protein Calretinin in Cochlear Afferent Fibers: A Possible Link to Vulnerability to Traumatic Noise
Sharma, K., Seo, Y.-W., & Yi, E. (2018) · Experimental Neurobiology · doi:10.5607/en.2018.27.5.397 · Cited by 16
Nanogrooved Surface-Patterns induce cellular organization and axonal outgrowth in neuron-like PC12-Cells
Klymov, A., Neves, C. T. R., Riet, J. T., Agterberg, M. J. H., Mylanus, E. A. M., Snik, A. F. M., Jansen, J. A., & Walboomers, X. F. (2015) · Hearing Research · doi:10.1016/j.heares.2014.12.009 · Cited by 16
Purinergic Modulation of Activity in the Developing Auditory Pathway
Jovanovic, S., & Milenković, I. (2020) · Neuroscience Bulletin · doi:10.1007/s12264-020-00586-4 · Cited by 14
Reciprocal synapses between inner hair cell spines and afferent dendrites in the organ of corti of the mouse
Sobkowicz, H. M., Slapnick, S. M., & August, B. K. (2003) · Synapse · doi:10.1002/syn.10241 · Cited by 14

Authors: Berglund, A. M., & Ryugo, D. K.
Affiliations: Massachusetts Eye and Ear Infirmary (US)
ORCID: Ryugo, D. K.
Venue: Journal of Comparative Neurology
Publisher: Wiley
Published: 1987-01-22
Volume: 255
Issue: 4
Pages: 560-570
ISSN: 0021-9967 (ISSN-L)
1096-9861
DOI: 10.1002/cne.902550408
OpenAlex: W2119585553
Cited by: 172
References: 34
Citations by year: 2026: 6 · 2025: 2 · 2024: 4 · 2023: 1 · 2022: 6 · 2021: 9 · 2020: 8 · 2019: 3 · 2018: 7 · 2016: 7 · 2015: 10 · 2014: 3 · 2013: 1 · 2012: 9
FWCI: 3.33
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 6470 d)
Locations: The Journal of Comparative Neurology (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute of General Medical Sciences (GM-07258)
National Institute of Neurological Disorders and Stroke (NS 20156, NS 13126)
Topics: Life Sciences › Neuroscience › Sensory Systems › Hearing, Cochlea, Tinnitus, Genetics
Life Sciences › Neuroscience › Neurology › Vestibular and auditory disorders
Health Sciences › Health Professions › Speech and Hearing › Hearing Loss and Rehabilitation
Keywords: spiral ganglion neurons, inner hair cells, outer hair cells, auditory nerve, radial fibers, hair cell innervation, mouse cochlea
MeSH terms: Animals, Ganglia, Hair Cells, Auditory, Male, Medical Illustration, Mice, Inbred Strains, Neurons, Mice

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Hair cell innervation by spiral ganglion neurons in the mouse

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks