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D. Albe‐Fessard, J. Boive, G. Grant, A. Levante (1975)
Labeling of cells in the medulla oblongata and the spinal cord of the monkey after injection of horseradish peroxidase in the thalamus, 1
F. Conde, H. Conde (1973)
Étude de la morphologie des cellules du noyau rouge du chat par la méthode de GolgiCox, 53
S. Ramón y Cajal (1895)
Atlas der pathologishcen Histologic des Nervensystems, 4
S. Gobel (1975a)
Golgi studies of the substantia gelatinosa neurons in the spinal trigeminal nucleus, 162
H. Waldeyer (1888)
Das Gorilla‐Rückenmark. Verlag der Konigl
S. Gobel (1975b)
Neurons with two axons in the substantia gelatinosa layer of the spinal trigeminal nucleus of the adult cat, 88
F. W. L. Kerr (1975)
Neuroanatomical substrates of nociception in the spinal cord, 1
D. D. Price, R. Dubner, J. W. Hu (1976)
Trigeminothalamic neurons in nucleus caudalis responsive to tactile, thermal, and nociceptive stimulation of the monkey's face, 39
F. W. L. Kerr (1970)
The organization of primary afferents in the subncleus caudalis of the trigeminal. A light and electron microscopic study of degeneration, 23
Y. Shigenaga, A. Sakai, K. Okada (1976)
Effects of tooth pulp stimulation in trigeminal nucleus caudalis and adjacent reticular formation in rat, 103
J. A. Beal, C. A. Fox (1976)
Afferent fibers in the substantia gelatinosa of the adult monkey (Macaca mulatta), 168
M. Rethelyi, J. Szentágothai (1973)
Handbook of Sensory Physiology, II
S. Gobel (1978)
Golgi studies of the neurons in layer II of the dorsal horn of the medulla (trigeminal nucleus caudalis), 180
H. J. Ralston (1968)
Dorsal root projections to dorsal horn neurons in the cat spinal cord, 132
H. Burton, A. Loewy (1976)
Descending projections from the marginal cell layer and other regions of monkey spinal cord, 116
J. Szentágothai (1964)
Neuronal and synaptic arrangement in the substantia gelatinosa Rolandi, 122
S. Hockfield, S. Gobel (1978)
Neurons in and near nucleus caudalis with long ascending projection axons demonstrated by retrograde labeling with horseradish peoxidase, 139
S. Ramón y Cajal (1911)
Histologie du Systeme Nerveux de l'Homme et des Vertebres, I
D. D. Price, D. J. Mayer (1975)
Neurophysiological characterization of the anterolateral quadrant neurons subserving pain in M. mulatta, 1
S. Gobel, J. M. Binck (1977)
Degenerative changes in primary trigeminal axons and in neurons in nucleus caudalis following tooth pulp extirpations in the cat, 132
T. Kumazawa, E. R. Perl, P. R. Burgess, D. Whitehorn (1975)
Ascending projections from marginal zone (lamina I) neurons of the spinal dorsal horn, 162
B. N. Christensen, E. R. Perl (1970)
Spinal neurons specifically excited by noxious or thermal stimuli: marginal zone of the dorsal horn, 33
S. Gobel, M. B. Purvis (1972)
Anatomical studies of the organization of the spinal V nucleus: The deep; bundles and the spinal V tract, 48
W. M. Falls, S. Gobel (1976)
A Golgi and EM study of the marginal and substantia gelatinosa layers of trigeminal nucleus caudalis in newborn kittens, 184
S. Gobel (1974)
Synaptic organization of the substantia gelatinosa glomeruli in the spinal trigeminal nucleus of the adult cat, 3
M. Lenhossek (1889)
Untersuchungen über die Entwickelung der Marscheide und den Faserverlauf in Rückenmarke der Maus, 33
T. Yokota (1975)
Excitation of units in marginal rim of trigeminal subnucleus caudalis elicited by tooth pulp stimulation, 95
D. D. Price, D. J. Mayer (1974)
Physiological laminar organization of the dorsal horn of M. mulatta, 79
L. Kruger, S. Saporta, S. G. Feldman (1977)
Pain in the Trigeminal Region
H. O. Handwerker, A. Iggo, M. Zimmerman (1975)
Segmental and supraspinal actions on the dorsal horn neurons responding to noxious and non‐noxious skin stiumuli, 1
T. Kumazawa, E. R. Perl (1976)
Sensory Functins of the skin in Primates with Special Reference to Man
R. Melzack, P. D. Wall (1965)
Pain mechanisms: a new theory, 150
M. A. Scheibel, A. B. Scheibel (1968)
Terminal axonal patterns in cat spinal cord. II. The dorsal horn, 9
D. L. Trevino, E. Carstens (1975)
Confirmation of the location of spinothalamic neurons in the cat and monkey by the retrograde transport of horseradish peroxidase, 98
W. D. Willis, D. L. Trevino, J. D. Coulter, R. A. Maunz (1974)
Responses of primate spinothalamic tract neurons to natural stimulation of hindlimb, 38
A. Coimbra, B. P. Sodre‐Borges, M. M. Magalheas (1974)
The substantia gelatinosa Rolandi of the rat. Fine structure cytochemistry (acid phosphatase) and changes after dorsal root section, 3
M. Rethelyi (1977)
Preterminal and terminal axon arborizations in the substantia gelatinosa of cat's spinal cord, 172
L. Heimer, P. D. Wall (1968)
The dorsal root distribution to the substantia gelatinosa of the rat with a note on the distribution in the cat, 6
A. Rustioni, S. Sanyal, H. G. J. M. Kuypers (1971)
A histochemical study of the distribution of the trigeminal divisins in the substantia geletinosa of the rat, 32
C. LaMotte (1977)
Distribution of the tact of Lissauer and the dorsal root fibers in the primate spinal cord, 172
M. Kuru (1949)
Sensory Paths in the Spinal Cord and Brain Stem of Man
J. L. Clark (1859)
Further researches on the gray substance of the spinal cord, 149
R. Dubner, S. Gobel, D. D. Price (1976)
Advances in Pain Research and Therapy, I
A. R. Light, E. R. Perl (1977)
Differential termination of large‐diameter and small‐diameter primary afferent fibers in the spinal dorsal gray matter as indicated by labeling with horseradish peroxiase, 6
J. A. Mosso, L. Kruger (1973)
Receptor categories represented in spinal trigeminal nucleus caudalis, 36
Two kinds of pyramidal neuro ns and two kinds of multipolar neurons have been identified in layer I in the adult cat on the basis of thier dendritic morphology. The spiny pyramid emits an apical dendrite which beings dividing within 50 μm of the cell body and gives rise to an extensive dendritic arbor in which some second and third order branches extend for over 100 μm. The primary branches of the basal dendrites divide into secondary branches within 20 μm of the cell body. At each of these divisions, one daughter secondary branch will turn 180° and course in the direction of the apical dendrite. It then undergoes further branching and becomes intermingled in the apical dendritic arbor. These recurrent basal dendrites and the apical dendrites are charcterized by numerous long‐necked spines. The other secondary basal branch either courses at right angles to the apical dendrite or droops basally away from it. Many of these basal dendrites are not as robust and extensive as the other dendritic branches. They may end without further branching or when they do branch they tend to be thinner and shorter with some showing signs of stunting. Smooth pyramids differ from the spiny pyramids in several respects. Their dendritic arbors contain fewer, more widely spaced spines and are more expansive than those of the spiny pyramids. While they still send branches into the apical arbors many branches run basally away from the cell body for considerable distances to give the entire dendritic field a more circular appearance. The compact multipolar neuron is found in the inner half of layer I. The long axis of its compact dendritic arbor (∼ 50 μm wide) is oriented in the rostrocaudal axis of the layer. Most of its dendritic branches lie to one side of the cell body squeezed between the axon bundles of the inner half of layer I. The loose multipolar neuron in found throughout the layer. Its loose dendritic arbor is at least 200 μm wide and, like the spiny pyramid, gives rise to several dendrites which terminate abruptly with little branching and without much change in diameter. The dendrites of all four layer I neurons are confined within layer I and its extensions into the spinal V tract. These four layer I neurons are considered to be Golgi type I projection neurons on the basis of the morphology of their initial axonal segment. Golgi type II inteneurons are not found in layer I.
The Journal of Comparative Neurology – Wiley
Published: Mar 15, 1979
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