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DEBRECENI EGYETEM EGYETEMI ÉS NEMZETI KÖNYVTÁR KENÉZY ÉLETTUDOMÁNYI KÖNYVTÁRA

4032 Debrecen, Egyetem tér 1. e ‐mail : publ ikac iok@l ib.unideb.hu

Iktatószám: DEENKÉTK /50/2012. Tételszám: Tárgy: Publikációs Lista-OTKA

Pályázó: Matesz Klára

Folyóiratcikkek (63)

Magyar nyelvű közlemények (1)

1. Földes I., Kern M., Matesz K.: Különböző porcok makromolekuláris komponenseinek vizsgálata

topooptikai reakciókkal.

Biológia 23, 45-54, 1975.

Idegen nyelvű ( Magyarországon megjelent ) közlemények (12)

2. Matesz, K., Bácskai, T., Székely, G.: Ascending and descending projections of the lateral vestibular

nucleus in the rat.

Acta Biol. Hung. 53 (1-2), 7-21, 2002.

IF:0.416

Idézetek összesen: 8

Független idézetek: 7 1. Нагаева, Д., Ахмадеев, А.: Состояние Периферических И Проводниковых

Центров Вестибулярного Анализатора При Конвульсивной Эпилепсии. М 45 Материалы II международной (IX итоговой) научно-практической конферен-ции молодых ученых.— (2011) Челябинск: Изд-во «Челябинская государст(TRUNCATED), , pp. 159.

2. Barmack, N.H.: Central vestibular system: Vestibular nuclei and posterior cerebellum. (2003) Brain Res Bull, 60 (5-6), pp. 511-541.

3. Tobias, C.A., Shumsky, J.S., Shibata, M., Tuszynski, M.H., Fischer, I., Tessler, A., Murray, M.: Delayed grafting of BDNF and NT-3 producing fibroblasts into the injured spinal cord stimulates sprouting, partially rescues axotomized red nucleus neurons from loss and atrophy, and provides limited regeneration. (2003) Exp Neurol, 184 (1), pp. 97-113.

4. Deumens, R., Koopmans, G.C., Joosten, E.A.J.: Regeneration of descending axon tracts after spinal cord injury. (2005) Prog Neurobiol, 77 (1-2), pp. 57-89.

5. Chiocchetti, R., Bombardi, C., Grandis, A., Mazzuoli, G., Gentile, A., Pisoni, L., Joechler, M., Lucchi, M.L.: Cytoarchitecture, morphology, and lumbosacral spinal cord projections of the red nucleus in cattle. (2006) Am J Vet Res, 67 (10), pp. 1662-1669.

6. Grandis, A., Bombardi, C., Travostini, B., Gentile, A., Joechler, M., Pisoni, L., Chiocchetti, R.: Vestibular nuclear complex in cattle: Topography,



morphology, cytoarchitecture and lumbo-sacral projections. (2007) Journal of Vestibular Research: Equilibrium and Orientation, 17 (1), pp. 9-24.

7. Shinder, M.E., Taube, J.S.: Differentiating ascending vestibular pathways to the cortex involved in spatial cognition. (2010) Journal of Vestibular Research: Equilibrium and Orientation, 20 (1-2), pp. 3-23.

Függő idézetek: 1 1. Deák, Á., Bácskai, T., Veress, G., Matesz, C.: Vestibular afferents to the

motoneurons of glossopharyngeal and vagus nerves in the frog, rana esculenta. (2009) Brain Res, 1286 , pp. 60-65.

3. Matesz, K., Nagy, E., Kulik, Á., Tönköl, A.: Projections of the medial and superior vestibular nuclei to

the brainstem and spinal cord in the rat.

Neurobiology. 5 (4), 489-493, 1997.


Függő idézetek: 4 1. Halasi, G., Bácskai, T., Matesz, C.: Connections of the superior vestibular

nucleus with the oculomotor and red nuclei in the rat: An electron microscopic study (2005) Brain Research Bulletin, 66 (4-6), pp. 532-535.

2. Bácskai, T., Székely, G., Matesz, C.: Ascending and descending projections of the lateral vestibular nucleus in the rat (2002) Acta Biologica Hungarica, 53 (1-2), pp. 7-21.

3. Matesz, C., Kulik, A., Bácskai, T.: Ascending and descending projections of the lateral vestibular nucleus in the frog Rana esculenta (2002) Journal of Comparative Neurology, 444 (2), pp. 115-128.

4. Matesz, C., Bácskai, T., Nagy, E., Halasi, G., Kulik, A.: Efferent connections of the vestibular nuclei in the rat: A neuromorphological study using PHA-L (2002) Brain Research Bulletin, 57 (3-4), pp. 313-315.

4. Kulik, Á., Polgár, E., Matesz, K., Kothalawala, D.S., Szűcs, P., Nagy, I.: Sub-population of capsaicin

sensitive primary afferent neurons in thoracic, lumbar and sacral dorsal root ganglion in young

rats revealed by stimulated cobalt uptake.

Acta Biol. Hung. 47 (1-4), 251-259, 1996.

IF:0.239

5. Matesz, K., Kulik, Á.: Connections of the torus semicircularis and oliva superior in the frog, Rana

esculenta: A Phaseolus vulgaris leucoagglutinin labeling study.

Acta Biol. Hung. 47, 287-301, 1996.

IF:0.239


Független idézetek: 6 1. González, M.J., Yáñez, J., Anadón, R.: Afferent and efferent connections of

the torus semicircularis in the sea lamprey: An experimental study. (1999) Brain Res, 826 (1), pp. 83-94.

2. Endepols, H., Walkowiak, W.: Integration of ascending and descending inputs in the auditory midbrain of anurans. (2000) Journal of Comparative Physiology - A Sensory, Neural, and Behavioral Physiology, 186 (12), pp. 1119-1133.

3. Sánchez-Camacho, C., Marín, O., Ten Donkelaar, H.J., González, A.: Descending supraspinal pathways in amphibians. I. A dextran amine tracing study of their cells of origin. (2001) J Comp Neurol, 434 (2), pp. 186-208.



4. Straka, H., Holler, S., Goto, F.: Patterns of canal and otolith afferent input convergence in frog second-order vestibular neurons. (2002) J Neurophysiol, 88 (5), pp. 2287-2301.

5. Straka, H., Dieringer, N.: Basic organization principles of the VOR: Lessons from frogs. (2004) Prog Neurobiol, 73 (4), pp. 259-309.

6. O'Connell, L.A., Ding, J.H., Ryan, M.J., Hofmann, H.A.: Neural distribution of the nuclear progesterone receptor in the túngara frog, physalaemus pustulosus. (2011) J Chem Neuroanat, 41 (3), pp. 137-147.

6. Kulik, Á., Matesz, K., Székely, G.: Mesencephalic projections of the cochlear nucleus in the frog,

Rana esculenta.

Acta Biol. Hung. 45 (2-4), 323-335, 1994.


Független idézetek: 9 1. Lowry, C., Richardson, C., Zoeller, T., Miller, L., Muske, L., Moore, F.:

Neuroanatomical distribution of vasotocin in a urodele amphibian (taricha granulosa) revealed by immunohistochemical and in situ hybridization techniques. (1997) J Comp Neurol, 385 (1), pp. 43-70.

2. Pollak, E., Lazar, G., Gabriel, R., Wang, S.: Localization and source of gamma aminobutyric acid immunoreactivity in the isthmic nucleus of the frog rana esculenta. (1999) Brain Res Bull, 48 (3), pp. 343-350.

3. Lazar, G.: Peptides in frog brain areas processing visual information. (2001) Microsc Res Tech, 54 (4), pp. 201-219.

4. Straka, H., Holler, S., Goto, F.: Patterns of canal and otolith afferent input convergence in frog second-order vestibular neurons RID C-6337-2011. (2002) J Neurophysiol, 88 (5), pp. 2287-2301.

5. Straka, H., Holler, S., Goto, F., Kolb, F., Gilland, E.: Differential spatial organization of otolith signals in frog vestibular nuclei RID C-6337-2011. (2003) J Neurophysiol, 90 (5), pp. 3501-3512.


7. Westhoff, G., Roth, G., Straka, H.: Topographic representation of vestibular and somatosensory signals in the anuran thalamus. (2004) Neuroscience, 124 (3), pp. 669-683.

8. Wilczynski, W., Endepols, H.: Central auditory pathways in anuran amphibians: The anatomical basis of hearing and sound communication. (2006) Hearing and sound communication in amphibians, , pp. 221-249.

9. Morona, R., Gonzalez, A.: Immunohistochemical localization of calbindin-D28k and calretinin in the brainstem of anuran and urodele amphibians. (2009) J Comp Neurol, 515 (5), pp. 503-537.

Függő idézetek: 3 1. Matesz, C., Kulik, A.: Connections of the torus semicircularis and oliva

superior in the frog, rana esculenta: A phaseolus vulgaris leucoagglutinin labeling study. (1996) Acta Biol Hung, 47 (1-4), pp. 287-301.

2. Kulik, A., Matesz, C.: Projections from the nucleus isthmi to the visual and auditory centres in the frog, rana esculenta. (1997) Journal of Brain Research-Journal Fur Hirnforschung, 38 (3), pp. 299-307.

3. Matesz, C., Kulik, A., Bacskai, T.: Ascending and descending projections of the lateral vestibular nucleus in the frog rana esculenta. (2002) J Comp Neurol, 444 (2), pp. 115-128.



7. Matesz, K.: Fine structure of the primary afferent vestibulocochlear terminals in the frog.

Acta Biol. Hung. 39 (2-3), 267-277, 1988.

IF:0.132


Független idézetek: 6 1. Fanardjian, V., Manvelyan, L., Zakarian, V., Pogossian, V., Nasoyan, A.:

Electrophysiological properties of the somatotopic organization of the vestibulospinal system in the frog. (1999) Neuroscience, 94 (3), pp. 845-857.

2. Birinyi, A., Straka, H., Matesz, C., Dieringer, N.: Location of dye-coupled second order and of efferent vestibular neurons labeled from individual semicircular canal or otolith organs in the frog. (2001) Brain Res, 921 (1-2), pp. 44-59.

3. Fanardjian, V., Manvelyan, L., Nasoyan, A.: Spatial distribution of the vestibulospinal neurons in the frog vestibular nuclei. (2001) Neuroscience, 104 (3), pp. 853-862.




Függő idézetek: 4 1. Bacskai, T., Matesz, C.: Primary afferent fibers establish dye-coupled

connections in the frog central nervous system. (2002) Brain Res Bull, 57 (3-4), pp. 317-319.


3. Racz, E., Bacskai, T., Halasi, G., Kovacs, E., Matesz, C.: Organization of dye-coupled cerebellar granule cells labeled from afferent vestibular and dorsal root fibers in the frog rana esculenta. (2006) J Comp Neurol, 496 (3), pp. 382-394.

4. Deak, A., Bacskai, T., Veress, G., Matesz, C.: Vestibular afferents to the motoneurons of glossopharyngeal and vagus nerves in the frog, rana esculenta RID C-9714-2009. (2009) Brain Res, 1286 , pp. 60-65.

8. Matesz, K., Székely, G.: The motor nuclei of the glossopharyngeal-vagal and the accessorius nerves

in the rat.

Acta Biol. Hung. 34 (2-3), 215-230, 1983.

IF:0.267


Független idézetek: 17 1. Bieger, D., Hopkins, D.: Viscerotopic Representation Of The Upper

Alimentary-Tract In The Medulla-Oblongata In The Rat - The Nucleus Ambiguus. (1987) J Comp Neurol, 262 (4), Pp. 546-562.

2. Oka, Y., Satou, M., Ueda, K.: Morphology And Distribution Of The Motor Neurons Of The Accessory Nerve (Nxi) In The Japanese Toad - A Cobaltic Lysine Study. (1987) Brain Res, 400 (2), Pp. 383-388.

3. Oka, Y., Takeuchi, H., Satou, M., Ueda, K.: Cobaltic Lysine Study Of The Morphology And Distribution Of The Cranial Nerve Efferent Neurons (Motoneurons And Preganglionic Parasympathetic Neurons) And Rostral



Spinal motoneurons in the japanese toad. (1987) J Comp Neurol, 259 (3), pp. 400-423.

4. Wake, D., Nishikawa, K., Dicke, U., Roth, G.: Organization of the motor nuclei in the cervical spinal-cord of salamanders. (1988) J Comp Neurol, 278 (2), pp. 195-208.

5. Rethelyi, M., Metz, C., Lund, P.: Distribution of neurons expressing calcitonin gene-related peptide mRNAs in the brain stem, spinal cord and dorsal root ganglia of rat and guinea-pig. (1989) Neuroscience, 29 (1), pp. 225-239.

6. Yajima, Y., Hayashi, Y.: Electrophysiological evidence for axonal branching of ambiguous laryngeal motoneurons. (1989) Brain Res, 478 (2), pp. 309-314.

7. Leong, S., Ling, E.: Vagus nerve and spinal-cord projecting neurons demonstrated by horseradish-peroxidase and different fluorescent dyes. (1991) Int J Neurosci, 57 (1-2), pp. 61-72.

8. Yoshida, Y., Tanaka, Y., Saito, T., Shimazaki, T., Hirano, M.: Peripheral nervous-system in the larynx - an anatomical study of the motor, sensory and autonomic nerve-fibers. (1992) Folia Phoniatr, 44 (5), pp. 194-219.

9. Brining, S.K., Smith, D.V.: Distribution and synaptology of glossopharyngeal afferent nerve terminals in the nucleus of the solitary tract of the hamster. (1996) J Comp Neurol, 365 (4), pp. 556-574.

10. Liinamaa, T.L., Keane, J., Richmond, F.J.R.: Distribution of motoneurons supplying feline neck muscles taking origin from the shoulder girdle. (1997) J Comp Neurol, 377 (2), pp. 298-312.

11. Yoshida, Y.: Central nervous system participation in phonation and deglutition - focus on the nucleus ambiguus. (2000) Japan Journal of Logopedics and Phoniatrics, 41 (2), pp. 95-110.

12. Hayakawa, T., Takanaga, A., Tanaka, K., Maeda, S., Seki, M.: Organization and distribution of the upper and lower esophageal motoneurons in the medulla and the spinal cord of the rat. (2002) Okajimas Folia Anat Jpn, 78 (6), pp. 263-280.

13. Hayakawa, T., Takanaga, A., Tanaka, K., Maeda, S., Seki, M.: Ultrastructure and synaptic organization of the spinal accessory nucleus of the rat. (2002) Anat Embryol, 205 (3), pp. 193-201.

14. Tsukamoto, K., Hayakawa, T., Maeda, S., Tanaka, K., Seki, M., Yamamura, T.: Projections to the alimentary canal from the dopaminergic neurons in the dorsal motor nucleus of the vagus of the rat. (2005) Autonomic Neuroscience: Basic and Clinical, 123 (1-2), pp. 12-18.

15. Ullah, M., Mansor, O., Ismail, Z.I.M., Kapitonova, M.Y., Sirajudeen, K.N.S.: Localization of the spinal nucleus of accessory nerve in rat: A horseradish peroxidase study. (2007) J Anat, 210 (4), pp. 428-438.

16. Cerimagic, D., Ivkic, G., Bilic, E.: Neuroanatomical basis of sandifer's syndrome: A new vagal reflex? (2008) Med Hypotheses, 70 (5), pp. 957-961.

17. Sienkiewicz, W., Dudek, A.: Sources of the motor and somatic sensory innervation of the trapezius muscle in the rat. (2010) Vet Med, 55 (5), pp. 242-252.

Függő idézetek: 3 1. Szekely, G., Matesz, C.: Topography And Organization Of Cranial Nerve

Nuclei In The Sand Lizard, Lacerta-Agilis. (1988) J Comp Neurol, 267 (4), Pp. 525-544.

2. Matesz, C., Birinyi, A., Kothalawala, D., Szekely, G.: Investigation Of The Dendritic Geometry Of Brain-Stem Motoneurons With Different Functions Using Multivariant Statistical Techniques In The Frog. (1995) Neuroscience, 65 (4), Pp. 1129-1144.

3. Matesz, C., Székely, G.: Organization Of The Ambiguus Nucleus In The Frog (Rana Esculenta). (1996) J Comp Neurol, 371 (2), Pp. 258-269.



9. Matesz, K.: Termination areas of primary afferent fibers of the trigeminal nerve in the rat.

Acta Biol. Hung. 34 (1), 31-43, 1983.

IF:0.267


Független idézetek: 15 1. Arvidsson, J., Pfaller, K.: Central projections of C4–C8 dorsal root ganglia in

the rat studied by anterograde transport of WGA‐HRP. (1990) J Comp Neurol, 292 (3), pp. 349-362.

2. Dallel, R., Raboisson, P., Woda, A., Sessle, B.: Properties of nociceptive and non-nociceptive neurons in trigeminal subnucleus oralis of the rat. (1990) Brain Res, 521 (1-2), pp. 95-106.

3. Marfurt, C.F., Rajchert, D.M.: Trigeminal primary afferent projections to “non‐trigeminal” areas of the rat central nervous system. (1991) J Comp Neurol, 303 (3), pp. 489-511.

4. Ter Horst, G., Copray, J., Liem, R., Van Willigen, J.: Projections from the rostral parvocellular reticular formation to pontine and medullary nuclei in the rat: Involvement in autonomic regulation and orofacial motor control. (1991) Neuroscience, 40 (3), pp. 735-758.

5. Raappana, P., Arvidsson, J.: Location, morphology, and central projections of mesencephalic trigeminal neurons innervating rat masticatory muscles studied by axonal transport of choleragenoid‐horseradish peroxidase. (1993) J Comp Neurol, 328 (1), pp. 103-114.

6. Usunoff, K.G., Marani, E., Schoen, J.H.: The trigeminal system in man. (1997) Adv Anat Embryol Cell Biol, 136 , pp. I-X, 1-126.

7. Malick, A., Burstein, R.: Cells of origin of the trigeminohypothalamic tract in the rat. (1998) J Comp Neurol, 400 (1), pp. 125-144.

8. May, P.J., Porter, J.D.: The distribution of primary afferent terminals from the eyelids of macaque monkeys. (1998) Experimental Brain Research, 123 (4), pp. 368-381.

9. Ndiaye, A., Pinganaud, G., Buisseret-Delmas, C., Buisseret, P., Vanderwerf, F.: Organization of trigeminocollicular connections and their relations to the sensory innervation of the eyelids in the rat. (2002) J Comp Neurol, 448 (4), pp. 373-387.

10. Monzani, D., Guidetti, G., Chiarini, L., Setti, G.: Combined effect of vestibular and craniomandibular disorders on postural behaviour. (2003) Acta otorhinolaryngologica italica, 23 (1), pp. 4-9.

11. Haenggeli, C.-., Pongstaporn, T., Doucet, J.R., Ryugo, D.K.: Projections from the spinal trigeminal nucleus to the cochlear nucleus in the rat. (2005) J Comp Neurol, 484 (2), pp. 191-205.

12. Panneton, W.M., Gan, Q., Juric, R.: Brainstem projections from recipient zones of the anterior ethmoidal nerve in the medullary dorsal horn. (2006) Neuroscience, 141 (2), pp. 889-906.

13. Satoh, Y., Ishizuka, K., Murakami, T.: Modulation of the jaw-opening reflex by stimulation of the vestibular nuclear complex in rats. (2009) Neurosci Lett, 457 (1), pp. 21-26.

14. Satoh, Y., Ishizuka, K., Murakami, T.: Modulation of cortically induced rhythmic jaw movements in rats by stimulation of the vestibular nuclear complex. (2010) Neurosci Res, 68 (4), pp. 307-314.

15. Novío Mallón S. Estudio experimental de las vías del dolor de la región de las vibrisas en el cobaya tricolor (cavia porcellus). Univ Santiago de Compostela; 2011.

Függő idézetek: 1 1. Székely, G., Matesz, C.: Topography and organization of cranial nerve nuclei

in the sand lizard, lacerta agilis. (1988) J Comp Neurol, 267 (4), pp. 525-544.



10. Lévai, G., Matesz, K., Székely, G.: Fine structure of dorsal root terminals in the dorsal horn of the

frog spinal cord.

Acta Biol. Acad. Sci. Hung. 33 (2-3), 231-246, 1982.

IF:0.208


Független idézetek: 4 1. Antal, M.: The Application Of Cobalt Labeling To Electron-Microscopic

Investigations Of Serial Sections. (1984) J Neurosci Methods, 12 (1), Pp. 69-77.

2. Oka, Y., Satou, M., Ueda, K.: An Improved Method For Correlative Light And Electron-Microscopic Examination Of Cobaltic-Lysine-Labeled Neurons. (1987) Neurosci Lett, 73 (2), Pp. 187-191.

3. Nagy, I., Sik, A., Polgar, E., Petko, M., Antal, M.: Combination Of Cobalt Labeling With Immunocytochemical Reactions For Electron-Microscopic Investigations On Frog Spinal-Cord. (1994) Microsc Res Tech, 28 (1), Pp. 60-66.

4. Jovanovic, K., Burke, R.E.: Morphology Of Brachial Segments In Mudpuppy (Necturus Maculosus) Spinal Cord Studied With Confocal And Electron Microscopy. (2004) J Comp Neurol, 471 (3), Pp. 361-385.

Függő idézetek: 8 1. Szekely, G., Levai, G., Matesz, K.: Primary Afferent Terminals In The Nucleus

Of The Solitary Tract Of The Frog - An Electron-Microscopic Study. (1983) Experimental Brain Research, 53 (1), Pp. 109-117.

2. Antal, M., Kraftsik, R., Szekely, G., Vanderloos, H.: Distal Dendrites Of Frog Motor Neurons - A Computer-Aided Electron-Microscopic Study Of Cobalt-Filled Cells. (1986) J Neurocytol, 15 (3), Pp. 303-310.

3. Matesz, C.: Fine Structure Of The Primary Afferent Vestibulocochlear Terminals In The Frog. (1988) Acta Biol Hung, 39 (2-3), Pp. 267.

4. Matesz, C.: Fine-Structure Of The Primary Afferent Vestibulocochlear Terminals In The Frog. (1988) Acta Biol Hung, 39 (2-3), Pp. 267-277.

5. Szekely, G., Nagy, I., Wolf, E., Nagy, P.: Spatial-Distribution Of Presynaptic And Postsynaptic Sites Of Axon Terminals In The Dorsal Horn Of The Frog Spinal-Cord. (1989) Neuroscience, 29 (1), Pp. 175-188.

6. Antal, M., Kraftsik, R., Szekely, G., Vanderloos, H.: Synapses On Motoneuron Dendrites In The Brachial Section Of The Frog Spinal-Cord - A Computer-Aided Electron-Microscopic Study Of Cobalt-Filled Cells. (1992) J Neurocytol, 21 (1), Pp. 34-49.

7. Matesz, C.: Synaptic Relations Of The Trigeminal Motoneurons In A Frog (Rana-Esculenta). (1994) Eur J Morphol, 32 (2-4), Pp. 117-121.

8. Székely, G.: An Approach To The Complexity Of The Brain. (2001) Brain Res Bull, 55 (1), Pp. 11-28.

11. Székely, G., Matesz, K., Antal, M.: Different dendritic arborization patterns of motoneurons in

various places of the rat's lumbosacral spinal cord.

Acta Biol. Acad. Sci. Hung. 31 (1-3), 305-319, 1980.

IF:0.239


Független idézetek: 2 1. Kitzman, P.: Alteration in axial motoneuronal morphology in the spinal cord

injured spastic rat. (2005) Exp Neurol, 192 (1), pp. 100-108. 2. Vrieseling, E., Arber, S.: Target-induced transcriptional control of dendritic

patterning and connectivity in motor neurons by the ETS gene Pea3. (2006) Cell, 127 (7), pp. 1439-1452.



Függő idézetek: 1 1. Nagy, I., Sik, A., Polgár, E., Petko, M., Antal, M.: Combination of cobalt

labelling with immunocytochemical reactions for electron microscopic investigations on frog spinal cord. (1994) Microsc Res Tech, 28 (1), pp. 60-66

12. Matesz, K., Székely, G.: The dorsomedial nuclear group of cranial nerve in the frog.

Acta Biol. Acad. Sci. Hung. 28 (4), 461-474, 1977.

IF:0.149


Független idézetek: 40 1. Lázár, G.: Long-term persistence, after eye-removal, of unmyelinated fibres in

the frog visual pathway. (1980) Brain Res, 199 (1), pp. 219-224. 2. Destombes, J., Durand, J., Gogan, P., Gueritaud, J., Horcholle-Bossavit, G.,

Tyc-Dumont, S.: Ultrastructural and electrophysiological properties of accessory abducens nucleus motoneurones: An intracellular horseradish peroxidase study in the cat. (1983) Neuroscience, 10 (4), pp. 1317-1332.

3. Lazar, G., Toth, P., Csank, G., Kicliter, E.: Morphology and location of tectal projection neurons in frogs: A study with hrp and cobalt‐filling. (1983) J Comp Neurol, 215 (1), pp. 108-120.

4. Schönenberger, N., Escher, G., Van Der Loos, H.: Axon number in oculomotor nerves in xenopus: Removal of one eye primordium affects both sides. (1983) Neurosci Lett, 41 (3), pp. 239-245.

5. Cochran, S., Dieringer, N., Precht, W.: Basic optokinetic-ocular reflex pathways in the frog. (1984) The Journal of neuroscience, 4 (1), pp. 43-57.

6. Knöpfel, T., Hess, B., Precht, W.: Responses of frog trochlear motoneurons to linear acceleration. (1984) Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology, 154 (2), pp. 233-240.

7. Donkelaar, H., Bangma, G., Boer-van Huizen, R.: The fasciculus longitudinalis medialis in the lizard varanus exanthematicus. (1985) Anat Embryol, 172 (2), pp. 205-215.

8. Roth, G., Wake, D.B.: The structure of the brainstem and cervical spinal cord in lungless salamanders (family plethodontidae) and its relation to feeding. (1985) J Comp Neurol, 241 (1), pp. 99-110.

9. Satou, M., Matsushima, T., Takeuchi, H., Ueda, K.: Tongue-muscle-controlling motoneurons in the japanese toad: Topography, morphology and neuronal pathways from the ‘snapping-evoking area’in the optic tectum. (1985) Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology, 157 (6), pp. 717-737.

10. Dieringer, N., Precht, W.: Functional organization of eye velocity and eye position signals in abducens motoneurons of the frog. (1986) Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology, 158 (2), pp. 179-194.

11. Naujoks‐Manteuffel, C., Manteuffel, G., Himstedt, W.: Localization of motoneurons innervating the extraocular muscles in salamandra salamandra L.(amphibia, urodela). (1986) J Comp Neurol, 254 (1), pp. 133-141.

12. Fritzsch, B., Sonntag, R.: The trochlear nerve of amphibians and its relation to proprioceptive fibers: A qualitative and quantitative HRP study. (1987) Anat Embryol, 177 (2), pp. 105-114.

13. Gonzalez, A., Munoz, M.: Distribution and morphology of abducens motoneurons innervating the lateral rectus and retractor bulbi muscles in the frog rana ridibunda. (1987) Neurosci Lett, 79 (1-2), pp. 29-34.

14. Oka, Y., Satou, M., Ueda, K.: An improved method for correlative light and electron microscopic examination of cobaltic-lysine-labelled neurons. (1987) Neurosci Lett, 73 (2), pp. 187-191.

15. Oka, Y., Takeuchi, H., Satou, M., Ueda, K.: Morphology and distribution of the preganglionic parasympathetic neurons of the facial, glossopharyngeal



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36. Bácskai, T., Matesz, K.: Primary afferent fibers establish dye-coupled connections in the frog central

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6. Winmill, R., Hedrick, M.: Gap junction blockade with carbenoxolone differentially affects fictive breathing in larval and adult bullfrogs. (2003) Respiratory Physiology & Neurobiology, 138 (2-3), pp. 239-251.

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37. Matesz, K., Kulik, Á., Bácskai, T.: Ascending and descending projections of the lateral vestibular

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4. Matesz, C., Modis, L., Halasi, G., Szigeti, Z.M., Felszeghy, S., Bacskai, T., Szekely, G.: Extracellular matrix molecules and their possible roles in the regeneration of frog nervous system. (2005) Brain Res Bull, 66 (4-6), pp. 526-531.

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38. Matesz, K., Bácskai, T., Nagy, É., Halasi, G., Kulik, Á.: Efferent connections of the vestibular nuclei

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12. Szabo, Z., Bacskai, T., Deak, A., Matesz, K., Veress, G., Sziklai, I.: Dendrodendritic connections between the cochlear efferent neurons in guinea pig. (2011) Neurosci Lett, 504 (3), pp. 195-198.

13. Szekely, G., Levai, G., Matesz, K.: Primary afferent terminals in the nucleus of the solitary tract of the frog - an electron-microscopic study. (1983) Experimental Brain Research, 53 (1), pp. 109-117.





Könyvek (1)

Idegen nyelvű ( külföldön megjelent ) könyvek (1)

64. Székely, G., Matesz, K.: The efferent system of cranial nerve nuclei: A comparative

neuromorphological study. Springer Verlag, Berlin, Heidelberg, New York, 1993.


Független idézetek: 19 1. Anderson, C., Keifer, J.: Properties of conditioned abducens nerve responses

in a highly reduced in vitro brain stem preparation from the turtle. (1999) J Neurophysiol, 81 (3), pp. 1242-1250.

2. Atobe, Y., Nakano, M., Kadota, T., Hisajima, T., Goris, R., Funakoshi, K.: Medullary efferent and afferent neurons of the facial nerve of the pit viper gloydius brevicaudus. (2004) J Comp Neurol, 472 (3), pp. 345-357.

3. Billig, I., Balaban, C.: Zonal organization of the vestibulo-cerebellar pathways controlling the horizontal eye muscles using two recombinant strains of pseudorabies virus. (2005) Neuroscience, 133 (4), pp. 1047-1059.


5. Blessing, W., Gai, W.: Chapter III caudal pons and medulla oblongata. (1997) Handbook of Chemical Neuroanatomy, 13 , pp. 139-186.

6. Borla, M., Palecek, B., Budick, S., O'Malley, D.: Prey capture by larval zebrafish: Evidence for fine axial motor control. (2002) Brain Behavior and Evolution, 60 (4), pp. 207-229.


8. Fritzsch, B.: Of mice and genes: Evolution of vertebrate brain development. (1998) Brain Behavior and Evolution, 52 (4-5), pp. 207-217.

9. Garel, S., Garcia-Dominguez, M., Charnay, P.: Control of the migratory pathway of facial branchiomotor neurones. (2000) Development, 127 (24), pp. 5297-5307.

10. Gilland, E., Baker, R.: Evolutionary patterns of cranial nerve efferent nuclei in vertebrates. (2005) Brain Behavior and Evolution, 66 (4), pp. 234-254.

11. Gonzalez, A., Lopez, J., Sanchez-Camacho, C., Marin, O.: Localization of choline acetyltransferase (ChAT) immunoreactivity in the brain of a caecilian amphibian, dermophis mexicanus (amphibia : Gymnophiona). (2002) J Comp Neurol, 448 (3), pp. 249-267.


13. Jones, M.P., Pierce, K.E., Jr., Ward, D.: Avian vision: A review of form and function with special consideration to birds of prey. (2007) Journal of Exotic Pet Medicine, 16 (2), pp. 69-87.

14. Landwehr, S., Dicke, U.: Distribution of GABA, glycine, and glutamate in neurons of the medulla oblongata and their projections to the midbrain tectum in plethodontid salamanders. (2005) J Comp Neurol, 490 (2), pp. 145-162.

15. Noden, D.M., Francis-West, P.: The differentiation and morphogenesis of craniofacial muscles. (2006) Developmental Dynamics, 235 (5), pp. 1194-1218.



16. Schmidt, A., Wake, D., Wake, M.: Motor nuclei of nerves innervating the tongue and hypoglossal musculature in a caecilian (amphibia: Gymnophiona), as revealed by HRP transport. (1996) J Comp Neurol, 370 (3), pp. 342-349.


18. Studer, M.: Initiation of facial motoneurone migration is dependent on rhombomeres 5 and 6. (2001) Development, 128 (19), pp. 3707-3716.

19. Vasilakos, K., Wilson, R., Kimura, N., Remmers, J.: Ancient gill and lung oscillators may generate the respiratory rhythm of frogs and rats. (2005) J Neurobiol, 62 (3), pp. 369-385.

Függő idézetek: 6 1. Bacskai, T., Veress, G., Halasi, G., Matesz, C.: Crossing dendrites of the


2. Birinyi, A., Szekely, G., Csapo, K., Matesz, C.: Quantitative morphological analysis of the motoneurons innervating muscles involved in tongue movements of the frog rana esculenta. (2004) J Comp Neurol, 470 (4), pp. 409-421.







Könyvrészletek (9)

Idegen nyelvű ( külföldön megjelent ) könyvrészletek (9)

65. Matesz, K., Birinyi, A., Rácz, É., Székely, G., Bácskai, T.: Organization of the hypoglossal nucleus in

the frog, Rana exculenta.

In: Tongue: Anatomy, Kinematics, Disaeses. Ed.: Hiroto Kato, Taiga Shimizu, Nova Science

Publishers, Hauppauge, USA, 1-11, 2011.

66. Matesz, K.: Descending control of spinal motor functions.

In: Motor functions of the spinal cord. Ed.: Andras Birinyi, Research Signpost, [Trivandrum], 80-

100, 2011.

67. Matesz, K., Bácskai, T., Deák, Á., Rácz, É., Veress, G., Székely, G.: Using of confocal laser

scanning microscope in the examination of neural network underlying the gaze and posture

control.

In: Research, Technology and Applications. Ed.: M. Kimura, Nova Science Publishers,

Hauppauge, USA, 205-210, 2009.

68. Matesz, K., Székely, G.: Brainstem and cranial nerves.

In: Encyclopeda of Neuroscience. Ed.: Larry R. Squire, Academic Press, Oxford, 449-455, 2009.

69. Székely, G., Matesz, K.: Brainstem/cranial nerves.

In: Encyclopedia of Neuroscience. Elsevier, New York, CD-ROM, 2004.

70. Mikó, I., Furka, I., Serfőző, J., Joós, G., Telek, B., Matesz, K., Hauck, M., Békési, L., Ignáth, T.:

Comparative study of haemotological and micro-morphological results in long-surviving spleen

autotransplants.

In: Chirurgische Forschung. Ed.: Uranus S, Zuckschwerdt Verlag, München, Bern, Wien, New

York, 50-55, 1994.

71. Székely, G., Matesz, K.: Comparative anatomy of the neural control of mastication.

In: Complex organismal functions : integration and evolution in vertebrates. Ed.: Wake D. B.,

Roth G, John Wiley and Sons, New York, 41-52, 1989.

72. Mikó, I., Furka, I., Joós, G., Matesz, K., Kovács, G., Sefcsik, I.: Changes to save functioning renal

parenchyma using absorbable synthetic suture matierials.

In: Chirurgische Forschung. Ed.: Eranus S, Zuckschwerdt Verlag, München, Bern, Wien, New

York, 165-170, 1984.



73. Módis, L., Matesz, K., Szabó, G., Pápay, A., Telek, B.: Functional fine structure of the osteocyte

capsule in exprimentally damaged bones.

In: Modern trends in orthopaedic surgery. Ed.: Bozdech Z., Horn V, Acta Fac. Med. Univ.

Brnensis, Purkyne Univ., Brno, Brno, 53-57, 1974.



Összesített tudománymetriai értékek

Folyóiratcikkek száma és impakt faktora: 63 (IF:124.648)

magyar nyelvű: 1 (IF:0)

idegen nyelvű ( Magyarországon megjelent ): 12 (IF:2.5)

idegen nyelvű ( külföldön megjelent ): 50 (IF:122.148)

Könyvek száma: 1

magyar nyelvű: 0

idegen nyelvű ( Magyarországon megjelenet ): 0

idegen nyelvű ( külföldön megjelent ): 1

Könyvrészletek száma: 9

magyar nyelvű: 0

idegen nyelvű ( Magyarországon megjelent ): 0


Konferenciacikkek száma: 0

magyar nyelvű: 0



Szabadalmak száma: 0

magyar nyelvű: 0


Egyéb közlemények száma: 0

magyar nyelvű: 0





Összes közlemény száma: 73

Összes közlemény száma ( utolsó 10 év ): 32

Összesített Impakt Faktor érték: 124.648

Összesített Impakt Faktor értek ( utolsó 10 év ): 69.357

Hivatkozások száma: 858

Hivatkozások száma ( utolsó 10 év ): 173

Összes független hivatkozások száma: 690

Összes független hivatkozások száma ( utolsó 10 év ): 131

Hirsch-index: 16



Legfontosabb közlemények

Utóbbi 5 év 5 legfontosabb közleménye

1. Deák, Á., Bácskai, T., Gaál, B., Rácz, É., Matesz, K.: Effect of unilateral labyrinthectomy on the

molecular composition of perineuronal nets in the lateral vestibular nucleus of the rat.

Neurosci. Lett. [Epub ahead of Print], 2012.

IF:2.055 (2010)

2. Bácskai, T., Veress, G., Halasi, G., Matesz, K.: Crossing dendrites of the hypoglossal motoneurons:

Possible morphological substrate of coordinated and synchronized tongue movements of the


Brain Res. 1313, 89-96, 2010.


IF:2.623



neuroanatomical tracing (2011) Journal of Chemical Neuroanatomy, 42 (3), pp. 157-183.


Dendrodendritic connections between the cochlear efferent neurons in guinea pig (2011) Neuroscience Letters, 504 (3), pp. 195-198.

3. Deák, Á., Bácskai, T., Veress, G., Matesz, K.: Vestibular afferents to the motoneurons of

glossopharyngeal and vagus nerves in the frog, Rana esculenta.

Brain Res. 1286, 60-65, 2009.


IF:2.463



Проекционной Системы Лягушки.(2011) Биолог. Журн. Армении, 2 (63), Pp. 43-47


Dendrodendritic connections between the cochlear efferent neurons in guinea pig. (2011) Neurosci Lett, 504 (3), pp. 195-198 .



4. Bácskai, T., Veress, G., Halasi, G., Deák, Á., Rácz, É., Székely, G., Matesz, K.: Dendrodendritic and

dendrosomatic contacts between oculomotor and trochlear motoneurons of the frog, Rana

esculenta.

Brain Res. Bull. 75 (2-4), 419-423, 2008.


IF:2.281


Független idézetek: 3 4. Campbell, R.E., Gaidamaka, G., Han, S.-., Herbison, A.E.: Dendro-dendritic

bundling and shared synapses between gonadotropin- releasing hormone neurons. (2009) Proc Natl Acad Sci U S A, 106 (26), pp. 10835-10840.

5. Campbell, R.E., Suter, K.J.: Redefining the gonadotrophin-releasing hormone neurone dendrite. (2010) J Neuroendocrinol, 22 (7), pp. 650-658.

6. Gottesman-Davis, A., Peusner, K.D.: Identification of vestibuloocular projection neurons in the developing chicken medial vestibular nucleus. (2010) J Neurosci Res, 88 (2), pp. 290-303.





5. Mészár, Z., Felszeghy, S., Veress, G., Matesz, K., Székely, G., Módis, L.: Hyaluronan accumulates

around differentiating neurons in spinal cord of chicken embryos.

Brain Res. Bull. 75 (2-4), 414-418, 2008.


IF:2.281


Független idézetek: 6 1. Krishnan, L.: Design of a biomimetic niche for adult progenitor cell selection

and differentiation. Adult Stem Cell Standardization, , pp. 149. 2. Hartwell, R., Lai, A., Ghahary, A.: Modulation of extracellular matrix through

keratinocyte-fbroblast crosstalk. (2009) Expert Review of Dermatology, 4 (6), pp. 623-635.

3. Eng, D., Caplan, M., Preul, M., Panitch, A.: Hyaluronan scaffolds: A balance between backbone functionalization and bioactivity. (2010) Acta Biomaterialia, 6 (7), pp. 2407-2414.

4. Jose, A., Krishnan, L.K.: Effect of matrix composition on differentiation of nestin-positive neural progenitors from circulation into neurons. (2010) Journal of neural engineering, 7 , pp. 036009.

5. Seidlits, S.K., Khaing, Z.Z., Petersen, R.R., Nickels, J.D., Vanscoy, J.E., Shear, J.B., Schmidt, C.E.: The effects of hyaluronic acid hydrogels with tunable mechanical properties on neural progenitor cell differentiation. (2010) Biomaterials, 31 (14), pp. 3930-3940.



6. Astachov, L., Nevo, Z., Aviv, M., Vago, R.: Crystalline calcium carbonate and hydrogels as microenvironment for stem cells. (2011) Frontiers in Bioscience, 16 (2), pp. 458-471.

Összesített Impakt Faktor érték: 11,703


Független hivatkozások száma: 11



Teljes életmű további 5 legfontosabb közleménye

1. Matesz, K., Székely, G.: The dorsomedial nuclear group of cranial nerve in the frog.

Acta Biol. Acad. Sci. Hung. 28 (4), 461-474, 1977.

IF:0.149


Független idézetek: 40 1. Lázár, G.: Long-term persistence, after eye-removal, of unmyelinated fibres in

the frog visual pathway. (1980) Brain Res, 199 (1), pp. 219-224. 2. Destombes, J., Durand, J., Gogan, P., Gueritaud, J., Horcholle-Bossavit, G.,

Tyc-Dumont, S.: Ultrastructural and electrophysiological properties of accessory abducens nucleus motoneurones: An intracellular horseradish peroxidase study in the cat. (1983) Neuroscience, 10 (4), pp. 1317-1332.

3. Lazar, G., Toth, P., Csank, G., Kicliter, E.: Morphology and location of tectal projection neurons in frogs: A study with hrp and cobalt‐filling. (1983) J Comp Neurol, 215 (1), pp. 108-120.

4. Schönenberger, N., Escher, G., Van Der Loos, H.: Axon number in oculomotor nerves in xenopus: Removal of one eye primordium affects both sides. (1983) Neurosci Lett, 41 (3), pp. 239-245.

5. Cochran, S., Dieringer, N., Precht, W.: Basic optokinetic-ocular reflex pathways in the frog. (1984) The Journal of neuroscience, 4 (1), pp. 43-57.

6. Knöpfel, T., Hess, B., Precht, W.: Responses of frog trochlear motoneurons to linear acceleration. (1984) Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology, 154 (2), pp. 233-240.

7. Donkelaar, H., Bangma, G., Boer-van Huizen, R.: The fasciculus longitudinalis medialis in the lizard varanus exanthematicus. (1985) Anat Embryol, 172 (2), pp. 205-215.

8. Roth, G., Wake, D.B.: The structure of the brainstem and cervical spinal cord in lungless salamanders (family plethodontidae) and its relation to feeding. (1985) J Comp Neurol, 241 (1), pp. 99-110.

9. Satou, M., Matsushima, T., Takeuchi, H., Ueda, K.: Tongue-muscle-controlling motoneurons in the japanese toad: Topography, morphology and neuronal pathways from the ‘snapping-evoking area’in the optic tectum. (1985) Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology, 157 (6), pp. 717-737.

10. Dieringer, N., Precht, W.: Functional organization of eye velocity and eye position signals in abducens motoneurons of the frog. (1986) Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology, 158 (2), pp. 179-194.

11. Naujoks‐Manteuffel, C., Manteuffel, G., Himstedt, W.: Localization of motoneurons innervating the extraocular muscles in salamandra salamandra L.(amphibia, urodela). (1986) J Comp Neurol, 254 (1), pp. 133-141.

12. Fritzsch, B., Sonntag, R.: The trochlear nerve of amphibians and its relation to proprioceptive fibers: A qualitative and quantitative HRP study. (1987) Anat Embryol, 177 (2), pp. 105-114.

13. Gonzalez, A., Munoz, M.: Distribution and morphology of abducens motoneurons innervating the lateral rectus and retractor bulbi muscles in the frog rana ridibunda. (1987) Neurosci Lett, 79 (1-2), pp. 29-34.

14. Oka, Y., Satou, M., Ueda, K.: An improved method for correlative light and electron microscopic examination of cobaltic-lysine-labelled neurons. (1987) Neurosci Lett, 73 (2), pp. 187-191.

15. Oka, Y., Takeuchi, H., Satou, M., Ueda, K.: Morphology and distribution of the preganglionic parasympathetic neurons of the facial, glossopharyngeal and vagus nerves in the japanese toad: A cobaltic lysine study. (1987) Brain Res, 400 (2), pp. 389-395.



16. Szabo, T., Lazar, G., Libouban, S., Toth, P., Ravaille, M.: Oculomotor system of the weakly electric fish gnathonemus petersii. (1987) J Comp Neurol, 264 (4), pp. 480-493.

17. Takei, K., Oka, Y., Satou, M., Ueda, K.: Distribution of motoneurons involved in the prey-catching behavior in the japanese toad, bufo japonicus. (1987) Brain Res, 410 (2), pp. 395-400.

18. Fritzsch, B., Sonntag, R.: The trochlear motoneurons of lampreys (lampetra fluviatilis): Location, morphology and numbers as revealed with horseradish peroxidase. (1988) Cell Tissue Res, 252 (2), pp. 223-229.

19. Roth, G., Nishikawa, K., Dicke, U., Wake, D.B.: Topography and cytoarchitecture of the motor nuclei in the brainstem of salamanders. (1988) J Comp Neurol, 278 (2), pp. 181-194.

20. Wake, D.B., Nishikawa, K.C., Dicke, U., Roth, G.: Organization of the motor nuclei in the cervical spinal cord of salamanders. (1988) J Comp Neurol, 278 (2), pp. 195-208.

21. Lazar, G., Bennani, S., Toth, P.: Neuronal pathways involved in the optokinetic head nystagmus of the frog. (1989) Acta Biol Hung, 40 (1-2), pp. 107-120.

22. Montgomery, N.M.: Somatomotor connectivity in the midbrain of< i> rana pipiens</i>(part 1 of 2). (1989) Brain Behav Evol, 34 (2), pp. 96-102.

23. Fritzsch, B., Sonntag, R.: Oculomotor (N III) motoneurons can innervate the superior oblique muscle of xenopus after larval trochlear (N IV) nerve surgery. (1990) Neurosci Lett, 114 (2), pp. 129-134.

24. Sokoloff, A.J.: Musculotopic organization of the hypoglossal nucleus in the grass frog, rana pipiens. (1991) J Comp Neurol, 308 (4), pp. 505-512.

25. Straka, H., Dieringer, N.: Internuclear neurons in the ocular motor system of frogs. (1991) J Comp Neurol, 312 (4), pp. 537-548.

26. Weerasuriya, A. In: Motor pattern generators in anuran prey capture. Visual structures and integrated functions; Springer-Verlag New York, Inc., (1991) pp. 255-70.

27. Straka, H., Dieringer, N.: Electrophysiological and pharmacological characterization of vestibular inputs to identified frog abducens motoneurons and internuclear neurons in vitro. (1993) Eur J Neurosci, 5 (3), pp. 251-260.

28. Puzdrowski, R., Leonard, R.: Vestibulo‐oculomotor connections in an elasmobranch fish, the atlantic stingray, dasyatis sabina. (1994) J Comp Neurol, 339 (4), pp. 587-597.

29. Muñoz, M., González, A.: The trochlear nucleus of the frog rana ridibunda: Localization, morphology and ultrastructure of identified motoneurons. (1995) Brain Res Bull, 36 (5), pp. 433-441.

30. Lázár, G., Pál, E.: Removal of cobalt-labeled neurons and nerve fibers by microglia from the frog's brain and spinal cord. (1996) Glia, 16 (2), pp. 101-107.

31. Schmidt, A., Wake, D.B., Wake, M.H.: Motor nuclei of nerves innervating the tongue and hypoglossal musculature in a caecilian (amphibia: Gymnophiona), as revealed by HRP transport. (1996) J Comp Neurol, 370 (3), pp. 342-349.

32. Marín, O., Smeets, W.J.A.J., González, A.: Distribution of choline acetyltransferase immunoreactivity in the brain of anuran (rana perezi, xenopus laevis) and urodele (pleurodeles waltl) amphibians. (1997) J Comp Neurol, 382 (4), pp. 499-534.

33. González, M.J., Pombal, M.A., Rodicio, M.C., Anadón, R.: Internuclear neurons of the ocular motor system of the larval sea lamprey. (1998) J Comp Neurol, 401 (1), pp. 1-15.

34. Puzdrowski, R.L.: Innervation of the medial rectus muscle in the ratfish, hydrolagus colliei. (1998) J Comp Neurol, 400 (4), pp. 571-579.

35. El Hassni, M., Bennis, M., Rio, J.P., Repérant, J.: Localization of motoneurons innervating the extraocular muscles in the chameleon (chamaeleo chameleon). (2000) Anat Embryol, 201 (1), pp. 63-74.

36. Hassni, M.E., Bennis, M., Rio, J., Reperant, J.: Localization of motoneurons innervating the extraocular muscles in the chameleon (chamaeleo chameleon). (2000) Brain Structure and Function, 201 (1), pp. 63-74.





39. Morona, R., González, A.: Immunohistochemical localization of calbindin-D28k and calretinin in the brainstem of anuran and urodele amphibians. (2009) J Comp Neurol, 515 (5), pp. 503-537.

40. Neuhuber, W., Schrödl, F.: Autonomic control of the eye and the iris. (2011) Autonomic Neuroscience: Basic and Clinical, 165 (1), pp. 67-79.

Függő idézetek: 11 1. Matesz, C.: Central projection of the VIIIth cranial nerve in the frog. (1979)

Neuroscience, 4 (12), pp. 2061-2071. 2. Szekely, G.: Order and plasticity in the nervous system. (1979) Trends

Neurosci, 2 , pp. 245-248. 3. Székely, G., Matesz, C.: The accessory motor nuclei of the trigeminal, facial,

and abducens nerves in the rat. (1982) J Comp Neurol, 210 (3), pp. 258-264. 4. Székely, G., Matesz, C.: Trigeminal motoneurons with disparate dendritic

geometry innervate different muscle groups in the frog. (1987) Neurosci Lett, 77 (2), pp. 161-165.

5. Matesz, C.: Development of the oculomotor and trochlear nuclei in the xenopus toad. (1990) Neurosci Lett, 116 (1-2), pp. 1-6.

6. Matesz, C., Birinyi, A., Kothalawala, D., Szekely, G.: Investigation of the dendritic geometry of brain stem motoneurons with different functions using multivariant statistical techniques in the frog. (1995) Neuroscience, 65 (4), pp. 1129-1144.


8. Birinyi, A., Szekely, G., Csapó, K., Matesz, C.: Quantitative morphological analysis of the motoneurons innervating muscles involved in tongue movements of the frog rana esculenta. (2004) J Comp Neurol, 470 (4), pp. 409-421.

9. Bacskai, T., Veress, G., Halasi, G., Deak, A., Racz, E., Szekely, G., Matesz, C.: Dendrodendritic and dendrosomatic contacts between oculomotor and trochlear motoneurons of the frog, rana esculenta. (2008) Brain Res Bull, 75 (2-4), pp. 419-423.



2. Matesz, K.: Peripheral and central distribution of fibers of the mesencephalic trigeminal root in the rat.

Neurosci. Lett. 27 (1), 13-17, 1981.


IF:2.873


Független idézetek: 77 1. Anadon, R., Demiguel, E., Gonzalezfuentes, M., Rodicio, C.: Hrp study of the

central components of the trigeminal nerve in the larval sea lamprey - organization and homology of the primary medullary and spinal nucleus of the trigeminus. (1989) J Comp Neurol, 283 (4), pp. 602-610.

2. Appenteng, K., Donga, R., Williams, R.: Morphological and electrophysiological determination of the projections of jaw-elevator muscle-



spindle afferents in rats. (1985) Journal of Physiology-London, 369 (DEC), pp. 93-113.

3. Arends, J., Dubbeldam, J.: Exteroceptive And Proprioceptive Afferents Of The Trigeminal And Facial Motor Nuclei In The Mallard (Anas-Platyrhynchos L). (1982) J Comp Neurol, 209 (3), Pp. 313-329.

4. Arvidsson, J., Pfaller, K.: Central projections of C4-C8 dorsal-root ganglia in the rat studied by anterograde transport of wga-hrp. (1990) J Comp Neurol, 292 (3), pp. 349-362.

5. Arvidsson, J., Raappana, P.: An hrp study of the central projections from primary sensory neurons innervating the rat masseter muscle. (1989) Brain Res, 480 (1-2), pp. 111-118.


7. Barnett, E., Perlman, S.: The olfactory nerve and not the trigeminal nerve is the major site of cns entry for mouse hepatitis-virus, strain jhm. (1993) Virology, 194 (1), pp. 185-191.

8. Borke, R., Nau, M., Ringler, R.: Brain-stem afferents of hypoglossal neurons in the rat. (1983) Brain Res, 269 (1), pp. 47-55.


10. Buisseretdelmas, C., Epelbaum, M., Buisseret, P.: The vestibular nuclei of the cat receive a primary afferent projection from receptors in extraocular-muscles. (1990) Experimental Brain Research, 81 (3), pp. 654-658.

11. BuisseretDelmas, C., Pinganaud, G., Compoint, C., Buisseret, P.: Projection from trigeminal nuclei to neurons of the mesencephalic trigeminal nucleus in rat. (1997) Neurosci Lett, 229 (3), pp. 189-192.

12. Byers, M., Dong, W.: Comparison of trigeminal receptor location and structure in the periodontal-ligament of different types of teeth from the rat, cat, and monkey. (1989) J Comp Neurol, 279 (1), pp. 117-127.

13. Chapotat, B., Stuart, M., Buda, C., Woda, A.: Demonstration with [C-14] 2-deoxyglucose of brain structures involved in the masticatory activity of the hedgehog (erinaceus-europaeus). (1990) Brain Res, 536 (1-2), pp. 139-145.

14. Cruccu, G., Truini, A., Priori, A.: Excitability of the human trigeminal motoneuronal pool and interactions with other brainstem reflex pathways. (2001) Journal of Physiology-London, 531 (2), pp. 559-571.


16. Dessem, D., Luo, P.: Jaw-muscle spindle afferent feedback to the cervical spinal cord in the rat. (1999) Experimental Brain Research, 128 (4), pp. 451-459.

17. Dessem, D., Taylor, A.: Morphology of jaw-muscle spindle afferents in the rat. (1989) J Comp Neurol, 282 (3), pp. 389-403.

18. Donga, R., Ishizuka, K., Satoh, Y., Scott, J., Murakami, T.: Physiological evidence in support of a direct projection by jaw muscle spindle afferents to the caudal medulla in the anaesthetized rat. (1999) Neurobiology of Mastication - from Molecular to Systems Approach, 1186 , pp. 270-274.

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2. Birinyi, A., Szekely, G., Csapo, K., Matesz, C.: Quantitative morphological analysis of the motoneurons innervating muscles involved in tongue movements of the frog rana esculenta. (2004) J Comp Neurol, 470 (4), pp. 409-421.





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