Chapter 12 Age-dependent effects of lesioning the mesocortical dopamine system upon prefrontal cortex morphometry and PFC-related behaviors

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Tennyson, V. M., Mytilineou, C., & Barrett, R. E. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901490208 · Cited by 69 · see citing works

Morphologic features of embryonic neocortex grafts in adult rats following frontal cortical ablation

Mufson, E. J., Labbe, R., & Stein, D. G. (1987) · Brain Research · doi:10.1016/0006-8993(87)91177-2 · Cited by 68 · see citing works

Morphometric analysis of prefrontal cortical development following neonatal lesioning of the dopaminergic mesocortical projection

Kalsbeek, A., Matthijssen, M. A. H., & Uylings, H. B. M. (1989) · Experimental Brain Research · doi:10.1007/bf00228899 · Cited by 66 · see citing works

Disappearance of hoarding and disorganization of eating behavior after ventral mesencephalic tegmentum lesions in rats.

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Assessment of the effects of neonatal subcutaneous 6-hydroxydopamine on noradrenergic and dopaminergic innervation of the cerebral cortex

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Differential effects of a two-minute open-field session on dopamine utilization in the frontal cortices of BALB/c and C57 BL/6 mice

Tassin, J., Hervé, D., Blanc, G., & Glowinski, J. (1980) · Neuroscience Letters · doi:10.1016/0304-3940(80)90063-4 · Cited by 65 · see citing works

Fetal neocortical transplants grafted to the cerebral cortex of newborn rats receive afferents from the basal forebrain, locus coeruleus and midline raphe

Castro, A. J., T�nder, N., Sunde, N. A., & Zimmer, J. (1988) · Experimental Brain Research · doi:10.1007/bf00247313 · Cited by 63 · see citing works

Distribution of catecholamines, serotonin, and their major metabolites in the rat cingulate, piriform-entorhinal, somatosensory, and visual cortex: A biochemical survey using high-performance liquid chromatography

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Sexual Behavior: Extreme Reduction of Postejaculatory Refractory Period by Midbrain Lesions in Male Rats

Barfield, R. J., Wilson, C. A., & McDonald, P. G. (1975) · Science · doi:10.1126/science.1138372 · Cited by 60 · see citing works

Perinatal Dopamine-Related Drugs Demasculinize Rats

Hull, E. M., Nishita, J. K., Bitran, D., & Dalterio, S. L. (1984) · Science · doi:10.1126/science.6719125 · Cited by 59 · see citing works

Increased caudate dopamine turnover may contribute to the recovery of motor function in marmosets treated with the dopaminergic neurotoxin MPTP

Rose, S., Nomoto, M., Kelly, E., Kilpatrick, G. J., Jenner, P. G., & MARSDEN, C. D. (1989) · Neuroscience Letters · doi:10.1016/0304-3940(89)90550-8 · Cited by 58 · see citing works

Chapter 20 Involvement of mesocorticolimbic dopaminergic systems in emotional states

Bertolucci-D'Angio, M., Serrano, A., Driscoll, P., & Scatton, B. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)62692-8 · Cited by 57 · see citing works

Neonatal frontal lesions in hamsters impair species-typical behaviors and reduce brain weight and neocortical thickness.

Kolb, B. E., & Whishaw, I. Q. (1985) · Behavioral Neuroscience · doi:10.1037//0735-7044.99.4.691 · Cited by 55 · see citing works

An economical, semi‐automatic system for measuring cellular tree structures in three dimensions, with special emphasis on Golgi‐impregnated neurons

Overdijk, J., Uylings, H. B. M., Kuypers, K., & Kamstra, A. W. (1978) · Journal of Microscopy · doi:10.1111/j.1365-2818.1978.tb00137.x · Cited by 54 · see citing works

MPP+ (1-methyl-4-phenylpyridine) is a neurotoxin to dopamine-, norepinephrine- and serotonin-containing neurons

Namura, I., Douillet, P., Sun, C. J., Pert, A., Cohen, R. M., & Chiueh, C. C. (1987) · European Journal of Pharmacology · doi:10.1016/0014-2999(87)90775-8 · Cited by 52 · see citing works

D-2 dopamine-receptors regulate the release of [3H]dopamine in rat cortical regions showing dopamine immunoreactive fibers

Plantjé, J. F., Steinbusch, H. W. M., Schipper, J., Dijcks, F. A., Verheijden, P. F. H. M., & Stoof, J. C. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90009-1 · Cited by 51 · see citing works

Evidence that [3H]Dopamine Is Taken Up and Released from Nondopaminergic Nerve Terminals in the Rat Substantia Nigra In Vitro

Kelly, E., Jenner, P. G., & MARSDEN, C. D. (1985) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1985.tb05485.x · Cited by 50 · see citing works

Effects of midbrain lesions on female sexual behavior in the rat

HERNDONJR, J. (1976) · Physiology & Behavior · doi:10.1016/0031-9384(76)90281-x · Cited by 47 · see citing works

Functional recovery after serial ablation of prefrontal cortex in the rat

Nonneman, A. J., & Kolb, B. E. (1979) · Physiology & Behavior · doi:10.1016/0031-9384(79)90334-2 · Cited by 47 · see citing works

Do Neurotransmitters, Neurohumors, and Hormones Specify Critical Periods?

Lauder, J. M., & Krebs, H. (1986) · Elsevier eBooks · doi:10.1016/b978-0-12-300271-6.50011-1 · Cited by 46 · see citing works

Development of cortical and nigro-neostriatal dopaminergic systems after destruction of central noradrenergic neurones in foetal or neonatal rats

Tassin, J., Velley, L., Stinus, L., Blanc, G., Glowinski, J., & Thierry, A. M. (1975) · Brain Research · doi:10.1016/0006-8993(75)90861-6 · Cited by 45 · see citing works

The origin of the monoaminergic innervation of immature rat neocortex: an ultrastructural analysis following lesions

Zečević, N., & Molliver, M. E. (1978) · Brain Research · doi:10.1016/0006-8993(78)90289-5 · Cited by 45 · see citing works

Early neurogenesis and synaptogenesis in cerebral cortex.

König, N., & Marty, R. (1981) · PubMed · Cited by 43 · see citing works

Partial protection by desmethylimipramine of the mesocortical dopamine neurones from the neurotoxic effect of 6-hydroxydopamine injected in ventral mesencephalic tegmentum. The role of noradrenergic innervation

Hervé, D., Studler, J., Blanc, G. ́., Glowinski, J., & Tassin, J. (1986) · Brain Research · doi:10.1016/0006-8993(86)90006-5 · Cited by 42 · see citing works

Prefrontal cortex: dense dopaminergic input in the newborn rat

Schmidt, R. H., Björklund, A., Lindvall, O., & Lorén, I. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90163-8 · Cited by 42 · see citing works

Neuronal and Extraneuronal Effects of Intracisternally Administered 6‐Hydroxydopamine on the Developing Rat Brain

Sievers, J., Klemm, H. P., Jenner, S., Baumgarten, H. G., & Berry, M. (1980) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1980.tb09645.x · Cited by 41 · see citing works

Dopamine‐β‐hydroxylase‐like immunoreactivity in the fetal cerebral cortex of the rat: Noradrenergic ascending pathways and terminal fields

Verney, C., Berger, B., Baulac, M., Helle, K. B., & Alvarez, C. (1984) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(84)90051-0 · Cited by 40 · see citing works

MPTP produces a mosaic-like pattern of terminal degeneration in the caudate nucleus of dog

Wilson, J. S., Turner, B. H., Morrow, G. D., & Hartman, P. J. (1987) · Brain Research · doi:10.1016/0006-8993(87)90857-2 · Cited by 40 · see citing works

Environmental and Genetic Determinants of Connectivity in the Central Nervous System — An Approach Through Dendritic Field Analysis

Berry, M., Bradley, P. B., & Borges, S. (1978) · Progress in brain research · doi:10.1016/s0079-6123(08)61020-1 · Cited by 39 · see citing works

Impairments of search behaviour in rats after haloperidol treatment, hippocampal or neocortical damage suggest a mesocorticolimbic role in cognition

Oades, R. D. (1981) · Biological Psychology · doi:10.1016/0301-0511(81)90021-1 · Cited by 39 · see citing works

Ontogeny of open field activity in rats after neonatal lesioning of the mesocortical dopaminergic projection

Kalsbeek, A., DEBRUIN, J., Matthijssen, M. A. H., & Uylings, H. B. M. (1989) · Behavioural Brain Research · doi:10.1016/s0166-4328(89)80079-8 · Cited by 39 · see citing works

Neonatal thermal lesions of the mesolimbocortical dopaminergic projection decrease food-hoarding behavior

Kalsbeek, A., de Bruin, J. P. C., Feenstra, M. G. P., Matthijssen, M. A. H., & Uylings, H. B. M. (1988) · Brain Research · doi:10.1016/0006-8993(88)90201-6 · Cited by 37 · see citing works

1-Methyl-4-phenylpyridine (MPP+): Regional dopamine neuron uptake, toxicity, and novel rotational behavior following dopamine receptor proliferation

Altar, C. A., Heikkila, R. E., Manzino, L., & Marien, M. R. (1986) · European Journal of Pharmacology · doi:10.1016/0014-2999(86)90573-x · Cited by 37 · see citing works

Spontaneous and graft-induced behavioral recovery after 6-hydroxydopamine lesion of the nucleus accumbens in the rat

Choulli, K., Herman, J. P., Rivet, J., Simon, H., & Moal, M. L. (1987) · Brain Research · doi:10.1016/0006-8993(87)91117-6 · Cited by 35 · see citing works

Neonatal frontal lesions in hamsters impair species-typical behaviors and reduce brain weight and neocortical thickness.

Kolb, B. E., & Whishaw, I. Q. (1985) · Behavioral Neuroscience · doi:10.1037/0735-7044.99.4.691 · Cited by 35 · see citing works

Prenatal neurotransmitter programming of postnatal receptor function

Miller, J. C., & Friedhoff, A. J. (1988) · Progress in brain research · doi:10.1016/s0079-6123(08)60523-3 · Cited by 34 · see citing works

Definitive disruption of spatial delayed alternation in rats after lesions in the ventral mesencephalic tegmentum

Simon, H., Scatton, B., & LeMoal, M. (1979) · Neuroscience Letters · doi:10.1016/0304-3940(79)96133-0 · Cited by 34 · see citing works

Synaptosomal uptake and release of dopamine in substantia nigra: Effects of γ-aminobutyric acid and substance P

Silbergeld, E. K., & Walters, J. R. (1979) · Neuroscience Letters · doi:10.1016/0304-3940(79)91491-5 · Cited by 34 · see citing works

Delayed-alternation performance after kainic acid lesions of the thalamic mediodorsal nucleus and the ventral tegmental area in the rat

KESSLER, J. (1981) · Behavioural Brain Research · doi:10.1016/0166-4328(81)90033-4 · Cited by 33 · see citing works

Structural and biochemical changes in rat cerebral cortex after neonatal 6-hydroxydopamine administration

Ont�niente, B., K�nig, N., Sievers, J., Jenner, S., Klemm, H. P., & Marty, R. (1980) · Anatomy and Embryology · doi:10.1007/bf00317649 · Cited by 31 · see citing works

Hypersensitivity to α-methyl-p-tyrosine suggests that behavioural recovery of rats receiving neonatal 6-OHDA lesions is mediated by residual catecholamine neurones

Rogers, D. C., & Dunnett, S. B. (1989) · Neuroscience Letters · doi:10.1016/0304-3940(89)90316-9 · Cited by 31 · see citing works

Role of residual anterior neocortex in recovery from neonatal prefrontal lesions in the rat

Vicedomini, J. P., Corwin, J. V., & Nonneman, A. J. (1982) · Physiology & Behavior · doi:10.1016/0031-9384(82)90196-2 · Cited by 29 · see citing works

Development of Dopamine - Containing Systems in the CNS

Buijs, R. M., Kalsbeek, A., & Voorn, P. (1992) · Data Archiving and Networked Services (DANS) · Cited by 27 · see citing works

Stress and Enhanced Dopamine Utilization in the Frontal Cortex: The Myth and the Realitya

Antelman, S. M., Knopf, S., Caggiula, A. R., Kocan, D. J., Lysle, D. T., & EDWARDS, D. J. (1988) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1988.tb42112.x · Cited by 27 · see citing works

Intracerebral dialysis monitoring of striatal dopamine release and metabolism in response to L-DOPA

Brannan, T. S., Knott, P. J., Kaufmann, H., Leung, L., & Yahr, M. D. (1989) · Journal of Neural Transmission · doi:10.1007/bf01677428 · Cited by 26 · see citing works

Stereotaxic operation in the neonatal rat; a novel and simple procedure

Hoorneman, E. M. D. (1985) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(85)90122-0 · Cited by 26 · see citing works

Enhanced dopamine metabolism after small lesions in the midbrain of the rat

Westerink, B. H. C., der Heyden, J. A. M. V., & Korf, J. (1978) · Life Sciences · doi:10.1016/0024-3205(78)90243-6 · Cited by 25 · see citing works

Development of the visual cortex of rats treated with 6-hydroxydopamine in early life

Ebersole, P., Parnavelas, J. G., & Blue, M. E. (1981) · Anatomy and Embryology · doi:10.1007/bf00301873 · Cited by 25 · see citing works

Monoamine and metabolite levels in the prefrontal cortex and the mesolimbic forebrain following neonatal lesions of the ventral tegmental area

Kalsbeek, A., Feenstra, M. G. P., van Galen, H., & Uylings, H. B. M. (1989) · Brain Research · doi:10.1016/0006-8993(89)91637-5 · Cited by 25 · see citing works

Effects of extended periods of reserpine and α‐methyl‐p‐tyrosine treatment on the development of the putamen in fetal rabbits

Tennyson, V. M., Gershon, P., Budininkas‐Schoenebeck, M., & Rothman, T. P. (1983) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(83)90033-3 · Cited by 25 · see citing works

Distorted development of intracerebral grafts: long-term maintenance of tyrosine hydroxylase-containing neurons in grafts of cortical tissue

Herman, J. P., Abrous, D. N., Vigny, A., Dulluc, J., & Moal, M. L. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90010-7 · Cited by 24 · see citing works

Effects of neonatal dopamine depletion on spatial ability during ontogeny.

Feeser, H. R., & Raskin, L. A. (1987) · Behavioral Neuroscience · doi:10.1037//0735-7044.101.6.812 · Cited by 22 · see citing works

Local connections in transplanted and normal cerebral cortex of rats

Fonseca, M., DeFelipe, J., & Fair�n, A. (1988) · Experimental Brain Research · doi:10.1007/bf00247584 · Cited by 22 · see citing works

Regulation of mating behaviour in the female rat by gonadotropin-releasing hormone in the ventral tegmental area: effects of selective destruction of the A10 dopamine neurones

Sirinathsinghji, D. J. S., Whittington, P. E., & Audsley, A. R. S. (1986) · Brain Research · doi:10.1016/0006-8993(86)90406-3 · Cited by 21 · see citing works

Effects of neonatal dopamine depletion on spatial ability during ontogeny.

Feeser, H. R., & Raskin, L. A. (1987) · Behavioral Neuroscience · doi:10.1037/0735-7044.101.6.812 · Cited by 19 · see citing works

Tactile-visual acquisition and reversal learning deficits in rats with prefrontal cortical lesions

Doar, B. P., Finger, S., & Almli, C. R. (1987) · Experimental Brain Research · doi:10.1007/bf00243317 · Cited by 15 · see citing works

Chapter 13 Is it possible to repair the damaged prefrontal cortex by neural tissue transplantation?

Dunnett, S. B. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)62685-0 · Cited by 14 · see citing works

Effect of intraventricular injections of 6-hydroxydopamine in neonatal rats on the catecholamine levels and tyrosine hydroxylase activity in brain regions at maturity

Peters, D. A., Pappas, B. A., Taub, H., & Saari, M. J. (1977) · Biochemical Pharmacology · doi:10.1016/0006-2952(77)90281-7 · Cited by 12 · see citing works

Neuropsychological Correlates of Early Parkinson's Disease: Evidence for Frontal Lobe Dysfunction

Levin, B. E., Llabre, M. M., & Weiner, W. J. (1988) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1988.tb42145.x · Cited by 12 · see citing works

Immunohistochemical analysis of the development of somatostatin in the reeler neocortex

Naus, C. C. G., & Bloom, F. E. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90153-8 · Cited by 12 · see citing works

Role of the caudate nucleus in recovery from neonatal mediofrontal cortex lesions in the rat

Vicedomini, J. P., Isaac, W. L., & Nonneman, A. J. (1984) · Developmental Psychobiology · doi:10.1002/dev.420170105 · Cited by 10 · see citing works

Effects of Neonatal 6-Hydroxydopamine Treatment on Cortical Development in Mice and Rats as Monitored by Developmental Changes of Gangliosides

Segler-Stahl, K., Rahmann, H., & Rösner, H. (2007) · Developmental Neuroscience · doi:10.1159/000112717 · Cited by 10 · see citing works

Sex differences in food hoarding behaviour of Long Evans rats

de Bruin, J. P. C. (1988) · Behavioural Processes · doi:10.1016/0376-6357(88)90002-2 · Cited by 8 · see citing works

Prenatal treatment with 6‐hydroxydopa and DSP 4: Biochemical, endocrinological and behavioural effects

König, N., Serrano, J., JONSSON, G., Malayal, F., & SZAFARCZYK, A. (1985) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(85)90039-5 · Cited by 6 · see citing works

The Heterogeneity of the Catecholamine Innervation of Cerebral Cortex

Reader, T. A., Ferron, A., Diop, L., Kolta, A., & Brière, R. (1988) · Springer eBooks · doi:10.1007/978-1-4613-0925-3_22 · Cited by 4 · see citing works

Morphological effects of chronic haloperidol administration on the postnatal development of the striatum

Iñiguez, C., Calle, F., Marshall, E., & Carreres, J. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90005-8 · Cited by 4 · see citing works

INSENSITIVITY OF EARLY POSTNATAL RAT-BRAIN DOPAMINERGIC SYSTEMS TO 1-METHYL-4-PHENYLPYRIDINIUM ION (MPP+)

Feenstra, M. G. P., Aj, V., Kalsbeek, A., & Rollema, H. (1990) · University of Groningen research database (University of Groningen / Centre for Information Technology) · Cited by 2 · see citing works

Chapter 3 Qualitative and quantitative comparison of the prefrontal cortex in rat and in primates, including humans

Uylings, H. B. M., & van Eden, C. G. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)62675-8 · Cited by 454 · see citing works

Development of prefrontal cortex

Kolk, S. M., & Rakic, P. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01137-9 · Cited by 378 · see citing works

Functional morphology of the endomysium in series fibered muscles

Trotter, J. A., & Purslow, P. P. (1992) · Journal of Morphology · doi:10.1002/jmor.1052120203 · Cited by 231 · see citing works

The functions of the preplate in development and evolution of the neocortex and hippocampus

Supèr, H., Soriano, E., & Uylings, H. B. M. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00005-8 · Cited by 221 · see citing works

Cytoarchitectonic and chemoarchitectonic characterization of the prefrontal cortical areas in the mouse

Werd, H. J. J. M. V. D., Rajkowska, G., Evers, P., & Uylings, H. B. M. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0247-z · Cited by 191 · see citing works

Development of the Human Cortex and the Concept of “Critical” or “Sensitive” Periods

Uylings, H. B. M. (2006) · Language Learning · doi:10.1111/j.1467-9922.2006.00355.x · Cited by 189 · see citing works

Organization of lumbosacral motoneuronal cell groups innervating hindlimb, pelvic floor, and axial muscles in the cat

VanderHorst, V., & Holstege, G. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970526)382:1 · Cited by 239 · see citing works

Gonadectomy Impairs T-Maze Acquisition in Adult Male Rats

Kritzer, M. F., McLaughlin, P. J., Smirlis, T., & Robinson, J. K. (2001) · Hormones and Behavior · doi:10.1006/hbeh.2001.1645 · Cited by 136 · see citing works

Chapter 8 The development of the rat prefrontal cortex : Its size and development of connections with thalamus, spinal cord and other cortical areas

van Eden, C. G., Kros, J. M., & Uylings, H. B. M. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)62680-1 · Cited by 135 · see citing works

Role of motor unit structure in defining function

Monti, R. J., Roy, R. R., & Edgerton, V. R. (2001) · Muscle & Nerve · doi:10.1002/mus.1083 · Cited by 117 · see citing works

Different mechanisms of glutamate-induced neuronal death between dopaminergic and non-dopaminergic neurons in rat mesencephalic culture

Sawada, H., Kawamura, T., Shimohama, S., AKAIKE, A., & Kimura, J. (1996) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19960215)43:4 · Cited by 52 · see citing works

Caudal medullary pathways to lumbosacral motoneuronal cell groups in the cat: Evidence for direct projections possibly representing the final common pathway for lordosis

VanderHorst, V., & Holstege, G. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903590308 · Cited by 105 · see citing works

Effects of gonadectomy on performance in operant tasks measuring prefrontal cortical function in adult male rats

Kritzer, M. F., Brewer, A., Montalmant, F., Davenport, M. J., & Robinson, J. K. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.07.005 · Cited by 98 · see citing works

The rat orbital and agranular insular prefrontal cortical areas: a cytoarchitectonic and chemoarchitectonic study

Werd, H. J. J. M. V. D., & Uylings, H. B. M. (2008) · Brain Structure and Function · doi:10.1007/s00429-007-0164-y · Cited by 73 · see citing works

'Roid rage in rats? Testosterone effects on aggressive motivation, impulsivity and tyrosine hydroxylase

Wood, R. I., Armstrong, A., Fridkin, V., Shah, V. D., Najafi, A. R., & Jakowec, M. W. (2012) · Physiology & Behavior · doi:10.1016/j.physbeh.2012.12.005 · Cited by 63 · see citing works

Continuous nicotine administration produces selective, age‐dependent structural alteration of pyramidal neurons from prelimbic cortex

Bergstrom, H. C., McDonald, C. G., French, H. T., & Smith, R. F. (2008) · Synapse · doi:10.1002/syn.20467 · Cited by 60 · see citing works

Changes in the neonatal gonadal hormonal environment prevent behavioral sparing and alter cortical morphogenesis after early frontal cortex lesions in male and female rats.

Kolb, B. E., & Stewart, J. (1995) · Behavioral Neuroscience · doi:10.1037//0735-7044.109.2.285 · Cited by 58 · see citing works

Neuromuscular specializations of the pharyngeal dilator muscles: II. Compartmentalization of the canine genioglossus muscle

Mu, L., & Sanders, I. (2000) · The Anatomical Record · doi:10.1002/1097-0185(20001101)260:3 · Cited by 57 · see citing works

Long-term Gonadectomy Affects the Density of Tyrosine Hydroxylase- but not Dopamine-beta-hydroxylase-, Choline Acetyltransferase- or Serotonin-immunoreactive Axons in the Medial Prefrontal Cortices of Adult Male Rats

Kritzer, M. F. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.3.282 · Cited by 56 · see citing works

Autism spectrum disorders pathogenesis: Toward a comprehensive model based on neuroanatomic and neurodevelopment considerations

Béopoulos, A., Géa, M., Fasano, A., & Iris, F. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.988735 · Cited by 54 · see citing works

Neuromuscular compartments and fiber‐type regionalization in the human inferior pharyngeal constrictor muscle

Mu, L., & Sanders, I. (2001) · The Anatomical Record · doi:10.1002/ar.10020 · Cited by 49 · see citing works

Movements elicited by electrical stimulation of muscles, nerves, intermediate spinal cord, and spinal roots in anesthetized and decerebrate cats

Aoyagi, Y., Mushahwar, V. K., Stein, R. B., & Procházka, A. (2004) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2003.823268 · Cited by 45 · see citing works

Chapter 24 Social behaviour and the prefrontal cortex

de Bruin, J. P. C. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)62696-5 · Cited by 41 · see citing works

Postnatal maturation of prefrontal pyramidal neurones is sensitive to a single early dose of methamphetamine in gerbils (Meriones unguiculatus)

Bläsing, B. E., Nossoll, M., Teuchert, G., & Dawirs, R. R. (2001) · Journal of Neural Transmission · doi:10.1007/s007020170101 · Cited by 40 · see citing works

Functional combination of tapering profiles and overlapping arrangements in nonspanning skeletal muscle fibers terminating intrafascicularly

Hijikata, T., Wakisaka, H., & Niida, S. (1993) · The Anatomical Record · doi:10.1002/ar.1092360403 · Cited by 33 · see citing works

Lateral rectus emg and contractile responses elicited by cat abducens motoneurons

Shall, M. S., & Goldberg, S. J. (1995) · Muscle & Nerve · doi:10.1002/mus.880180905 · Cited by 32 · see citing works

Neonatal lesions of the ventral tegmental area affect monoaminergic responses to stress in the medial prefrontal cortex and other dopamine projection areas in adulthood

Feenstra, M. G. P., Kalsbeek, A., & van Galen, H. (1992) · Brain Research · doi:10.1016/0006-8993(92)91545-p · Cited by 30 · see citing works

Neuroanatomical correlates of sparing of function after neonatal medial prefrontal cortex lesions in rats

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Perturbed Developmental Serotonin Signaling Affects Prefrontal Catecholaminergic Innervation and Cortical Integrity

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