Academic literature on the topic 'Substantia innominata'

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Journal articles on the topic "Substantia innominata"

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Oikawa, Hirobumi, Makoto Sasaki, Shigeru Ehara, and Takashi Abe. "Substantia innominata: MR findings in Parkinson?s disease." Neuroradiology 46, no. 10 (2004): 817–21. http://dx.doi.org/10.1007/s00234-004-1257-4.

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Grove, Elizabeth A. "Efferent connections of the substantia innominata in the rat." Journal of Comparative Neurology 277, no. 3 (1988): 347–64. http://dx.doi.org/10.1002/cne.902770303.

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WENK, G. L. "Pharmacological Manipulation of the Substantia Innominata-Cortical Cholinergic Pathway." Annals of the New York Academy of Sciences 444, no. 1 Memory Dysfun (1985): 541–42. http://dx.doi.org/10.1111/j.1749-6632.1985.tb37640.x.

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Mori, Norio, Shuzo Hoshino, and Hisashi Kumashiro. "Comparison between substantia innominata and amygdala kindling in rats." Brain Research 534, no. 1-2 (1990): 329–31. http://dx.doi.org/10.1016/0006-8993(90)90151-z.

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Ota, Kazuki, Takanari Kitazono, Hiroaki Ooboshi, et al. "Role of substantia innominata in cerebral blood flow autoregulation." Brain Research 1135 (March 2007): 146–53. http://dx.doi.org/10.1016/j.brainres.2006.12.017.

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Khanamiryan, T. V. "Participation of the substantia innominata in differential inhibition in cats." Neuroscience and Behavioral Physiology 18, no. 1 (1988): 4–9. http://dx.doi.org/10.1007/bf01186898.

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Zhu, Zhenggang, Qingqing Ma, Lu Miao, et al. "A substantia innominata-midbrain circuit controls a general aggressive response." Neuron 109, no. 9 (2021): 1540–53. http://dx.doi.org/10.1016/j.neuron.2021.03.002.

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Hanyu, Haruo, Soichiro Shimizu, Yuriko Tanaka, Kentaro Hirao, Toshihiko Iwamoto, and Kimihiko Abe. "MR features of the substantia innominata and therapeutic implications in dementias." Neurobiology of Aging 28, no. 4 (2007): 548–54. http://dx.doi.org/10.1016/j.neurobiolaging.2006.02.009.

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Formaggio, E., A. C. Dalfini, F. Fazzini, G. Fumagalli, and C. Chiamulera. "GABAergic neurons expressing p75 in rat substantia innominata and nucleus basalis." Molecular and Cellular Neuroscience 46, no. 3 (2011): 625–32. http://dx.doi.org/10.1016/j.mcn.2011.01.002.

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Grove, Elizabeth A. "Neural associations of the substantia innominata in the rat: Afferent connections." Journal of Comparative Neurology 277, no. 3 (1988): 315–46. http://dx.doi.org/10.1002/cne.902770302.

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Dissertations / Theses on the topic "Substantia innominata"

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Boyes, Barry Edward. "Molecular cloning of the human Substantia innominata : characterization of a brain large mRNA." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/30960.

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Brain tissue samples were collected from individuals with histologically and biochemically confirmed Alzheimer's Disease (AD), as well as from a group of individuals without any signs of neurological disease (NNC). Ribonucleic acid (RNA) was extracted from these tissues, characterized by several chemical methods, and the yields were compared between AD and NNC groups. High molecular weight RNA could be effectively extracted from frozen postmortem human brain. In comparison to the NNC group, tissue RNA levels were reduced in the AD hippocampus, but not in the temporal cortex or substantia innom
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Wilhelmi, Eckbert. "Die neuronale Verschaltung der thalamo-amygdalofugalen Projektion zum cholinergen basalen Vorderhirn (Substantia innominata)." [S.l.] : [s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=962905860.

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Wilhelmi, Eckbert [Verfasser]. "Die neuronale Verschaltung der thalamo-amygdalofugalen Projektion zum cholinergen basalen Vorderhirn (Substantia innominata) / von Eckbert Wilhelmi." 2000. http://d-nb.info/962905860/34.

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Book chapters on the topic "Substantia innominata"

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Wood, P. L., and P. McQuade. "Substantia Innominata — Cortical Cholinergic Pathway: Regulatory Afferents." In Advances in Behavioral Biology. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5194-8_98.

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Napier, T. Celeste, Mary Beth Muench, Renata J. Maslowski, and George Battaglia. "Is Dopamine a Neurotransmitter within the Ventral Pallidum/Substantia Innominata?" In Advances in Experimental Medicine and Biology. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4757-0145-6_9.

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Carnes, Kenneth M., and Joseph L. Price. "Demonstration of Individual Fibers from the Substantia Innominata to the Frontal Cortex of the Rat, Using Phaseolus Vulgaris Leucoagglutinin (PHA-L)." In Neurobiology of Amino Acids, Peptides and Trophic Factors. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1721-0_15.

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Zaborszky, Laszlo, and Peter Gombkoto. "The Cholinergic Multicompartmental Basal Forebrain Microcircuit." In Handbook of Brain Microcircuits, edited by Gordon M. Shepherd and Sten Grillner. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190636111.003.0015.

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The basal forebrain (BF) is composed of an affiliation of structures, including the medial septum, ventral pallidum (VP), vertical diagonal band (VDB) and horizontal diagonal band (HDB) nuclei, substantia innominata/extended amygdala (SI/EA), and peripallidal regions. Together, they constitute one of the most extensive multicompartmental microcircuits in the brain. A prominent feature of the mammalian BF is the presence of aggregated and nonaggregated, large, cholinergic neurons, which project to the cerebral cortex, the hippocampal complex, and the amygdala. This highly complex system has been implicated in cortical activation, attention, motivation, and memory, as well as neuropsychiatric disorders such as Alzheimer’s disease, Parkinson’s disease, schizophrenia, and drug abuse. Advances in modern tracing, genetic, and refined pharmacological techniques have dramatically increased the understanding of how the BF cholinergic system can support both phasic acetylcholine (ACh) release in attention, memory, and sensory processing and tonic ACh release over broad cortical areas as part of a general arousal effect.
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Bernabeu, Ignacio, Monica Marazuela, and Felipe F. Casanueva. "General concepts of hypothalamus-pituitary anatomy." In Oxford Textbook of Endocrinology and Diabetes. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199235292.003.2004.

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The hypothalamus is the part of the diencephalon associated with visceral, autonomic, endocrine, affective, and emotional behaviour. It lies in the walls of the third ventricle, separated from the thalamus by the hypothalamic sulcus. The rostral boundary of the hypothalamus is roughly defined as a line through the optic chiasm, lamina terminalis, and anterior commissure, and an imaginary line extending from the posterior commissure to the caudal limit of the mamillary body represents the caudal boundary. Externally, the hypothalamus is bounded rostrally by the optic chiasm, laterally by the optic tract, and posteriorly by the mamillary bodies. Dorsolaterally, the hypothalamus extends to the medial edge of the internal capsule (Fig. 2.1.1) (1). The complicated anatomy of this area of the central nervous system (CNS) is the reason why, for a long time, little was known about its anatomical organization and functional significance. Even though the anatomy of the hypothalamus is well established it does not form a well-circumscribed region. On the contrary, it is continuous with the surrounding parts of the CNS: rostrally, with the septal area of the telencephalon and anterior perforating substance; anterolaterally with the substantia innominata; and caudally with the central grey matter and the tegmentum of the mesencephalon. The ventral portion of the hypothalamus and the third ventricular recess form the infundibulum, which represents the most proximal part of the neurohypophysis. A bulging region posterior to the infundibulum is the tuber cinereum, and the zone that forms the floor of the third ventricle is called the median eminence. The median eminence represents the final point of convergence of pathways from the CNS on the peripheral endocrine system and it is supplied by primary capillaries of the hypophyseal portal vessels. The median eminence is the anatomical interface between the brain and the anterior pituitary. Ependymal cells lining the floor of the third ventricle have processes that traverse the width of the median eminence and terminate near the portal perivascular space; these cells, called tanycytes, provide a structural and functional link between the cerebrospinal fluid (CSF) and the perivascular space of the pituitary portal vessels. The conspicuous landmarks of the ventral surface of the brain can be used to divide the hypothalamus into three parts: anterior (preoptic and supraoptic regions), middle (tuberal region), and caudal (mamillary region). Each half of the hypothalamus is also divided into a medial and lateral zone. The medial zone contains the so-called cell-rich areas with well-defined nuclei. The scattered cells of the lateral hypothalamic area have long overlapping dendrites, similar to the cells of the reticular formation. Some of these neurons send axons directly to the cerebral cortex and others project down into the brainstem and spinal cord.
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Marson, James, and Katy Ferris. "4. Contract III: contractual terms and statutory protection." In Business Law Concentrate. Oxford University Press, 2019. http://dx.doi.org/10.1093/he/9780198840602.003.0004.

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Each Concentrate revision guide is packed with essential information, key cases, revision tips, exam Q&As, and more. Concentrates show you what to expect in a law exam, what examiners are looking for, and how to achieve extra marks. This chapter discusses contractual terms and statutory protection. Parties to a contract may express terms and/or terms may be implied. The sources and effects of implied terms are essential to the rights of the parties and obligations imposed on them. Terms can be implied through the courts, through customs, and from statute. Terms are identified as conditions, warranties, or innominate and this distinction is relevant when identifying remedies for breach. Statutes regulate the rights and obligations applicable to consumers and traders. These include the Sale of Goods Act 1979, the Unfair Contract Terms Act 1977, and the substantial changes in contracts between consumers and traders introduced through the Consumer Rights Act 2015.
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