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Last updated: 20 February 2023

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1

Book, Adam A., Ronald G. Wiley, and John B. Schweitzer. "192 IgG-saporin." Acta Neuropathologica 89, no. 6 (1995): 519–26. http://dx.doi.org/10.1007/bf00571506.

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2

Book, Adam A., Ronald G. Wiley, and John B. Schweitzer. "192 IgG-saporin." Acta Neuropathologica 89, no. 6 (May 1, 1995): 519–26. http://dx.doi.org/10.1007/s004010050283.

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3

Grindstaff, Ryan J., Regina R. Grindstaff, and J. Thomas Cunningham. "Baroreceptor sensitivity of rat supraoptic vasopressin neurons involves noncholinergic neurons in the DBB." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 279, no. 5 (November 1, 2000): R1934—R1943. http://dx.doi.org/10.1152/ajpregu.2000.279.5.r1934.

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Previous studies suggest that cholinergic neurons in the diagonal band of Broca (DBB) participate in the baroreceptor-mediated inhibition of phasic vasopressin neurons in the supraoptic nucleus (SON). To test this hypothesis, extracellular recordings were obtained from putative vasopressin SON neurons of anesthetized rats injected with the cholinergic immunotoxin 192 IgG-saporin (0.8 μg/μl) in the DBB. Baroreceptor sensitivity of neurons was tested with brief phenylephrine-induced (10 μg/10 μl iv) increases in blood pressure of at least 40 mmHg. In rats injected with vehicle or unconjugated saporin, 19 of 21 and 18 of 20 phasic neurons, respectively, were inhibited by increased blood pressure. In rats injected with 192 IgG-saporin, which significantly reduced the number of choline acetyltransferase (ChAT)-positive DBB neurons, 33 of 36 phasic neurons were inhibited. Normal rats and rats with DBB saporin injections received rhodamine bead injections into the perinuclear zone (PNZ) to retrogradely label DBB neurons, and their brains were stained for ChAT. ChAT-positive DBB neurons were not retrogradely labeled from the PNZ. Together, these results indicate that the pathway relaying baroreceptor information to the SON involves noncholinergic DBB neurons.
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4

Harrell, Lindy E., Dee Parsons, and Krystyna Kolasa. "Hippocampal sympathetic ingrowth occurs following 192-IgG–Saporin administration." Brain Research 911, no. 2 (August 2001): 158–62. http://dx.doi.org/10.1016/s0006-8993(01)02626-9.

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5

Blanco-Centurion, Carlos A., Anjelica Shiromani, Elizabeth Winston, and Priyattam J. Shiromani. "Effects of hypocretin-1 in 192-IgG-saporin-lesioned rats." European Journal of Neuroscience 24, no. 7 (October 2006): 2084–88. http://dx.doi.org/10.1111/j.1460-9568.2006.05074.x.

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6

Moga, Margaret M. "192 IgG-saporin abolishes p75 neurotrophin receptor immunoreactivity in rat SCN." NeuroReport 9, no. 14 (October 1998): 3197–200. http://dx.doi.org/10.1097/00001756-199810050-00012.

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7

Wrenn, Craige C., and Ronald G. Wiley. "The behavioral functions of the cholinergic basalforebrain : lessons from 192 IgG‐SAPORIN." International Journal of Developmental Neuroscience 16, no. 7-8 (November 1998): 595–602. http://dx.doi.org/10.1016/s0736-5748(98)00071-9.

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8

Burk, Joshua A., Matthew W. Lowder, and Kathleen E. Altemose. "Attentional demands for demonstrating deficits following intrabasalis infusions of 192 IgG-saporin." Behavioural Brain Research 195, no. 2 (December 2008): 231–38. http://dx.doi.org/10.1016/j.bbr.2008.09.006.

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9

Pappas, B. A., C. M. Davidson, T. Fortin, S. Nallathamby, G. A. S. Park, E. Mohr, and R. G. Wiley. "192 IgG-saporin lesion of basal forebrain cholinergic neurons in neonatal rats." Developmental Brain Research 96, no. 1-2 (October 1996): 52–61. http://dx.doi.org/10.1016/0165-3806(96)00095-8.

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10

Sachdev, Robert N. S., Shao-Ming Lu, Ron G. Wiley, and Ford F. Ebner. "Role of the Basal Forebrain Cholinergic Projection in Somatosensory Cortical Plasticity." Journal of Neurophysiology 79, no. 6 (June 1, 1998): 3216–28. http://dx.doi.org/10.1152/jn.1998.79.6.3216.

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Sachdev, Robert N. S., Shao-Ming Lu, Ron G. Wiley, and Ford F. Ebner. Role of the basal forebrain cholinergic projection in somatosensory cortical plasticity. J. Neurophysiol. 79: 3216–3228, 1998. Trimming all but two whiskers in adult rats produces a predictable change in cortical cell-evoked responses characterized by increased responsiveness to the two intact whiskers and decreased responsiveness to the trimmed whiskers. This type of synaptic plasticity in rat somatic sensory cortex, called “whisker pairing plasticity,” first appears in cells above and below the layer IV barrels. These are also the cortical layers that receive the densest cholinergic inputs from the nucleus basalis. The present study assesses whether the cholinergic inputs to cortex have a role in regulating whisker pairing plasticity. To do this, cholinergic basal forebrain fibers were eliminated using an immunotoxin specific for these fibers. A monoclonal antibody to the low-affinity nerve growth factor receptor 192 IgG, conjugated to the cytotoxin saporin, was injected into cortex to eliminate cholinergic fibers in the barrel field. The immunotoxin reduces acetylcholine esterase (AChE)-positive fibers in S1 cortex by >90% by 3 wk after injection. Sham-depleted animals in which either saporin alone or saporin unconjugated to 192 IgG is injected into the cortex produces no decrease in AChE-positive fibers in cortex. Sham-depleted animals show the expected plasticity in barrel column neurons. In contrast, no plasticity develops in the ACh-depleted, 7-day whisker-paired animals. These results support the conclusion that the basal forebrain cholinergic projection to cortex is an important facilitator of synaptic plasticity in mature cortex.
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11

Galani, Rodrigue, Hélène Jeltsch, Olivia Lehmann, Fabrice Bertrand, and Jean-Christophe Cassel. "Effects of 192 IgG-saporin on acetylcholinesterase histochemistry in male and female rats." Brain Research Bulletin 58, no. 2 (June 2002): 179–86. http://dx.doi.org/10.1016/s0361-9230(02)00775-x.

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12

Lehmann, Olivia, Hélène Jeltsch, Christine Lazarus, Laurent Tritschler, Fabrice Bertrand, and Jean-Christophe Cassel. "Combined 192 IgG-saporin and 5,7-dihydroxytryptamine lesions in the male rat brain." Pharmacology Biochemistry and Behavior 72, no. 4 (July 2002): 899–912. http://dx.doi.org/10.1016/s0091-3057(02)00752-9.

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13

Pereira, Patricia Marques, Dulce Papy-Garcia, Denis Barritault, Franck Chiappini, Rolf Jackisch, Sarah Schimchowitsch, and Jean-Christophe Cassel. "Protective Effects of a synthetic glycosaminoglycan mimetic (OTR4132) in a rat immunotoxic lesion model of septohippocampal cholinergic degeneration." Glycoconjugate Journal 39, no. 1 (February 2022): 107–30. http://dx.doi.org/10.1007/s10719-022-10047-x.

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AbstractUsing a partial hippocampal cholinergic denervation model, we assessed the effects of the RGTA® named OTR4132, a synthetic heparan-mimetic biopolymer with neuroprotective/neurotrophic properties. Long-Evans male rats were injected with the cholinergic immunotoxin 192 IgG-saporin into the medial septum/diagonal band of Broca (0.37 µg); vehicle injections served as controls. Immediately after surgery, OTR4132 was injected into the lateral ventricles (0.25 µg/5 µl/rat) or intramuscularly (1.5 mg/kg). To determine whether OTR4132 reached the lesion site, some rats received intracerebroventricular (ICV) or intramuscular (I.M.) injections of fluorescent OTR4132. Rats were sacrificed at 4, 10, 20, or 60 days post-lesion (DPL). Fluorescein-labeled OTR4132 injected ICV or I.M. was found in the lesion from 4 to 20 DPL. Rats with partial hippocampal cholinergic denervation showed decreases in hippocampal acetylcholinesterase reaction products and in choline acetyltransferase-positive neurons in the medial septum. These lesions were the largest at 10 DPL and then remained stable until 60 DPL. Both hippocampal acetylcholinesterase reaction products and choline acetyltransferase-positive neurons in the medial septum effects were significantly attenuated in OTR4132-treated rats. These effects were not related to competition between OTR4132 and 192 IgG-saporin for the neurotrophin receptor P75 (p75NTR), as OTR4132 treatment did not alter the internalization of Cy3-labelled 192 IgG. OTR4132 was more efficient at reducing the acetylcholinesterase reaction products and choline acetyltransferase-positive neurons than a comparable heparin dose used as a comparator. Using the slice superfusion technique, we found that the lesion-induced decrease in muscarinic autoreceptor sensitivity was abolished by intramuscular OTR4132. After partial cholinergic damage, OTR4132 was able to concentrate at the brain lesion site possibly due to the disruption of the blood-brain barrier and to exert structural and functional effects that hold promises for neuroprotection/neurotrophism.
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14

Pappas, Bruce A., and Nicole Sherren. "Neonatal 192 IgG-saporin lesion of forebrain cholinergic neurons: focus on the life span?" Neuroscience & Biobehavioral Reviews 27, no. 4 (June 2003): 365–76. http://dx.doi.org/10.1016/s0149-7634(03)00067-8.

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15

Ricceri, Laura, Christine Hohmann, and Joanne Berger-Sweeney. "Early neonatal 192 IgG saporin induces learning impairments and disrupts cortical morphogenesis in rats." Brain Research 954, no. 2 (November 2002): 160–72. http://dx.doi.org/10.1016/s0006-8993(02)03172-4.

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16

Botly, L. C. P., and E. De Rosa. "Cholinergic Deafferentation of the Neocortex Using 192 IgG-Saporin Impairs Feature Binding In Rats." Journal of Neuroscience 29, no. 13 (April 1, 2009): 4120–30. http://dx.doi.org/10.1523/jneurosci.0654-09.2009.

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17

Pallera, Arnel M., John B. Schweitzer, Adam A. Book, and Ronald G. Wiley. "192 IgG-Saporin Causes a Major Loss of Synaptic Content in Rat Olfactory Bulb." Experimental Neurology 127, no. 2 (June 1994): 265–77. http://dx.doi.org/10.1006/exnr.1994.1102.

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18

Birthelmer, Anja, Esther Dommes, Hélène Jeltsch, Jean-Christophe Cassel, and Rolf Jackisch. "Septal grafts and evoked acetylcholine release in the rat hippocampus after 192 IgG-saporin lesions." NeuroReport 13, no. 7 (May 2002): 973–76. http://dx.doi.org/10.1097/00001756-200205240-00015.

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19

Sherren, Nicole, Bruce A. Pappas, and Teresa Fortin. "Neural and behavioral effects of intracranial 192 IgG-saporin in neonatal rats: sexually dimorphic effects?" Developmental Brain Research 114, no. 1 (April 1999): 49–62. http://dx.doi.org/10.1016/s0165-3806(99)00018-8.

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20

Potter, P. "Lesion of septal-hippocampal neurons with 192 IgG-saporin alters function of M1 muscarinic receptors." Neuropharmacology 38, no. 4 (April 1, 1999): 579–86. http://dx.doi.org/10.1016/s0028-3908(98)00207-x.

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21

Book, A. A., R. G. Wiley, and J. B. Schweitzer. "DESTRUCTION OF CHOLINERGIC NEURONS IN THE BASAL FOREBRAIN OF THE RAT BY 192 IgG-SAPORIN." Journal of Neuropathology and Experimental Neurology 52, no. 3 (May 1993): 286. http://dx.doi.org/10.1097/00005072-199305000-00104.

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22

Holley, Lee Ann, Ronald G. Wiley, Douglas A. Lappi, and Martin Sarter. "Cortical cholinergic deafferentation following the intracortical infusion of 192 IgG-saporin: a quantitative histochemical study." Brain Research 663, no. 2 (November 1994): 277–86. http://dx.doi.org/10.1016/0006-8993(94)91274-2.

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23

Bannon, Anthony W., Peter Curzon, Karen L. Gunther, and Michael W. Decker. "Effects of intraseptal injection of 192-IgG-saporin in mature and aged Long-Evans rats." Brain Research 718, no. 1-2 (April 1996): 25–36. http://dx.doi.org/10.1016/0006-8993(95)01568-x.

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24

Scott Janis, L., Marylou M. Glasier, Zoltan Fulop, and Donald G. Stein. "Intraseptal injections of 192 IgG saporin produce deficits for strategy selection in spatial-memory tasks." Behavioural Brain Research 90, no. 1 (January 1998): 23–34. http://dx.doi.org/10.1016/s0166-4328(97)00078-8.

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25

Perry, TracyAnn, Helen Hodges, and Jeffrey A. Gray. "Behavioural, histological and immunocytochemical consequences following 192 IgG-saporin immunolesions of the basal forebrain cholinergic system." Brain Research Bulletin 54, no. 1 (January 2001): 29–48. http://dx.doi.org/10.1016/s0361-9230(00)00413-5.

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26

Rastogi, Shweta, Sumithra Unni, Sumit Sharma, T. Rao Laxmi, and Bindu M. Kutty. "Cholinergic immunotoxin 192 IgG-SAPORIN alters subicular theta–gamma activity and impairs spatial learning in rats." Neurobiology of Learning and Memory 114 (October 2014): 117–26. http://dx.doi.org/10.1016/j.nlm.2014.05.008.

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27

Ricceri, Laura. "Behavioral patterns under cholinergic control during development: lessons learned from the selective immunotoxin 192 IgG saporin." Neuroscience & Biobehavioral Reviews 27, no. 4 (June 2003): 377–84. http://dx.doi.org/10.1016/s0149-7634(03)00068-x.

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28

Bailey, Aileen M., Meghan L. Rudisill, Emily J. Hoof, and Michelle L. Loving. "192 IgG-saporin lesions to the nucleus basalis magnocellularis (nBM) disrupt acquisition of learning set formation." Brain Research 969, no. 1-2 (April 2003): 147–59. http://dx.doi.org/10.1016/s0006-8993(03)02294-7.

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29

Holschneider, D. P., Jerene J. Waite, Andrew F. Leuchter, Nancy Y. Walton, and Oscar U. Scremin. "Changes in electrocortical power and coherence in response to the selective cholinergic immunotoxin 192 IgG-saporin." Experimental Brain Research 126, no. 2 (May 4, 1999): 270–80. http://dx.doi.org/10.1007/s002210050736.

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30

Pain, L., H. Jeltsch, O. Lehmann, C. Lazarus, F. Z. Laalou, and J. C. Cassel. "Central cholinergic depletion induced by 192 IgG-Saporin alleviates the sedative effects of propofol in rats." British Journal of Anaesthesia 85, no. 6 (December 2000): 869–73. http://dx.doi.org/10.1093/bja/85.6.869.

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31

Book, Adam A., Ronald G. Wiley, and John B. Schweitzer. "192 IgG-saporin : I. Specific Lethality for Cholinergic Neurons in the Basal Forebrain of the Rat." Journal of Neuropathology and Experimental Neurology 53, no. 1 (January 1994): 95–102. http://dx.doi.org/10.1097/00005072-199401000-00012.

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32

Steckler, T., A. B. Keith, R. G. Wiley, and A. Sahgal. "Cholinergic lesions by 192 IgG-saporin and short-term recognition memory: Role of the septohippocampal projection." Neuroscience 66, no. 1 (May 1995): 101–14. http://dx.doi.org/10.1016/0306-4522(94)00603-3.

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33

Kapás, Levente, Ferenc Obál, Adam A. Book, John B. Schweitzer, Ronald G. Wiley, and James M. Krueger. "The effects of immunolesions of nerve growth factor-receptive neurons by 192 IgG-saporin on sleep." Brain Research 712, no. 1 (March 1996): 53–59. http://dx.doi.org/10.1016/0006-8993(95)01431-4.

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34

Waite, Jerene J., Mark L. Wardlow, Andrew C. Chen, Douglas A. Lappi, Ronald G. Wiley, and Leon J. Thal. "Time course of cholinergic and monoaminergic changes in rat brain after immunolesioning with 192 IgG-saporin." Neuroscience Letters 169, no. 1-2 (March 1994): 154–58. http://dx.doi.org/10.1016/0304-3940(94)90379-4.

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35

Book, Adam A., Ronald G. Wiley, and John B. Schweitzer. "Specificity of 192 IgG-saporin for NGF receptor-positive cholinergic basal forebrain neurons in the rat." Brain Research 590, no. 1-2 (September 1992): 350–55. http://dx.doi.org/10.1016/0006-8993(92)91121-t.

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36

Turchi, Janita, and Martin Sarter. "Cortical cholinergic inputs mediate processing capacity: effects of 192 IgG-saporin-induced lesions on olfactory span performance." European Journal of Neuroscience 12, no. 12 (December 2000): 4505–14. http://dx.doi.org/10.1046/j.1460-9568.2000.01347.x.

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37

Turchi, Janita, and Martin Sarter. "Cortical cholinergic inputs mediate processing capacity: effects of 192 IgG-saporin-induced lesions on olfactory span performance." European Journal of Neuroscience 12, no. 12 (December 2000): 4505–14. http://dx.doi.org/10.1111/j.1460-9568.2000.01347.x.

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38

Jeong, Da Un, Won Seok Chang, Yong Sup Hwang, Dongkyu Lee, and Jin Woo Chang. "Decrease of GABAergic Markers and Arc Protein Expression in the Frontal Cortex by Intraventricular 192 IgG-Saporin." Dementia and Geriatric Cognitive Disorders 32, no. 1 (2011): 70–78. http://dx.doi.org/10.1159/000330741.

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39

Hernández-Melesio, M. Alejandra, Dinora González-Esquivel, Alma Ortíz-Plata, Alicia Sánchez-Mendoza, Aurora Sánchez-García, Mireya Alcaraz-Zubeldia, Camilo Ríos, and Francisca Pérez-Severiano. "Molsidomine modulates the cNOS activity in an experimental model of cholinergic damage induced by 192-IgG saporin." Neuroscience Letters 491, no. 2 (March 2011): 133–37. http://dx.doi.org/10.1016/j.neulet.2011.01.023.

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40

Wenk, GL, JD Stoehr, G. Quintana, S. Mobley, and RG Wiley. "Behavioral, biochemical, histological, and electrophysiological effects of 192 IgG-saporin injections into the basal forebrain of rats." Journal of Neuroscience 14, no. 10 (October 1, 1994): 5986–95. http://dx.doi.org/10.1523/jneurosci.14-10-05986.1994.

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41

Leblanc, C. J., T. W. Deacon, B. R. Whatley, J. Dinsmore, L. Lin, and O. Isacson. "Morris Water Maze Analysis of 192-IgG-Saporin-Lesioned Rats and Porcine Cholinergic Transplants to the Hippocampus." Cell Transplantation 8, no. 1 (January 1999): 131–42. http://dx.doi.org/10.1177/096368979900800105.

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42

Jouvenceau, Anne, Jean-Marie Billard, Yvon Lamour, and Patrick Dutar. "Potentiation of glutamatergic EPSPs in rat CA1 hippocampal neurons after selective cholinergic denervation by 192 IgG-saporin." Synapse 26, no. 3 (July 1997): 292–300. http://dx.doi.org/10.1002/(sici)1098-2396(199707)26:3<292::aid-syn10>3.0.co;2-y.

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43

Quinlivan, Mitchell, Sylvie Chalon, Jackie Vergote, Jasmine Henderson, Andrew Katsifis, Michael Kassiou, and Denis Guilloteau. "Decreased vesicular acetylcholine transporter and α4β2 nicotinic receptor density in the rat brain following 192 IgG-saporin immunolesioning." Neuroscience Letters 415, no. 2 (March 2007): 97–101. http://dx.doi.org/10.1016/j.neulet.2006.08.065.

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44

Sarter, Martin, John P. Bruno, Lee Ann H. Miner, and Jill McGaughy. "Development of a method for intraparenchymal infusions of 192 IgG-saporin: a comment on Pizzo et al. (1999)." Journal of Neuroscience Methods 96, no. 2 (March 2000): 169–70. http://dx.doi.org/10.1016/s0165-0270(99)00196-x.

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45

Fadel, Jim, Holly Moore, Martin Sarter, and John P. Bruno. "Trans-Synaptic Stimulation of Cortical Acetylcholine Release after Partial 192 IgG-Saporin-Induced Loss of Cortical Cholinergic Afferents." Journal of Neuroscience 16, no. 20 (October 15, 1996): 6592–600. http://dx.doi.org/10.1523/jneurosci.16-20-06592.1996.

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46

Walsh, T. J., C. D. Herzog, C. Gandhi, R. W. Stackman, and R. G. Wiley. "Injection of IgG 192-saporin into the medial septum produces cholinergic hypofunction and dose-dependent working memory deficits." Brain Research 726, no. 1-2 (July 1996): 69–79. http://dx.doi.org/10.1016/0006-8993(96)00271-5.

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47

Angelucci, Francesco, Francesca Gelfo, Paola De Bartolo, Carlo Caltagirone, and Laura Petrosini. "BDNF concentrations are decreased in serum and parietal cortex in immunotoxin 192 IgG-Saporin rat model of cholinergic degeneration." Neurochemistry International 59, no. 1 (August 2011): 1–4. http://dx.doi.org/10.1016/j.neuint.2011.04.010.

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48

Ricceri, Laura, Alessandro Usiello, Angela Valanzano, Gemma Calamandrei, Karyn Frick, and Joanne Berger-Sweeney. "Neonatal 192 IgG-saporin lesions of basal forebrain cholinergic neurons selectively impair response to spatial novelty in adult rats." Behavioral Neuroscience 113, no. 6 (1999): 1204–15. http://dx.doi.org/10.1037/0735-7044.113.6.1204.

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49

Walsh, T. J., R. M. Kelly, K. D. Dougherty, R. W. Stackman, R. G. Wiley, and C. L. Kutscher. "Behavioral and neurobiological alterations induced by the immunotoxin 192-IgG-saporin: cholinergic and non-cholinergic effects following i.c.v. injection." Brain Research 702, no. 1-2 (December 1995): 233–45. http://dx.doi.org/10.1016/0006-8993(95)01050-x.

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50

Singh, Vivekanand, and John B. Schweitzer. "Loss of p75 nerve growth factor receptor mRNA containing neurons in rat forebrain after intraventricular IgG 192-saporin administration." Neuroscience Letters 194, no. 1-2 (July 1995): 117–20. http://dx.doi.org/10.1016/0304-3940(95)11744-h.

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