These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 14980722)

  • 21. The role of the basolateral amygdala in stimulus-reward memory and extinction memory consolidation and in subsequent conditioned cued reinstatement of cocaine seeking.
    Fuchs RA; Feltenstein MW; See RE
    Eur J Neurosci; 2006 May; 23(10):2809-13. PubMed ID: 16817884
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Intracranial self-stimulation recovers learning and memory capacity in basolateral amygdala-damaged rats.
    Segura-Torres P; Aldavert-Vera L; Gatell-Segura A; Redolar-Ripoll D; Morgado-Bernal I
    Neurobiol Learn Mem; 2010 Jan; 93(1):117-26. PubMed ID: 19761861
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Activating a memory system focuses connectivity toward its central structure.
    Boucard A; Mons N; Micheau J; Noguès X
    Behav Brain Res; 2009 Dec; 204(1):226-34. PubMed ID: 19539661
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Glucocorticoid enhancement of dorsolateral striatum-dependent habit memory requires concurrent noradrenergic activity.
    Goodman J; Leong KC; Packard MG
    Neuroscience; 2015 Dec; 311():1-8. PubMed ID: 26470808
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Amygdala central nucleus function is necessary for learning but not expression of conditioned visual orienting.
    McDannald M; Kerfoot E; Gallagher M; Holland PC
    Eur J Neurosci; 2004 Jul; 20(1):240-8. PubMed ID: 15245496
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The role of dopamine in the dorsomedial striatum in place and response learning.
    Lex B; Sommer S; Hauber W
    Neuroscience; 2011 Jan; 172():212-8. PubMed ID: 21056091
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Lesions of the dorsolateral striatum impair the acquisition of a simplified stimulus-response dependent conditional discrimination task.
    Featherstone RE; McDonald RJ
    Neuroscience; 2005; 136(2):387-95. PubMed ID: 16226388
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Longitudinal axis of the hippocampus: both septal and temporal poles of the hippocampus support water maze spatial learning depending on the training protocol.
    de Hoz L; Knox J; Morris RG
    Hippocampus; 2003; 13(5):587-603. PubMed ID: 12921349
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Empirical tests of the functional significance of amygdala-based modulation of hippocampal representations: evidence for multiple memory consolidation pathways.
    McDonald RJ; Lo Q; King AL; Wasiak TD; Hong NS
    Eur J Neurosci; 2007 Mar; 25(5):1568-80. PubMed ID: 17425583
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Complementary roles for the amygdala and hippocampus during different phases of appetitive information processing.
    Holahan MR
    Neurobiol Learn Mem; 2005 Sep; 84(2):124-31. PubMed ID: 16046157
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Effects of fimbria-fornix, hippocampus, and amygdala lesions on discrimination between proximal locations.
    Chai SC; White NM
    Behav Neurosci; 2004 Aug; 118(4):770-84. PubMed ID: 15301603
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Effects of persistent cocaine self-administration on amygdala-dependent and dorsal striatum-dependent learning in rats.
    Udo T; Ugalde F; DiPietro N; Eichenbaum HB; Kantak KM
    Psychopharmacology (Berl); 2004 Jul; 174(2):237-45. PubMed ID: 14726992
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Differential effects of massed and spaced training on place and response learning: A memory systems perspective.
    Wingard JC; Goodman J; Leong KC; Packard MG
    Behav Processes; 2015 Sep; 118():85-9. PubMed ID: 26047523
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A triple dissociation of memory systems: hippocampus, amygdala, and dorsal striatum.
    McDonald RJ; White NM
    Behav Neurosci; 1993 Feb; 107(1):3-22. PubMed ID: 8447956
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Exposure to predator odor influences the relative use of multiple memory systems: role of basolateral amygdala.
    Leong KC; Packard MG
    Neurobiol Learn Mem; 2014 Mar; 109():56-61. PubMed ID: 24333118
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Expression of a conditioned place preference or spatial navigation task following muscimol-induced inactivations of the amygdala or dorsal hippocampus: A double dissociation in the retrograde direction.
    McDonald RJ; Yim TT; Lehmann H; Sparks FT; Zelinski EL; Sutherland RJ; Hong NS
    Brain Res Bull; 2010 Aug; 83(1-2):29-37. PubMed ID: 20542095
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dorsal striatum and stimulus-response learning: lesions of the dorsolateral, but not dorsomedial, striatum impair acquisition of a simple discrimination task.
    Featherstone RE; McDonald RJ
    Behav Brain Res; 2004 Apr; 150(1-2):15-23. PubMed ID: 15033275
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Learning and memory functions of the Basal Ganglia.
    Packard MG; Knowlton BJ
    Annu Rev Neurosci; 2002; 25():563-93. PubMed ID: 12052921
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Parallel processing across neural systems: implications for a multiple memory system hypothesis.
    Mizumori SJ; Yeshenko O; Gill KM; Davis DM
    Neurobiol Learn Mem; 2004 Nov; 82(3):278-98. PubMed ID: 15464410
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The dorsolateral striatum selectively mediates extinction of habit memory.
    Goodman J; Ressler RL; Packard MG
    Neurobiol Learn Mem; 2016 Dec; 136():54-62. PubMed ID: 27663194
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.