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from disinhibition from the light responsive GRP neurons. The 3h delay between light exposure and its effect on GRP+ neurons suggests that the mechanism involves the loss of GABAdependent inhibition at ZT 17-21 results from receptor internalization. Disclosures: J.J. Le Sauter, None; P. Witkovsky, None; R. Cloues, None; R. Silver, None. Poster 574. Entrainment and Phase Shifts: Neurons, Transmitters, Genes, and Proteins Location: South Hall A Time: Tuesday, October 20, 2009, 8:00 am - 12:00 noon Program#/Poster#: 574.4/FF54 Topic: E.08.a. Entrainment and phase shifts Support: NIH grant NS37919 Title: The SCN response to light in the subjective day is augmented by activity Authors: *E. RODRIGUEZ 1 , J. LESAUTER 2 , R. SILVER 1 ; 1 Psychology, Columbia Univ., New York, NY; 2 Psychology, Barnard Col., New York, NY Abstract: It is well established that the SCN responds to photic input during the night but not during the day. Here, we investigated whether the SCN’s response to light is determined by the prior light-dark (LD) cycle or by the animal’s rest/activity cycle. We tested whether activity induction by temporal food restriction (FR) or awakening by movement of the home cage influence daytime responses to a light pulse. Mice expressing GFP in gastrin-releasing peptide (GRP) cells were housed individually with a running wheel, entrained to a 12:12 LD cycle, and placed in one of 6 groups (n=6/group). Animals in a food anticipatory activity (FAA) paradigm had food access restricted to ZT 6-14 (FAA+ group), while controls were fed at libitum (Undisturbed groups). After 5 days FR, they were maintained in constant darkness from lights off (ZT12) until a 30 min light pulse the next day starting at CT3.5 (FAA+ LP+ and Undisturbed LP+); controls received no light pulse (FAA+LP−, Undisturbed LP−). Two other groups (Awaken) were fed ad libitum and kept awake (at CT3.5-4) by gentle shaking of their home cage by an experimenter wearing infrared goggles to see in the dark. Of these Awaken animals, one group was exposed to a light pulse as above (Awaken LP+) while the controls received no light (Awaken LP-). All mice were sacrificed at CT5. For fluorescent immunohistochemistry, every third 40µm SCN slice was processed for c-FOS, arginine-vasopressin (AVP) and GFP. AVP was used to delineate the core and shell SCN. AVP-outlined images were quantified by two independent experimenters. Contrary to expectation, a light pulse during the subjective day led to a small but significant increase in the number of c-FOS expressing cells. The number of light
induced c-FOS cells was significantly increased if animals were active due to FAA or awakened by the experimenter. The effect of activity is supported by a positive correlation between the number of wheel revolutions and the number of c-FOS cells in the SCN. Surprisingly, c-FOS was not observed in GRP cells, a subpopulation of SCN cells that respond to light during the subjective night. In the absence of a light-pulse, the animals in the Awakened condition had more shell (not core) c-FOS compared to the Undisturbed condition. There was no difference between FAA and Awakened groups in c-FOS in either the presence or absence of light. These results suggest that the SCN responds to light during the subjective day and that activity, whether endogenously organized or exogenously driven, enhances this response. Disclosures: E. Rodriguez, None; J. LeSauter, None; R. Silver, None. Poster 574. Entrainment and Phase Shifts: Neurons, Transmitters, Genes, and Proteins Location: South Hall A Time: Tuesday, October 20, 2009, 8:00 am - 12:00 noon Program#/Poster#: 574.5/FF55 Topic: E.08.a. Entrainment and phase shifts Support: UMDNJ foundation Title: Membrane guanylate cyclase in circadian rhythms Authors: *V. VENKATARAMAN 1 , R. SWANSON 1 , A. KRISHNAN 1 , T. DUDA 2 ; 1 Cell Biol., UMDNJ, Stratford, NJ; 2 Salus Univ., Elkins Park, PA Abstract: Cyclic GMP plays a critical role in setting the phase in circadian rhythms. However, the mechanism by which it is regulated is unclear. The results from this study suggest that membrane guanylate cyclase is the source and that its activity is regulated by the neuronal calcium sensor protein neurocalcin δ. This would also enable a tight coupling of the system to calcium, which is already an established regulator of generation and maintenance of circadian rhythms. Disclosures: V. Venkataraman, None; R. Swanson, None; A. Krishnan, None; T. Duda, None. Poster
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When citing an abstract from the 20
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specification. Supported by the NIH
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Poster 505. Cell Lineage and Cell F
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Location: South Hall A Time: Tuesda
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mammalian Suppressor of Hairless (R
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Abstract: In spite of the considera
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Abstract: The dorsal root ganglia (
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Genome Canada Title: Pannexin 2, a
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Authors: *T. ROITBAK, L. A. CUNNING
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never express mature neuronal genes
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NIH Neuroscience Blueprint Title: A
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1 Dept. of Anatomy, Ajou Univ. Sch.
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Poster 506. Neurogenesis II Locatio
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from ND7 cells, showed an increase
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functions of the NZF/MyTgene family
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NIH T32 MH018268-24 Solnit Integrat
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pathway and its transient transloca
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(82±12%) in the number of GABAergi
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constructs were tagged with or coin
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Title: How do GFAP-expressing neura
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Disclosures: A. Pignatelli, None; J
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Disclosures: J.H. Lim, None; S.D. M
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Poster 507. Stem Cells: Basic Biolo
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significant changes in gene express
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embryonic period of rat corticogene
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PRIN 2005 Title: Death resistant ne
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Topic: A.03.b. Stem cells: Basic bi
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during development as well as betwe
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fate of MAPCs within the CNS is not
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Torsten and Ragnar Söderberg’s F
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Support: FNRS - Belgium Title: Prob
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Inserm Osteoarticular research gran
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animals (p
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Abstract: Currently there are no ef
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Time: Tuesday, October 20, 2009, 8:
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Poster 508. Development and Organiz
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Poster 508. Development and Organiz
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Disclosures: M. Nebieridze , None;
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Disclosures: Y. Kim, None; R. Sincl
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Disclosures: A. Haessly, None; B. S
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the connection at the level of the
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due to a per- or post-synaptic func
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suggest that ambient temperature ma
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509. Molecular Mechanisms Regulatin
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stationary neurons, the migration s
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Ser473 and Thr308 in the null cereb
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maintained in culture in medium sup
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development, may alter the proper m
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Program#/Poster#: 510.2/B35 Topic:
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Poster 510. Regeneration: PNS Locat
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Disclosures: D. Wu , None; A. Raafa
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Disclosures: R.M. Grumbles, None; C
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ody response, but interfered with a
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properties of sensory nerve grafts.
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510. Regeneration: PNS Location: So
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domains that are known to promote c
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Support: CIHR AHFMR Title: Side-to-
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Disclosures: X. Jing, None; T. Wang
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development and has been implicated
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Abstract: Peripheral nerve gaps tha
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Program#/Poster#: 510.23/B56 Topic:
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Poster 510. Regeneration: PNS Locat
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promote the elongation of intact ne
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examined the consequences on axonal
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using co-immunoprecipitation and di
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Abstract: A hallmark feature of NMD
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not by AMPA stimulation. Importantl
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phosphorylation site. We have gener
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damage has been reported to be a co
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have not been found previously in c
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Abstract: In the barrel cortex, fee
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Authors: *H. MAEJIMA 1 , S. SAKANO
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Poster 511. Glutamate Receptors: Ge
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indicating the presence of the two
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significance of the structure of Gl
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elicited by kainate and glutamate,
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the GluRdelta2 receptor in the lurc
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mediated inhibition, generated by s
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Poster 513. GABA-A Receptors: Physi
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As etomidate concentrations increas
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Authors: *J. ADAMS, T. G. SMART; Ne
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Poster 513. GABA-A Receptors: Physi
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Topic: B.02.o. GABA(A) receptors: P
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Master scholarship CONACyT Title: M
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these cells. α3KO mice showed an e
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Authors: *M. L. MCCRACKEN 1 , L. M.
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514. Glycine Receptors Location: So
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Poster 514. Glycine Receptors Locat
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glycine induced chloride currents.
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Authors: F. WELTZIEN 1 , I. PAARMAN
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Program#/Poster#: 514.10/B117 Topic
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occurs by interaction with splicing
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Disclosures: Y. Kim, None; L.O. Tru
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forebrain regions and that the α2
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Abstract: The postnatal development
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Program#/Poster#: 515.1/C1 Topic: B
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Disclosures: C. Tai, None; B.A. Mac
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this is indicative of changes in tw
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NISWENDER 1 , C. D. WEAVER 3 , C. W
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Program#/Poster#: 515.8/C8 Topic: B
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Poster 515. Muscarinic Receptors Lo
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515. Muscarinic Receptors Location:
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(OxoM) was significantly greater in
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phosphorylation, microdialysis and
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516. Serotonin Receptors II Locatio
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5-HT1A signaling pathways and mecha
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produced a similar phenotype to tra
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1 2 Dept Woman Child Hlth., Karolin
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Poster 516. Serotonin Receptors II
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to be formed in order to allow Gi/o
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TPH1 & 2 knockout mice. Another imp
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several behaviors in rodents report
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NIH Grant DA025412 ACADIA Pharmaceu
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Poster 516. Serotonin Receptors II
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pattern congaing). Results were the
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Abstract: Serotonin receptors in pr
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Topic: B.04.a. Sodium channels: Phy
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persistent sodium current is engage
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Authors: J.-H. WANG 1 , *N. CHEN 2
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Given the fact that the AIS of moto
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517. Sodium Channels: Physiology II
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hyperpolarized resting membrane pot
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with longer pulses. Macroscopic ina
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Support: Brain Research Trust Medic
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Poster 517. Sodium Channels: Physio
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channels activity at 2 mM Ca 2+ rev
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Title: The effect of 1-octanol on s
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NIH Grant 1F31NS059190 NIH Grant T3
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change alters CaV3.2 gating and act
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secondary dendrites. Ratiometric im
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Program#/Poster#: 518.10/C64 Topic:
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AA016852 AA017048 Title: Acute effe
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tools capable of distinguishing amo
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the most common mechanisms of chann
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Program#/Poster#: 519.3/C72 Topic:
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Title: Neurofibromin, CRMP-2 and pr
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Poster 519. Voltage-Dependent Calci
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IHCs or OHCs but may rather be caus
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Abstract: Voltage-gated calcium (Ca
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Support: NS029967 Title: Isoform-sp
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cells. The most prominent RIM1 effe
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messengers. One is the chemically m
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Abstract: A dominant form of presyn
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CONACyT Title: Gating charges per c
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US-Israel Binational Sci Fnd #20053
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Disclosures: P.M. Paez, None; D.J.
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variants. Therefore, the alternativ
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the prediction is that a BK-like cu
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Abstract: Modulation of ion channel
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Authors: *E. PETROFF; Biol. and Mol
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DNASTAR, Inc Title: Differential tr
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520. Calcium-Activated Potassium Ch
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of SK channels and had little effec
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pathway, consisting of axons from l
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Title: Loss of dendritic Ih results
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Poster 521. Ion Channels and Diseas
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causes pure familial hemiplegic mig
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may involve spontaneously occuring
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Abstract: Mutations in voltage-gate
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facilitate efflux at a distance fro
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Abstract: Voltage gated calcium cha
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that this channel regulates the mor
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521. Ion Channels and Disease Locat
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These results indicate that neurona
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ise to a reduced number of Kv1.1 su
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Title: Cholesterol elevation impair
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Poster 521. Ion Channels and Diseas
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alterations in ion channel expressi
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Abstract: Over the past 5 years an
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Abstract: Glial-derived primary bra
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fluorescent sensor that responds to
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adjacent synapses and were subseque
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Title: Photodamaging the ribbon dis
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Program#/Poster#: 522.9/E34 Topic:
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assembly, creating an energetic bar
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dependent fusion of a SV. We optica
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type of exocytotic vesicle and cell
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Support: NIH Grant GM081809 NIH Gra
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522. Neurtransmitter Release: Docki
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labeling showed extensive co-locali
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protein which is also implicated in
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NINDS UO1-NS058213 NIDA P50DA005274
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523. Modulation: Mechanisms of Acti
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Poster 523. Modulation: Mechanisms
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effect of the secondly applied drug
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Abstract: Transient, non-catastroph
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523. Modulation: Mechanisms of Acti
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sites, as it decreased the amplitud
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Abstract: NMDA receptors are critic
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Support: AHAF NIH Grant NS055804 Ti
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524. LTP: Physiology and Behavior I
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Moreover, the expression of some fo
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mg/kg/day) or saline during 3 days
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control levels in the presence of p
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the novel object recognition task,
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524. LTP: Physiology and Behavior I
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stimulation of the contralateral CA
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effects on cognitive functions, par
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escaling and convergence to a commo
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Abstract: We demonstrate here for t
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input resistance (RN = 108.24 ± 20
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nerve conduction block phenomenon,
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Authors: *K. M. CRISP; St Olaf Col.
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correlations and defined electrical
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Authors: T. F. BECKHAUSER 1 , C. V.
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Topic: C.02.n. Animal and experimen
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Program#/Poster#: 526.4/G27 Topic:
Page 437 and 438:
different ages. Authors thank Dr. C
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Abstract: The cholinergic neurotran
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Topic: C.02.n. Animal and experimen
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Support: Alzheimer's Association AP
Page 445 and 446:
Page 447 and 448:
2. Doraiswamy, P.M., et al. J Geron
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excess of Aβ in the brain. We have
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Authors: *S. M. KRANTIC 1 , W. YU 2
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Disclosures: M. Lange, None; R. Sow
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Poster 526. Alzheimer's Disease: Ex
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sham and lesion groups were able to
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e phagocytically compromised during
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Alzheimer's Association IIRG-02-375
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Disclosures: C. Perez Cruz, Abbott,
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necessarily precede one to another.
Page 467 and 468:
Title: γ-Secretase activity altera
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were elevated by treatment with the
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effects in the brain without any me
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Univ. of Maryland, College Park, MD
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membrane synthesis. For instance, d
Page 477 and 478:
Program#/Poster#: 527.13/H26 Topic:
Page 479 and 480:
Program#/Poster#: 527.15/H28 Topic:
Page 481 and 482:
clarify its distribution in human t
Page 483 and 484:
Topic: C.02.d. Beta and gamma secre
Page 485 and 486:
Page 487 and 488:
Collectively, these findings, taken
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consolidated memories (remembering)
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plaque and tangle model (Bi-TAPP) w
Page 493 and 494:
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pattern reminiscent of our previous
Page 497 and 498:
Authors: *N. W. SEEDS 1 , S. FABBRO
Page 499 and 500:
Page 501 and 502:
learning performance in the Morris
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immunoprecipitation/Western blottin
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Authors: *L. F. YAMASHITA, A. A. BO
Page 507 and 508:
AG10688 Title: Neuronal colocalizat
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Disclosures: M.A. King, None; M.L.
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in the compromised cerebral vascula
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cognition has come from transgenic
Page 515 and 516:
Support: NIH Grant RO1 AG20159 Titl
Page 517 and 518:
Page 519 and 520:
were down-regulated. In contrast, g
Page 521 and 522:
Title: Nicotine treatment of mild c
Page 523 and 524:
oth AD Tg mice and young adult/aged
Page 525 and 526:
Poster 529. Treatments: Alzheimer's
Page 527 and 528:
excised 30 minutes and 3 hours afte
Page 529 and 530:
Authors: *C. HOLSCHER 1 , V. A. GAU
Page 531 and 532:
Page 533 and 534:
inhibit the protective action of AP
Page 535 and 536:
of connectivity among neurons resul
Page 537 and 538:
Title: Addressing the challenge of
Page 539 and 540:
Page 541 and 542:
Page 543 and 544:
Disclosures: L.J. Street, None; S.
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significantly. When the nitrites le
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absence of vision. The present stud
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Title: PIB binding in Parkinson dis
Page 551 and 552:
Page 553 and 554:
cortex, pre-supplementary motor are
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aetiology of VH in PD is unknown .H
Page 557 and 558:
Employment (full or part-time); U.
Page 559 and 560:
neurons. These results suggest that
Page 561 and 562:
long-term levodopa therapy. It has
Page 563 and 564:
Page 565 and 566:
a 6 h period by a neurologist blind
Page 567 and 568:
Program#/Poster#: 530.19/J29 Topic:
Page 569 and 570:
eductions, respectively, in LID to
Page 571 and 572:
Authors: *E. L. PRANSKI, N. V. DALA
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530. Parkinson's Disease: Human Rel
Page 575 and 576:
console, CE was measured into 5 con
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Support: NIH Grant 5T32GM007507 NIH
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deficiency leads specifically to ta
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months of age, with no differences
Page 583 and 584:
Title: Dietary selenium deficiency
Page 585 and 586:
Page 587 and 588:
have greater autoreceptor inhibitio
Page 589 and 590:
DFG Transregio SFB TR3 A11 and D12
Page 591 and 592:
poorly ubiquitinated when compared
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using the “tet-off” system. Whe
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Topic: C.03.d. Transgenic and relat
Page 597 and 598:
531. Parkinson's Disease: Models II
Page 599 and 600:
Poster 531. Parkinson's Disease: Mo
Page 601 and 602:
Disclosures: M. Herzig, None; P. Sc
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oxygen species in neurons is preven
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Perugia, Perugia, Italy; 4 Ctr. of
Page 607 and 608:
Topic: C.03.f. Mechanisms and degen
Page 609 and 610:
Page 611 and 612:
Poster 532. Parkinson's Disease: Ra
Page 613 and 614:
(100µg/50µl) or cyRADfV (negative
Page 615 and 616:
Abstract: The inferior colliculus (
Page 617 and 618:
Program#/Poster#: 532.14/L2 Topic:
Page 619 and 620:
Disclosures: K.B. Dupre, None; K.L.
Page 621 and 622:
loss of DA neurons 10 months after
Page 623 and 624:
enhancer synphillin. We are current
Page 625 and 626:
Grad. Sch. of Science, Kyoto Univ.,
Page 627 and 628:
Page 629 and 630:
Page 631 and 632:
transiently reversed in DA-depleted
Page 633 and 634:
and by Filter-trap assays and FCS (
Page 635 and 636:
members of the Bcl-2 family. In add
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Biomedicine and Dept. of Biochem.,
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Title: Pathogenic mechanism and sma
Page 641 and 642:
Abstract: Huntington’s disease (H
Page 643 and 644:
Authors: *M. SHIMOJO; Univ. Kentuck
Page 645 and 646:
Program#/Poster#: 533.13/L28 Topic:
Page 647 and 648:
Poster 533. Huntington's Disease an
Page 649 and 650:
iochemical properties. To further v
Page 651 and 652:
aberrant chromatin remodeling is a
Page 653 and 654:
oligomeric or protofibrillar forms
Page 655 and 656:
neurodegeneration in the striatum a
Page 657 and 658:
study of HD is how this polyQ-expan
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Title: Androgen receptor antagonist
Page 661 and 662:
Program#/Poster#: 533.28/M5 Topic:
Page 663 and 664:
Disclosures: R. Schneider, None; A.
Page 665 and 666:
Disclosures: S.J. Bissel, None; G.
Page 667 and 668:
duodenal epithelium to the blood st
Page 669 and 670:
Authors: *D. GRIS 1 , Z. YE 1 , H.
Page 671 and 672:
1 2 3 Physiol., Univ. of Toronto, T
Page 673 and 674:
Pioneer Fund Title: Induction of au
Page 675 and 676:
Disclosures: B.A. Faucheux, None; J
Page 677 and 678:
mTOR activation. Since STI1 has imp
Page 679 and 680:
Authors: *A. BACHIS 1 , V. AVDOSHIN
Page 681 and 682:
Authors: *S. G. KOHAMA 1 , S. G. KR
Page 683 and 684:
Poster 535. Aging of the Nervous Sy
Page 685 and 686:
Abstract: Oxidative stress is assoc
Page 687 and 688:
Page 689 and 690:
Program#/Poster#: 535.8/M30 Topic:
Page 691 and 692:
Title: 13C isotopic incorporation s
Page 693 and 694:
Page 695 and 696:
patent or other intellectual proper
Page 697 and 698:
Abstract: The serotonergic system i
Page 699 and 700:
Disclosures: M.C. Mitschelen, None;
Page 701 and 702:
ml water/day. Results: A multivaria
Page 703 and 704:
Abstract: Neurodegenerative disorde
Page 705 and 706:
Authors: *G. L. BECKER 1 , P. J. HU
Page 707 and 708:
RESNICK 1 ; 1 Natl. Inst. On Aging/
Page 709 and 710:
Disclosures: D.H. Salat, None; S.Y.
Page 711 and 712:
Page 713 and 714:
Disclosures: B. Setlow, None; D.S.
Page 715 and 716:
Disclosures: B. Levant, Friesland F
Page 717 and 718:
Disclosures: K. Hashimoto-Torii, No
Page 719 and 720:
Abstract: Methylphenidate (MPH) tre
Page 721 and 722:
Page 723 and 724:
and examined the function of STRAD
Page 725 and 726:
Fédération des Maladies Orpheline
Page 727 and 728:
above are either absent or altered
Page 729 and 730:
NSF predoctoral fellowship Title: L
Page 731 and 732:
Topic: C.06.k. Animal models and me
Page 733 and 734:
NARSAD, B. Research Grant (principa
Page 735 and 736:
neuropathology in these human devel
Page 737 and 738:
Abstract: Determining the timing of
Page 739 and 740:
Topic: C.06.d. Developmental disord
Page 741 and 742:
mTOR hyperactivity at the cellular
Page 743 and 744:
Authors: *K. E. WATKINS 1 , N. A. B
Page 745 and 746:
Program#/Poster#: 537.3/O3 Topic: C
Page 747 and 748:
p=0.43) with converging values in t
Page 749 and 750:
Topic: C.06.j. ADHD, SLI, dyslexia
Page 751 and 752:
Dcdc2 in mice, behavioral features
Page 753 and 754:
the role for this gene in the etiol
Page 755 and 756:
Page 757 and 758:
examining functional-anatomic devel
Page 759 and 760:
inhibit on 50% of stop-trials. Stop
Page 761 and 762:
Support: Finnish Cultural Foundatio
Page 763 and 764:
Poster 537. Developmental Disorders
Page 765 and 766:
stimulus. In our fMRI design, prosa
Page 767 and 768:
Killam scholarship NSERC scholarshi
Page 769 and 770:
Topic: C.07.j. Animal models Suppor
Page 771 and 772:
538. Epilepsy: Inflammation and Imm
Page 773 and 774:
538. Epilepsy: Inflammation and Imm
Page 775 and 776:
different brain regions. This study
Page 777 and 778:
pilocarpine-induced SE leads to hip
Page 779 and 780:
pilocarpine induces prolonged SE re
Page 781 and 782:
NS051445-04 Title: Increased incide
Page 783 and 784:
Poster 539. Epilepsy: Anticonvulsan
Page 785 and 786:
(dentate gyrus subfield) hippocampu
Page 787 and 788:
Authors: *T. M. WYCKHUYS 1 , P. BOO
Page 789 and 790:
Page 791 and 792:
Page 793 and 794:
(saline, 0.2 mls, i.p.), LY379268 (
Page 795 and 796:
Authors: *K. K. AKULA 1 , S. K. KUL
Page 797 and 798:
Page 799 and 800:
ecto-ATPase inhibitor ARL 67156. In
Page 801 and 802:
protected confirming the anticonvul
Page 803 and 804:
NIH Grants R01NS048216 AHA Establis
Page 805 and 806:
Page 807 and 808:
Poster 540. Ischemia: Glia Location
Page 809 and 810:
dependent degradation of spectrin w
Page 811 and 812:
Abstract: CD36, a multi-functional
Page 813 and 814:
Title: Different mononuclear cell p
Page 815 and 816:
Page 817 and 818:
Disclosures: C.C. Pegg, None; M.A.
Page 819 and 820:
show that DHPG activates extracellu
Page 821 and 822:
Abstract: Ethyl pyruvate (EP), a si
Page 823 and 824:
Title: The relative roles of neuron
Page 825 and 826:
Page 827 and 828:
2 Wilke et al., 2004, J Neuropathol
Page 829 and 830:
attentional lapses, and depressed m
Page 831 and 832:
Program#/Poster#: 541.1/R4 Topic: C
Page 833 and 834:
performance, evolving white matter
Page 835 and 836:
within these networks between healt
Page 837 and 838:
Support: The Rockefeller University
Page 839 and 840:
and ROI analyses revealed no areas
Page 841 and 842:
Support: JIEDDO-001 Mid-Atlantic MI
Page 843 and 844:
diminished overall capacity to inte
Page 845 and 846:
DOD PT075675 Marshall Goldberg Fund
Page 847 and 848:
Poster 542. Spinal Cord Injury: Fro
Page 849 and 850:
indicate that acupuncture significa
Page 851 and 852:
einnervate their distal targets. To
Page 853 and 854:
Page 855 and 856:
Disclosures: S. Veiga, None; K. Irv
Page 857 and 858:
Blood β-hydroxybutyrate levels of
Page 859 and 860:
NIH Grant NS31193 New York State Co
Page 861 and 862:
Page 863 and 864:
EMG, trains of motor unit potential
Page 865 and 866:
the area of residual myelin in the
Page 867 and 868:
upregulation of genes in the A-HX g
Page 869 and 870:
carried out to confirm differences
Page 871 and 872:
Program#/Poster#: 542.23/T2 Topic:
Page 873 and 874:
of damage across spinal sections th
Page 875 and 876:
physiologic characteristics they sh
Page 877 and 878:
Page 879 and 880:
Page 881 and 882:
Disclosures: A. Jayaraman, None; J.
Page 883 and 884:
plasticity, we also tested E2’s a
Page 885 and 886:
Abstract: The 'Progesterone in Brai
Page 887 and 888:
Topic: C.11.h. Neuroprotective mech
Page 889 and 890:
543. Cell Death Mechanisms; Mitocho
Page 891 and 892:
Disclosures: C.C. Aguirre, None; A.
Page 893 and 894:
low doses (Ec50 less than 5nM), esp
Page 895 and 896:
Abstract: We reported before that 1
Page 897 and 898:
Authors: *K. D. YI, J. W. SIMPKINS;
Page 899 and 900:
Authors: L. XIE, E. POTEET, W. LI,
Page 901 and 902:
against cognitive decline and memor
Page 903 and 904:
and mitochondrial function are esse
Page 905 and 906:
Page 907 and 908:
vesicles, broken and disorganized c
Page 909 and 910:
Abstract: Increasing evidence sugge
Page 911 and 912:
Poster 544. Neurotoxicity: Toxins I
Page 913 and 914:
ain after i.m. injection. The highl
Page 915 and 916:
Support: FCT- Grant POCI/SAU-FCF/58
Page 917 and 918:
Poster 544. Neurotoxicity: Toxins I
Page 919 and 920:
Results revealed DAT complexes pres
Page 921 and 922:
Title: D. melanogaster: A new model
Page 923 and 924:
Support: NIH Grant P20 RR16454 USAM
Page 925 and 926:
Support: Department of Chemistry WS
Page 927 and 928:
Title: The striatal neurokinin-1 an
Page 929 and 930:
visualized using fluorescent phallo
Page 931 and 932:
Authors: *A. C. VALENCIA 1 , J. MOR
Page 933 and 934:
Support: NIH/NIA/IRP FAPESP Brazil
Page 935 and 936:
FONDECYT Grant 1090353 Title: Diffe
Page 937 and 938:
Page 939 and 940:
endothelial interactions. This will
Page 941 and 942:
of CD200 in immune-regulation and d
Page 943 and 944:
temporal concentration increases of
Page 945 and 946:
Alzheimer’s Association (KA) AG24
Page 947 and 948:
Page 949 and 950:
Topic: C.11.m. Neuroinflammation: C
Page 951 and 952:
Disclosures: R.F. Silva, None; S.L.
Page 953 and 954:
vessels in the neonatal mouse brain
Page 955 and 956:
death within 24 hours. This charact
Page 957 and 958:
(bDC). These bDCs share a remarkabl
Page 959 and 960:
proliferation. It is now evident th
Page 961 and 962:
Abstract: Negative symptoms (avolit
Page 963 and 964:
546. Schizophrenia and Bi-polar Dis
Page 965 and 966:
Poster 546. Schizophrenia and Bi-po
Page 967 and 968:
Authors: *M. S. MILELLA, F. PASSARE
Page 969 and 970:
Page 971 and 972:
mice. EGR-1 protein levels were ele
Page 973 and 974:
Abstract: α2 norepinephrine (NE) r
Page 975 and 976:
psychotic symptoms with PPI impairm
Page 977 and 978:
startle response were examined betw
Page 979 and 980:
Topic: C.15.d. Animal models Suppor
Page 981 and 982:
Page 983 and 984:
antagonist MLA (0.1 mM; 0.5µL), si
Page 985 and 986:
that these Nf1+/- RGC phenotypes re
Page 987 and 988:
cell-cell integrity, DNA fragmentat
Page 989 and 990:
found a significant decrease in pro
Page 991 and 992:
subcellular localization during a c
Page 993 and 994:
Authors: *D. BUCHMAN, J. ILLES; Med
Page 995 and 996:
Poster 548. Mood Disorders: Human B
Page 997 and 998:
Authors: *A. J. HOLMES 1 , R. BOGDA
Page 999 and 1000:
Support: KAKENHI (20790841) Title:
Page 1001 and 1002:
Program#/Poster#: 548.8/W26 Topic:
Page 1003 and 1004:
Page 1005 and 1006:
together, this study demonstrates t
Page 1007 and 1008:
depressed compared to nondepressed
Page 1009 and 1010:
1 Dept of Biol. Res., Lundbeck Res.
Page 1011 and 1012:
Disclosures: C.H. Duman, None; M. B
Page 1013 and 1014:
egulatory effects including glucose
Page 1015 and 1016:
Topic: C.16.f. Mood disorders: Expe
Page 1017 and 1018:
Page 1019 and 1020:
Disclosures: U.C. Campbell, None; S
Page 1021 and 1022:
eward-related effects of the TRI, D
Page 1023 and 1024:
Authors: E. ZHANG 1 , R. C. C. CHAN
Page 1025 and 1026:
Title: Neuroplastic changes associa
Page 1027 and 1028:
Poster 549. Mood Disorders: Experim
Page 1029 and 1030:
fluoxetine. No significant changes
Page 1031 and 1032:
Title: Peripheral infusion of the p
Page 1033 and 1034:
Abstract: In recent years it has be
Page 1035 and 1036:
Topic: C.17.bb. Neural plasticity,
Page 1037 and 1038:
increased AMPA/NMDA ratio with prol
Page 1039 and 1040:
nucleus accumbens (NAc) and the ext
Page 1041 and 1042:
Disclosures: B.A. Grueter, None; R.
Page 1043 and 1044:
electrophysiological experiments sh
Page 1045 and 1046:
IL; 3 Psychiatry, Yale Univ. Sch. o
Page 1047 and 1048:
550. Neural Plasticity, Dependence,
Page 1049 and 1050:
Disclosures: Z.R. Daruwalla, None;
Page 1051 and 1052:
development or expression of behavi
Page 1053 and 1054:
Fondation pour la Recherche Medical
Page 1055 and 1056:
550. Neural Plasticity, Dependence,
Page 1057 and 1058:
Poster 550. Neural Plasticity, Depe
Page 1059 and 1060:
persistence of these neuroadaptatio
Page 1061 and 1062:
Title: Toluene intoxication: Struct
Page 1063 and 1064:
Program#/Poster#: 551.1/Y4 Topic: C
Page 1065 and 1066:
highest dose of cocaine and ampheta
Page 1067 and 1068:
they had access to either a single
Page 1069 and 1070:
Abstract: Background: We have previ
Page 1071 and 1072:
Page 1073 and 1074:
Poster 551. Behavioral Pharmacology
Page 1075 and 1076:
each group), and the respective sur
Page 1077 and 1078:
adolescence with amphetamine demons
Page 1079 and 1080:
of CART mRNA levels in relation to
Page 1081 and 1082:
locomotor stimulation at low to mod
Page 1083 and 1084:
Abstract: It is well known that the
Page 1085 and 1086:
552. Alcohol: Neural Mechanisms II
Page 1087 and 1088:
Disclosures: Y. Chen, None; S.F. Le
Page 1089 and 1090:
educed basal glutamate levels (appr
Page 1091 and 1092:
Abstract: Poly-drug abuse may be pr
Page 1093 and 1094:
Title: Ethanol increases GAPDH-TIEG
Page 1095 and 1096:
Page 1097 and 1098:
expressing microglia (OX6) observed
Page 1099 and 1100:
consumption by C57Bl/6J mice. The r
Page 1101 and 1102:
Abstract: Ethanol may be consumed f
Page 1103 and 1104:
Page 1105 and 1106:
Poster 552. Alcohol: Neural Mechani
Page 1107 and 1108:
ain tissues of different treated gr
Page 1109 and 1110:
Authors: I. G. BARBOSA LUNA, J. M.
Page 1111 and 1112:
Topic: C.17.e. Alcohol: Neural mech
Page 1113 and 1114:
553. Cocaine, Methylphenidate, and
Page 1115 and 1116:
Poster 553. Cocaine, Methylphenidat
Page 1117 and 1118:
period rats were trained to self-ad
Page 1119 and 1120:
sodium butyrate injected immediatel
Page 1121 and 1122:
non-responders spent the majority o
Page 1123 and 1124:
Title: The effects of adrenalectomy
Page 1125 and 1126:
Program#/Poster#: 553.12/Z25 Topic:
Page 1127 and 1128:
NIH Grant R01 MH49469 NIH Grant F31
Page 1129 and 1130:
Disclosures: D.R. Ramirez, None; X.
Page 1131 and 1132:
at the basolateral amygdala (BLA).
Page 1133 and 1134:
Title: Sex differences in cocaine p
Page 1135 and 1136:
553. Cocaine, Methylphenidate, and
Page 1137 and 1138:
Disclosures: M.T. McCoy, Department
Page 1139 and 1140:
Abstract: Manganese enhanced magnet
Page 1141 and 1142:
Disclosures: T.Z. Ramsoy, None; K.S
Page 1143 and 1144:
and removal of the 22 N-terminal am
Page 1145 and 1146:
methamphetamine induced more extens
Page 1147 and 1148:
Page 1149 and 1150:
Disclosures: J. Nickell, None; A. V
Page 1151 and 1152:
Poster 554. Methamphetamine and Rel
Page 1153 and 1154:
Disclosures: K.A. Horner, None; Y.E
Page 1155 and 1156:
male and female CRF-R2 knockout (KO
Page 1157 and 1158:
Page 1159 and 1160:
Page 1161 and 1162:
The findings support the idea that
Page 1163 and 1164:
T32HL076133 Title: The acute effect
Page 1165 and 1166:
Abstract: Methamphetamine (METH) ab
Page 1167 and 1168:
Authors: *N. CAI, B. LADENHEIM, M.
Page 1169 and 1170:
Royal Gloden Jubilee PhD Program Ti
Page 1171 and 1172:
mediated by vasoactive eicosanoids.
Page 1173 and 1174:
Title: Dendrodendritic transmission
Page 1175 and 1176:
Page 1177 and 1178:
Page 1179 and 1180:
synapses between ET cells and GABAe
Page 1181 and 1182:
we demonstrate that the activation
Page 1183 and 1184:
had no consistent effect on mIPSCs
Page 1185 and 1186:
Authors: *N. KANG 1 , M. J. BAUM 2
Page 1187 and 1188:
NIH Grant DC006972 Title: The locat
Page 1189 and 1190:
Poster 555. Olfactory Bulb: Synapse
Page 1191 and 1192:
excitatory to inhibitory shift betw
Page 1193 and 1194:
ange of preferred AM frequencies de
Page 1195 and 1196:
Authors: *D. P. KNUDSEN 1 , T. Q. G
Page 1197 and 1198:
Title: Laminar dependent representa
Page 1199 and 1200:
Abstract: The auditory cortex is in
Page 1201 and 1202:
Page 1203 and 1204:
and savannah forest scenes (60 seco
Page 1205 and 1206:
consonant discriminations can be pe
Page 1207 and 1208:
Authors: *N. HIGGINS 1 , D. A. STOR
Page 1209 and 1210:
Title: Local field potentials and s
Page 1211 and 1212:
Title: Neuronal response latency an
Page 1213 and 1214:
Page 1215 and 1216:
Disclosures: J.M. Bouskila, None; M
Page 1217 and 1218:
favored the hypothesis that eCBs fu
Page 1219 and 1220:
1 2 3 Devers Eye Inst., Portland, O
Page 1221 and 1222:
Title: Tropisetron as a neuroprotec
Page 1223 and 1224:
Page 1225 and 1226:
premature ganglion cells. These res
Page 1227 and 1228:
Tectal EP amplitudes did not signif
Page 1229 and 1230:
esponses over time. The initial lig
Page 1231 and 1232:
Page 1233 and 1234:
amplitude is set by a balance of Ca
Page 1235 and 1236:
Kv4.2 was determined by immunohisto
Page 1237 and 1238:
Disclosures: H. Kim, None; J. Lee,
Page 1239 and 1240:
We have previously identified the c
Page 1241 and 1242:
Depolarizing a ‘donor’ cone eli
Page 1243 and 1244:
Title: The impact of temporal frequ
Page 1245 and 1246:
Poster 558. Visual Motion: Neural M
Page 1247 and 1248:
motion alone to that evoked by the
Page 1249 and 1250:
Support: NIH Grant AG17596 NIH Gran
Page 1251 and 1252:
Page 1253 and 1254:
Further, the central CCG peak was n
Page 1255 and 1256:
Authors: *Y. GU 1 , G. C. DEANGELIS
Page 1257 and 1258:
Poster 558. Visual Motion: Neural M
Page 1259 and 1260:
velocity signals are processed thro
Page 1261 and 1262:
model shows how vector decompositio
Page 1263 and 1264:
and whole-cell recordings. Tectal n
Page 1265 and 1266:
effector and object in a retinal fr
Page 1267 and 1268:
motion axis (George et al, 2002). I
Page 1269 and 1270:
Abstract: Motion aftereffects (MAE)
Page 1271 and 1272:
Topic: D.06.e. Pursuit Support: MRC
Page 1273 and 1274:
these changes in the symmetry of th
Page 1275 and 1276:
Authors: *C. J. COLLINS, R. ACKERLE
Page 1277 and 1278:
Poster 559. Pursuit Eye Movements L
Page 1279 and 1280:
task. While fixating a stationary s
Page 1281 and 1282:
559. Pursuit Eye Movements Location
Page 1283 and 1284:
suggest that NOT serves as an impor
Page 1285 and 1286:
eye position at the end of the sacc
Page 1287 and 1288:
To explicitly test the causal contr
Page 1289 and 1290:
Authors: *J. MARUTA 1 , M. SUH 2 ,
Page 1291 and 1292:
Page 1293 and 1294:
administration of BPN (100 ng/kg/2x
Page 1295 and 1296:
alter morphine-induced CPP and/or a
Page 1297 and 1298:
Topic: D.08.bb. Opioids Support: NI
Page 1299 and 1300:
greater than morphine. Of note, the
Page 1301 and 1302:
the possible relevance of the arach
Page 1303 and 1304:
560. Opioids: Mechanism of Action L
Page 1305 and 1306:
Poster 560. Opioids: Mechanism of A
Page 1307 and 1308:
560. Opioids: Mechanism of Action L
Page 1309 and 1310:
with either MOR (1 µg), FEN (1 ng)
Page 1311 and 1312:
Authors: A. DOGRUL 1 , *M. H. OSSIP
Page 1313 and 1314:
sensitive enough to demonstrate agi
Page 1315 and 1316:
Poster 560. Opioids: Mechanism of A
Page 1317 and 1318:
injected with CFA in the masseter a
Page 1319 and 1320:
Title: Effect of interleukin-8 rece
Page 1321 and 1322:
Page 1323 and 1324:
Poster 561. Neuropathic Pain: Infla
Page 1325 and 1326:
Clark AK, Yip PK, Grist J, Gentry C
Page 1327 and 1328:
all 10 baseline images before lamin
Page 1329 and 1330:
dorsal horn in models of pain creat
Page 1331 and 1332:
Authors: P. FELDMAN 1 , H. JUNG 2 ,
Page 1333 and 1334:
Page 1335 and 1336:
Topic: D.08.t. Mechanisms of neurop
Page 1337 and 1338:
Poster 561. Neuropathic Pain: Infla
Page 1339 and 1340:
Disclosures: T. Berta, None; Y. Liu
Page 1341 and 1342:
Disclosures: O. Rosenthal, Unilever
Page 1343 and 1344:
staircase procedure based on a two-
Page 1345 and 1346:
Abstract: The brain needs to encode
Page 1347 and 1348:
Program#/Poster#: 562.8/DD25 Topic:
Page 1349 and 1350:
562. Tactile Stimulation and Proces
Page 1351 and 1352:
Page 1353 and 1354:
Page 1355 and 1356:
compared to the evoked response to
Page 1357 and 1358:
Authors: *S. YEO 1,2 , I.-H. CHOE 3
Page 1359 and 1360:
Program#/Poster#: 562.19/DD36 Topic
Page 1361 and 1362:
week 1, 36±38% after week 2, 55±3
Page 1363 and 1364:
Morton Cure Paralysis Fund Title: A
Page 1365 and 1366:
Topic: D.10.a. Plasticity Support:
Page 1367 and 1368:
Page 1369 and 1370:
of hyperreflexia after SCI and open
Page 1371 and 1372:
Authors: *E. M. ANDREWS 1,2 , Q. F.
Page 1373 and 1374:
Page 1375 and 1376:
NeuN, calbindin (CB), neuron specif
Page 1377 and 1378:
and Synapsin-I proteins. The functi
Page 1379 and 1380:
well as in decerebrated cats by spi
Page 1381 and 1382:
Support: Canadian Institute of Heal
Page 1383 and 1384:
564. Rhythmic Movements: Afferent C
Page 1385 and 1386:
organization forms a potent and dur
Page 1387 and 1388:
antagonists to the rostral bath had
Page 1389 and 1390:
Page 1391 and 1392:
sensillae (CS). Two types of reacti
Page 1393 and 1394:
flexion signals from the tibia (Bä
Page 1395 and 1396:
Topic: D.11.d. Afferent control Sup
Page 1397 and 1398:
Poster 564. Rhythmic Movements: Aff
Page 1399 and 1400:
p0.05). To assess the CabPK influen
Page 1401 and 1402:
Program#/Poster#: 564.21/DD72 Topic
Page 1403 and 1404:
Page 1405 and 1406:
in behavioral experiments with inta
Page 1407 and 1408:
Abstract: A fundamental problem of
Page 1409 and 1410:
Page 1411 and 1412:
Topic: D.11.b. Connectivity Support
Page 1413 and 1414:
sustained activity pattern was corr
Page 1415 and 1416:
examine the organization of the ves
Page 1417 and 1418:
Support: CIHR 79416 Will-to-Win Sch
Page 1419 and 1420:
Poster 565. Rhythmic Motor Networks
Page 1421 and 1422:
document modulation of MIo neuron a
Page 1423 and 1424:
abuse also trigger the release of t
Page 1425 and 1426:
1 2 Behavioral Neurosci Br., NIDA,
Page 1427 and 1428:
Page 1429 and 1430:
566. Basal Ganglia: Transmitters an
Page 1431 and 1432:
dopaminergic cells in the posterior
Page 1433 and 1434:
Program#/Poster#: 566.11/EE26 Topic
Page 1435 and 1436:
Poster 566. Basal Ganglia: Transmit
Page 1437 and 1438:
Disclosures: T. Lerner, None; A.C.
Page 1439 and 1440:
Abstract: Cbln1 (precerebellin) is
Page 1441 and 1442:
Authors: S. TAI, *L. LEUNG; Univ. W
Page 1443 and 1444:
Topic: D.15.a. Transmitters and neu
Page 1445 and 1446:
Page 1447 and 1448:
Poster 567. Basal Ganglia: Electrop
Page 1449 and 1450:
external pallidum are known to exhi
Page 1451 and 1452:
nature of synchronous beta oscillat
Page 1453 and 1454:
Page 1455 and 1456:
smaller subset entrained to theta-b
Page 1457 and 1458:
Abstract: We have previously traine
Page 1459 and 1460:
Support: DA 06886 DA 04551 T32 Trai
Page 1461 and 1462:
Page 1463 and 1464:
and movement, using a paradigm desi
Page 1465 and 1466:
mechanism thought to prevent the br
Page 1467 and 1468:
A brain area that has been closely
Page 1469 and 1470:
Abstract: It is now widely believed
Page 1471 and 1472:
Authors: E. BRAZHNIK, I. AVILA, N.
Page 1473 and 1474:
Poster 567. Basal Ganglia: Electrop
Page 1475 and 1476:
chronic stroke. The present data su
Page 1477 and 1478:
controls its own load in maintainin
Page 1479 and 1480:
Topic: D.17.d. Stroke, damage, or d
Page 1481 and 1482:
task (0.11). There was a positive c
Page 1483 and 1484:
Res. Inst., Kyoto Univ., Inuyama, J
Page 1485 and 1486:
Poster 568. Stroke: Damage or Disea
Page 1487 and 1488:
glial (myoinositol, mIn), and gluta
Page 1489 and 1490:
Topic: D.17.d. Stroke, damage, or d
Page 1491 and 1492:
Page 1493 and 1494:
Disclosures: S. Churchill, None; D.
Page 1495 and 1496:
daily life. Although studies in hea
Page 1497 and 1498:
Abstract: Many activities of daily
Page 1499 and 1500:
Page 1501 and 1502:
These preliminary data suggests tha
Page 1503 and 1504:
568. Stroke: Damage or Disease - Me
Page 1505 and 1506:
Page 1507 and 1508:
final position. In contrast, the PO
Page 1509 and 1510:
Recently, the relationship between
Page 1511 and 1512:
Authors: E. CHANG 1 , *J. T. KING 2
Page 1513 and 1514:
Title: Retinoic acid stimulates est
Page 1515 and 1516:
Program#/Poster#: 569.7/EE98 Topic:
Page 1517 and 1518:
Disclosures: B.W. Bakkum, None; L.
Page 1519 and 1520:
specific to E2. In support, pharmac
Page 1521 and 1522:
not (reproductively-senescent). We
Page 1523 and 1524:
Topic: E.01.d. Steroids and plastic
Page 1525 and 1526:
Interestingly, none of these estrog
Page 1527 and 1528:
spatio-temporal subcellular distrib
Page 1529 and 1530:
Title: Maternal care and perinatal
Page 1531 and 1532:
Disclosures: K.M. Olesen, None; N.
Page 1533 and 1534:
Intriguingly, the autonomic respons
Page 1535 and 1536:
measured plasma norepinephrine (NE)
Page 1537 and 1538:
Authors: E. T. GILBREATH 1 , J. L.
Page 1539 and 1540:
Authors: *R. P. GAYKEMA, G. C. THAC
Page 1541 and 1542:
Support: NSERC Canadian Foundation
Page 1543 and 1544:
Page 1545 and 1546:
associated with differences in both
Page 1547 and 1548:
571. Parental Behavior Location: So
Page 1549 and 1550:
571. Parental Behavior Location: So
Page 1551 and 1552:
attained had over 10 times the numb
Page 1553 and 1554:
Page 1555 and 1556:
that this average round-the-clock m
Page 1557 and 1558:
maternal experience. Our preliminar
Page 1559 and 1560:
divergent paternal responses. P. ca
Page 1561 and 1562:
castration reduces the amount of hu
Page 1563 and 1564:
e related. In this study, sexually
Page 1565 and 1566:
Authors: *K. M. SEIP 1 , J. I. MORR
Page 1567 and 1568: Authors: *D. POPA, E. BREEN, L. DUG
Page 1569 and 1570: Topic: E.04.b. Respiratory regulati
Page 1571 and 1572: Authors: N. R. NELSON 1 , *M. BEHAN
Page 1573 and 1574: eceptor antagonists AP-5 and/or CNQ
Page 1575 and 1576: Program#/Poster#: 572.9/FF14 Topic:
Page 1577 and 1578: Location: South Hall A Time: Tuesda
Page 1579 and 1580: Disclosures: A.T. Takakura, None; M
Page 1581 and 1582: dye “DiI” into the carotid body
Page 1583 and 1584: Authors: J.-H. ZHANG 1,2 , S. J. FU
Page 1585 and 1586: Support: NSERC Grant Department of
Page 1587 and 1588: Location: South Hall A Time: Tuesda
Page 1589 and 1590: (WT) obtained from the same colony,
Page 1591 and 1592: the activity of npEW-Ucn1 system du
Page 1593 and 1594: defeated and instead exposed to emp
Page 1595 and 1596: Title: Pre-locus coeruleus neurons
Page 1597 and 1598: 573. Stress-Modulated Brain Pathway
Page 1599 and 1600: Poster 573. Stress-Modulated Brain
Page 1601 and 1602: estraint stress starting one week p
Page 1603 and 1604: increases VTA BDNF, which may influ
Page 1605 and 1606: t=3.177, df=12). Early and delayed
Page 1607 and 1608: CORT with the antagonist of GR or M
Page 1609 and 1610: paradigm designed to induce variabl
Page 1611 and 1612: Abstract: Neurogenesis in the hippo
Page 1613 and 1614: Title: Chronic corticosterone expos
Page 1615 and 1616: Program#/Poster#: 574.1/FF51 Topic:
Page 1617: 574. Entrainment and Phase Shifts:
Page 1621 and 1622: Poster 574. Entrainment and Phase S
Page 1623 and 1624: Ca2+i leak rate through RyR in vivo
Page 1625 and 1626: neuroprotection or neuronal death.
Page 1627 and 1628: phase to one that is consistent wit
Page 1629 and 1630: Disclosures: N. Atkins, None; S. Re
Page 1631 and 1632: Disclosures: L.S. Zhang , None; C.
Page 1633 and 1634: of withdrawal from morphine, the bl
Page 1635 and 1636: Title: Preliminary study of the exp
Page 1641 and 1642: Similar to the results with clock g
Page 1643 and 1644: investigation is necessary to ident
Page 1645 and 1646: Poster 575. Maintenance and Executi
Page 1647 and 1648: (color judgment) while at the same
Page 1649 and 1650: Intelligence and Processing Speed c
Page 1651 and 1652: Abstract: How the brain maintains s
Page 1653 and 1654: MA; 2 The Picower Inst. for Learnin
Page 1655 and 1656: Time: Tuesday, October 20, 2009, 8:
Page 1659 and 1660: The study proceeded in two stages.
Page 1661 and 1662: NIH Grant AG0925 NSF Graduate Resea
Page 1665 and 1666: eak, a surprising recognition task
Page 1667 and 1668: Title: Behavioral and neural eviden
Page 1669 and 1670:
Topic: F.01.f. Working memory Suppo
Page 1671 and 1672:
Page 1673 and 1674:
perceived each odor contributed to
Page 1675 and 1676:
Program#/Poster#: 576.3/FF105 Topic
Page 1677 and 1678:
in the subliminal condition. These
Page 1679 and 1680:
with rPMC, and rPMC with rPC. There
Page 1681 and 1682:
premotor regions, but modulated mor
Page 1683 and 1684:
did not notice the delay. From this
Page 1685 and 1686:
Page 1687 and 1688:
evidence by influencing the represe
Page 1689 and 1690:
Authors: *R. M. KALWANI, J. I. GOLD
Page 1691 and 1692:
Results: RT for correct responses w
Page 1693 and 1694:
Title: Dissociable components of ob
Page 1695 and 1696:
Authors: *G. C. DE GUZMAN 1 , J. LA
Page 1697 and 1698:
Poster 577. Communication and Self:
Page 1699 and 1700:
esponse creation compared to contro
Page 1701 and 1702:
A Grant-in-Aid for Scientific Resea
Page 1703 and 1704:
Page 1705 and 1706:
egions previously implicated as the
Page 1707 and 1708:
NINDS grant NS048229-04 ONR Contrac
Page 1709 and 1710:
577. Communication and Self: Other
Page 1711 and 1712:
compared to that in the familiar fa
Page 1713 and 1714:
to make it possible to scan the bra
Page 1715 and 1716:
phylogenetically highly conserved n
Page 1717 and 1718:
Topic: F.01.l. Social cognition Sup
Page 1719 and 1720:
Support: CREST, 17022035 KAKENHI, 2
Page 1721 and 1722:
Poster 578. Executive Function: Ani
Page 1723 and 1724:
Disclosures: C.T. Miller, None; X.
Page 1725 and 1726:
Poster 578. Executive Function: Ani
Page 1727 and 1728:
trials were match trials and half w
Page 1729 and 1730:
Authors: *M. ISODA 1,2 , K. YAKO 1,
Page 1731 and 1732:
Page 1733 and 1734:
neural coding perspective the funct
Page 1735 and 1736:
induced cognitive impairments. Alth
Page 1737 and 1738:
Program#/Poster#: 579.6/GG21 Topic:
Page 1739 and 1740:
Poster 579. Executive Function: Rod
Page 1741 and 1742:
ehavioral and temporal information
Page 1743 and 1744:
ecause this ability in nonhuman ani
Page 1745 and 1746:
few information are available regar
Page 1747 and 1748:
Authors: *S. GARCIA, F. PAPALEO, L.
Page 1749 and 1750:
and cognitive flexibility occurs in
Page 1751 and 1752:
Title: Prenatal protein malnutritio
Page 1753 and 1754:
Employment (full or part-time); R.
Page 1755 and 1756:
correlates of behavioral performanc
Page 1757 and 1758:
Abstract: Like the proverbial moth
Page 1759 and 1760:
Support: Roche-Palo Alto Department
Page 1761 and 1762:
Page 1763 and 1764:
Page 1765 and 1766:
eward sensitivity. Results: BMI imp
Page 1767 and 1768:
1999). Here, we examined the time c
Page 1769 and 1770:
Support: NIH Grant MH48404 Pittsbur
Page 1771 and 1772:
Page 1773 and 1774:
Page 1775 and 1776:
581. Adult Neurogenesis and Cogniti
Page 1777 and 1778:
During neurogenesis, immature denta
Page 1779 and 1780:
training with the post-US cue was n
Page 1781 and 1782:
gross structural neurological chang
Page 1783 and 1784:
Authors: R. M. ALEKSEJEV 1 , *J. AM
Page 1785 and 1786:
Authors: *C. L. PICKENS 1 , T. ADAM
Page 1787 and 1788:
582. Stress and Behavior Location:
Page 1789 and 1790:
582. Stress and Behavior Location:
Page 1791 and 1792:
Support: HHMI (AMS) NIH Grant DA201
Page 1793 and 1794:
Program#/Poster#: 582.11/GG73 Topic
Page 1795 and 1796:
Poster 582. Stress and Behavior Loc
Page 1797 and 1798:
Poster 583. Reward: Motivated Behav
Page 1799 and 1800:
system. Ten healthy, normal-weight
Page 1801 and 1802:
medial shell amplify ‘liking’ r
Page 1803 and 1804:
Authors: *S. E. ROSS 1 , J. W. ALDR
Page 1805 and 1806:
Topic: F.03.a. Reward Support: NIH
Page 1807 and 1808:
Title: Activation of nucleus accumb
Page 1809 and 1810:
Page 1811 and 1812:
Disclosures: R. Sharf, None; M. Sar
Page 1813 and 1814:
Disclosures: M. Baudonnat, None; J.
Page 1815 and 1816:
RD for a block of trials. In the re
Page 1817 and 1818:
Abstract: Operant tasks have been u
Page 1819 and 1820:
Topic: F.03.a. Reward Title: The di
Page 1821 and 1822:
Page 1823 and 1824:
levels stabilized (13 cycles), both
Page 1825 and 1826:
during development in the Bengalese
Page 1827 and 1828:
Authors: P. V. LOVELL, *C. V. MELLO
Page 1829 and 1830:
Page 1831 and 1832:
Disclosures: L. Remage-Healey, None
Page 1833 and 1834:
examined behavioral and neural resp
Page 1835 and 1836:
tegmental area (VTA) cell activatio
Page 1837 and 1838:
millisecond before initiation of si
Page 1839 and 1840:
lateral song transmission from tuto
Page 1841 and 1842:
Authors: *B. A. PAWLISCH 1,2 , S. A
Page 1843 and 1844:
Page 1845 and 1846:
number of round DCX-ir cells (diffe
Page 1847 and 1848:
Title: LC/MS/MS analysis of in vivo
Page 1849 and 1850:
previously exposed to novel objects
Page 1851 and 1852:
controlling the adhesion, growth an
Page 1853 and 1854:
MS). Previously this approach had b
Page 1855 and 1856:
Topic: G.01. Molecular, Biochemical
Page 1857 and 1858:
585. Molecular Methods to Monitor a
Page 1859 and 1860:
586. Imaging Techniques VI Location
Page 1861 and 1862:
post injury as compared to that of
Page 1863 and 1864:
apoptosis (1). In the last decade m
Page 1865 and 1866:
Page 1867 and 1868:
such as axons. EdU signal was prese
Page 1869 and 1870:
Page 1871 and 1872:
Aβ. Tissue sections co-stained wit
Page 1873 and 1874:
Support: AEG: Natl. Defense Science
Page 1875 and 1876:
Poster 586. Imaging Techniques VI L
Page 1877 and 1878:
Disclosures: Y. Ogawa, None; K. Osa
Page 1879 and 1880:
Authors: *Z. ZENG 1 , S. O'MALLEY 2
Page 1881 and 1882:
activation, along with the morpholo
Page 1883 and 1884:
vivo. Because co-infectivity of AAV
Page 1885 and 1886:
Authors: *L. C. FLORES, R. GALVEZ,
Page 1887 and 1888:
Authors: J. A. CURRY, A. MOSS, S. T
Page 1889 and 1890:
Authors: *A. E. KALYUZHNY 1 , J. P.
Page 1891 and 1892:
Agence Nationale de Recherche grant
Page 1893 and 1894:
587. Electrophysiological Recording
Page 1895 and 1896:
587. Electrophysiological Recording
Page 1897 and 1898:
procedures allowed the reliable ide
Page 1899 and 1900:
completion IA HA injections. Method
Page 1901 and 1902:
Poster 587. Electrophysiological Re
Page 1903 and 1904:
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