about
Modulating central gain in tinnitus: changes in nitric oxide synthase in the ventral cochlear nucleus.Neural changes accompanying tinnitus following unilateral acoustic trauma in the guinea pig.Changes in the response properties of inferior colliculus neurons relating to tinnitusRepresentation of individual elements of a complex call sequence in primary auditory cortex.A novel behavioural approach to detecting tinnitus in the guinea pig.Processing of communication calls in Guinea pig auditory cortex.Morphological and physiological characteristics of laminar cells in the central nucleus of the inferior colliculus.Cortical inactivation by cooling in small animals.Onset neurones in the anteroventral cochlear nucleus project to the dorsal cochlear nucleusChanges in density of brainstem afferents in ferret primary auditory cortex (AI) during postnatal developmentPhase-locked responses to pure tones in the auditory thalamus.NADPH-diaphorase activity in activated astrocytes represents inducible nitric oxide synthase.Histological Basis of Laminar MRI Patterns in High Resolution Images of Fixed Human Auditory CortexReductions in cortical alpha activity, enhancements in neural responses and impaired gap detection caused by sodium salicylate in awake guinea pigs.Callosal connections of the ferret primary auditory cortex.Localization of cholecystokinin in the dentate commissural-associational system of the mouse and rat.Intrinsic inter- and intralaminar connections and their relationship to the tonotopic map in cat primary auditory cortex.Interconnections of auditory areas in the guinea pig neocortex.Morphology of physiologically characterised ventral cochlear nucleus stellate cells.Relationship of afferent inputs to the lattice of high NADPH-diaphorase activity in the mouse superior colliculus.Laminar differences in the response properties of cells in the primary auditory cortex.Different representations of tooth chatter and purr call in guinea pig auditory cortex.Gap-induced reductions of evoked potentials in the auditory cortex: a possible objective marker for the presence of tinnitus.Representation of the purr call in the guinea pig primary auditory cortex.Organisation of binaural interactions in the primary and dorsocaudal fields of the guinea pig auditory cortex.A ventrorostral belt is adjacent to the guinea pig primary auditory cortex.Correction: Processing of Communication Calls in Guinea Pig Auditory Cortex.Chemoarchitectonic organization of the cat primary auditory cortex.Responses to the purr call in three areas of the guinea pig auditory cortex.Effects of the cannabinoid CB1 agonist ACEA on salicylate ototoxicity, hyperacusis and tinnitus in guinea pigs.Location of cells giving phase-locked responses to pure tones in the primary auditory cortex.Origin of high acetylcholinesterase activity in the mouse superior colliculus.Comparison of penicillin epileptogenesis in rat somatosensory and motor cortex.Histochemical demonstration of sensory maps in the rat and mouse cerebral cortex.Lattice of high oxidative metabolism in the intermediate grey layer of the rat and hamster superior colliculus.Spatial relationship of NADPH-diaphorase and acetylcholinesterase lattices in the rat and mouse superior colliculus.Activated astrocytes of the mouse hippocampus contain high levels of NADPH-diaphorase.Spatial relationship of histochemically demonstrable patches in the mouse superior colliculus.Evidence for a direct, short latency projection from the dorsal cochlear nucleus to the auditory thalamus in the guinea pig.Phase-locked responses to pure tones in the primary auditory cortex.
P50
Q30416124-A104DBE0-F8D7-4B18-BE3B-6BD0C8A5E67EQ30425806-FE0FBCD6-1E18-48D8-BEE7-E38ABAA5DC3FQ30427763-829BAFD3-ADF1-4AC0-9517-4AD4D2D2AA7EQ30447506-1520EF6A-99B3-4D96-811A-C06350F3D6E8Q30456272-5DF38E74-B554-4A60-8A5B-A36F55CD2671Q30459827-AB41104D-C789-4E4D-89D6-537D4519E0FAQ30464412-00B31894-0760-45E0-AEFC-519E720B5EAEQ30474890-789AECEF-A74B-4576-972F-FA766B531274Q30492660-0DC370FA-B52A-47FF-8208-7CFC44B24DEAQ33880593-88EFC1D8-92BC-4495-A506-4259DE8AE26DQ34663507-1F70DA16-93AC-4204-818A-20DEA677BD27Q36675667-A9650B2F-5C61-46DC-B4AD-46731CAF9007Q37318601-B29CB870-F279-4E89-BFE2-54707A298076Q39174973-70AB5E70-185F-475D-BBD0-D6621E4E6E67Q40879421-E72BBB39-909C-4089-A60E-F04AE6929692Q41452965-296EC4B1-C8A6-4E7E-8D15-EAE34213BC49Q43412262-502BD567-43B4-4F05-AFF5-FE96555D8F7AQ43926667-64E4A0A8-5D74-44B2-BA26-6AB6BACF8C3FQ44573305-33AF0CAA-1BA5-45B3-B992-C59C427565C9Q44644919-B0E7A741-13D3-4C9D-9CBD-B8732248645BQ45722940-7C25B875-FE57-42D1-9B81-9107C1B3D92DQ46275649-AD2276C8-70FF-4EBB-9194-74EA3A19DFB6Q46345401-404D2147-19A5-48FE-8108-F16213A1D328Q46518145-58596699-8711-45DD-BDC8-A24C54197AC5Q46740711-FB9B2C0B-C9F1-4BAD-B020-36449541CE40Q46749945-4100A827-21B2-4544-BD1E-AA64623FFD41Q46767455-76FEDDF0-A659-49D9-A50C-33EE01F82B40Q46976286-FB6461AC-A30E-4AC5-81C3-798F3827D01AQ46986526-68A08DCB-F9C7-4A54-A1F1-97D280117CA6Q47107982-A1190EFD-DEBF-408E-8407-804189B3DA7AQ48128343-AE44CD76-533B-46C0-9C88-533BD74A6CDEQ48167247-55A2260C-2967-453C-AB34-6231882F7E86Q48203396-4DF6D941-93CD-48FA-8CCB-E0437B262CD8Q48219810-467DB69A-D28F-47FD-97AC-7CB1B0D8C3D6Q48287488-54B590AE-EF89-4AFF-9A6C-2DAEC2EC3BD8Q48291706-50CE75DA-50C7-40E5-865A-EBCDD0298970Q48409940-D3DBE394-6F66-49A9-A3AC-3517E050F773Q48416512-462423F8-60A2-49C3-B1E2-81DCAD7192CAQ48474067-453229FC-FDB9-41EE-9516-019996E402BEQ48475922-B0B98B54-7112-4DAE-823B-67F83F03DAD8
P50
description
chercheur
@fr
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Mark Wallace
@ast
Mark Wallace
@en
Mark Wallace
@es
Mark Wallace
@fr
Mark Wallace
@nl
Mark Wallace
@sl
type
label
Mark Wallace
@ast
Mark Wallace
@en
Mark Wallace
@es
Mark Wallace
@fr
Mark Wallace
@nl
Mark Wallace
@sl
prefLabel
Mark Wallace
@ast
Mark Wallace
@en
Mark Wallace
@es
Mark Wallace
@fr
Mark Wallace
@nl
Mark Wallace
@sl
P108
P106
P21
P31
P496
0000-0001-6894-4903