(Q45010775)

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Heritable differences in the dopaminergic regulation of sensorimotor gating. II. Temporal, pharmacologic and generational analyses of apomorphine effects on prepulse inhibition

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Europe PubMed Central

PubMed publication ID

8 December 2017

Heritable differences in the dopaminergic regulation of sensorimotor gating. II. Temporal, pharmacologic and generational analyses of apomorphine effects on prepulse inhibition (English)

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Europe PubMed Central

PubMed publication ID

8 December 2017

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Neal R. Swerdlow

1

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Neal R Swerdlow

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8 December 2017

author name string

Jody M Shoemaker

2

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Europe PubMed Central

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8 December 2017

Pamela P Auerbach

3

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Europe PubMed Central

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8 December 2017

Leia Pitcher

4

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8 December 2017

Jana Goins

5

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8 December 2017

Amanda Platten

6

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8 December 2017

publication date

21 May 2003

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8 December 2017

Psychopharmacology

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8 December 2017

174

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8 December 2017

4

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8 December 2017

452-462

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8 December 2017

Assessing the validity of an animal model of deficient sensorimotor gating in schizophrenic patients

1 reference

https://api.crossref.org/works/10.1007%2FS00213-003-1480-4

21 January 2018

Animal models of deficient sensorimotor gating: what we know, what we think we know, and what we hope to know soon

1 reference

https://api.crossref.org/works/10.1007%2FS00213-003-1480-4

21 January 2018

Effects of pergolide on sensorimotor gating of the startle reflex in rats

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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A D2 dopamine receptor agonist disrupts sensorimotor gating in rats. Implications for dopaminergic abnormalities in schizophrenia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Dopamine characteristics in different rat genotypes: the relation to absence epilepsy

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Sensitivity to the dopaminergic regulation of prepulse inhibition in rats: Evidence for genetic, but not environmental determinants

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Human studies of prepulse inhibition of startle: normal subjects, patient groups, and pharmacological studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Presidential Address, 1974. The more or less startling effects of weak prestimulation

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Normalization of information processing deficits in schizophrenia with clozapine

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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PHNO, a selective dopamine D2 receptor agonist, does not reduce prepulse inhibition of the startle reflex in rats

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Do D1/D2 interactions regulate prepulse inhibition in rats?

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Dopaminergic stimulation disrupts sensorimotor gating in the rat

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Startle gating deficits occur across prepulse intensities in schizophrenic patients

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Differential effects of apomorphine on prepulse inhibition of acoustic startle reflex in two rat strains

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Prepulse startle deficit in the Brown Norway rat: a potential genetic model

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Auditory information processing in rat genotypes with different dopaminergic properties

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Enhancement of the acoustic startle response in rats by the dopamine D1 receptor agonist SKF 82958

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Central dopamine hyperactivity in rats mimics abnormal acoustic startle response in schizophrenics

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Toward understanding the biology of a complex phenotype: rat strain and substrain differences in the sensorimotor gating-disruptive effects of dopamine agonists.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Heritable differences in the dopaminergic regulation of sensorimotor gating. I. Apomorphine effects on startle gating in albino and hooded outbred rat strains and their F1 and N2 progeny

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Comparative genetics of albinism

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Pharmacological studies of prepulse inhibition models of sensorimotor gating deficits in schizophrenia: a decade in review

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

based on heuristic

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Sensitivity to sensorimotor gating-disruptive effects of apomorphine in two outbred parental rat strains and their F1 and N2 progeny

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Prestimulus effects on human startle reflex in normals and schizophrenics

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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New evidence for presence of tyrosinase in substantia nigra, forebrain and midbrain

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Rat strain differences in the ability to disrupt sensorimotor gating are limited to the dopaminergic system, specific to prepulse inhibition, and unrelated to changes in startle amplitude or nucleus accumbens dopamine receptor sensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Genetic differences in startle gating-disruptive effects of apomorphine: evidence for central mediation

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https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Effective neuroleptic medication removes prepulse inhibition deficits in schizophrenia patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Petit mal epilepsy and parkinsonian tremor: hypothesis of a common pacemaker

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300359

12 December 2020

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Identifiers

10.1007/S00213-003-1480-4

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

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