UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Atypical behaviour and connectivity in SHANK3-mutant macaques

Nature (London), 2019-06, Vol.570 (7761), p.326-331

2019

Volltextzugriff (PDF)

Genetic Influence on Eye Movements to Complex Scenes at Short Timescales

Current biology, 2017-11, Vol.27 (22), p.3554-3560.e3

2017

Volltextzugriff (PDF)

Human CFEOM1 Mutations Attenuate KIF21A Autoinhibition and Cause Oculomotor Axon Stalling

Neuron (Cambridge, Mass.), 2014-04, Vol.82 (2), p.334-349

2014

Volltextzugriff (PDF)

Analyses of the MAPT , PGRN , and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS

Parkinsonism & related disorders, 2013-01, Vol.19 (1), p.15-20

2013

Volltextzugriff (PDF)

Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS

Human molecular genetics, 2015-09, Vol.24 (17), p.4948-4957

2015

Volltextzugriff (PDF)

A cerebellar learning model of vestibulo-ocular reflex adaptation in wild-type and mutant mice

The Journal of neuroscience, 2014-05, Vol.34 (21), p.7203-7215

2014

Volltextzugriff (PDF)

Spatial gradients and multidimensional dynamics in a neural integrator circuit

Nature neuroscience, 2011-09, Vol.14 (9), p.1150-1159

2011

Volltextzugriff (PDF)

Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Nature genetics, 2006-11, Vol.38 (11), p.1242-1244

2006

Volltextzugriff (PDF)

Eye movement dysfunction in first-degree relatives of patients with schizophrenia: A meta-analytic evaluation of candidate endophenotypes

Brain and cognition, 2008-12, Vol.68 (3), p.436-461

2008

Volltextzugriff (PDF)

Loss of α-calcitonin gene-related peptide (αCGRP) reduces the efficacy of the Vestibulo-ocular Reflex (VOR)

The Journal of neuroscience, 2014-07, Vol.34 (31), p.10453-10458

2014

Volltextzugriff (PDF)

Does COMT val158met polymorphism influence P50 sensory gating, eye tracking or saccadic inhibition dysfunctions in schizophrenia?

Psychiatry research, 2016-12, Vol.246, p.738-744

2016

Volltextzugriff (PDF)

Anticipatory oculomotor responses in parents of children with attention deficit hyperactivity disorder

Psychiatric genetics, 2020-06, Vol.30 (3), p.65-72

2020

Volltextzugriff (PDF)

New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32

JAMA neurology, 2013-06, Vol.70 (6), p.764

2013

Volltextzugriff (PDF)

Defining and Quantifying the Social Phenotype in Autism

The American journal of psychiatry, 2002-06, Vol.159 (6), p.895-908

2002

Volltextzugriff (PDF)

Heritability and reliability of P300, P50 and duration mismatch negativity

Behavior genetics, 2006-11, Vol.36 (6), p.845-857

2006

Volltextzugriff (PDF)

Measuring the optokinetic response of zebrafish larvae

Nature protocols, 2006-12, Vol.1 (5), p.2448-2451

Brockerhoff, Susan E

2006

Volltextzugriff (PDF)

Retinoic acid deficiency impairs the vestibular function

The Journal of neuroscience, 2013-03, Vol.33 (13), p.5856-5866

2013

Volltextzugriff (PDF)

TUBB3 E410K syndrome with osteoporosis and cough syncope in a patient previously diagnosed with atypical Moebius syndrome

Brain & development (Tokyo. 1979), 2018-03, Vol.40 (3), p.233-237

2018

Volltextzugriff (PDF)

Association of DISC1, BDNF, and COMT polymorphisms with exploratory eye movement of schizophrenia in a Chinese Han population

Psychiatric genetics, 2016-12, Vol.26 (6), p.258-265

2016

Volltextzugriff (PDF)

Viewing Social Scenes: A Visual Scan-Path Study Comparing Fragile X Syndrome and Williams Syndrome

Journal of autism and developmental disorders, 2013-08, Vol.43 (8), p.1880-1894

2013

Volltextzugriff (PDF)

Development of oculomotor circuitry independent of hox3 genes

Nature communications, 2014-06, Vol.5 (1), p.4221-4221, Article 4221

2014

Volltextzugriff (PDF)

The influence of dopamine-related genes on perceptual stability

The European journal of neuroscience, 2013-11, Vol.38 (9), p.3378-3383

2013

Volltextzugriff (PDF)

Genome-wide scans of genetic variants for psychophysiological endophenotypes: Introduction to this special issue of Psychophysiology

Psychophysiology, 2014-12, Vol.51 (12), p.1201-1202

Iacono, William G.

2014

Volltextzugriff (PDF)

Identifcation of a Novel Mutation p.I240T in the FRMD7 gene in a Family with Congenital Nystagmus

Scientific reports, 2013-10, Vol.3 (1), p.3084-3084, Article 3084

2013

Volltextzugriff (PDF)

Serotonin transporter gene promoter region polymorphism and selective processing of emotional images

Biological psychology, 2010-03, Vol.83 (3), p.260-265

2010

Volltextzugriff (PDF)

1 – 25 von 2.390

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.171)
Mit Volltextzugriff
(1.950)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

5 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(4)
... seit 90 Tagen
(15)

Menü

Weitere Dienste

Einstellungen

Atypical behaviour and connectivity in SHANK3-mutant macaques

Genetic Influence on Eye Movements to Complex Scenes at Short Timescales

Human CFEOM1 Mutations Attenuate KIF21A Autoinhibition and Cause Oculomotor Axon Stalling

Analyses of the MAPT , PGRN , and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS

Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS

A cerebellar learning model of vestibulo-ocular reflex adaptation in wild-type and mutant mice

Spatial gradients and multidimensional dynamics in a neural integrator circuit

Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Eye movement dysfunction in first-degree relatives of patients with schizophrenia: A meta-analytic evaluation of candidate endophenotypes

Loss of α-calcitonin gene-related peptide (αCGRP) reduces the efficacy of the Vestibulo-ocular Reflex (VOR)

Does COMT val158met polymorphism influence P50 sensory gating, eye tracking or saccadic inhibition dysfunctions in schizophrenia?

Anticipatory oculomotor responses in parents of children with attention deficit hyperactivity disorder

New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32

Defining and Quantifying the Social Phenotype in Autism

Heritability and reliability of P300, P50 and duration mismatch negativity

Measuring the optokinetic response of zebrafish larvae

Retinoic acid deficiency impairs the vestibular function

TUBB3 E410K syndrome with osteoporosis and cough syncope in a patient previously diagnosed with atypical Moebius syndrome

Association of DISC1, BDNF, and COMT polymorphisms with exploratory eye movement of schizophrenia in a Chinese Han population

Viewing Social Scenes: A Visual Scan-Path Study Comparing Fragile X Syndrome and Williams Syndrome

Development of oculomotor circuitry independent of hox3 genes

The influence of dopamine-related genes on perceptual stability

Genome-wide scans of genetic variants for psychophysiological endophenotypes: Introduction to this special issue of Psychophysiology

Identifcation of a Novel Mutation p.I240T in the FRMD7 gene in a Family with Congenital Nystagmus

Serotonin transporter gene promoter region polymorphism and selective processing of emotional images

Suchergebnisse filtern