(Q36487730)

14 August 2017

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title

The role of mutagenesis in defining genes in behaviour (English)

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14 August 2017

2

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14 August 2017

Sofia I H Godinho

1

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14 August 2017

publication date

1 June 2006

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European Journal of Human Genetics

14 August 2017

published in

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14 August 2017

volume

14

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14 August 2017

issue

6

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14 August 2017

page(s)

651-659

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201545

14 August 2017

exact match

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Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouse

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Suppressor screen in Mpl-/- mice: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling

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ZIC2 and Sp3 repress Sp1-induced activation of the human D1A dopamine receptor gene.

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

21 January 2018

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Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith--Lemli--Opitz syndrome

21 January 2018

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Strain differences in three measures of ethanol intoxication in mice: the screen, dowel and grip strength tests

21 January 2018

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Beneficial effects of the kappa opioid receptor agonist U-50488H in experimental acute brain and spinal cord injury

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Depression: a new animal model sensitive to antidepressant treatments

21 January 2018

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The quantiative measurement of motor inco-ordination in naive mice using an acelerating rotarod

21 January 2018

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Preliminary evidence for reduced social interactions in Chakragati mutants modeling certain symptoms of schizophrenia

21 January 2018

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Dominance behavior: a phylogenetic analysis in the mouse

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

Expanded characterization of the social interaction abnormalities in mice lacking Dvl1

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.

21 January 2018

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7 January 2021

Spontaneous locomotor hyperactivity in a mouse mutant with a deletion including the Snap gene on chromosome 2

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

7 January 2021

Coloboma hyperactive mutant mice exhibit regional and transmitter-specific deficits in neurotransmission.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

7 January 2021

Mutagenesis and behavioral screening for altered circadian activity identifies the mouse mutant, Wheels

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

7 January 2021

Comprehensive observational assessment: Ia. A systematic, quantitative procedure for assessing the behavioral and physiologic state of the mouse

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

7 January 2021

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

7 January 2021

Impaired motor learning performance in cerebellar En-2 mutant mice.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

7 January 2021

Modification of the acoustic startle response in hearing-impaired C57BL/6J mice: prepulse augmentation and prolongation of prepulse inhibition.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

7 January 2021

Phosphagens and intracellular pH in intact rabbit smooth muscle studied by 31P-NMR

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201545

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201545

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14 August 2017

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