(Q48161604)

9 February 2018

title

Behavioral characterization of mdx3cv mice deficient in C-terminal dystrophins. (English)

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9 February 2018

author name string

Vaillend C

series ordinal

1

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9 February 2018

Ungerer A

series ordinal

2

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9 February 2018

publication date

1 July 1999

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9 February 2018

published in

Neuromuscular Disorders

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9 February 2018

volume

9

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9 February 2018

issue

5

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9 February 2018

page(s)

296-304

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9 February 2018

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Duchenne muscular dystrophy gene product is not identical in muscle and brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Dystrophin in the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

The central nervous system in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Deletion status and intellectual impairment in Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

X chromosome-linked muscular dystrophy (mdx) in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Passive avoidance behaviour deficit in the mdx mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Influence of dystrophin-gene mutation on mdx mouse behavior. I. Retention deficits at long delays in spontaneous alternation and bar-pressing tasks.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Spatial learning and hippocampal long-term potentiation are not impaired in mdx mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Spatial discrimination learning and CA1 hippocampal synaptic plasticity in mdx and mdx3cv mice lacking dystrophin gene products.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

mdx mice show progressive weakness and muscle deterioration with age

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Differential expression of dystrophin isoforms in strains of mdx mice with different mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Neurogenetic basis of cognition: Facts and hypotheses

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Effects of lateral amygdala lesions on the responses to novelty in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

HOMOGENEITY OF SINGLE TRIAL RESPONSE TENDENCIES AND SPONTANEOUS ALTERNATION IN THE T-MAZE.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Intertrial interval dependent effect of lateral hypothalamic stimulation on spontaneous alternation behavior in a T-maze

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Operant discrimination learning and operant bar-pressing rates in inbred and heterogeneous laboratory mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

The effect of hippocampal lesions on extinction and “hypothesis” behavior in rats

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Dystrophin expression in the hair cells of the cochlea

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Dystrophin expression in the human retina is required for normal function as defined by electroretinography

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Dystrophin and its isoforms

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Unusual behavioral phenotypes of inbred mouse strains.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

Cognitive impairment in Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900029-2

7 January 2021

10.1016/S0960-8966(99)00029-2

Identifiers

DOI

1 reference

9 February 2018

release_fr56g7hlpngzpjvi35liba6yru

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fr56g7hlpngzpjvi35liba6yru

24 November 2022

mapped directly with Wikidata item

PubMed ID

10407849

1 reference

9 February 2018