(Q50313568)

English

Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.

scientific article published on 21 May 2007

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17517686%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17517686%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

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30 December 2019

Jeffrey L. Noebels

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30 December 2019

James R. Lupski

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James R Lupski

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30 December 2019

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Richard Paylor

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30 December 2019

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Weimin Bi

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30 December 2019

Xin Shi

3

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30 December 2019

Lisa A Yuva-Paylor

4

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30 December 2019

Barbara A Antalffy

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30 December 2019

Alica Goldman

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30 December 2019

Jong W Yoo

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30 December 2019

Dawna L Armstrong

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30 December 2019

publication date

21 May 2007

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30 December 2019

Human Molecular Genetics

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30 December 2019

16

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30 December 2019

15

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30 December 2019

1802-1813

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30 December 2019

Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Interstitial deletion of (17)(p11.2p11.2) in nine patients

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Cognitive and adaptive behavior profiles in Smith-Magenis syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Mutations in RAI1 associated with Smith-Magenis syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Cloning of a retinoic acid-induced gene, GT1, in the embryonal carcinoma cell line P19: neuron-specific expression in the mouse brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2).

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

A million dollar question: does LTP = memory?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Dexras1 potentiates photic and suppresses nonphotic responses of the circadian clock

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM128

21 January 2018

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