Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. (Q50313568)

From Wikidata

Jump to navigation Jump to search

scientific article published on 21 May 2007

Language	Label	Description	Also known as
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

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

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)

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

1 reference

based on heuristic

inferred from title

2

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

Jeffrey L. Noebels

8

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

James R. Lupski

11

object named as

James R Lupski

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

10

object named as

Richard Paylor

1 reference

Europe PubMed Central

PubMed publication ID

30 December 2019

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

author name string

Weimin Bi

1

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

Xin Shi

3

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

Lisa A Yuva-Paylor

4

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

Barbara A Antalffy

5

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

Alica Goldman

6

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

Jong W Yoo

7

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

Dawna L Armstrong

9

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

publication date

21 May 2007

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

Human Molecular Genetics

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

16

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

15

1 reference

Europe PubMed Central

PubMed publication ID

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

30 December 2019

1802-1813

1 reference

Europe PubMed Central

PubMed publication ID

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

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

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50313568&oldid=2118800082"