(Q42655901)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22742499%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

title

In a shake of a lamb's tail: using genomics to unravel a cause of chondrodysplasia in Texel sheep (English)

1 reference

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6 February 2020

0 references

6

1 reference

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6 February 2020

author name string

X Zhao

1

1 reference

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6 February 2020

S K Onteru

2

1 reference

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6 February 2020

S Piripi

3

1 reference

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6 February 2020

K G Thompson

4

1 reference

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6 February 2020

H T Blair

5

1 reference

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6 February 2020

M F Rothschild

7

1 reference

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6 February 2020

publication date

1 July 2012

1 reference

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6 February 2020

1 reference

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6 February 2020

volume

43 Suppl 1

1 reference

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6 February 2020

page(s)

9-18

1 reference

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Microphthalmia in Texel sheep is associated with a missense mutation in the paired-like homeodomain 3 (PITX3) gene

6 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2052.2011.02304.X

A single-base change in the tyrosine kinase II domain of ovine FGFR3 causes hereditary chondrodysplasia in sheep

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2052.2011.02304.X

Protein localization of SLC26A2 (DTDST) in rat kidney

21 January 2018

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Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites

21 January 2018

1 reference

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Hyposulfatemia, growth retardation, reduced fertility, and seizures in mice lacking a functional NaSi-1 gene.

21 January 2018

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Abnormal sulfate metabolism in vitamin D-deficient rats.

21 January 2018

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Identification of the Finnish founder mutation for diastrophic dysplasia (DTD).

21 January 2018

1 reference

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The ABCs of solute carriers: physiological, pathological and therapeutic implications of human membrane transport proteinsIntroduction

21 January 2018

1 reference

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The human renal sodium sulfate cotransporter (SLC13A1; hNaSi-1) cDNA and gene: organization, chromosomal localization, and functional characterization.

21 January 2018

1 reference

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Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases

21 January 2018

1 reference

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Functional and structural characterization of the zebrafish Na+-sulfate cotransporter 1 (NaS1) cDNA and gene (slc13a1).

21 January 2018

1 reference

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An expressed fgf4 retrogene is associated with breed-defining chondrodysplasia in domestic dogs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2052.2011.02304.X

On the Sulfation Pattern of Polysaccharides in the Extracellular Matrix of Sheep with Chondrodysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2052.2011.02304.X

The estrogen receptor locus is associated with a major gene influencing litter size in pigs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2052.2011.02304.X

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

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Genetic polymorphism in varietal identification and genetic improvement

21 January 2018

1 reference

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Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2052.2011.02304.X

Inherited chondrodysplasia in Texel sheep

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2052.2011.02304.X

An association study of 20 candidate genes with cryptorchidism in Siberian Husky dogs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2052.2011.02304.X

A novel nonsense mutation in the DMP1 gene identified by a genome-wide association study is responsible for inherited rickets in Corriedale sheep

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2052.2011.02304.X

Restriction fragment length polymorphisms in genetic improvement: methodologies, mapping and costs

21 January 2018

1 reference

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