(Q24308809)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

title

Association of PKD2 (polycystin 2) mutations with left-right laterality defects (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

Polycystin 2, transient receptor potential cation channel

6 February 2020

main subject

1 reference

determination of liver left/right asymmetry

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Stanislas Bataille

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Karin Dahan

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Stephane Burtey

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

author name string

Nathalie Demoulin

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Marie-Pierre Audrézet

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Michel Godin

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Michel Fontès

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Yves Pirson

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Olivier Devuyst

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

language of work or name

English

0 references

publication date

29 June 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Kidney Diseases

6 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

volume

58

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

page(s)

456-460

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21719175%20AND%20SRC:MED&resulttype=core&format=json

Disorders of left-right asymmetry: heterotaxy and situs inversus

6 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Discordant organ laterality in monozygotic twins with primary ciliary dyskinesia

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Dextrocardia and coronal alignment of thoracic curve: a population study

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Nodal flow and the generation of left-right asymmetry.

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer's vesicle are required for specification of the zebrafish left-right axis

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Somatic inactivation of Pkd2 results in polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Two populations of node monocilia initiate left-right asymmetry in the mouse

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

The ion channel polycystin-2 is required for left-right axis determination in mice

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Fluid flow and broken symmetry

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Extrarenal manifestations of autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Clinical practice. Autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

A homozygous mutation in INVS causing juvenile nephronophthisis with abnormal reactivity of the Wnt/beta-catenin pathway

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Breaking symmetry: a clinical overview of left-right patterning.

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Lack of a laterality phenotype in Pkd1 knock-out embryos correlates with absence of polycystin-1 in nodal cilia

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Zebrafish curly up encodes a Pkd2 ortholog that restricts left-side-specific expression of southpaw

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Polycystin-2 immunolocalization and function in zebrafish

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

Unified criteria for ultrasonographic diagnosis of ADPKD.

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021

A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group

1 reference

https://api.crossref.org/works/10.1053%2FJ.AJKD.2011.05.015

7 January 2021