(Q24318443)

regulation of hippo signaling

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Peter Nürnberg

16

0 references

Gudrun Nürnberg

9

0 references

Bernhard Schermer

21

0 references

Thomas Benzing

17

0 references

author name string

Valeska Frank

1

0 references

Sandra Habbig

2

0 references

Malte P Bartram

3

0 references

Tobias Eisenberger

4

0 references

Hermine E Veenstra-Knol

5

0 references

Christian Decker

6

0 references

Reinder A C Boorsma

7

0 references

Heike Göbel

8

0 references

Anabel Griessmann

10

0 references

Mareike Franke

11

0 references

Lori Borgal

12

0 references

Priyanka Kohli

13

0 references

Linus A Völker

14

0 references

Jörg Dötsch

15

0 references

Hanno J Bolz

18

0 references

Colin Johnson

19

0 references

Erica H Gerkes

20

0 references

Carsten Bergmann

PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD).

22

0 references

language of work or name

English

0 references

publication date

1 June 2013

0 references

published in

Human Molecular Genetics

0 references

volume

22

0 references

issue

11

0 references

page(s)

2177-85

0 references

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Altered Hippo signalling in polycystic kidney disease.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

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/10.1093%2FHMG%2FDDT070

7 January 2021

Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

TRPP2 and autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

The Hippo pathway regulates Wnt/beta-catenin signaling

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

A molecular mechanism that links Hippo signalling to the inhibition of Wnt/β-catenin signalling

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

c-myc as an inducer of polycystic kidney disease in transgenic mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Autosomal dominant polycystic kidney disease: the last 3 years

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Cilium-generated signaling and cilia-related disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

The primary cilium: a signalling centre during vertebrate development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

When pathways collide: collaboration and connivance among signalling proteins in development.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Perinatal deaths in a family with autosomal dominant polycystic kidney disease and a PKD2 mutation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

1 reference

7 January 2021

Homo- and heterodimeric interactions between the gene products of PKD1 and PKD2

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Connective tissue growth factor induces apoptosis in human breast cancer cell line MCF-7.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Nephrocystin-4 regulates Pyk2-induced tyrosine phosphorylation of nephrocystin-1 to control targeting to monocilia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

TEAD transcription factors mediate the function of TAZ in cell growth and epithelial-mesenchymal transition

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

C-myc-induced apoptosis in polycystic kidney disease is Bcl-2 and p53 independent

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

The ciliopathy disease protein NPHP9 promotes nuclear delivery and activation of the oncogenic transcriptional regulator TAZ.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Clinical spectrum and pathogenesis of nephronophthisis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Hippo pathway inhibits Wnt signaling to restrain cardiomyocyte proliferation and heart size

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Intrinsic proinflammatory signaling in podocytes contributes to podocyte damage and prolonged proteinuria

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Nek8 regulates the expression and localization of polycystin-1 and polycystin-2

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Nephronophthisis: disease mechanisms of a ciliopathy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

Loss of the ciliary kinase Nek8 causes left-right asymmetry defects

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

CTGF and chronic kidney fibrosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021

BCL-2: pro-or anti-oxidant?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT070

7 January 2021