(Q28586772)

31 January 2017

title

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis (English)

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GLIS family zinc finger 2

31 January 2017

0 references

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GOA release 2020-03-11

author

Peter Nürnberg

15

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Friedhelm Hildebrandt

16

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Gudrun Nürnberg

12

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Edgar A. Otto

Edgar Otto

5

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Massimo Attanasio

Massimo Attanasio

1

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Dominik Seelow

Dominik Seelow

11

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Christian Becker

13

Christian Becker

1 reference

31 January 2017

10

John A. Sayer

1 reference

31 January 2017

9

Juliana Helou

1 reference

31 January 2017

14

Albert E. Chudley

1 reference

31 January 2017

author name string

N. Henriette Uhlenhaut

2

1 reference

31 January 2017

Vitor H. Sousa

3

1 reference

31 January 2017

John F. O'Toole

4

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31 January 2017

Katrin Anlag

6

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31 January 2017

Claudia Klugmann

7

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31 January 2017

Anna-Corina Treier

8

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31 January 2017

Mathias Treier

17

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31 January 2017

language of work or name

English

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publication date

1 August 2007

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31 January 2017

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31 January 2017

volume

39

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31 January 2017

issue

8

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31 January 2017

page(s)

1018–1024

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A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

31 January 2017

cites work

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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

7 January 2021

Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease?

1 reference

7 January 2021

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

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7 January 2021

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7 January 2021

Genetics and pathogenesis of polycystic kidney disease.

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7 January 2021

Genomic structure of the gene encoding the human GLI-related, Krüppel-like zinc finger protein GLIS2.

1 reference

7 January 2021

Characterization of Glis2, a novel gene encoding a Gli-related, Krüppel-like transcription factor with transactivation and repressor functions. Roles in kidney development and neurogenesis

1 reference

7 January 2021

Characterization of the nephrocystin/nephrocystin-4 complex and subcellular localization of nephrocystin-4 to primary cilia and centrosomes

1 reference

7 January 2021

Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function

1 reference

7 January 2021

Progressive renal fibrosis in murine polycystic kidney disease: an immunohistochemical observation

1 reference

7 January 2021

Intrarenal cells, not bone marrow-derived cells, are the major source for regeneration in postischemic kidney

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7 January 2021

Sonic Hedgehog-induced activation of the Gli1 promoter is mediated by GLI3

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7 January 2021

GLI3-dependent transcriptional repression of Gli1, Gli2 and kidney patterning genes disrupts renal morphogenesis

1 reference

7 January 2021

Structure and function of the feed-forward loop network motif

1 reference

7 January 2021

Renal fibrosis and the origin of the renal fibroblast

1 reference

7 January 2021

Genetic profiling of epithelial cells expressing E-cadherin repressors reveals a distinct role for Snail, Slug, and E47 factors in epithelial-mesenchymal transition

1 reference

7 January 2021

Toward a unified theory of renal progression

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7 January 2021

Mechanisms of TGF-beta signaling from cell membrane to the nucleus

1 reference

7 January 2021

Chemokines and chemokine receptors are involved in the resolution or progression of renal disease.

1 reference

7 January 2021

Connective-tissue growth factor (CTGF) modulates cell signalling by BMP and TGF-beta

1 reference

7 January 2021

Regulation of PDGF and its receptors in fibrotic diseases

1 reference

7 January 2021

Integrated actions of transforming growth factor-beta1 and connective tissue growth factor in renal fibrosis

1 reference

7 January 2021

Interleukin-1beta-induced transdifferentiation of renal proximal tubular cells is mediated by activation of JNK and p38 MAPK

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7 January 2021

Molecular requirements for epithelial-mesenchymal transition during tumor progression

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7 January 2021

Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism.

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7 January 2021

Hedgehog signalling in the mouse requires intraflagellar transport proteins

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7 January 2021

Identifiers

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31 January 2017

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