TSPAN12 regulates retinal vascular development by promoting Norrin- but not Wnt-induced FZD4/beta-catenin signaling (Q24336628)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19837033 AND SRC:MED&resulttype=core&format=json

10 February 2020

title

TSPAN12 regulates retinal vascular development by promoting Norrin- but not Wnt-induced FZD4/beta-catenin signaling (English)

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10 February 2020

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GOA release 2020-03-11

author

Harald J Junge

1

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10 February 2020

Weilan Ye

9

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10 February 2020

author name string

Stacey Yang

2

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10 February 2020

Jeremy B Burton

3

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10 February 2020

Kim Paes

4

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10 February 2020

Xiao Shu

5

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10 February 2020

Dorothy M French

6

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10 February 2020

Mike Costa

7

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10 February 2020

Dennis S Rice

8

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10 February 2020

language of work or name

English

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publication date

1 October 2009

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19837033 AND SRC:MED&resulttype=core&format=json

10 February 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19837033 AND SRC:MED&resulttype=core&format=json

10 February 2020

volume

139

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10 February 2020

issue

2

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10 February 2020

page(s)

299-311

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10 February 2020

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Development of the retinal vasculature

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Nrarp coordinates endothelial Notch and Wnt signaling to control vessel density in angiogenesis

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

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Knockout mouse models to study Wnt signal transduction.

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Appearance of new tetraspanin genes during vertebrate evolution.

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Sequence and expression of seven new tetraspans

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Localization of the Norrie disease gene mRNA by in situ hybridization

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Insights into Wnt binding and signalling from the structures of two Frizzled cysteine-rich domains

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

WNT7b mediates macrophage-induced programmed cell death in patterning of the vasculature

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Mutant Frizzled 4 associated with vitreoretinopathy traps wild-type Frizzled in the endoplasmic reticulum by oligomerization

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Tetraspanin functions and associated microdomains

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Wnt/beta-catenin signaling is required for CNS, but not non-CNS, angiogenesis

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Norrie Disease Protein (Norrin) Forms Disulfide-linked Oligomers Associated with the Extracellular Matrix

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Mutational analysis of Norrin-Frizzled4 recognition

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Wnt signaling: multiple pathways, multiple receptors, and multiple transcription factors

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

The Wnt signaling pathway in familial exudative vitreoretinopathy and Norrie disease

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Wnt/beta-catenin signaling controls development of the blood-brain barrier

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

A model for familial exudative vitreoretinopathy caused by LPR5 mutations

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Wnt induces LRP6 signalosomes and promotes dishevelled-dependent LRP6 phosphorylation

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Canonical Wnt signaling regulates organ-specific assembly and differentiation of CNS vasculature

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Alternative wnt signaling is initiated by distinct receptors.

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Mutations in the Norrie disease gene: a new mutation in a Japanese family

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Role of the Norrie disease pseudoglioma gene in sprouting angiogenesis during development of the retinal vasculature

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Expression of the type I diabetes-associated gene LRP5 in macrophages, vitamin A system cells, and the Islets of Langerhans suggests multiple potential roles in diabetes

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Evolution and Classification of Cystine Knot-Containing Hormones and Related Extracellular Signaling Molecules

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Wnt signals across the plasma membrane to activate the beta-catenin pathway by forming oligomers containing its receptors, Frizzled and LRP.

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Frizzled receptor dimerization is sufficient to activate the Wnt/beta-catenin pathway.

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled-4 gene

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

Vascular defects and sensorineural deafness in a mouse model of Norrie disease.

1 reference

https://api.crossref.org/works/10.1016/J.CELL.2009.07.048

7 January 2021

10.1016/J.CELL.2009.07.048

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19837033 AND SRC:MED&resulttype=core&format=json

10 February 2020

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017