Memo has a novel role in S1P signaling and is [corrected] crucial for vascular development (Q30413877)

22 August 2017

Memo has a novel role in S1P signaling and is [corrected] crucial for vascular development (English)

1 reference

22 August 2017

10

Sarah Spiegel

1 reference

22 August 2017

Shunya Kondo

1

1 reference

22 August 2017

Alessia Bottos

2

1 reference

22 August 2017

Jeremy C Allegood

3

1 reference

22 August 2017

Regis Masson

4

1 reference

22 August 2017

Francisca G Maurer

5

1 reference

22 August 2017

Christel Genoud

6

1 reference

22 August 2017

Patrick Kaeser

7

1 reference

22 August 2017

Andrea Huwiler

8

1 reference

22 August 2017

Masato Murakami

9

1 reference

22 August 2017

Nancy E Hynes

11

1 reference

22 August 2017

language of work or name

English

0 references

publication date

8 April 2014

1 reference

22 August 2017

1 reference

22 August 2017

9

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22 August 2017

4

1 reference

22 August 2017

e94114

1 reference

Creative Commons Attribution 4.0 International

22 August 2017

start time

8 April 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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The sphingosine-1-phosphate receptors S1P1, S1P2, and S1P3 function coordinately during embryonic angiogenesis

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The mTOR inhibitor RAD001 sensitizes tumor cells to DNA-damaged induced apoptosis through inhibition of p21 translation.

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G-protein-coupled receptor S1P1 acts within endothelial cells to regulate vascular maturation.

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Sphingosine 1-phosphate (S1P) receptor subtypes S1P1 and S1P3, respectively, regulate lymphocyte recirculation and heart rate

21 January 2018

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Promotion of lymphocyte egress into blood and lymph by distinct sources of sphingosine-1-phosphate

21 January 2018

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Loss of Memo, a novel FGFR regulator, results in reduced lifespan

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10.1371/JOURNAL.PONE.0094114

26 November 2018

Identifiers

DOI

1 reference

22 August 2017

0 references

1 reference

22 August 2017

PubMed publication ID

24714781

1 reference