RASA1 mutations may cause hereditary capillary malformations without arteriovenous malformations. (Q54540655)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18363760%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

RASA1 mutations may cause hereditary capillary malformations without arteriovenous malformations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18363760%20AND%20SRC:MED&resulttype=core&format=json

arteriovenous malformation

4 January 2020

main subject

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18363760%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

author name string

D Bercovich

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18363760%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

E Sprecher

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18363760%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

M Lapidot

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18363760%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

language of work or name

English

0 references

publication date

20 March 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18363760%20AND%20SRC:MED&resulttype=core&format=json

British Journal of Dermatology

4 January 2020

published in

1 reference

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4 January 2020

volume

158

1 reference

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4 January 2020

page(s)

1035-1040

1 reference

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4 January 2020

issue

5

1 reference

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Vascular malformations: Part I.

4 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2008.08493.X

Vascular malformations: localized defects in vascular morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2008.08493.X

Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2008.08493.X

Vascular system defects and neuronal apoptosis in mice lacking ras GTPase-activating protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2008.08493.X

Role of p120 Ras-GAP in directed cell movement

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2008.08493.X

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2008.08493.X

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2008.08493.X

Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2008.08493.X

Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas")

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2008.08493.X