(Q28145448)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508515%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

title

Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas (English)

1 reference

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31 October 2019

1

1 reference

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31 October 2019

author name string

Jung HH

2

1 reference

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31 October 2019

Labauge P

3

1 reference

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31 October 2019

Houtteville JP

4

1 reference

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31 October 2019

Lescoat C

5

1 reference

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31 October 2019

Cecillon M

6

1 reference

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31 October 2019

Marechal E

7

1 reference

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31 October 2019

Joutel A

8

1 reference

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31 October 2019

Bach JF

9

1 reference

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31 October 2019

Tournier-Lasserve E

10

1 reference

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31 October 2019

language of work or name

English

0 references

publication date

1 October 1999

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31 October 2019

1 reference

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31 October 2019

volume

23

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31 October 2019

page(s)

189-193

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31 October 2019

issue

2

1 reference

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Cerebral cavernous malformations. Incidence and familial occurrence

31 October 2019

cites work

1 reference

7 January 2021

A gene responsible for cavernous malformations of the brain maps to chromosome 7q

1 reference

7 January 2021

Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.

1 reference

7 January 2021

A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans

1 reference

7 January 2021

Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig

1 reference

7 January 2021

Association of Krev-1/rap1a with Krit1, a novel ankyrin repeat-containing protein encoded by a gene mapping to 7q21-22

1 reference

7 January 2021

All in the family? New insights and questions regarding interconnectivity of Ras, Rap1 and Ral.

1 reference

7 January 2021

Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de Neurochirurgie.

1 reference

7 January 2021

Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families.

1 reference

7 January 2021

1 reference

7 January 2021

1 reference

7 January 2021

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

1 reference

7 January 2021

Endothelial apoptosis in Braf-deficient mice

1 reference

7 January 2021

The Rap1 GTPase functions as a regulator of morphogenesis in vivo

1 reference

7 January 2021

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

7 January 2021

A tool for analyzing and annotating genomic sequences

1 reference

7 January 2021

Identifiers

DOI

10.1038/13815

2 references

Consolidated OpenCitations Corpus – April 2017

1664808

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508515%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1664808

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

1664808