Cerebral cavernous malformations: somatic mutations in vascular endothelial cells (Q33477821)

27 July 2017

title

Cerebral cavernous malformations: somatic mutations in vascular endothelial cells (English)

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27 July 2017

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Judith Gault

1

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27 July 2017

Issam A Awad

2

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27 July 2017

Peter Recksiek

3

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27 July 2017

Robert Shenkar

4

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27 July 2017

Robert Breeze

5

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27 July 2017

Michael Handler

6

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27 July 2017

Bette K Kleinschmidt-DeMasters

7

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27 July 2017

language of work or name

English

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publication date

1 July 2009

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27 July 2017

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27 July 2017

volume

65

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27 July 2017

issue

1

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27 July 2017

page(s)

138-44; discussion 144-5

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A two-hit mechanism causes cerebral cavernous malformations: complete inactivation of CCM1, CCM2 or CCM3 in affected endothelial cells

27 July 2017

cites work

1 reference

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Biallelic somatic and germline mutations in cerebral cavernous malformations (CCMs): evidence for a two-hit mechanism of CCM pathogenesis

21 June 2018

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A PP2A phosphatase high density interaction network identifies a novel striatin-interacting phosphatase and kinase complex linked to the cerebral cavernous malformation 3 (CCM3) protein

21 June 2018

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Declining cellular fitness with age promotes cancer initiation by selecting for adaptive oncogenic mutations.

21 June 2018

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KRIT-1/CCM1 is a Rap1 effector that regulates endothelial cell cell junctions

21 June 2018

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Krit 1 interactions with microtubules and membranes are regulated by Rap1 and integrin cytoplasmic domain associated protein-1

21 June 2018

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CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformations

21 June 2018

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Deletions in CCM2 are a common cause of cerebral cavernous malformations

21 June 2018

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CCM3 mutations are uncommon in cerebral cavernous malformations

21 June 2018

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Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus

21 June 2018

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A Quantitative Measurement of the Human Somatic Mutation Rate

21 June 2018

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Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations

21 June 2018

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Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations.

21 June 2018

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Pathobiology of human cerebrovascular malformations: basic mechanisms and clinical relevance

21 June 2018

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Mutations within the MGC4607 gene cause cerebral cavernous malformations

21 June 2018

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Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations

21 June 2018

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Molecular genetic investigations in the CCM1 gene in sporadic cerebral cavernomas

21 June 2018

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Mutation and expression analysis of the KRIT1 gene associated with cerebral cavernous malformations (CCM1)

21 June 2018

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KRIT1 association with the integrin-binding protein ICAP-1: a new direction in the elucidation of cerebral cavernous malformations (CCM1) pathogenesis

21 June 2018

1 reference

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Interaction between krit1 and icap1alpha infers perturbation of integrin beta1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation

21 June 2018

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PCR amplification introduces errors into mononucleotide and dinucleotide repeat sequences

21 June 2018

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Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)

21 June 2018

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TFAR19, a novel apoptosis-related gene cloned from human leukemia cell line TF-1, could enhance apoptosis of some tumor cells induced by growth factor withdrawal

21 June 2018

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

21 June 2018

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Mutation and cancer: statistical study of retinoblastoma

21 June 2018

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Krit1 modulates beta 1-integrin-mediated endothelial cell proliferation

21 June 2018

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ccm1 cell autonomously regulates endothelial cellular morphogenesis and vascular tubulogenesis in zebrafish

31 October 2018

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Proteomic identification of the cerebral cavernous malformation signaling complex

31 October 2018

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Study of cerebral cavernous malformation in Spain and Portugal: high prevalence of a 14 bp deletion in exon 5 of MGC4607 (CCM2 gene).

31 October 2018

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Large germline deletions and duplication in isolated cerebral cavernous malformation patients

31 October 2018

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Genotype-phenotype correlations in cerebral cavernous malformations patients

31 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722441

santa and valentine pattern concentric growth of cardiac myocardium in the zebrafish

31 October 2018

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Ultrastructural characteristics of hemorrhagic, nonhemorrhagic, and recurrent cavernous malformations

31 October 2018

1 reference

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Biallelic somatic and germ line CCM1 truncating mutations in a cerebral cavernous malformation lesion.

31 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722441

Multiple spinal cavernous malformations with atypical phenotype after prior irradiation: case report

31 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722441

Ccm1 is required for arterial morphogenesis: implications for the etiology of human cavernous malformations.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722441

Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans-heterozygous mutations.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722441

Ultrastructural pathological features of cerebrovascular malformations: a preliminary report.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722441

Probable clonal origin of neurofibrosarcoma in a patient with hereditary neurofibromatosis.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722441

Search for loss of heterozygosity and mutation analysis of KRIT1 gene in CCM patients

31 October 2018

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Denaturing high-performance liquid chromatography using the WAVE DNA fragment analysis system

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12 December 2020

[Variable progression of autosomal dominant polycystic kidney disease: genetic and molecular counterparts]

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12 December 2020

Gene therapy for haemophilia

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12 December 2020

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Identifiers

DOI

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27 July 2017

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27 July 2017

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