Neuronal expression of the Ccm2 gene in a new mouse model of cerebral cavernous malformations. (Q48657154)

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16 January 2020

title

Neuronal expression of the Ccm2 gene in a new mouse model of cerebral cavernous malformations (English)

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16 January 2020

1

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16 January 2020

Sudha Srinivasan

3

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16 January 2020

author name string

Teresa L Squire

2

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16 January 2020

Elizabeth Huang

4

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16 January 2020

Jon S Zawistowski

5

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16 January 2020

Hiroaki Matsunami

6

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16 January 2020

Laura P Hale

7

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16 January 2020

Douglas A Marchuk

8

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16 January 2020

publication date

7 February 2006

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16 January 2020

number of pages

10

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inferred from page(s)

published in

Mammalian Genome

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16 January 2020

volume

17

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16 January 2020

issue

2

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16 January 2020

page(s)

119-128

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

16 January 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-005-0098-8

KRIT1/cerebral cavernous malformation 1 protein localizes to vascular endothelium, astrocytes, and pyramidal cells of the adult human cerebral cortex

21 January 2018

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12 December 2020

Mutations within the MGC4607 gene cause cerebral cavernous malformations

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12 December 2020

Wiring the vascular circuitry: from growth factors to guidance cues

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12 December 2020

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

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12 December 2020

Applications of magnetic resonance microscopy.

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12 December 2020

Rac-MEKK3-MKK3 scaffolding for p38 MAPK activation during hyperosmotic shock.

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Krev1 interaction trapped-1/cerebral cavernous malformation-1 protein expression during early angiogenesis.

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12 December 2020

Ultrastructural pathological features of cerebrovascular malformations: a preliminary report.

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12 December 2020

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

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12 December 2020

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

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12 December 2020

The natural history of cavernous malformations.

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12 December 2020

Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult

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12 December 2020

A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

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12 December 2020

Common cues in vascular and axon guidance

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12 December 2020

Astrocyte-endothelial interactions and blood-brain barrier permeability

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Pathology of cerebral vascular malformations

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12 December 2020

Selective ablation of v integrins in the central nervous system leads to cerebral hemorrhage, seizures, axonal degeneration and premature death

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12 December 2020

Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas

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12 December 2020

Genetics of cerebral cavernous malformations

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12 December 2020

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

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12 December 2020

Ultrastructural and immunocytochemical evidence that an incompetent blood-brain barrier is related to the pathophysiology of cavernous malformations

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12 December 2020

KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

GFAP promoter directs astrocyte-specific expression in transgenic mice

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12 December 2020

Magnetic resonance imaging at microscopic resolution reveals subtle morphological changes in a mouse model of dopaminergic hyperfunction.

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12 December 2020

CCM1 and CCM2 protein interactions in cell signaling: implications for cerebral cavernous malformations pathogenesis

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12 December 2020

Magnetic resonance histology for morphologic phenotyping.

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12 December 2020

Bodenin: a novel murine gene expressed in restricted areas of the brain

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12 December 2020