Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management. - Wikidata - awgldk - TriplyDB

Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management.

Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management.

http://www.wikidata.org/entity/Q38003193

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Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations Cutaneous venous malformations related to KRIT1 mutation: case report and literature review.Signaling pathways and the cerebral cavernous malformations proteins: lessons from structural biology.Cerebral cavernous malformations in the setting of focal epilepsies: pathological findings, clinical characteristics, and surgical treatment principles.KRIT1 loss of function causes a ROS-dependent upregulation of c-Jun Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas.A Novel KRIT1/CCM1 Gene Insertion Mutation Associated with Cerebral Cavernous Malformations in a Chinese Family.The anatomical location and laterality of orbital cavernous haemangiomas.Up-regulation of c-Fos associated with neuronal apoptosis following intracerebral hemorrhage.

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Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management.

http://www.wikidata.org/entity/Q38003193

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J.1399-0004.2012.01892.X

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Clinical Genetics

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Genetic and cellular basis of ...... tions for clinical management.

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A La Camera

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G Tredici

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L Goitre

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M C Patrosso

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P2860

KRIT1 regulates the homeostasis of intracellular reactive oxygen species

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

Mutations within the MGC4607 gene cause cerebral cavernous malformations

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

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

CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformations

Cerebral cavernous malformation protein CCM1 inhibits sprouting angiogenesis by activating DELTA-NOTCH signaling.

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

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

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

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10.1111/J.1399-0004.2012.01892.X

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1

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Saverio Francesco Retta

Alberto Citterio

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