Results 151 to 160 of about 2,293 (187)

Unilateral Dermatomal Cavernous Hemangiomatosis Responding to Dabigatran. [PDF]

open access: yesIndian Dermatol Online J
Baskaran N, Singh S, Bishnoi A, Vinay K.
europepmc   +1 more source

Recurrent somatic copy number alterations in resected cerebral cavernous malformations. [PDF]

open access: yesHum Genomics
Ressler AK   +11 more
europepmc   +1 more source

Headache in Cerebral Cavernous Malformations: Clinical, Genetic, and Neuroimaging Associations. [PDF]

open access: yesJ Clin Med
Shiran T   +7 more
europepmc   +1 more source

Expression of CCM2 and CCM3 During Mouse Gonadogenesis [PDF]

open access: yesJournal of Assisted Reproduction and Genetics, 2015
WOS: 000363272800010PubMed ID: 26386873Three cerebral cavernous malformation (CCM) proteins, CCM1, CCM2, and CCM3, regulate cell-cell adhesion, cell shape and polarity, and most likely cell adhesion to extracellular matrix.
Aylin Yaba   +2 more
exaly   +6 more sources

Novel CCM1, CCM2, and CCM3 Mutations in Patients With Cerebral Cavernous Malformations: In-Frame Deletion in CCM2 Prevents Formation of a CCM1/CCM2/CCM3 Protein Complex

open access: yesHuman Mutation, 2008
Cerebral cavernous malformations (CCM) are prevalent cerebrovascular lesions predisposing to chronic headaches, epilepsy, and hemorrhagic stroke. Using a combination of direct sequencing and MLPA analyses, we identified 15 novel and eight previously ...
Mario Habek   +2 more
exaly   +5 more sources

A Japanese Case of Successful Surgical Resection of Cerebral Cavernous Malformations With a CCM2 Mutation [PDF]

open access: yesNeurology and Clinical Neuroscience, 2022
Cerebral cavernous malformations (CCMs) are congenital abnormalities of cerebral vessels. Surgical resection is rarely considered for the control of epilepsy in a first seizure patient with vascular malformation.
Mami Takemoto   +2 more
exaly   +2 more sources

CCM3 Interacts With CCM2 Indicating Common Pathogenesis for Cerebral Cavernous Malformations

Neurogenetics, 2007
Individuals carrying a mutation in one of the three cerebral cavernous malformation genes (CCM1/KRIT1, CCM2, CCM3) cannot be clinically distinguished, raising the possibility that they act within common molecular pathways. In this study, we demonstrate that CCM3 (PDCD10) coprecipitates and colocalizes with CCM2. We also show that CCM3 directly binds to
Ute Felbor, Elisa Schleider, Sonja Stahl
exaly   +3 more sources

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