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Journal Abstract Search

407 related items for PubMed ID: 28745674

  • 1. [Gene mutations in patients with hereditary cavernous malformations].
    Belousova OB, Bulygina ES, Okishev DN, Prohorchuk EB, Tsygankova SV, Pronin IN, Shishkina LV, Ryzhova MV, Skryabin KG, Konovalov AN.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2017; 117(6):66-72. PubMed ID: 28745674
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  • 8. Differential angiogenesis function of CCM2 and CCM3 in cerebral cavernous malformations.
    Zhu Y, Wu Q, Xu JF, Miller D, Sandalcioglu IE, Zhang JM, Sure U.
    Neurosurg Focus; 2010 Sep; 29(3):E1. PubMed ID: 20809750
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  • 10. Genetic Screening of Pediatric Cavernous Malformations.
    Merello E, Pavanello M, Consales A, Mascelli S, Raso A, Accogli A, Cama A, Valeria C, De Marco P.
    J Mol Neurosci; 2016 Oct; 60(2):232-8. PubMed ID: 27561926
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  • 11. DNA promoter methylation of CCM genes in human cerebral cavernous malformations: Importance of confirming MSP data through sequencing.
    Saban D, Larisch J, Nickel AC, Pierscianek D, Dammann P, Sure U, Zhu Y.
    Eur J Med Genet; 2020 Dec; 63(12):104090. PubMed ID: 33122157
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  • 12. Mutation analysis of CCM1, CCM2 and CCM3 genes in a cohort of Italian patients with cerebral cavernous malformation.
    D'Angelo R, Marini V, Rinaldi C, Origone P, Dorcaratto A, Avolio M, Goitre L, Forni M, Capra V, Alafaci C, Mareni C, Garrè C, Bramanti P, Sidoti A, Retta SF, Amato A.
    Brain Pathol; 2011 Mar; 21(2):215-24. PubMed ID: 21029238
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  • 14. 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.
    Stahl S, Gaetzner S, Voss K, Brackertz B, Schleider E, Sürücü O, Kunze E, Netzer C, Korenke C, Finckh U, Habek M, Poljakovic Z, Elbracht M, Rudnik-Schöneborn S, Bertalanffy H, Sure U, Felbor U.
    Hum Mutat; 2008 May; 29(5):709-17. PubMed ID: 18300272
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