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Journal Abstract Search

154 related items for PubMed ID: 16455310

  • 1. Patterns of expression of the three cerebral cavernous malformation (CCM) genes during embryonic and postnatal brain development.
    Petit N, Blécon A, Denier C, Tournier-Lasserve E.
    Gene Expr Patterns; 2006 Jun; 6(5):495-503. PubMed ID: 16455310
    [Abstract] [Full Text] [Related]

  • 2. Recent insights into cerebral cavernous malformations: the molecular genetics of CCM.
    Riant F, Bergametti F, Ayrignac X, Boulday G, Tournier-Lasserve E.
    FEBS J; 2010 Mar; 277(5):1070-5. PubMed ID: 20096038
    [Abstract] [Full Text] [Related]

  • 3. Mutation and expression analysis of the KRIT1 gene associated with cerebral cavernous malformations (CCM1).
    Kehrer-Sawatzki H, Wilda M, Braun VM, Richter HP, Hameister H.
    Acta Neuropathol; 2002 Sep; 104(3):231-40. PubMed ID: 12172908
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  • 4. Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.
    Battistini S, Rocchi R, Cerase A, Citterio A, Tassi L, Lando G, Patrosso MC, Galli R, Brunori P, Sgrò DL, Pitillo G, Lo Russo G, Marocchi A, Penco S.
    Arch Neurol; 2007 Jun; 64(6):843-8. PubMed ID: 17562932
    [Abstract] [Full Text] [Related]

  • 5. Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus.
    Liquori CL, Berg MJ, Squitieri F, Ottenbacher M, Sorlie M, Leedom TP, Cannella M, Maglione V, Ptacek L, Johnson EW, Marchuk DA.
    Hum Mutat; 2006 Jan; 27(1):118. PubMed ID: 16329096
    [Abstract] [Full Text] [Related]

  • 6. PDCD10, the gene mutated in cerebral cavernous malformation 3, is expressed in the neurovascular unit.
    Tanriover G, Boylan AJ, Diluna ML, Pricola KL, Louvi A, Gunel M.
    Neurosurgery; 2008 Apr; 62(4):930-8; discussion 938. PubMed ID: 18496199
    [Abstract] [Full Text] [Related]

  • 7. Genomic causes of multiple cerebral cavernous malformations in a Japanese population.
    Tsutsumi S, Ogino I, Miyajima M, Ikeda T, Shindo N, Yasumoto Y, Ito M, Arai H.
    J Clin Neurosci; 2013 May; 20(5):667-9. PubMed ID: 23485406
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformations.
    Sirvente J, Enjolras O, Wassef M, Tournier-Lasserve E, Labauge P.
    J Eur Acad Dermatol Venereol; 2009 Sep; 23(9):1066-72. PubMed ID: 19453802
    [Abstract] [Full Text] [Related]

  • 10. Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations.
    Cavé-Riant F, Denier C, Labauge P, Cécillon M, Maciazek J, Joutel A, Laberge-Le Couteulx S, Tournier-Lasserve E.
    Eur J Hum Genet; 2002 Nov; 10(11):733-40. PubMed ID: 12404106
    [Abstract] [Full Text] [Related]

  • 11. A novel deletion mutation in CCM1 gene (krit1) is detected in a Chinese family with cerebral cavernous malformations.
    Ji BH, Qin W, Sun T, Feng GY, He L, Wang YJ.
    Yi Chuan Xue Bao; 2006 Feb; 33(2):105-10. PubMed ID: 16529293
    [Abstract] [Full Text] [Related]

  • 12. Clinical features of cerebral cavernous malformations patients with KRIT1 mutations.
    Denier C, Labauge P, Brunereau L, Cavé-Riant F, Marchelli F, Arnoult M, Cecillon M, Maciazek J, Joutel A, Tournier-Lasserve E, Sociéte Française de Neurochirgurgie, Sociéte de Neurochirurgie de Langue Française.
    Ann Neurol; 2004 Feb; 55(2):213-20. PubMed ID: 14755725
    [Abstract] [Full Text] [Related]

  • 13. Spectrum of genotype and clinical manifestations in cerebral cavernous malformations.
    Gault J, Sain S, Hu LJ, Awad IA.
    Neurosurgery; 2006 Dec; 59(6):1278-84; discussion 1284-5. PubMed ID: 17277691
    [Abstract] [Full Text] [Related]

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  • 15. Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult.
    Denier C, Gasc JM, Chapon F, Domenga V, Lescoat C, Joutel A, Tournier-Lasserve E.
    Mech Dev; 2002 Sep; 117(1-2):363-7. PubMed ID: 12204286
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  • 17. Identification of an Arg35X mutation in the PDCD10 gene in a patient with cerebral and multiple spinal cavernous malformations.
    Lee ST, Choi KW, Yeo HT, Kim JW, Ki CS, Cho YD.
    J Neurol Sci; 2008 Apr 15; 267(1-2):177-81. PubMed ID: 18035376
    [Abstract] [Full Text] [Related]

  • 18. Identification of a c.601C>G mutation in the CCM1 gene in a kindred with multiple skin, spinal and cerebral cavernous malformations.
    Haghighi A, Fathi D, Shahbazi M, Motahari MM, Friedman B.
    J Neurol Sci; 2013 Nov 15; 334(1-2):97-101. PubMed ID: 24007869
    [Abstract] [Full Text] [Related]

  • 19. Cerebral cavernous malformations: from CCM genes to endothelial cell homeostasis.
    Fischer A, Zalvide J, Faurobert E, Albiges-Rizo C, Tournier-Lasserve E.
    Trends Mol Med; 2013 May 15; 19(5):302-8. PubMed ID: 23506982
    [Abstract] [Full Text] [Related]

  • 20. C329X in KRIT1 is a founder mutation among CCM patients in Sardinia.
    Cau M, Loi M, Melis M, Congiu R, Loi A, Meloni C, Serrenti M, Addis M, Melis MA.
    Eur J Med Genet; 2009 May 15; 52(5):344-8. PubMed ID: 19454328
    [Abstract] [Full Text] [Related]

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