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    Results: 1 to 20 of 42

    1.

    Identification of the Kelch family protein Nd1-L as a novel molecular interactor of KRIT1.

    Guazzi P, Goitre L, Ferro E, Cutano V, Martino C, Trabalzini L, Retta SF.

    PLoS One. 2012;7(9):e44705. doi: 10.1371/journal.pone.0044705. Epub 2012 Sep 6.

    PMID:
    22970292
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    The importance of susceptibility-weighted imaging in familial cerebral cavernous malformation.

    Bulakci M, Kalelioglu T, Kiris A.

    Arch Neurol. 2012 Oct;69(10):1376-7. No abstract available.

    PMID:
    22825481
    [PubMed - indexed for MEDLINE]
    3.

    STK25 protein mediates TrkA and CCM2 protein-dependent death in pediatric tumor cells of neural origin.

    Costa B, Kean MJ, Ast V, Knight JD, Mett A, Levy Z, Ceccarelli DF, Badillo BG, Eils R, König R, Gingras AC, Fainzilber M.

    J Biol Chem. 2012 Aug 24;287(35):29285-9. doi: 10.1074/jbc.C112.345397. Epub 2012 Jul 10.

    PMID:
    22782892
    [PubMed - indexed for MEDLINE]
    4.

    Familial cerebral cavernous malformation.

    Dziedzic T, Kunert P, Matyja E, Ziora-Jakutowicz K, Sidoti A, Marchel A.

    Folia Neuropathol. 2012;50(2):152-8.

    PMID:
    22773461
    [PubMed - indexed for MEDLINE]
    5.

    Crystallization and preliminary crystallographic studies of CCM3 in complex with the C-terminal domain of MST4.

    Xu X, Wang X, Ding J, Wang DC.

    Acta Crystallogr Sect F Struct Biol Cryst Commun. 2012 Jul 1;68(Pt 7):760-3. doi: 10.1107/S1744309112016843. Epub 2012 Jun 27.

    PMID:
    22750858
    [PubMed - indexed for MEDLINE]
    6.

    Crystallization and preliminary X-ray analysis of the C-terminal domain of CCM2, part of a novel adaptor protein involved in cerebral cavernous malformations.

    Wang X, Ding J, Wang D.

    Acta Crystallogr Sect F Struct Biol Cryst Commun. 2012 Jun 1;68(Pt 6):683-6. doi: 10.1107/S1744309112016181. Epub 2012 May 23.

    PMID:
    22684070
    [PubMed - indexed for MEDLINE]
    7.

    PDCD10 interacts with STK25 to accelerate cell apoptosis under oxidative stress.

    Zhang H, Ma X, Deng X, Chen Y, Mo X, Zhang Y, Zhao H, Ma D.

    Front Biosci. 2012 Jun 1;17:2295-305.

    PMID:
    22652780
    [PubMed - indexed for MEDLINE]
    8.

    An analysis of flow dynamics in cerebral cavernous malformation and orbital cavernous angioma using indocyanine green videoangiography.

    Murakami K, Endo T, Tominaga T.

    Acta Neurochir (Wien). 2012 Jul;154(7):1169-75. doi: 10.1007/s00701-012-1354-9. Epub 2012 May 3.

    PMID:
    22552434
    [PubMed - indexed for MEDLINE]
    9.

    CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: a case-control study.

    D'Angelo R, Scimone C, Rinaldi C, Trimarchi G, Italiano D, Bramanti P, Amato A, Sidoti A.

    Int J Mol Med. 2012 Jun;29(6):1113-20. doi: 10.3892/ijmm.2012.927. Epub 2012 Feb 28.

    PMID:
    22378217
    [PubMed - indexed for MEDLINE]
    10.

    Spontaneous resolution of a Chiari malformation Type I and syrinx after supratentorial craniotomy for excision of a cavernous malformation.

    Miele WR, Schirmer CM, Yao KC, Heilman CB.

    J Neurosurg. 2012 May;116(5):1054-9. doi: 10.3171/2012.1.JNS11580. Epub 2012 Feb 10.

    PMID:
    22324421
    [PubMed - indexed for MEDLINE]
    11.

    Adaptor protein cerebral cavernous malformation 3 (CCM3) mediates phosphorylation of the cytoskeletal proteins ezrin/radixin/moesin by mammalian Ste20-4 to protect cells from oxidative stress.

    Fidalgo M, Guerrero A, Fraile M, Iglesias C, Pombo CM, Zalvide J.

    J Biol Chem. 2012 Mar 30;287(14):11556-65. doi: 10.1074/jbc.M111.320259. Epub 2012 Jan 30.

    PMID:
    22291017
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    12.

    Angioleiomyomas of the dura: rare entities that lack KRIT1 mutations.

    Conner TM, Waziri A, Kleinschmidt-Demasters BK.

    Am J Surg Pathol. 2012 Apr;36(4):526-33. doi: 10.1097/PAS.0b013e31823def98.

    PMID:
    22261708
    [PubMed - indexed for MEDLINE]
    13.

    Treatment of pediatric patients with cerebral cavernous malformation.

    Alexiou GA, Prodromou N, Moschovi M.

    J Clin Neurosci. 2012 Feb;19(2):339. doi: 10.1016/j.jocn.2011.10.002. Epub 2011 Dec 29. No abstract available.

    PMID:
    22209396
    [PubMed - indexed for MEDLINE]
    14.

    Protein phosphatase 2a (PP2A) binds within the oligomerization domain of striatin and regulates the phosphorylation and activation of the mammalian Ste20-Like kinase Mst3.

    Gordon J, Hwang J, Carrier KJ, Jones CA, Kern QL, Moreno CS, Karas RH, Pallas DC.

    BMC Biochem. 2011 Oct 10;12:54. doi: 10.1186/1471-2091-12-54.

    PMID:
    21985334
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    15.

    Clinical features and microsurgical treatment of pediatric patients with cerebral cavernous malformation.

    Song J, Qiao N, Xie L, Qiu T, Li P, Wu J, Zhu W, Chen L, He KM, Zhang N, Mao Y, Zhao Y.

    J Clin Neurosci. 2011 Oct;18(10):1303-7. doi: 10.1016/j.jocn.2011.01.033. Epub 2011 Jul 26.

    PMID:
    21795052
    [PubMed - indexed for MEDLINE]
    16.

    Molecular recognition of leucine-aspartate repeat (LD) motifs by the focal adhesion targeting homology domain of cerebral cavernous malformation 3 (CCM3).

    Li X, Ji W, Zhang R, Folta-Stogniew E, Min W, Boggon TJ.

    J Biol Chem. 2011 Jul 22;286(29):26138-47. doi: 10.1074/jbc.M110.211250. Epub 2011 Jun 1.

    PMID:
    21632544
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    17.

    CCM2 expression during prenatal development and adult human neocortex.

    Tanriover G, Sozen B, Gunel M, Demir N.

    Int J Dev Neurosci. 2011 Aug;29(5):509-14. doi: 10.1016/j.ijdevneu.2011.04.006. Epub 2011 May 4.

    PMID:
    21569831
    [PubMed - indexed for MEDLINE]
    18.

    A founder mutation in the Ashkenazi Jewish population affecting messenger RNA splicing of the CCM2 gene causes cerebral cavernous malformations.

    Gallione CJ, Solatycki A, Awad IA, Weber JL, Marchuk DA.

    Genet Med. 2011 Jul;13(7):662-6. doi: 10.1097/GIM.0b013e318211ff8b.

    PMID:
    21543988
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    19.

    Mutations in 2 distinct genetic pathways result in cerebral cavernous malformations in mice.

    Chan AC, Drakos SG, Ruiz OE, Smith AC, Gibson CC, Ling J, Passi SF, Stratman AN, Sacharidou A, Revelo MP, Grossmann AH, Diakos NA, Davis GE, Metzstein MM, Whitehead KJ, Li DY.

    J Clin Invest. 2011 May;121(5):1871-81. doi: 10.1172/JCI44393. Epub 2011 Apr 1. Erratum in: J Clin Invest. 2012 May 1;122(5):1948.

    PMID:
    21490399
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    20.

    In vitro characterization of the angiogenic phenotype and genotype of the endothelia derived from sporadic cerebral cavernous malformations.

    Zhu Y, Wu Q, Fass M, Xu JF, You C, Müller O, Sandalcioglu IE, Zhang JM, Sure U.

    Neurosurgery. 2011 Sep;69(3):722-31; discussion 731-2. doi: 10.1227/NEU.0b013e318219569f.

    PMID:
    21471841
    [PubMed - indexed for MEDLINE]

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