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Items: 1 to 20 of 24

1.

Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.

Dupré N, Verlaan DJ, Hand CK, Laurent SB, Turecki G, Davenport WJ, Acciarri N, Dichgans J, Ohkuma A, Siegel AM, Rouleau GA.

Can J Neurol Sci. 2003 May;30(2):122-8.

PMID:
12774951
2.

Vascular morphogenesis: tales of two syndromes.

Marchuk DA, Srinivasan S, Squire TL, Zawistowski JS.

Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R97-112. Review.

3.

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.

4.

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. Epub 2002 Jun 26.

PMID:
12172908
5.

KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein.

Gunel M, Laurans MS, Shin D, DiLuna ML, Voorhees J, Choate K, Nelson-Williams C, Lifton RP.

Proc Natl Acad Sci U S A. 2002 Aug 6;99(16):10677-82. Epub 2002 Jul 24.

6.

KRIT1 association with the integrin-binding protein ICAP-1: a new direction in the elucidation of cerebral cavernous malformations (CCM1) pathogenesis.

Zawistowski JS, Serebriiskii IG, Lee MF, Golemis EA, Marchuk DA.

Hum Mol Genet. 2002 Feb 15;11(4):389-96.

7.
8.

Cavernous angiomas of the nervous system in Italy: clinical and genetic study.

Squitieri F, Maglione V, Buzzi MG, Nargi E, Novelletto A, Cannella M, Simonelli M, Colonnese C, Simonelli P, Innocenzi G, Gagliardi FM, Caruso R, Ragona G, Cantore GP.

Neurol Sci. 2000 Jun;21(3):129-34.

PMID:
11076000
9.

Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1).

Sahoo T, Johnson EW, Thomas JW, Kuehl PM, Jones TL, Dokken CG, Touchman JW, Gallione CJ, Lee-Lin SQ, Kosofsky B, Kurth JH, Louis DN, Mettler G, Morrison L, Gil-Nagel A, Rich SS, Zabramski JM, Boguski MS, Green ED, Marchuk DA.

Hum Mol Genet. 1999 Nov;8(12):2325-33.

10.

Pathology of cerebral vascular malformations.

Zabramski JM, Henn JS, Coons S.

Neurosurg Clin N Am. 1999 Jul;10(3):395-410. Review.

PMID:
10419567
11.

Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families.

Laberge S, Labauge P, Maréchal E, Maciazek J, Tournier-Lasserve E.

Eur J Hum Genet. 1999 May-Jun;7(4):499-504.

12.

Interaction of the integrin beta1 cytoplasmic domain with ICAP-1 protein.

Zhang XA, Hemler ME.

J Biol Chem. 1999 Jan 1;274(1):11-9.

13.

Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.

Craig HD, Günel M, Cepeda O, Johnson EW, Ptacek L, Steinberg GK, Ogilvy CS, Berg MJ, Crawford SC, Scott RM, Steichen-Gersdorf E, Sabroe R, Kennedy CT, Mettler G, Beis MJ, Fryer A, Awad IA, Lifton RP.

Hum Mol Genet. 1998 Nov;7(12):1851-8.

14.

Bodenin: a novel murine gene expressed in restricted areas of the brain.

Faisst AM, Gruss P.

Dev Dyn. 1998 Jun;212(2):293-303.

15.

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

Serebriiskii I, Estojak J, Sonoda G, Testa JR, Golemis EA.

Oncogene. 1997 Aug 28;15(9):1043-9.

17.

A locus for cerebral cavernous malformations maps to chromosome 7q in two families.

Marchuk DA, Gallione CJ, Morrison LA, Clericuzio CL, Hart BL, Kosofsky BE, Louis DN, Gusella JF, Davis LE, Prenger VL.

Genomics. 1995 Jul 20;28(2):311-4.

PMID:
8530042
18.

The natural history of familial cavernous malformations: results of an ongoing study.

Zabramski JM, Wascher TM, Spetzler RF, Johnson B, Golfinos J, Drayer BP, Brown B, Rigamonti D, Brown G.

J Neurosurg. 1994 Mar;80(3):422-32.

PMID:
8113854
19.

Angiographically occult vascular malformations: a correlative study of features on magnetic resonance imaging and histological examination.

Tomlinson FH, Houser OW, Scheithauer BW, Sundt TM Jr, Okazaki H, Parisi JE.

Neurosurgery. 1994 May;34(5):792-9; discussion 799-800.

PMID:
8052376
20.

A gene responsible for cavernous malformations of the brain maps to chromosome 7q.

Dubovsky J, Zabramski JM, Kurth J, Spetzler RF, Rich SS, Orr HT, Weber JL.

Hum Mol Genet. 1995 Mar;4(3):453-8.

PMID:
7795602
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