277 related articles for article (PubMed ID: 15046662)
1. KRIT1/cerebral cavernous malformation 1 protein localizes to vascular endothelium, astrocytes, and pyramidal cells of the adult human cerebral cortex.
Guzeloglu-Kayisli O; Amankulor NM; Voorhees J; Luleci G; Lifton RP; Gunel M
Neurosurgery; 2004 Apr; 54(4):943-9; discussion 949. PubMed ID: 15046662
[TBL] [Abstract][Full Text] [Related]
2. Interaction between krit1 and icap1alpha infers perturbation of integrin beta1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation.
Zhang J; Clatterbuck RE; Rigamonti D; Chang DD; Dietz HC
Hum Mol Genet; 2001 Dec; 10(25):2953-60. PubMed ID: 11741838
[TBL] [Abstract][Full Text] [Related]
3. Vertebral hemangiomas associated with familial cerebral cavernous malformation: segmental disease expression. Case report.
Clatterbuck RE; Cohen B; Gailloud P; Murphy K; Rigamonti D
J Neurosurg; 2002 Sep; 97(2 Suppl):227-30. PubMed ID: 12296684
[TBL] [Abstract][Full Text] [Related]
4. Novel KRIT1/CCM1 mutation in a patient with retinal cavernous hemangioma and cerebral cavernous malformation.
Reddy S; Gorin MB; McCannel TA; Tsui I; Straatsma BR
Graefes Arch Clin Exp Ophthalmol; 2010 Sep; 248(9):1359-61. PubMed ID: 20306072
[TBL] [Abstract][Full Text] [Related]
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; 99(16):10677-82. PubMed ID: 12140362
[TBL] [Abstract][Full Text] [Related]
6. Mutations in KRIT1 in familial cerebral cavernous malformations.
Zhang J; Clatterbuck RE; Rigamonti D; Dietz HC
Neurosurgery; 2000 May; 46(5):1272-7; discussion 1277-9. PubMed ID: 10807272
[TBL] [Abstract][Full Text] [Related]
7. 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
[TBL] [Abstract][Full Text] [Related]
8. A splice-site mutation in CCM1/KRIT1 is associated with retinal and cerebral cavernous hemangioma.
Kitzmann AS; Pulido JS; Ferber MJ; Highsmith WE; Babovic-Vuksanovic D
Ophthalmic Genet; 2006 Dec; 27(4):157-9. PubMed ID: 17148043
[TBL] [Abstract][Full Text] [Related]
9. Identification of a novel KRIT1 mutation in an Italian family with cerebral cavernous malformation by the protein truncation test.
Marini V; Ferrera L; Dorcaratto A; Viale G; Origone P; Mareni C; Garrè C
J Neurol Sci; 2003 Aug; 212(1-2):75-8. PubMed ID: 12810002
[TBL] [Abstract][Full Text] [Related]
10. Increased number of white matter lesions in patients with familial cerebral cavernous malformations.
Golden MJ; Morrison LA; Kim H; Hart BL
AJNR Am J Neuroradiol; 2015 May; 36(5):899-903. PubMed ID: 25556204
[TBL] [Abstract][Full Text] [Related]
11. A Novel CCM1/KRIT1 Heterozygous Nonsense Mutation (c.1864C>T) Associated with Familial Cerebral Cavernous Malformation: a Genetic Insight from an 8-Year Continuous Observational Study.
Yang C; Nicholas VH; Zhao J; Wu B; Zhong H; Li Y; Xu Y
J Mol Neurosci; 2017 Apr; 61(4):511-523. PubMed ID: 28255959
[TBL] [Abstract][Full Text] [Related]
12. Structural basis for the disruption of the cerebral cavernous malformations 2 (CCM2) interaction with Krev interaction trapped 1 (KRIT1) by disease-associated mutations.
Fisher OS; Liu W; Zhang R; Stiegler AL; Ghedia S; Weber JL; Boggon TJ
J Biol Chem; 2015 Jan; 290(5):2842-53. PubMed ID: 25525273
[TBL] [Abstract][Full Text] [Related]
13. CCM2 expression parallels that of CCM1.
Seker A; Pricola KL; Guclu B; Ozturk AK; Louvi A; Gunel M
Stroke; 2006 Feb; 37(2):518-23. PubMed ID: 16373645
[TBL] [Abstract][Full Text] [Related]
14. Large Cystic Cavernous Malformation in Infant with Novel KRIT1 Gene Abnormality.
Lu VM; Daniels DJ
World Neurosurg; 2019 Oct; 130():304-305. PubMed ID: 31326642
[TBL] [Abstract][Full Text] [Related]
15. A Novel KRIT1/CCM1 Gene Insertion Mutation Associated with Cerebral Cavernous Malformations in a Chinese Family.
Wang H; Pan Y; Zhang Z; Li X; Xu Z; Suo Y; Li W; Wang Y
J Mol Neurosci; 2017 Feb; 61(2):221-226. PubMed ID: 28160210
[TBL] [Abstract][Full Text] [Related]
16. Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1.
Choquet H; Trapani E; Goitre L; Trabalzini L; Akers A; Fontanella M; Hart BL; Morrison LA; Pawlikowska L; Kim H; Retta SF
Free Radic Biol Med; 2016 Mar; 92():100-109. PubMed ID: 26795600
[TBL] [Abstract][Full Text] [Related]
17. Identification of Krit1B: a novel alternative splicing isoform of cerebral cavernous malformation gene-1.
Retta SF; Avolio M; Francalanci F; Procida S; Balzac F; Degani S; Tarone G; Silengo L
Gene; 2004 Jan; 325():63-78. PubMed ID: 14697511
[TBL] [Abstract][Full Text] [Related]
18. Cerebral cavernous malformations: mutations in Krit1.
Verlaan DJ; Davenport WJ; Stefan H; Sure U; Siegel AM; Rouleau GA
Neurology; 2002 Mar; 58(6):853-7. PubMed ID: 11914398
[TBL] [Abstract][Full Text] [Related]
19. Cutaneous venous malformations related to KRIT1 mutation: case report and literature review.
Grippaudo FR; Piane M; Amoroso M; Longo B; Penco S; Chessa L; Giubettini M; Santanelli F
J Mol Neurosci; 2013 Oct; 51(2):442-5. PubMed ID: 23828392
[TBL] [Abstract][Full Text] [Related]
20. Frequency of retinal cavernomas in 60 patients with familial cerebral cavernomas: a clinical and genetic study.
Labauge P; Krivosic V; Denier C; Tournier-Lasserve E; Gaudric A
Arch Ophthalmol; 2006 Jun; 124(6):885-6. PubMed ID: 16769843
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
