INTERACTION BETWEEN KRIT1 AND MALCAVERNIN
- 1 February 2007
- journal article
- research article
- Published by Wolters Kluwer Health in Neurosurgery
- Vol. 60 (2) , 353-359
- https://doi.org/10.1227/01.neu.0000249268.11074.83
Abstract
OBJECTIVE. Cerebral cavernous malformations (CCM) are a relatively common autosomal dominant disorder leading to the formation of vascular malformationKeywords
This publication has 14 references indexed in Scilit:
- Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous MalformationsAmerican Journal of Human Genetics, 2003
- Cerebral cavernous malformationsNeurology, 2002
- Ultrastructural and immunocytochemical evidence that an incompetent blood-brain barrier is related to the pathophysiology of cavernous malformationsJournal of Neurology, Neurosurgery & Psychiatry, 2001
- KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformationHuman Molecular Genetics, 2000
- Mutations in the Gene Encoding KRIT1, a Krev-1/rap1a Binding Protein, Cause Cerebral Cavernous Malformations (CCM1)Human Molecular Genetics, 1999
- Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasNature Genetics, 1999
- Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27Human Molecular Genetics, 1998
- ICAP-1, a Novel β1 Integrin Cytoplasmic Domain–associated Protein, Binds to a Conserved and Functionally Important NPXY Sequence Motif of β1 IntegrinThe Journal of cell biology, 1997
- An analysis of the natural history of cavernous angiomasJournal of Neurosurgery, 1991
- Cerebral Cavernous MalformationsNew England Journal of Medicine, 1988