KRIT1 gene

Known as: KRIT1, ankyrin repeat containing, KRIT1, CAM 
This gene plays a role in signal transduction and is involved in vascular morphogenesis.
National Institutes of Health

Papers overview

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Highly Cited
2005
Highly Cited
2005
Cerebral cavernous malformations (CCMs) are hamartomatous vascular malformations characterized by abnormally enlarged capillary… (More)
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Highly Cited
2004
Highly Cited
2004
Cerebral cavernous malformations (CCM) are hamartomatous vascular malformations characterized by abnormally enlarged capillary… (More)
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Highly Cited
2003
Highly Cited
2003
Cerebral cavernous malformations (CCMs) are congenital vascular anomalies of the central nervous system that can result in… (More)
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Highly Cited
2002
Highly Cited
2002
Mutations in KRIT1, a protein initially identified based on a yeast two-hybrid interaction with the RAS-family GTPase RAP1A, are… (More)
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Highly Cited
2002
Highly Cited
2002
Mutations in Krev1 interaction trapped gene 1 (KRIT1) cause cerebral cavernous malformation, an autosomal dominant disease… (More)
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Review
2002
Review
2002
OBJECTIVE To find mutations in the recently identified additional exons of the Krit1 gene that causes CCM1, a disease… (More)
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Highly Cited
2001
Highly Cited
2001
Cerebral cavernous malformation (CCM) is a common autosomal dominant disorder characterized by venous sinusoids that predispose… (More)
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Highly Cited
1999
Highly Cited
1999
Cavernous angiomas are vascular malformations mostly located in the central nervous system and characterized by enlarged… (More)
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Highly Cited
1999
Highly Cited
1999
Cerebral cavernous malformations (CCM) are congenital vascular anomalies of the brain that can cause significant neurological… (More)
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Highly Cited
1997
Highly Cited
1997
Krev-1/rap1A is an evolutionarily conserved Ras-family GTPase whose cellular function remains unclear, but which has been… (More)
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