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Cerebral Cavernous Malformations Protein
Known as:
Krev Interaction Trapped 1
, Cerebral Cavernous Malformations 1
, Ankyrin Repeat-Containing Protein KRIT1
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Ankyrin Repeat-Containing Protein KRIT1, encoded by the CCM1 gene, interacts with ICAP-1 and may be involved in bidirectional signaling between…
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National Institutes of Health
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Related topics
Related topics
15 relations
Angiogenic Process
Ankyrin Repeat
Binding Proteins
Brain
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformations
F. Riant
,
S. Odent
,
+4 authors
Elizabeth Tournier-Lasserve
Clinical Genetics
2014
Corpus ID: 30326150
Loss‐of‐function mutations in CCM1/KRIT1, CCM2/MGC4607 and CCM3/PDCD10 genes are identified in the vast majority of familial…
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2012
2012
Angioleiomyomas of the Dura: Rare Entities That Lack KRIT1 Mutations
T. M. Conner
,
A. Waziri
,
B. Kleinschmidt-DeMasters
American Journal of Surgical Pathology
2012
Corpus ID: 13054873
Angioleiomyomas (ALMs) are cutaneous and soft tissue lesions usually seen in the lower extremities of middle-aged women. The…
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2011
2011
In Vitro Characterization of the Angiogenic Phenotype and Genotype of the Endothelia Derived From Sporadic Cerebral Cavernous Malformations
Yuan Zhu
,
Qun Wu
,
+6 authors
U. Sure
Neurosurgery
2011
Corpus ID: 33554025
BACKGROUND:Cerebral cavernous malformation (CCM) is mainly a disorder of endothelial cells. Although the endothelial function of…
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2011
2011
A novel CCM1 gene mutation causes cerebral cavernous malformation in a Chinese family
Yao Zhao
,
Li-qian Xie
,
+8 authors
Y. Mao
Journal of clinical neuroscience
2011
Corpus ID: 35440244
2005
2005
A Novel Gene Mutation (1292 Deletion) in a Chinese Family with Cerebral Cavernous Malformations
Y. Mao
,
Yao Zhao
,
+5 authors
Guo-Yuan Yang
Neurosurgery
2005
Corpus ID: 6398096
OBJECTIVE:Hereditary cerebral cavernous malformations (CCMs) are characterized by focal abnormalities of small blood vessels in…
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2003
2003
Molecular genetic investigations in the CCM1 gene in sporadic cerebral cavernomas
P. Reich
,
J. Winkler
,
Andreas Straube
,
H. J. Steiger
,
A. Peraud
Neurology
2003
Corpus ID: 36335171
Objective: Cerebral cavernous malformations (CCM) occur in familial and sporadic forms that cannot be distinguished by phenotype…
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2003
2003
[A novel Krit-1 mutation in Han family with cerebral cavernous malformation].
Yulun Xu
,
Ji-zong Zhao
,
Bing-quan Wu
,
H. Zhong
,
Shuo Wang
,
W. Heng
Zhonghua bing li xue za zhi = Chinese journal of…
2003
Corpus ID: 25468116
OBJECTIVE To detect the mutations of Krit-1 gene that cause familial cerebral cavernous malformation (CCM) in the Han ethnic…
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2001
2001
Identification of eight novel 5'-exons in cerebral capillary malformation gene-1 (CCM1) encoding KRIT1.
I. Eerola
,
Brendan A.S. McIntyre
,
M. Vikkula
Biochimica et Biophysica Acta
2001
Corpus ID: 39958401
1999
1999
Human-mouse comparative mapping of the genomic region containing CDK6: localization of an evolutionary breakpoint
James W. Thomas
,
S. Lee-Lin
,
E. Green
Mammalian Genome
1999
Corpus ID: 29043668
The striking success of the ongoing Human Genome Project has resulted in the formulation of accelerated plans for completing the…
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Highly Cited
1983
Highly Cited
1983
Tissue-specific expression of a chicken calmodulin pseudogene lacking intervening sequences.
J. P. Stein
,
R. Munjaal
,
L. Lagacé
,
E. Lai
,
B. O’Malley
,
A. Means
Proceedings of the National Academy of Sciences…
1983
Corpus ID: 41996005
An eel calmodulin cDNA probe has been used to isolate a calmodulin gene from a chicken DNA library. Sequence analysis revealed…
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