Novel Murine Models of Cerebral Cavernous Malformations-Reference-Cited by-同舟云学术

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Novel Murine Models of Cerebral Cavernous Malformations

Published:2020-07-24 Issue:4 Volume:23 Page:651-666
ISSN:0969-6970
Container-title:Angiogenesis
language:en
Short-container-title:Angiogenesis

Author:

Detter Matthew R.^ORCID,Shenkar Robert^ORCID,Benavides Christian R.,Neilson Catherine A.,Moore Thomas,Lightle Rhonda,Hobson Nicholas,Shen Le,Cao Ying,Girard Romuald,Zhang Dongdong,Griffin Erin,Gallione Carol J.,Awad Issam A.^ORCID,Marchuk Douglas A.^ORCID

Funder

National Institute of Neurological Disorders and Stroke

National Heart, Lung, and Blood Institute

National Institutes of Health

Fondation Leducq

American Heart Association

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Clinical Biochemistry,Physiology

Link

https://link.springer.com/content/pdf/10.1007/s10456-020-09736-8.pdf

Reference73 articles.

1. Rigamonti D, Hadley MN, Drayer BP, Johnson PC, Hoenig-Rigamonti K, Knight JT et al (1988) Cerebral cavernous malformations. Incidence and familial occurrence. N Engl J Med 319(6):343–347. https://doi.org/10.1056/nejm198808113190605

2. Knudson AG Jr (1971) Mutation and cancer: statistical study of retinoblastoma. Proc Natl Acad Sci USA 68(4):820–823

3. Sahoo T, Johnson EW, Thomas JW, Kuehl PM, Jones TL, Dokken CG et al (1999) Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1). Hum Mol Genet 8(12):2325–2333

4. Laberge-le Couteulx S, Jung HH, Labauge P, Houtteville JP, Lescoat C, Cecillon M et al (1999) Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas. Nat Genet 23(2):189–193. https://doi.org/10.1038/13815

5. Liquori CL, Berg MJ, Siegel AM, Huang E, Zawistowski JS, Stoffer T et al (2003) Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations. Am J Hum Genet 73(6):1459–1464. https://doi.org/10.1086/380314

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