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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 1 |
2009 | 1 |
2010 | 1 |
2011 | 1 |
2014 | 1 |
2017 | 1 |
2024 | 0 |
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6 results
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Page 1
Combined HMG-COA reductase and prenylation inhibition in treatment of CCM.
Proc Natl Acad Sci U S A. 2017 May 23;114(21):5503-5508. doi: 10.1073/pnas.1702942114. Epub 2017 May 12.
Proc Natl Acad Sci U S A. 2017.
PMID: 28500274
Free PMC article.
Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration.
Louvi A, Nishimura S, Günel M.
Louvi A, et al.
Development. 2014 Mar;141(6):1404-15. doi: 10.1242/dev.093526.
Development. 2014.
PMID: 24595293
Free PMC article.
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Apoptotic functions of PDCD10/CCM3, the gene mutated in cerebral cavernous malformation 3.
Chen L, Tanriover G, Yano H, Friedlander R, Louvi A, Gunel M.
Chen L, et al.
Stroke. 2009 Apr;40(4):1474-81. doi: 10.1161/STROKEAHA.108.527135. Epub 2009 Feb 26.
Stroke. 2009.
PMID: 19246713
Free PMC article.
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Loss of cerebral cavernous malformation 3 (Ccm3) in neuroglia leads to CCM and vascular pathology.
Louvi A, Chen L, Two AM, Zhang H, Min W, Günel M.
Louvi A, et al.
Proc Natl Acad Sci U S A. 2011 Mar 1;108(9):3737-42. doi: 10.1073/pnas.1012617108. Epub 2011 Feb 14.
Proc Natl Acad Sci U S A. 2011.
PMID: 21321212
Free PMC article.
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Stabilization of VEGFR2 signaling by cerebral cavernous malformation 3 is critical for vascular development.
He Y, Zhang H, Yu L, Gunel M, Boggon TJ, Chen H, Min W.
He Y, et al.
Sci Signal. 2010 Apr 6;3(116):ra26. doi: 10.1126/scisignal.2000722.
Sci Signal. 2010.
PMID: 20371769
Free PMC article.
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A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigation.
Bilguvar K, Bydon M, Bayrakli F, Ercan-Sencicek AG, Bayri Y, Mason C, DiLuna ML, Seashore M, Bronen R, Lifton RP, State M, Gunel M.
Bilguvar K, et al.
J Neurosurg. 2007 Dec;107(6 Suppl):495-9. doi: 10.3171/PED-07/12/495.
J Neurosurg. 2007.
PMID: 18154020
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