Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 2
1964 2
1974 1
1984 1
1985 2
1986 1
1991 2
1992 1
1997 1
1999 1
2000 1
2002 1
2003 2
2004 1
2005 2
2006 1
2007 3
2008 1
2009 3
2010 1
2012 2
2013 1
2014 2
2017 1
2018 3
2019 3
2020 2
2021 6
2022 11
2023 14
2024 7

Text availability

Article attribute

Article type

Publication date

Search Results

77 results

Results by year

Filters applied: . Clear all
The following term was not found in PubMed: Smerpitak
Page 1
Conflict of Interest Disclosures.
[No authors listed] [No authors listed] Global Spine J. 2023 May;13(2_suppl):568S-591S. doi: 10.1177/21925682231173597. Global Spine J. 2023. PMID: 37222100 Free PMC article. No abstract available.
KRIT-1/CCM1 is a Rap1 effector that regulates endothelial cell cell junctions.
Glading A, Han J, Stockton RA, Ginsberg MH. Glading A, et al. J Cell Biol. 2007 Oct 22;179(2):247-54. doi: 10.1083/jcb.200705175. J Cell Biol. 2007. PMID: 17954608 Free PMC article.
Cerebral cavernous malformation (CCM), a disease associated with defective endothelial junctions, result from autosomal dominant CCM1 mutations that cause loss of KRIT-1 protein function, though how the loss of KRIT-1 leads to CCM is obscure. ...Rap1 activity regula …
Cerebral cavernous malformation (CCM), a disease associated with defective endothelial junctions, result from autosomal dominant CCM1 mutati …
Control of cell adhesion dynamics by Rap1 signaling.
Boettner B, Van Aelst L. Boettner B, et al. Curr Opin Cell Biol. 2009 Oct;21(5):684-93. doi: 10.1016/j.ceb.2009.06.004. Epub 2009 Jul 16. Curr Opin Cell Biol. 2009. PMID: 19615876 Free PMC article. Review.
In this review we will discuss more recently revealed roles of Rap1 signaling by primarily focusing on functions of the Rap1 effectors RIAM, KRIT-1/CCM1 and AF-6/Afadin in junctional regulation of the vascular system and in epithelial cells. ...
In this review we will discuss more recently revealed roles of Rap1 signaling by primarily focusing on functions of the Rap1 effectors RIAM, …
Suspicion after inheritance.
Villegas-Romero I, Domínguez-Gómez M, Linares-Barrios M. Villegas-Romero I, et al. Actas Dermosifiliogr (Engl Ed). 2021 May 13:S0001-7310(21)00179-4. doi: 10.1016/j.ad.2020.02.012. Online ahead of print. Actas Dermosifiliogr (Engl Ed). 2021. PMID: 33992619 Free article. English, Spanish. No abstract available.
CCM1 and the second life of proteins in adhesion complexes.
van den Berg MC, Burgering BM. van den Berg MC, et al. Cell Adh Migr. 2014;8(2):146-57. doi: 10.4161/cam.28437. Cell Adh Migr. 2014. PMID: 24714220 Free PMC article. Review.
Here we discuss nuclear functions of adhesion complex proteins with a special focus on the CCM-1/KRIT-1 protein, which may turn out to be yet another adhesion complex protein with a second life....
Here we discuss nuclear functions of adhesion complex proteins with a special focus on the CCM-1/KRIT-1 protein, which may turn out t …
Plasma Nitridation Effect on β-Ga2O3 Semiconductors.
Kim S, Kim M, Kim J, Hwang WS. Kim S, et al. Nanomaterials (Basel). 2023 Mar 28;13(7):1199. doi: 10.3390/nano13071199. Nanomaterials (Basel). 2023. PMID: 37049293 Free PMC article.
Occlusive membranes for guided regeneration of inflamed tissue defects.
Choi W, Mangal U, Park JY, Kim JY, Jun T, Jung JW, Choi M, Jung S, Lee M, Na JY, Ryu DY, Kim JM, Kwon JS, Koh WG, Lee S, Hwang PTJ, Lee KJ, Jung UW, Cha JK, Choi SH, Hong J. Choi W, et al. Nat Commun. 2023 Nov 24;14(1):7687. doi: 10.1038/s41467-023-43428-3. Nat Commun. 2023. PMID: 38001080 Free PMC article.
[A novel Krit-1 mutation in Han family with cerebral cavernous malformation].
Xu YL, Zhao JZ, Wu BQ, Zhong HH, Wang S, Heng WJ. Xu YL, et al. Zhonghua Bing Li Xue Za Zhi. 2003 Jun;32(3):220-5. Zhonghua Bing Li Xue Za Zhi. 2003. PMID: 12882686 Chinese.
OBJECTIVE: To detect the mutations of Krit-1 gene that cause familial cerebral cavernous malformation (CCM) in the Han ethnic origin. ...Two families (A and B) and 8 apparently sporadic individuals affected with CCM were screened for mutations of Krit-1 gene. Member …
OBJECTIVE: To detect the mutations of Krit-1 gene that cause familial cerebral cavernous malformation (CCM) in the Han ethnic origin. …
77 results