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

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1998 1
2004 1
2005 2
2006 2
2007 3
2009 9
2010 8
2011 20
2012 16
2013 12
2014 16
2015 13
2016 8
2017 9
2018 9
2019 7
2020 10
2021 8
2022 5
2023 4
2024 0

Text availability

Article attribute

Article type

Publication date

PubMed (GeneRIF) for id: 59

142 results

Results by year

Filters applied: . Clear all
Page 1
A highly penetrant ACTA2 mutation of thoracic aortic disease.
Bobba CM, Azarrafiy R, Spratt JR, Hendrickson J, Martin TD, Arnaoutakis GJ, Jeng EI, Beaver TM. Bobba CM, et al. J Cardiothorac Surg. 2023 Dec 4;18(1):352. doi: 10.1186/s13019-023-02420-0. J Cardiothorac Surg. 2023. PMID: 38044429 Free PMC article.
A comparative study of the epiligament of the medial collateral and anterior cruciate ligaments in the human knee: Immunohistochemical analysis of CD 34, α-smooth muscle actin and vascular endothelial growth factor in relation to epiligament theory.
Georgiev GP, Tubbs RS, Olewnik Ł, Zielinska N, Telang M, Ananiev J, Dimitrova IN, Slavchev SA, Yordanov Y, LaPrade RF, Ruzik K, Landzhov B. Georgiev GP, et al. Knee. 2022 Dec;39:78-90. doi: 10.1016/j.knee.2022.07.013. Epub 2022 Sep 28. Knee. 2022. PMID: 36179587 Free article.
Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort.
van den Bersselaar LM, Verhagen JMA, Bekkers JA, Kempers M, Houweling AC, Baars M, Overwater E, Hilhorst-Hofstee Y, Barge-Schaapveld DQCM, Rompen E, Krapels IPC, Dulfer E, Wessels MW, Loeys BL, Verhagen HJM, Maugeri A, Roos-Hesselink JW, Brüggenwirth HT, van de Laar IMBH. van den Bersselaar LM, et al. Genet Med. 2022 Oct;24(10):2112-2122. doi: 10.1016/j.gim.2022.07.009. Epub 2022 Sep 2. Genet Med. 2022. PMID: 36053285 Free article.
ACTA2-Related Dysgyria: An Under-Recognized Malformation of Cortical Development.
Subramanian S, Biswas A, Alves CAPF, Sudhakar SV, Shekdar KV, Krishnan P, Shroff M, Taranath A, Arrigoni F, Aldinger KA, Leventer RJ, Dobyns WB, Mankad K. Subramanian S, et al. AJNR Am J Neuroradiol. 2022 Jan;43(1):146-150. doi: 10.3174/ajnr.A7364. Epub 2021 Dec 2. AJNR Am J Neuroradiol. 2022. PMID: 34857515 Free PMC article.
142 results