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
1947 1
1951 1
1958 3
1972 1
1973 1
1974 1
1975 2
1977 1
1978 2
1979 1
1982 1
1983 1
1985 1
1986 4
1987 4
1988 1
1989 3
1990 2
1991 8
1992 4
1993 3
1994 2
1995 3
1996 2
1998 2
1999 1
2000 3
2001 2
2002 1
2004 2
2005 1
2011 3
2012 2
2013 2
2014 3
2015 4
2016 6
2017 7
2018 14
2019 12
2020 6
2021 8
2022 12
2023 8
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

138 results

Results by year

Filters applied: . Clear all
Page 1
A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3.
Schepers D, Tortora G, Morisaki H, MacCarrick G, Lindsay M, Liang D, Mehta SG, Hague J, Verhagen J, van de Laar I, Wessels M, Detisch Y, van Haelst M, Baas A, Lichtenbelt K, Braun K, van der Linde D, Roos-Hesselink J, McGillivray G, Meester J, Maystadt I, Coucke P, El-Khoury E, Parkash S, Diness B, Risom L, Scurr I, Hilhorst-Hofstee Y, Morisaki T, Richer J, Désir J, Kempers M, Rideout AL, Horne G, Bennett C, Rahikkala E, Vandeweyer G, Alaerts M, Verstraeten A, Dietz H, Van Laer L, Loeys B. Schepers D, et al. Among authors: verstraeten a. Hum Mutat. 2018 May;39(5):621-634. doi: 10.1002/humu.23407. Epub 2018 Mar 6. Hum Mutat. 2018. PMID: 29392890 Free PMC article.
Meester-Loeys Syndrome.
Meester JAN, De Kinderen P, Verstraeten A, Loeys B. Meester JAN, et al. Among authors: verstraeten a. Adv Exp Med Biol. 2021;1348:265-272. doi: 10.1007/978-3-030-80614-9_12. Adv Exp Med Biol. 2021. PMID: 34807424
SMAD6-deficiency in human genetic disorders.
Luyckx I, Verstraeten A, Goumans MJ, Loeys B. Luyckx I, et al. Among authors: verstraeten a. NPJ Genom Med. 2022 Nov 21;7(1):68. doi: 10.1038/s41525-022-00338-5. NPJ Genom Med. 2022. PMID: 36414630 Free PMC article. Review.
Aetiology and management of hereditary aortopathy.
Verstraeten A, Luyckx I, Loeys B. Verstraeten A, et al. Nat Rev Cardiol. 2017 Apr;14(4):197-208. doi: 10.1038/nrcardio.2016.211. Epub 2017 Jan 19. Nat Rev Cardiol. 2017. PMID: 28102232 Review.
Novel Association of the NOTCH Pathway Regulator MIB1 Gene With the Development of Bicuspid Aortic Valve.
Tessler I, Albuisson J, Piñeiro-Sabarís R, Verstraeten A, Kamber Kaya HE, Siguero-Álvarez M, Goudot G, MacGrogan D, Luyckx I, Shpitzen S, Levin G, Kelman G, Reshef N, Mananet H, Holdcraft J, Muehlschlegel JD, Peloso GM, Oppenheim O, Cheng C, Mazzella JM, Andelfinger G, Mital S, Eriksson P, Billon C, Heydarpour M, Dietz HC, Jeunemaitre X, Leitersdorf E, Sprinzak D, Blacklow SC, Body SC, Carmi S, Loeys B, de la Pompa JL, Gilon D, Messas E, Durst R. Tessler I, et al. Among authors: verstraeten a. JAMA Cardiol. 2023 Aug 1;8(8):721-731. doi: 10.1001/jamacardio.2023.1469. JAMA Cardiol. 2023. PMID: 37405741 Free PMC article.
The Genetics and Typical Traits of Thoracic Aortic Aneurysm and Dissection.
Rodrigues Bento J, Meester J, Luyckx I, Peeters S, Verstraeten A, Loeys B. Rodrigues Bento J, et al. Among authors: verstraeten a. Annu Rev Genomics Hum Genet. 2022 Aug 31;23:223-253. doi: 10.1146/annurev-genom-111521-104455. Annu Rev Genomics Hum Genet. 2022. PMID: 36044906 Free article. Review.
TGF-β signalopathies as a paradigm for translational medicine.
Cannaerts E, van de Beek G, Verstraeten A, Van Laer L, Loeys B. Cannaerts E, et al. Among authors: verstraeten a. Eur J Med Genet. 2015 Dec;58(12):695-703. doi: 10.1016/j.ejmg.2015.10.010. Epub 2015 Oct 24. Eur J Med Genet. 2015. PMID: 26598797 Review.
138 results