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Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome.
Aoki Y, Niihori T, Banjo T, Okamoto N, Mizuno S, Kurosawa K, Ogata T, Takada F, Yano M, Ando T, Hoshika T, Barnett C, Ohashi H, Kawame H, Hasegawa T, Okutani T, Nagashima T, Hasegawa S, Funayama R, Nagashima T, Nakayama K, Inoue S, Watanabe Y, Ogura T, Matsubara Y. Aoki Y, et al. Among authors: ogura t. Am J Hum Genet. 2013 Jul 11;93(1):173-80. doi: 10.1016/j.ajhg.2013.05.021. Epub 2013 Jun 20. Am J Hum Genet. 2013. PMID: 23791108 Free PMC article.
Importance of endothelial Hey1 expression for thoracic great vessel development and its distal enhancer for Notch-dependent endothelial transcription.
Watanabe Y, Seya D, Ihara D, Ishii S, Uemoto T, Kubo A, Arai Y, Isomoto Y, Nakano A, Abe T, Shigeta M, Kawamura T, Saito Y, Ogura T, Nakagawa O. Watanabe Y, et al. Among authors: ogura t. J Biol Chem. 2020 Dec 18;295(51):17632-17645. doi: 10.1074/jbc.RA120.015003. J Biol Chem. 2020. PMID: 33454003 Free PMC article.
[No title available]
[No authors listed] [No authors listed] PMID: 33067358
Fibroblast growth factor 10 gene regulation in the second heart field by Tbx1, Nkx2-5, and Islet1 reveals a genetic switch for down-regulation in the myocardium.
Watanabe Y, Zaffran S, Kuroiwa A, Higuchi H, Ogura T, Harvey RP, Kelly RG, Buckingham M. Watanabe Y, et al. Among authors: ogura t. Proc Natl Acad Sci U S A. 2012 Nov 6;109(45):18273-80. doi: 10.1073/pnas.1215360109. Epub 2012 Oct 23. Proc Natl Acad Sci U S A. 2012. PMID: 23093675 Free PMC article.
2,386 results