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Year Number of Results
2008 1
2010 2
2011 1
2018 3
2021 1
2024 0

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PubMed for id: 47086044

7 results

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Page 1
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Motta M, Fasano G, Gredy S, Brinkmann J, Bonnard AA, Simsek-Kiper PO, Gulec EY, Essaddam L, Utine GE, Guarnetti Prandi I, Venditti M, Pantaleoni F, Radio FC, Ciolfi A, Petrini S, Consoli F, Vignal C, Hepbasli D, Ullrich M, de Boer E, Vissers LELM, Gritli S, Rossi C, De Luca A, Ben Becher S, Gelb BD, Dallapiccola B, Lauri A, Chillemi G, Schuh K, Cavé H, Zenker M, Tartaglia M. Motta M, et al. Am J Hum Genet. 2021 Nov 4;108(11):2112-2129. doi: 10.1016/j.ajhg.2021.09.007. Epub 2021 Oct 8. Am J Hum Genet. 2021. PMID: 34626534 Free PMC article.
Mir-126 is a conserved modulator of lymphatic development.
Kontarakis Z, Rossi A, Ramas S, Dellinger MT, Stainier DYR. Kontarakis Z, et al. Dev Biol. 2018 May 15;437(2):120-130. doi: 10.1016/j.ydbio.2018.03.006. Epub 2018 Mar 15. Dev Biol. 2018. PMID: 29550364 Free article.
miR-126 regulates angiogenic signaling and vascular integrity.
Fish JE, Santoro MM, Morton SU, Yu S, Yeh RF, Wythe JD, Ivey KN, Bruneau BG, Stainier DY, Srivastava D. Fish JE, et al. Dev Cell. 2008 Aug;15(2):272-84. doi: 10.1016/j.devcel.2008.07.008. Dev Cell. 2008. PMID: 18694566 Free PMC article.