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Fingolimod inhibits PDGF-B-induced migration of vascular smooth muscle cell by down-regulating the S1PR1/S1PR3 pathway.
Biochimie. 2012 Dec;94(12):2523-31. doi: 10.1016/j.biochi.2012.07.002. Epub 2012 Jul 22.
Biochimie. 2012.
PMID: 22828274
Fingolimod potentiates the effects of sunitinib malate in a rat breast cancer model.
Mousseau Y, Mollard S, Faucher-Durand K, Richard L, Nizou A, Cook-Moreau J, Baaj Y, Qiu H, Plainard X, Fourcade L, Funalot B, Sturtz FG.
Mousseau Y, et al. Among authors: baaj y.
Breast Cancer Res Treat. 2012 Jul;134(1):31-40. doi: 10.1007/s10549-011-1903-6. Epub 2011 Dec 9.
Breast Cancer Res Treat. 2012.
PMID: 22160641
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In vitro 3D angiogenesis assay in egg white matrix: comparison to Matrigel, compatibility to various species, and suitability for drug testing.
Mousseau Y, Mollard S, Qiu H, Richard L, Cazal R, Nizou A, Vedrenne N, Rémi S, Baaj Y, Fourcade L, Funalot B, Sturtz FG.
Mousseau Y, et al. Among authors: baaj y.
Lab Invest. 2014 Mar;94(3):340-9. doi: 10.1038/labinvest.2013.150. Epub 2014 Jan 6.
Lab Invest. 2014.
PMID: 24395110
Free article.
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How can grafted breast cancer models be optimized?
Mollard S, Mousseau Y, Baaj Y, Richard L, Cook-Moreau J, Monteil J, Funalot B, Sturtz FG.
Mollard S, et al. Among authors: baaj y.
Cancer Biol Ther. 2011 Nov 15;12(10):855-64. doi: 10.4161/cbt.12.10.18139. Epub 2011 Nov 15.
Cancer Biol Ther. 2011.
PMID: 22057217
Free PMC article.
Review.
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Multiplex detection and genotyping of point mutations involved in charcot-marie-tooth disease using a hairpin microarray-based assay.
Baaj Y, Magdelaine C, Ubertelli V, Valat C, Mousseau Y, Qiu H, Funalot B, Vallat JM, Sturtz FG.
Baaj Y, et al.
Res Lett Biochem. 2009;2009:960560. doi: 10.1155/2009/960560. Epub 2009 Jun 11.
Res Lett Biochem. 2009.
PMID: 22820753
Free PMC article.
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A highly specific microarray method for point mutation detection.
Baaj Y, Magdelaine C, Ubertelli V, Valat C, Talini L, Soussaline F, Khomyakova E, Funalot B, Vallat JM, Sturtz FG.
Baaj Y, et al.
Biotechniques. 2008 Jan;44(1):119-26. doi: 10.2144/000112630.
Biotechniques. 2008.
PMID: 18254389
Free article.
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A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA gene.
Chautard R, Laroche-Raynaud C, Lia AS, Chazelas P, Derouault P, Sturtz F, Baaj Y, Veauville-Merllié A, Acquaviva C, Favreau F, Faye PA.
Chautard R, et al. Among authors: baaj y.
BMC Med Genomics. 2020 Jan 29;13(1):12. doi: 10.1186/s12920-020-0665-6.
BMC Med Genomics. 2020.
PMID: 31996215
Free PMC article.
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Pharmacoresistant Epilepsy in Childhood: Think of the Cerebral Folate Deficiency, a Treatable Disease.
Mafi S, Laroche-Raynaud C, Chazelas P, Lia AS, Derouault P, Sturtz F, Baaj Y, Froget R, Rio M, Benoist JF, Poumeaud F, Favreau F, Faye PA.
Mafi S, et al. Among authors: baaj y.
Brain Sci. 2020 Oct 22;10(11):762. doi: 10.3390/brainsci10110762.
Brain Sci. 2020.
PMID: 33105619
Free PMC article.
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