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6篇 您的检索式:作者名="Hofer EL"
    题名 作者 年代 出处 被引量
1Cardiomyogenic differentiation of human bone marrow mesenchymal ceils: Role of cardiac extract from neonatal rat cardiomyocytes 显示文摘Labovsky V Hofer EL Feldman L 2010Differentiation2010,79,:1
2Ultrafine particles cause cytoskeletal dysfunctions in macrophages 显示文摘MOLLER W HOFER T ZIESENIS A at el 2002Toxicol Appl Pharmacol2002,182,3:1
3The efficacy of exeimer laser (308 nm) for vitiligo at different body sites 显示文摘Hofer A Hassan AS Legat FJ eL al 2006J Eur Aead Dermatol Venereol2006,20,5:1
4Cardiomyogenic differentiationof human bone marrow mesenchymal cells:Role of cardiac extract fromneonatal rat cardiomyocytes显示文摘Labovsky V Hofer EL Feldman L 2010Differentiation2010,79,2:1
5Mesenchymal stromal cells,colony-forming unit fibroblasts,from bone marrow of untreated ad-vanced breast and lung cancer patients suppress fibroblast colony for-mation from healthy marrow显示文摘Hofer EL Labovsky V La Russa V 2010Stem Cells Dev2010,19,:1
6QT-GWAS:A novel method for unveiling biosynthetic loci affecting qualitative metabolic traits显示文摘Although the plant kingdom provides an enormous diversity of metabolites with potentially beneficial applications for humankind,a large fraction of these metabolites and their biosynthetic pathways remain unknown.Resolving metabolite structures and their biosynthetic pathways is key to gaining biological understanding andto allow metabolic engineering.In orderto retrieve novel biosynthetic genes involved in specialized metabolism,we developed a novel untargeted method designated as qualitative trait GWAs(QT-GWAS)that subjects qualitative metabolic traits to a genome-wide association study,while the conventional metabolite GWAS(mGWAS)mainly considers the quantitative variation of metabolites.As a proof of the validity of QT-GWAS,23 and 15of the retrieved associations identified in Arabidopsis thaliana by QTGWAS and mGWAS,respectively,were supported by previous research.Furthermore,seven genemetabolite associations retrieved by QT-GWAS were confirmed in this study through reverse genetics combined with metabolomics and/or in vitro enzyme assays.As such,we established that CYTOCHROME P450706A5(CYP706A5)is involved in the biosynthesis of chroman derivatives,UDP-GLYCOSYLTRANSFERASE 76C3(UGT76C3)is able tohexosylate guanine in vitro and in planta,and SULFOTRANSFERASE 202B1(SULT202B1)catalyzes the sulfation of neolignans in vitro.Collectively,our study demonstrates that the untargeted QT-GWAS method can retrieve valid gene-metabolite associations at the level of enzyme-encoding genes,even new associations that cannot be found by the conventional mGwAs,providing a new approach for dissecting qualitative metabolic traits.Marlies Brouckaert Meng Peng RenéHofer lias El Houari Chiarina Darrah Veronique Storme Yvan Saeys Ruben Vanholme Geert Goeminne Vitaliy I.Timokhin John Ralph Kris Morreel Wout Boerjan 2023Molecular Plant2023,16,7:0
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