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EWS-FLI-1 expression triggers a Ewing's sarcoma initiation program in primary human mesenchymal stem cells Riggi, Nicolo; Suva, Mario-Luca; Suva, Domizio; Cironi, Luisa; ... Stamenkovic, Ivan 2008
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EWS-FLI-1 modulates miRNA145 and SOX2 expression to initiate mesenchymal stem cell reprogramming toward Ewing sarcoma cancer stem cells Riggi, Nicolo; Suva, Mario-Luca; De Vito, Claudio; Provero, Paolo; ... Stamenkovic, Ivan 2010
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Expanding the phenotype of fragile X-associated tremor/ataxia syndrome: a new female case Horvath, Judit; Burkhard, Pierre; Morris, Michael Andréw; Bottani, Armand; ... Delavelle, Jacqueline 2007
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Experimental approaches to lymphocyte migration in dermatology in vitro and in vivo Radeke, Heinfried H.; Ludwig, Ralf J.; Boehncke, Wolf-Henning 2005
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Exploring venlafaxine pharmacokinetic variability with a phenotyping approach, a multicentric french-swiss study (MARVEL study) Lloret-Linares, Célia; Daali, Youssef; Chevret, Sylvie; Nieto, Isabelle; ... Bellivier, Frank 2017
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Expression of an activated Notch4(int-3) oncoprotein disrupts morphogenesis and induces an invasive phenotype in mammary epithelial cells in vitro Soriano, Jesus; Uyttendaele, Hendrik; Kitajewski, Jan; Montesano, Roberto 2000
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Expression of mitofusin 2(R94Q) in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A Cartoni, Romain; Arnaud, Estelle; Médard, Jean-Jacques; Poirot, Olivier; ... Martinou, Jean-Claude 2010
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Extensive natural variation for cellular hydrogen peroxide release is genetically controlled Attar Cohen, Homa; Bedard, Karen; Migliavacca Voeffray, Eugenia Linda; Gagnebin, Maryline; ... Antonarakis, Stylianos 2012
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Fatty acid amide hydrolase deficiency enhances intraplaque neutrophil recruitment in atherosclerotic mice Lenglet, Sébastien; Thomas, Aurélien; Soehnlein, Oliver; Montecucco, Fabrizio; ... Steffens, Sabine 2013
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FGFR3 and p53 protein expressions in patients with pTa and pT1 urothelial bladder cancer Mhawech-fauceglia, Paulette; Cheney, R. T.; Fischer, G.; Beck, A.; Herrmann, François 2006
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Fibrinogen gene mutations accounting for congenital afibrinogenemia Neerman Arbez, Marguerite 2001
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Fibrinogen Krakow: a novel hypo/dysfibrinogenemia mutation in fibrinogen gamma chain (Asn325Ile) affecting fibrin clot structure and function Undas, Anetta; Zdziarska, Joanna; Iwaniec, Teresa; Stepien, Ewa; ... Neerman Arbez, Marguerite 2009
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Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study Ehret, Georg Benedikt; O'Connor, Ashley A.; Weder, Alan; Cooper, Richard S.; Chakravarti, Aravinda 2009
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Formation of multivesicular endosomes in Dictyostelium Marchetti, Anna; Mercanti, Valentina; Cornillon, Sophie Marie; Alibaud, Laethitia; ... Cosson, Pierre 2004
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Formation of new chromatin domains determines pathogenicity of genomic duplications Franke, Martin; Ibrahim, Daniel M; Andrey, Guillaume; Schwarzer, Wibke; ... Mundlos, Stefan 2016
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Frailty syndrome: a transitional state in a dynamic process Lang, Pierre Olivier; Michel, Jean-Pierre; Zekry Berger, Dina Selma 2009
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Function of major histocompatibility complex class II promoters requires cooperative binding between factors RFX and NF-Y Reith, Walter; Siegrist, Claire-Anne; Durand, Bénédicte; Barras, Emmanuele; Mach, Bernard 1994
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Functional analysis of T cell subsets from mice bearing the lpr gene Davignon, J. L.; Budd, R. C.; Ceredig, R.; Piguet, P. F.; ... Izui, Shozo 1985
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Functional equivalence and rescue among group 11 Hox gene products in vertebral patterning Zakany, Jozsef; Gerard, Matthieu; Favier, B.; Potter, S.S.; Duboule, Denis 1996
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Functional genetic variation of human miRNAs and phenotypic consequences Borel, Christelle; Antonarakis, Stylianos 2008
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