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 TitleAuthors / EditorsDate
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Epidermal growth factor receptor overexpression is common and not correlated to gene copy number in ependymoma Friedrich, Carsten; Von Bueren, André; Kolevatova, Larissa; Bernreuther, Christian; ... Glatzel, Markus 2016
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Bimodal expression of PHO84 is modulated by early termination of antisense transcription Castelnuovo, Manuele; Rahman, Samir; Guffanti, Elisa; Infantino, Valentina; ... Zenklusen, Daniel 2013
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Developmental expression and organisation of fibrinogen genes in the zebrafish Fish, Richard; Vorjohann, Silja; Bena, Frédérique; Fort, Alexandre; Neerman-Arbez, Marguerite 2012
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Persistence of recipient-type endothelium after allogeneic hematopoietic stem cell transplantation Mueller, Regula J; Stussi, Georg; Puga Yung, Gisella; Nikolic, Milica; ... Seebach, Jorg Dieter 2011
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Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanoma Valsesia, Armand; Rimoldi, Donata; Martinet, Danielle; Ibberson, Mark; ... Stevenson, Brian J 2011
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Glioblastoma with signet-ring morphology Pusztaszeri, Marc; Lobrinus, Johannes Alexander 2010
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Clonal heterogeneity and chromosomal instability at disease presentation in high hyperdiploid acute lymphoblastic leukemia Talamo, Anna; Chalandon, Yves; Marazzi, Alfio; Jotterand, Martine 2010
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De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic features Makrythanasis, Periklis; Moix, Isabelle; Gimelli, Stefania; Fluss, Joel Victor; ... Bottani, Armand 2010
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Array-CGH analysis in a patient with WAGR syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation Gimelli, Stefania; Divizia, Maria Teresa; Lerone, Margherita; Bricco, Lara; ... Gimelli, Giorgio 2010
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Extensive biliary intraepithelial neoplasia (BilIN) and multifocal early intrahepatic cholangiocarcinoma in non-biliary cirrhosis Rougemont-Pidoux, Anne-Laure; Genevay-Infante, Muriel; Mckee, Thomas Alexander; Gremaud, Magali; ... Rubbia-Brandt, Laura 2010
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Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients Martinet, Danielle; Filges, Isabel; Besuchet Schmutz, Nathalie; Morris, Michael Andréw; ... Bena, Frédérique 2008
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Chondroid cystic malformation of the lung with trisomy 8 mosaicism: a new cystic lung malformation Bouron-Dal Soglio, Dorothee; Rougemont-Pidoux, Anne-Laure; De Buys Roessingh, Anthony S.; Fetni, Raouf; ... Fournet, Jean-Christophe 2008
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Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21 Lyle, Robert; Prandini, Paola; Osoegawa, Kazutoyo; ten Hallers, Boudewijn; ... Antonarakis, Stylianos 2007
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The prognostic significance of cytogenetic aberrations in childhood acute myeloid leukaemia. A study of the Swiss Paediatric Oncology Group (SPOG) Betts, David R; Ammann, Roland A; Hirt, Andreas; Hengartner, Heinz; ... Niggli, Felix K 2007
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Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions Howald, C.; Merla, Giuseppe; Digilio, M. C.; Amenta, S.; ... Reymond, Alexandre 2006
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Human splicing factor SF3a, but not SF1, is essential for pre-mRNA splicing in vivo Tanackovic Abbas-Terki, Goranka; Kraemer, Angela 2005
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The transcription factor RFX3 directs nodal cilium development and left-right asymmetry specification Bonnafe, E.; Touka, M.; Ait-Lounis, Aouatef; Baas, Dominique; ... Reith, Walter 2004
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No association between DUP25 and anxiety disorders Henrichsen, C. N.; Delorme, Richard; Boucherie, Maria; Marelli, Dominique; ... Dahoun, Sophie 2004
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BRU1, a novel link between responses to DNA damage and epigenetic gene silencing in Arabidopsis Takeda, Shin; Tadele, Zerihun; Hofmann, Ingo; Probst, Aline V.; ... Paszkowski, Jerzy 2004
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Two means of transcriptional reactivation within heterochromatin Probst, Aline V.; Fransz, Paul F.; Paszkowski, Jerzy; Mittelsten Scheid, Ortrun 2003
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