Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart
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* Corresponding author: Jonathan Pevsner pevsner@kennedykrieger.org
Genome Biology 2005, 6:R107 doi:10.1186/gb-2005-6-13-r107
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Julien Laffaire, Isabelle Rivals, Luce Dauphinot, Fabien Pasteau, Rosine Wehrle, Benoit Larrat, Tania Vitalis, Randal X Moldrich, Jean Rossier, Ralph Sinkus, Yann Herault, Isabelle Dusart, Marie-Claude Potier BMC Genomics 2009, 10:138 (30 March 2009) |
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Profiling expression changes caused by a segmental aneuploid in maize Irina Makarevitch, Ronald L Phillips, Nathan M Springer BMC Genomics 2008, 9:7 (10 January 2008) |
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Anna Conti, Floriana Fabbrini, Paola D'Agostino, Rosa Negri, Dario Greco, Rita Genesio, Maria D'Armiento, Carlo Olla, Dario Paladini, Mariastella Zannini, Lucio Nitsch BMC Genomics 2007, 8:268 (7 August 2007) |
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Gene expression variation in Down's syndrome mice allows prioritization of candidate genes Marc Sultan, Ilaria Piccini, Daniela Balzereit, Ralf Herwig, Nidhi G Saran, Hans Lehrach, Roger H Reeves, Marie-Laure Yaspo Genome Biology 2007, 8:R91 (25 May 2007) RNA from eight Ts65Dn mice (a model of Down syndrome) and eight euploid mice were analysed by real-time PCR to examine inter-individual gene expression levels as a function of trisomy. |
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Chi-Ming Li, Meirong Guo, Martha Salas, Nicole Schupf, Wayne Silverman, Warren B Zigman, Sameera Husain, Dorothy Warburton, Harshwardhan Thaker, Benjamin Tycko BMC Medical Genetics 2006, 7:24 (15 March 2006) Differential over-expression of chromosome 21 genes in trisomy 21 fibroblasts and fetal hearts may help explain the occurrence of cardiac defects and autoimmune diseases in patients with Down syndrome.
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