Resultados da pesquisa - Turro, Ernest

Phenotype Similarity Regression for Identifying the Genetic Determinants of Rare Diseases Por Greene, Daniel, Richardson, Sylvia, Turro, Ernest

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ontologyX: a suite of R packages for working with ontological data Por Greene, Daniel, Richardson, Sylvia, Turro, Ernest

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A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases Por Greene, Daniel, Richardson, Sylvia, Turro, Ernest

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Hybrid Mice Reveal Parent-of-Origin and Cis- and Trans-Regulatory Effects in the Retina Por Shen, Susan Q., Turro, Ernest, Corbo, Joseph C.

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BGX: a Bioconductor package for the Bayesian integrated analysis of Affymetrix GeneChips Por Turro, Ernest, Bochkina, Natalia, Hein, Anne-Mette K, Richardson, Sylvia

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MMBGX: a method for estimating expression at the isoform level and detecting differential splicing using whole-transcript Affymetrix arrays Por Turro, Ernest, Lewin, Alex, Rose, Anna, Dallman, Margaret J., Richardson, Sylvia

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MMBGX: a method for estimating expression at the isoform level and detecting differential splicing using whole-transcript Affymetrix arrays Por Turro, Ernest, Lewin, Alex, Rose, Anna, Dallman, Margaret J., Richardson, Sylvia

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Inherited platelet disorders: toward DNA-based diagnosis Por Lentaigne, Claire, Freson, Kathleen, Laffan, Michael A., Turro, Ernest, Ouwehand, Willem H.

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Fgf and Esrrb integrate epigenetic and transcriptional networks that regulate self-renewal of trophoblast stem cells Por Latos, Paulina A., Goncalves, Angela, Oxley, David, Mohammed, Hisham, Turro, Ernest, Hemberger, Myriam

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Haplotype and isoform specific expression estimation using multi-mapping RNA-seq reads Por Turro, Ernest, Su, Shu-Yi, Gonçalves, Ângela, Coin, Lachlan JM, Richardson, Sylvia, Lewin, Alex

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Extensive Co-Operation between the Epstein-Barr Virus EBNA3 Proteins in the Manipulation of Host Gene Expression and Epigenetic Chromatin Modification Por White, Robert E., Groves, Ian J., Turro, Ernest, Yee, Jade, Kremmer, Elisabeth, Allday, Martin J.

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Correction: Induction of p16(INK4a) Is the Major Barrier to Proliferation when Epstein-Barr Virus (EBV) Transforms Primary B Cells into Lymphoblastoid Cell Lines Por Skalska, Lenka, White, Robert E., Parker, Gillian A., Turro, Ernest, Sinclair, Alison J., Paschos, Kostas, Allday, Martin J.

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PIGO deficiency: palmoplantar keratoderma and novel mutations Por Morren, Marie-Anne, Jaeken, Jaak, Visser, Gepke, Salles, Isabelle, Van Geet, Chris, Simeoni, Ilenia, Turro, Ernest, Freson, Kathleen

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Extensive compensatory cis-trans regulation in the evolution of mouse gene expression Por Goncalves, Angela, Leigh-Brown, Sarah, Thybert, David, Stefflova, Klara, Turro, Ernest, Flicek, Paul, Brazma, Alvis, Odom, Duncan T., Marioni, John C.

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Transcription Factor Levels after Forward Programming of Human Pluripotent Stem Cells with GATA1, FLI1, and TAL1 Determine Megakaryocyte versus Erythroid Cell Fate Decision Por Dalby, Amanda, Ballester-Beltrán, Jose, Lincetto, Chiara, Mueller, Annett, Foad, Nicola, Evans, Amanda, Baye, James, Turro, Ernest, Moreau, Thomas, Tijssen, Marloes R., Ghevaert, Cedric

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Altered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathy Por Burley, Kate, Whyte, Claire S., Westbury, Sarah K., Walker, Mary, Stirrups, Kathleen E., Turro, Ernest, Chapman, Oliver G., Reilly-Stitt, Christopher, Mutch, Nicola J., Mumford, Andrew D.

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A novel missense variant in SLC18A2 causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets Por Padmakumar, Manisha, Jaeken, Jaak, Ramaekers, Vincent, Lagae, Lieven, Greene, Daniel, Thys, Chantal, Van Geet, Chris, BioResource, NIHR, Stirrups, Kathleen, Downes, Kate, Turro, Ernest, Freson, Kathleen

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Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia Por Cornish, Naomi, Aungraheeta, M. Riyaad, FitzGibbon, Lucy, Burley, Kate, Alibhai, Dominic, Collins, Janine, Greene, Daniel, Downes, Kate, Westbury, Sarah K., Turro, Ernest, Mumford, Andrew D.

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MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases Por Ratnaike, Thiloka E, Greene, Daniel, Wei, Wei, Sanchis-Juan, Alba, Schon, Katherine R, van den Ameele, Jelle, Raymond, Lucy, Horvath, Rita, Turro, Ernest, Chinnery, Patrick F

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mRNA structural elements immediately upstream of the start codon dictate dependence upon eIF4A helicase activity Por Waldron, Joseph A., Tack, David C., Ritchey, Laura E., Gillen, Sarah L., Wilczynska, Ania, Turro, Ernest, Bevilacqua, Philip C., Assmann, Sarah M., Bushell, Martin, Le Quesne, John

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