Arama Sonuçları - Turro, Ernest

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  1. 1
    Phenotype Similarity Regression for Identifying the Genetic Determinants of Rare Diseases

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

    Baskı/Yayın Bilgisi 2016
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  2. 2
    ontologyX: a suite of R packages for working with ontological data

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

    Baskı/Yayın Bilgisi 2017
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  3. 3
    A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases

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

    Baskı/Yayın Bilgisi 2017
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  4. 4
    Hybrid Mice Reveal Parent-of-Origin and Cis- and Trans-Regulatory Effects in the Retina

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

    Baskı/Yayın Bilgisi 2014
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  5. 5
    BGX: a Bioconductor package for the Bayesian integrated analysis of Affymetrix GeneChips

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

    Baskı/Yayın Bilgisi 2007
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  6. 6
    MMBGX: a method for estimating expression at the isoform level and detecting differential splicing using whole-transcript Affymetrix arrays

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

    Baskı/Yayın Bilgisi 2010
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  7. 7
    MMBGX: a method for estimating expression at the isoform level and detecting differential splicing using whole-transcript Affymetrix arrays

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

    Baskı/Yayın Bilgisi 2010
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  8. 8
    Inherited platelet disorders: toward DNA-based diagnosis

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

    Baskı/Yayın Bilgisi 2016
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  9. 9
    Fgf and Esrrb integrate epigenetic and transcriptional networks that regulate self-renewal of trophoblast stem cells

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

    Baskı/Yayın Bilgisi 2015
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  10. 10
    Haplotype and isoform specific expression estimation using multi-mapping RNA-seq reads

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

    Baskı/Yayın Bilgisi 2011
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  11. 11
    Extensive Co-Operation between the Epstein-Barr Virus EBNA3 Proteins in the Manipulation of Host Gene Expression and Epigenetic Chromatin Modification

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

    Baskı/Yayın Bilgisi 2010
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  12. 12
    Correction: Induction of p16(INK4a) Is the Major Barrier to Proliferation when Epstein-Barr Virus (EBV) Transforms Primary B Cells into Lymphoblastoid Cell Lines

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

    Baskı/Yayın Bilgisi 2013
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  13. 13
    PIGO deficiency: palmoplantar keratoderma and novel mutations

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

    Baskı/Yayın Bilgisi 2017
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  14. 14
    Extensive compensatory cis-trans regulation in the evolution of mouse gene expression

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

    Baskı/Yayın Bilgisi 2012
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  15. 15
    Transcription Factor Levels after Forward Programming of Human Pluripotent Stem Cells with GATA1, FLI1, and TAL1 Determine Megakaryocyte versus Erythroid Cell Fate Decision

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

    Baskı/Yayın Bilgisi 2018
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  16. 16
    Altered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathy

    Altered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathy Yazar: 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.

    Baskı/Yayın Bilgisi 2016
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  17. 17
    A novel missense variant in SLC18A2 causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets

    A novel missense variant in SLC18A2 causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets Yazar: 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

    Baskı/Yayın Bilgisi 2019
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  18. 18
    Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia

    Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia Yazar: 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.

    Baskı/Yayın Bilgisi 2020
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  19. 19
    MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases

    MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases Yazar: 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

    Baskı/Yayın Bilgisi 2021
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  20. 20
    mRNA structural elements immediately upstream of the start codon dictate dependence upon eIF4A helicase activity

    mRNA structural elements immediately upstream of the start codon dictate dependence upon eIF4A helicase activity Yazar: 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

    Baskı/Yayın Bilgisi 2019
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