Résultats de la recherche - David A. Sweetser

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  1. 1
    The nucleotide sequence of the rat liver fatty acid-binding protein gene. Evidence that exon 1 encodes an oligopeptide domain shared by a family of proteins which bind hydrophobic ligands.

    The nucleotide sequence of the rat liver fatty acid-binding protein gene. Evidence that exon 1 encodes an oligopeptide domain shared by a family of proteins which bind hydrophobic... par David A. Sweetser, John B. Lowe, Jeffrey I. Gordon

    Publié 1986
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  2. 2
    Tle4 controls both developmental acquisition and early post-natal maturation of corticothalamic projection neuron identity

    Tle4 controls both developmental acquisition and early post-natal maturation of corticothalamic projection neuron identity par María J. Galazo, David A. Sweetser, Jeffrey D. Macklis

    Publié 2023
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  3. 3
    Rat cellular retinol-binding protein II: use of a cloned cDNA to define its primary structure, tissue-specific expression, and developmental regulation.

    Rat cellular retinol-binding protein II: use of a cloned cDNA to define its primary structure, tissue-specific expression, and developmental regulation. par E Li, Laurie Demmer, David A. Sweetser, D E Ong, Jeffrey I. Gordon

    Publié 1986
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  4. 4
    Transgenic mice containing intestinal fatty acid-binding protein-human growth hormone fusion genes exhibit correct regional and cell-specific expression of the reporter gene in their small intestine.

    Transgenic mice containing intestinal fatty acid-binding protein-human growth hormone fusion genes exhibit correct regional and cell-specific expression of the reporter gene in the... par David A. Sweetser, S M Hauft, Peter C. Hoppe, E H Birkenmeier, Jeffrey I. Gordon

    Publié 1988
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  5. 5
    Mechanisms underlying generation of gradients in gene expression within the intestine: an analysis using transgenic mice containing fatty acid binding protein-human growth hormone fusion genes.

    Mechanisms underlying generation of gradients in gene expression within the intestine: an analysis using transgenic mice containing fatty acid binding protein-human growth hormone... par David A. Sweetser, E H Birkenmeier, Peter C. Hoppe, Daniel W. McKeel, J I Gordon

    Publié 1988
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  6. 6
    Human liver fatty acid binding protein. Isolation of a full length cDNA and comparative sequence analyses of orthologous and paralogous proteins.

    Human liver fatty acid binding protein. Isolation of a full length cDNA and comparative sequence analyses of orthologous and paralogous proteins. par John B. Lowe, Mark S. Boguski, David A. Sweetser, Nabil A. Elshourbagy, John M. Taylor, Jeffrey I. Gordon

    Publié 1985
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  7. 7
    Discovering chemical modifiers of oncogene-regulated hematopoietic differentiation

    Discovering chemical modifiers of oncogene-regulated hematopoietic differentiation par Jing-Ruey Joanna Yeh, Kathleen M. Munson, Kamaleldin E. Elagib, Adam N. Goldfarb, David A. Sweetser, Randall T. Peterson

    Publié 2009
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  8. 8
    The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships.

    The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships. par David A. Sweetser, E H Birkenmeier, Ivana Klisak, Susan Zollman, R S Sparkes, T. Mohandas, Aldons J. Lusis, Jeffrey I. Gordon

    Publié 1987
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  9. 9
    The cellular retinol binding protein II gene. Sequence analysis of the rat gene, chromosomal localization in mice and humans, and documentation of its close linkage to the cellular retinol binding protein gene.

    The cellular retinol binding protein II gene. Sequence analysis of the rat gene, chromosomal localization in mice and humans, and documentation of its close linkage to the cellular... par Laurie Demmer, E H Birkenmeier, David A. Sweetser, M S Levin, Susan Zollman, R S Sparkes, T. Mohandas, Aldons J. Lusis, Jeffrey I. Gordon

    Publié 1987
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  10. 10
    Novel Compound Heterozygous Mutations Expand the Recognized Phenotypes of <i>FARS2</i>-Linked Disease

    Novel Compound Heterozygous Mutations Expand the Recognized Phenotypes of <i>FARS2</i>-Linked Disease par Melissa Walker, Kyle Mohler, Kyle W. Hopkins, Derek H. Oakley, David A. Sweetser, Michael Ibba, Matthew P. Frosch, Ronald L. Thibert

    Publié 2016
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  11. 11
    Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia

    Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia par Soheil Meshinchi, William G. Woods, Derek L. Stirewalt, David A. Sweetser, Jonathan D. Buckley, Thomas K. Tjoa, Irwin D. Bernstein, Jerald P. Radich

    Publié 2001
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  12. 12
    Loss of TLE1 and TLE4 from the del(9q) commonly deleted region in AML cooperates with AML1-ETO to affect myeloid cell proliferation and survival

    Loss of TLE1 and TLE4 from the del(9q) commonly deleted region in AML cooperates with AML1-ETO to affect myeloid cell proliferation and survival par Farshid Dayyani, Jianfeng Wang, Jing-Ruey Joanna Yeh, E. Ahn, Erica M. Tobey, Dong‐Er Zhang, Irwin D. Bernstein, Randall T. Peterson, David A. Sweetser

    Publié 2008
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  13. 13
    AML1-ETO mediates hematopoietic self-renewal and leukemogenesis through a COX/β-catenin signaling pathway

    AML1-ETO mediates hematopoietic self-renewal and leukemogenesis through a COX/β-catenin signaling pathway par Yiyun Zhang, Jianfeng Wang, Justin C. Wheat, Xi Chen, Shan Jin, Hossein Sadrzadeh, Amir T. Fathi, Randall T. Peterson, Andrew L. Kung, David A. Sweetser, Jing-Ruey Joanna Yeh

    Publié 2013
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  14. 14
    Tle1 tumor suppressor negatively regulates inflammation in vivo and modulates NF-κB inflammatory pathway

    Tle1 tumor suppressor negatively regulates inflammation in vivo and modulates NF-κB inflammatory pathway par Selvi Ramasamy, Borja Sáez, Subhankar Mukhopadhyay, Daching Ding, Alwiya M. Ahmed, Xi Chen, Ferdinando Pucci, Rae’e Yamin, Jianfeng Wang, Mikaël J. Pittet, Cassandra M. Kelleher, David T. Scadden, David A. Sweetser

    Publié 2016
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  15. 15
    Mutations in the neutral sphingomyelinase gene SMPD3 implicate the ceramide pathway in human leukemias

    Mutations in the neutral sphingomyelinase gene SMPD3 implicate the ceramide pathway in human leukemias par Woo‐Jae Kim, Ross A. Okimoto, Louise E. Purton, Meagan Goodwin, Sara M. Haserlat, Farshid Dayyani, David A. Sweetser, Andrea I. McClatchey, Olivier Bernard, A. Thomas Look, Daphne W. Bell, David T. Scadden, Daniel A. Haber

    Publié 2008
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  16. 16
    Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing

    Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing par Mark Consugar, Daniel Navarro-Gomez, Emily Place, Kinga M. Bujakowska, Maria E Sousa, Zoë Fonseca-Kelly, Daniel G. Taub, Maria Janessian, Dan Yi Wang, Elizabeth D. Au, Katherine B. Sims, David A. Sweetser, Anne B. Fulton, Qin Liu, Janey L. Wiggs, Xiaowu Gai, Eric A. Pierce

    Publié 2014
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  17. 17
    De novo missense variants in<i>HECW2</i>are associated with neurodevelopmental delay and hypotonia

    De novo missense variants in<i>HECW2</i>are associated with neurodevelopmental delay and hypotonia par Esther R. Berko, Megan T. Cho, Christine M. Eng, Yunru Shao, David A. Sweetser, Jessica L. Waxler, Nathaniel H. Robin, Fallon Brewer, Sandra Donkervoort, Payam Mohassel, Carsten G. Bönnemann, Martin G. Bialer, Christine Moore, Lynne A. Wolfe, Cynthia J. Tifft, Yufeng Shen, Kyle Retterer, Francisca Millan, Wendy K. Chung

    Publié 2016
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  18. 18
    Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate–binding region

    Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate–binding region par McKenna Kelly, Meredith Park, Ivana Mihalek, Anne Rochtus, Marie Gramm, Eduardo Pérez‐Palma, Erika Axeen, Christina Hung, Heather E. Olson, Lindsay C. Swanson, Irina Anselm, Lauren C. Briere, Frances A. High, David A. Sweetser, Saima Kayani, Molly Snyder, Sophie Calvert, Ingrid E. Scheffer, Edward Yang, Jeff L. Waugh, Dennis Lal, Olaf A. Bodamer, Annapurna Poduri

    Publié 2019
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  19. 19
    A genome-wide DNA methylation signature for SETD1B-related syndrome

    A genome-wide DNA methylation signature for SETD1B-related syndrome par I. Krzyzewska, Saskia M. Maas, Peter Henneman, K. Lip, A. Venema, Kristin Barañano, Anna Chassevent, Erfan Aref‐Eshghi, Anthonie J. van Essen, Tokiko Fukuda, Hiroko Ikeda, M. Jacquemont, H.-G. Kim, Audrey Labalme, M. E. Suzanne Lewis, Gaëtan Lesca, Irene Madrigal, Sonal Mahida, Naomichi Matsumoto, Raquel Rabionet, Evica Rajcan‐Separovic, Ying Qiao, Bekim Sadiković, Hirotomo Saitsu, David A. Sweetser, Mariëlle Alders, Marcel M.A.M. Mannens

    Publié 2019
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  20. 20
    Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing

    Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing par Chloe M. Reuter, Jennefer N. Kohler, Devon Bonner, Diane B. Zastrow, Liliana Fernández, Annika M. Dries, Shruti Marwaha, Jean M. Davidson, Elly Brokamp, Matthew Herzog, Joyce Hong, Ellen F. Macnamara, Jill A. Rosenfeld, Kelly Schoch, Rebecca C. Spillmann, Joseph Loscalzo, Joel B. Krier, Joan M. Stoler, David A. Sweetser, Christina G.S. Palmer, John A. Phillips, Vandana Shashi, David A. Adams, Yaping Yang, Euan A. Ashley, Paul G. Fisher, John J. Mulvihill, Jonathan A. Bernstein, Matthew T. Wheeler

    Publié 2019
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