Ohcanbohtosat - David A. Sweetser
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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... Dahkki David A. Sweetser, S M Hauft, Peter C. Hoppe, E H Birkenmeier, Jeffrey I. Gordon
Almmustuhtton 1988Artigo -
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Mechanisms underlying generation of gradients in gene expression within the intestine: an analysis using transgenic mice containing fatty acid binding protein-human growth hormone... Dahkki David A. Sweetser, E H Birkenmeier, Peter C. Hoppe, Daniel W. McKeel, J I Gordon
Almmustuhtton 1988Artigo -
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Human liver fatty acid binding protein. Isolation of a full length cDNA and comparative sequence analyses of orthologous and paralogous proteins. Dahkki John B. Lowe, Mark S. Boguski, David A. Sweetser, Nabil A. Elshourbagy, John M. Taylor, Jeffrey I. Gordon
Almmustuhtton 1985Artigo -
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The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships. Dahkki David A. Sweetser, E H Birkenmeier, Ivana Klisak, Susan Zollman, R S Sparkes, T. Mohandas, Aldons J. Lusis, Jeffrey I. Gordon
Almmustuhtton 1987Artigo -
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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... Dahkki Laurie Demmer, E H Birkenmeier, David A. Sweetser, M S Levin, Susan Zollman, R S Sparkes, T. Mohandas, Aldons J. Lusis, Jeffrey I. Gordon
Almmustuhtton 1987Artigo -
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Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia Dahkki Soheil Meshinchi, William G. Woods, Derek L. Stirewalt, David A. Sweetser, Jonathan D. Buckley, Thomas K. Tjoa, Irwin D. Bernstein, Jerald P. Radich
Almmustuhtton 2001Artigo -
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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 Dahkki 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
Almmustuhtton 2008Artigo -
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AML1-ETO mediates hematopoietic self-renewal and leukemogenesis through a COX/β-catenin signaling pathway Dahkki 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
Almmustuhtton 2013Artigo -
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Tle1 tumor suppressor negatively regulates inflammation in vivo and modulates NF-κB inflammatory pathway Dahkki 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
Almmustuhtton 2016Artigo -
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Mutations in the neutral sphingomyelinase gene SMPD3 implicate the ceramide pathway in human leukemias Dahkki 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
Almmustuhtton 2008Artigo -
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Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing Dahkki 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
Almmustuhtton 2014Artigo -
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De novo missense variants in<i>HECW2</i>are associated with neurodevelopmental delay and hypotonia Dahkki 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
Almmustuhtton 2016Artigo -
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Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate–binding region Dahkki 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
Almmustuhtton 2019Artigo -
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A genome-wide DNA methylation signature for SETD1B-related syndrome Dahkki 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
Almmustuhtton 2019Artigo -
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Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing Dahkki 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
Almmustuhtton 2019Artigo
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Laktáseaddji fáttát
Biology
Gene
Genetics
Medicine
Mutation
Phenotype
Biochemistry
Bioinformatics
Cancer research
Disease
Exome sequencing
Internal medicine
Cell biology
Exome
Exon
Missense mutation
Molecular biology
Computational biology
Gene expression
Immunology
Pathology
Pediatrics
Stem cell
Binding protein
Gene knockdown
Genetic testing
Genome
Haematopoiesis
Hypotonia
Peptide sequence