Výsledky vyhledávání - Molly Weaver

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  1. 1
    Dual Origin of Tissue-Specific Progenitor Cells in <i>Drosophila</i> Tracheal Remodeling

    Dual Origin of Tissue-Specific Progenitor Cells in <i>Drosophila</i> Tracheal Remodeling Autor Molly Weaver, Mark A. Krasnow

    Vydáno 2008
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  2. 2
    Tissue interactions pattern the mesenchyme of the embryonic mouse lung

    Tissue interactions pattern the mesenchyme of the embryonic mouse lung Autor Molly Weaver, Lorene Batts, Brigid L.M. Hogan

    Vydáno 2003
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  3. 3
    <i>Aspergillus fumigatus</i>Variant with Decreased Susceptibility to Multiple Antifungals

    <i>Aspergillus fumigatus</i>Variant with Decreased Susceptibility to Multiple Antifungals Autor S. Arunmozhi Balajee, Molly Weaver, Alexander Imhof, Jennifer L. Gribskov, Kieren A. Marr

    Vydáno 2004
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  4. 4
    Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies

    Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies Autor Karen Stephens, Molly Weaver, Kathleen A. Leppig, Kyoko Maruyama, Peter D. Emanuel, Michelle M. Le Beau, Kevin Shannon

    Vydáno 2006
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  5. 5
    Functional Interactions of Genes Mediating Convergent Extension,knypekandtrilobite,during the Partitioning of the Eye Primordium in Zebrafish

    Functional Interactions of Genes Mediating Convergent Extension,knypekandtrilobite,during the Partitioning of the Eye Primordium in Zebrafish Autor Florence L. Marlow, Fried Zwartkruis, Jarema Malicki, Stephan C. F. Neuhauss, Leïla Abbas, Molly Weaver, Wolfgang Driever, Lilianna Solnica‐Krezel

    Vydáno 1998
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  6. 6
    Sequencing newly replicated DNA reveals widespread plasticity in human replication timing

    Sequencing newly replicated DNA reveals widespread plasticity in human replication timing Autor R. Scott Hansen, Sean Thomas, Richard Sandstrom, Theresa K. Canfield, Robert E. Thurman, Molly Weaver, Michael O. Dorschner, Stanley M. Gartler, J Stamatoyannopoulos

    Vydáno 2009
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  7. 7
    Genome‐Scale Mapping of DNase I Hypersensitivity

    Genome‐Scale Mapping of DNase I Hypersensitivity Autor Sam John, Peter J. Sabo, Theresa K. Canfield, Kristen Lee, Shinny Vong, Molly Weaver, Hao Wang, Jeff Vierstra, Alex Reynolds, Robert E. Thurman, J Stamatoyannopoulos

    Vydáno 2013
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  8. 8
    Widespread plasticity in CTCF occupancy linked to DNA methylation

    Widespread plasticity in CTCF occupancy linked to DNA methylation Autor Hao Wang, Matthew T. Maurano, Hongzhu Qu, Katherine E. Varley, Jason Gertz, Florencia Pauli, Kristen Lee, Theresa Canfield, Molly Weaver, Richard Sandstrom, Robert E. Thurman, Rajinder Kaul, R Myers, J Stamatoyannopoulos

    Vydáno 2012
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  9. 9
    Zebrafish globin switching occurs in two developmental stages and is controlled by the LCR

    Zebrafish globin switching occurs in two developmental stages and is controlled by the LCR Autor Jared J. Ganis, Nelson Hsia, Eirini Trompouki, Jill L. O. de Jong, Anthony DiBiase, John S. Lambert, Zhiying Jia, Peter J. Sabo, Molly Weaver, Richard Sandstrom, J Stamatoyannopoulos, Yi Zhou, Leonard I. Zon

    Vydáno 2012
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  10. 10
    An expansive human regulatory lexicon encoded in transcription factor footprints

    An expansive human regulatory lexicon encoded in transcription factor footprints Autor Shane Neph, Jeff Vierstra, Andrew B. Stergachis, Alex Reynolds, Eric Haugen, Benjamin Vernot, Robert E. Thurman, Sam John, Richard Sandstrom, Audra Johnson, Matthew T. Maurano, Richard Humbert, Eric Rynes, Hao Wang, Shinny Vong, Kristen Lee, Daniel Bates, Morgan Diegel, Vaughn Roach, Douglas Dunn, Jun Neri, Anthony Schafer, R. Scott Hansen, Tanya Kutyavin, Erika Giste, Molly Weaver, Theresa K. Canfield, Peter J. Sabo, Miaohua Zhang, Gayathri Balasundaram, Rachel Byron, Michael J. MacCoss, Joshua M. Akey, M. A. Bender, Mark Groudine, Rajinder Kaul, J Stamatoyannopoulos

    Vydáno 2012
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  11. 11
    Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

    Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1 Autor Gemma L. Carvill, Sinéad B. Heavin, Simone C. Yendle, Jacinta M. McMahon, Brian J. O’Roak, Joseph Cook, Adiba Khan, Michael O. Dorschner, Molly Weaver, Sophie Calvert, Stephen Malone, Geoff Wallace, Thorsten Stanley, Ann Bye, Andrew Bleasel, Katherine B. Howell, Sara Kivity, Mark T. Mackay, Victoria Rodriguez‐Casero, Richard Webster, Amos D. Korczyn, Zaid Afawi, Nathanel Zelnick, Tally Lerman‐Sagie, Dorit Lev, Rikke S. Møller, Deepak Gill, Danielle M. Andrade, Jeremy L. Freeman, Lynette G. Sadleir, Jay Shendure, Samuel F. Berkovic, Ingrid E. Scheffer, Heather C. Mefford

    Vydáno 2013
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  12. 12
    Mapping and sequencing of structural variation from eight human genomes

    Mapping and sequencing of structural variation from eight human genomes Autor Jeffrey M. Kidd, Gregory M. Cooper, William F. Donahue, Hillary S. Hayden, Nick Sampas, Tina Graves, Nancy F. Hansen, Brian Teague, Can Alkan, Francesca Antonacci, Eric Haugen, Troy Zerr, N. Alice Yamada, Peter Tsang, Tera L. Newman, Eray Tüzün, Ze Cheng, Heather Ebling, Nadeem Tusneem, Robert David, Will Gillett, Karen A. Phelps, Molly Weaver, David J. Saranga, Adrianne Brand, Wei Tao, Erik Gustafson, Kevin McKernan, Lin Chen, Maika Malig, Joshua D. Smith, Joshua M. Korn, Steven A. McCarroll, David Altshuler, Daniel A. Peiffer, Michael O. Dorschner, J Stamatoyannopoulos, David A. Schwartz, Deborah A. Nickerson, James C. Mullikin, Richard K. Wilson, Laurakay Bruhn, Maynard V. Olson, Rajinder Kaul, Andrew R. Smith, Evan E. Eichler

    Vydáno 2008
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  13. 13
    Association of<i>MTOR</i>Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism

    Association of<i>MTOR</i>Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism Autor Ghayda Mirzaa, Catarina D. Campbell, Nadia Solovieff, Carleton P. Goold, Laura A. Jansen, Suchithra Menon, Andrew E. Timms, Valerio Conti, Jonathan Biag, Carissa Olds, Evan A. Boyle, Sarah Collins, Gisele E. Ishak, Sandra L. Poliachik, Katta M. Girisha, Kit San Yeung, Brian Hon‐Yin Chung, Elisa Rahikkala, Sonya A. Gunter, Sharon S. McDaniel, Colleen Macmurdo, Jonathan A. Bernstein, Beth Martin, Rebecca Leary, Scott Mahan, Shanming Liu, Molly Weaver, Michael O. Dorschner, Shalini N. Jhangiani, Donna M. Muzny, Eric Boerwinkle, Richard A. Gibbs, James R. Lupski, Jay Shendure, Russell P. Saneto, Edward J. Novotny, Christopher J. Wilson, William R. Sellers, Michael Morrissey, Robert F. Hevner, Jeffrey G. Ojemann, Renzo Guerrini, Leon O. Murphy, Wendy Winckler, William B. Dobyns

    Vydáno 2016
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  14. 14
    The accessible chromatin landscape of the human genome

    The accessible chromatin landscape of the human genome Autor Robert E. Thurman, Eric Rynes, Richard Humbert, Jeff Vierstra, Matthew T. Maurano, Eric Haugen, Nathan C. Sheffield, Andrew B. Stergachis, Hao Wang, Benjamin Vernot, Kavita S. Garg, Sam John, Richard Sandstrom, Daniel Bates, Lisa Boatman, Theresa K. Canfield, Morgan Diegel, Douglas Dunn, Abigail K. Ebersol, Tristan Frum, Erika Giste, Audra Johnson, Ericka M. Johnson, Tanya Kutyavin, Bryan R. Lajoie, Bum-Kyu Lee, Kristen Lee, Darin London, Dimitra M. Lotakis, Shane Neph, Fidencio Neri, Éric Nguyen, Hongzhu Qu, Alex Reynolds, Vaughn Roach, Alexias Safi, Minerva E. Sanchez, Amartya Sanyal, Anthony Shafer, Jeremy M. Simon, Lingyun Song, Shinny Vong, Molly Weaver, Yongqi Yan, Zhancheng Zhang, Zhuzhu Zhang, Boris Lenhard, Muneesh Tewari, Michael O. Dorschner, R. Scott Hansen, Patrick A. Navas, George Stamatoyannopoulos, Vishwanath R. Iyer, Jason D. Lieb, Shamil Sunyaev, Joshua M. Akey, Peter J. Sabo, Rajinder Kaul, Terrence S. Furey, Job Dekker, Gregory E. Crawford, J Stamatoyannopoulos

    Vydáno 2012
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  15. 15
    Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

    Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project Autor Ewan Birney, J Stamatoyannopoulos, Anindya Dutta, Roderic Guigó, T Gingeras, Elliott H. Margulies, Zhiping Weng, M Snyder, Emmanouil T. Dermitzakis, Robert E. Thurman, Michael S. Kuehn, Christopher M. Taylor, Shane Neph, Christof Koch, Saurabh Asthana, Ankit Malhotra, Ivan Adzhubei, Jason Greenbaum, Robert Andrews, Paul Flicek, Patrick J. Boyle, Hua Cao, N. P. Carter, Gayle K. Clelland, Sean Davis, Nathan Day, Pawandeep Dhami, Shane C. Dillon, Michael O. Dorschner, Heike Fiegler, Paul G. Giresi, Jeff Goldy, Michael Hawrylycz, Andrew Haydock, Richard Humbert, Keith James, Brett Johnson, Ericka M. Johnson, Tristan Frum, Elizabeth Rosenzweig, Neerja Karnani, Kirsten Lee, Grégory Lefebvre, Patrick A. Navas, Fidencio Neri, Stephen C. J. Parker, Peter J. Sabo, Richard Sandstrom, Anthony Shafer, David Vetrie, Molly Weaver, Sarah Wilcox, Man Yu, Francis S. Collins, Job Dekker, Jason D. Lieb, Thomas D. Tullius, Gregory E. Crawford, Shamil Sunyaev, William Stafford Noble, Ian Dunham, Alexandre Reymond, Philipp Kapranov, Joel Rozowsky, Deyou Zheng, Robert Castelo, Adam Frankish, Jennifer Harrow, Srinka Ghosh, Albin Sandelin, Ivo L. Hofacker, Robert Baertsch, Damian Keefe, Sujit Dike, Jill Cheng, Heather A. Hirsch, Edward A. Sekinger, Julien Lagarde, Josep F. Abril, Atif Shahab, Christoph Flamm, Claudia Fried, Jörg Hackermüller, Jana Hertel, Manja Lindemeyer, Kristin Missal, Andrea Tanzer, Stefan Washietl, Jan O. Korbel, Olof Emanuelsson, Jakob Skou Pedersen, Nancy Holroyd, Ruth Taylor, David Swarbreck, Nicholas Matthews, Mark Dickson, Daryl J. Thomas, Matthew T. Weirauch, James Gilbert, Jörg Drenkow

    Vydáno 2007
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