Výsledky vyhledávání - Brooke Gardiner

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  1. 1
    Dynamic transcription programs during ES cell differentiation towards mesoderm in serum versus serum-freeBMP4 culture

    Dynamic transcription programs during ES cell differentiation towards mesoderm in serum versus serum-freeBMP4 culture Autor Stephen J. Bruce, Brooke Gardiner, Leslie Burke, Milena Gongora, Sean M. Grimmond, Andrew C. Perkins

    Vydáno 2007
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  2. 2
    Brief Report: Intestinal Dysbiosis in Ankylosing Spondylitis

    Brief Report: Intestinal Dysbiosis in Ankylosing Spondylitis Autor Mary‐Ellen Costello, Francesco Ciccia, Dana Willner, Nicole M. Warrington, Philip C. Robinson, Brooke Gardiner, Mhairi Marshall, Tony Kenna, G Triolo, Matthew A. Brown

    Vydáno 2014
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  3. 3
    Transcriptional analysis of early lineage commitment in human embryonic stem cells

    Transcriptional analysis of early lineage commitment in human embryonic stem cells Autor Andrew L. Laslett, Sean M. Grimmond, Brooke Gardiner, Lincon A. Stamp, Adelia Lin, Susan M. Hawes, Sam Wormald, David J. Nikolic‐Paterson, David N. Haylock, Martín F. Pera

    Vydáno 2007
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  4. 4
    A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells

    A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells Autor Michael R. Tallack, Tom Whitington, Wai Shan Yuen, Elanor N. Wainwright, Janelle R. Keys, Brooke Gardiner, Ehsan Nourbakhsh, Nicole Cloonan, Sean M. Grimmond, Timothy L. Bailey, Andrew C. Perkins

    Vydáno 2010
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  5. 5
    Regulated post-transcriptional RNA cleavage diversifies the eukaryotic transcriptome

    Regulated post-transcriptional RNA cleavage diversifies the eukaryotic transcriptome Autor Tim R. Mercer, Marcel E. Dinger, Cameron P. Bracken, Gabriel Kolle, Jan M. Szubert, Darren Korbie, Marjan Askarian-Amiri, Brooke Gardiner, Gregory J. Goodall, Sean M. Grimmond, John S. Mattick

    Vydáno 2010
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  6. 6
    Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6

    Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6 Autor Duncan B. Sparrow, Aideen M. McInerney‐Leo, Zoran Gucev, Brooke Gardiner, Mhairi Marshall, Paul Leo, Deborah L. Chapman, Velibor Tasić, Abduhadi Shishko, Matthew A. Brown, Emma L. Duncan, Sally L. Dunwoodie

    Vydáno 2013
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  7. 7
    Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects

    Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects Autor Aideen M. McInerney‐Leo, Duncan B. Sparrow, Jessica Harris, Brooke Gardiner, Mhairi Marshall, Victoria C. O׳Reilly, Hongjun Shi, Matthew A. Brown, Paul Leo, Andreas Zankl, Sally L. Dunwoodie, Emma L. Duncan

    Vydáno 2014
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  8. 8
    Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation

    Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation Autor Marcel E. Dinger, Paulo Amaral, Tim R. Mercer, Ken C. Pang, Stephen J. Bruce, Brooke Gardiner, Marjan Askarian-Amiri, Kelin Ru, Giulia Soldà, Cas Simons, Susan M. Sunkin, Mark L. Crowe, Sean M. Grimmond, Andrew C. Perkins, John S. Mattick

    Vydáno 2008
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  9. 9
    Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60

    Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60 Autor Aideen M. McInerney‐Leo, Miriam Schmidts, Claudio R. Cortés, Paul Leo, Blanca Gener, Andrew D. Courtney, Brooke Gardiner, Jessica Harris, Yeping Lu, Mhairi Marshall, Peter Scambler, Philip L. Beales, Matthew A. Brown, Andreas Zankl, Hannah M. Mitchison, Emma L. Duncan, Carol Wicking

    Vydáno 2013
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  10. 10
    MicroRNAs and their isomiRs function cooperatively to target common biological pathways

    MicroRNAs and their isomiRs function cooperatively to target common biological pathways Autor Nicole Cloonan, Shivangi Wani, Qinying Xu, Jian Gu, Kristi Lea, Sheila J. Heater, Cátálin Bárbácioru, Anita L Steptoe, Hilary C. Martin, Ehsan Nourbakhsh, Keerthana Krishnan, Brooke Gardiner, Xiaohui Wang, Kátia Nones, Jason A. Steen, Nicholas Matigian, David Wood, Karin S. Kassahn, Nicola Waddell, Jill Shepherd, Clarence Lee, Jeff Ichikawa, Kevin McKernan, Kelli Bramlett, Scott Kuersten, Sean M. Grimmond

    Vydáno 2011
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  11. 11
    Mutations in the Gene Encoding IFT Dynein Complex Component WDR34 Cause Jeune Asphyxiating Thoracic Dystrophy

    Mutations in the Gene Encoding IFT Dynein Complex Component WDR34 Cause Jeune Asphyxiating Thoracic Dystrophy Autor Miriam Schmidts, Julia Vodopiutz, Sonia Christou-Savina, Claudio R. Cortés, Aideen M. McInerney‐Leo, Richard D. Emes, Heleen H. Arts, Beyhan Tüysüz, Jason K. D’Silva, Paul Leo, Tom Giles, Machteld M. Oud, Jessica Harris, Marion Koopmans, Mhairi Marshall, Nursel Elçioğlu, Alma Kuechler, Detlef Böckenhauer, Anthony T. Moore, Louise C. Wilson, Andreas Janecke, Matthew E. Hurles, Warren Emmet, Brooke Gardiner, Berthold Streubel, Belinda Dopita, Andreas Zankl, Hülya Kayserili, Peter Scambler, Matthew A. Brown, Philip L. Beales, Carol Wicking, Emma L. Duncan, Hannah M. Mitchison

    Vydáno 2013
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  12. 12
    Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans

    Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans Autor Jan Halbritter, Albane A. Bizet, Miriam Schmidts, Jonathan D. Porath, Daniela A. Braun, Heon Yung Gee, Aideen M. McInerney‐Leo, Pauline Krug, Emilie Filhol, Erica E. Davis, Rannar Airik, Peter G. Czarnecki, Anna Lehman, Peter Trnka, Patrick Nitschké, Christine Bôle‐Feysot, Markus Schueler, Bertrand Knebelmann, Stéphane Burtey, Attila J. Szabó, Kálmán Tory, Paul Leo, Brooke Gardiner, Fiona A. McKenzie, Andreas Zankl, Matthew A. Brown, Jane Hartley, Eamonn R. Maher, Chunmei Li, Michel R. Leroux, Peter Scambler, Shing H. Zhan, Steven J.M. Jones, Hülya Kayserili, Beyhan Tüysüz, Khemchand N Moorani, Alexandru R. Constantinescu, Ian D. Krantz, Bernard S. Kaplan, Jagesh V. Shah, Toby W. Hurd, Dan Doherty, Nicholas Katsanis, Emma L. Duncan, Edgar A. Otto, Philip L. Beales, Hannah M. Mitchison, Sophie Saunier, Friedhelm Hildebrandt

    Vydáno 2013
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  13. 13
    Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture

    Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture Autor Hou‐Feng Zheng, Vincenzo Forgetta, Yi‐Hsiang Hsu, Karol Estrada, Alberto Roselló‐Díez, Paul Leo, Chitra Lekha Dahia, Kyung Hyun Park‐Min, Jonathan H. Tobias, Charles Kooperberg, Aaron Kleinman, Unnur Styrkársdóttir, Yongmei Liu, Charlotta Uggla, Daniel S. Evans, Carrie M. Nielson, Klaudia Walter, U. Pettersson, Shane McCarthy, Joel Eriksson, Tony Kwan, Mila Jhamai, Katerina Trajanoska, Yasin Memari, Josine L. Min, Jie Huang, Petr Danecek, Beth Wilmot, Rui Li, Wen‐Chi Chou, Lauren E. Mokry, Alireza Moayyeri, Melina Claussnitzer, Chia‐Ho Cheng, Warren Cheung, Carolina Medina‐Gómez, Bing Ge, Shu‐Huang Chen, Kwangbom Choi, Ling Oei, James A. Fraser, Robert Kraaij, Matthew Hibbs, Celia L. Gregson, Denis Paquette, Albert Hofman, Carl Wibom, Gregory J. Tranah, Mhairi Marshall, Brooke Gardiner, Katie Cremin, Paul L. Auer, Li Hsu, Susan M. Ring, Joyce Y. Tung, Gudmar Thorleifsson, Anke W. Enneman, Natasja M. van Schoor, C.P.G.M. de Groot, Nathalie van der Velde, Beatrice Melin, John P. Kemp, Claus Christiansen, Adrian Sayers, Yanhua Zhou, Sophie Caldérari, Frank J.A. van Rooij, Chris Carlson, Annette Peters, Soizik Berlivet, Josée Dostie, André G. Uitterlinden, Stephen R. Williams, Charles R. Farber, Daniel Grinberg, Andrea Z. LaCroix, Jeff Haessler, Daniel I. Chasman, Franco Giulianini, Lynda M. Rose, Paul M. Ridker, John A. Eisman, Tuan V. Nguyen, Jacqueline R. Center, Xavier Nogués, Natalia García‐Giralt, Lenore J. Launer, Vilmundur Guðnason, Dan Mellström, Liesbeth Vandenput, Najaf Amin, Cornelia M. van Duijn, Magnus K. Karlsson, Östen Ljunggren, Olle Svensson, Göran Hallmans, François Rousseau, Sylvie Giroux, J L Bussière, Pascal P. Arp

    Vydáno 2015
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  14. 14
    Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes

    Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes Autor Andrew V. Biankin, Nicola Waddell, Karin S. Kassahn, Marie‐Claude Gingras, Lakshmi Muthuswamy, Amber L. Johns, David K. Miller, Peter J. Wilson, Ann‐Marie Patch, Jianmin Wu, David K. Chang, Mark J. Cowley, Brooke Gardiner, Sarah Song, Ivon Harliwong, Senel Idrisoglu, Craig Nourse, Ehsan Nourbakhsh, Suzanne Manning, Shivangi Wani, Milena Gongora, Marina Pajic, Christopher J. Scarlett, Anthony J. Gill, Andreia V. Pinho, Ilse Rooman, Matthew J. Anderson, Oliver Holmes, Conrad Leonard, Darrin F. Taylor, Scott Wood, Qinying Xu, Kátia Nones, J. Lynn Fink, Angelika N. Christ, Timothy J. C. Bruxner, Nicole Cloonan, Gabriel Kolle, Felicity Newell, Mark Pinese, R. Scott Mead, Jeremy L. Humphris, Warren Kaplan, Marc D. Jones, Emily K. Colvin, Adnan Nagrial, Emily S. Humphrey, Angela Chou, Venessa Chin, Lorraine A. Chantrill, Amanda Mawson, Jaswinder S. Samra, James G. Kench, Jessica A. Lovell, Roger J. Daly, Neil D. Merrett, Christopher W. Toon, Krishna Epari, Nam Q. Nguyen, Andrew P. Barbour, Nikolajs Zeps, Nipun Kakkar, Fengmei Zhao, Yuan Wu, Min Wang, Donna M. Muzny, William E. Fisher, F. Charles Brunicardi, Sally E. Hodges, Jeffrey G. Reid, Jennifer Drummond, Kyle Chang, Yi Han, Lora Lewis, Huyen Dinh, Christian Buhay, Timothy A. Beck, Lee E. Timms, Michelle Sam, Kimberly Begley, Andrew Brown, Deepa Pai, Ami Panchal, Nicholas Buchner, Richard de Borja, Robert E. Denroche, Christina K. Yung, Stefano Serra, Nicole Onetto, Debabrata Mukhopadhyay, Ming‐Sound Tsao, Patricia A. Shaw, Gloria M. Petersen, Steven Gallinger, Ralph H. Hruban, Anirban Maitra, Christine A. Iacobuzio‐Donahue, Richard D. Schulick, Christopher L. Wolfgang, Richard A. Morgan

    Vydáno 2012
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