Search Results - Jonathan G.L. Mullins

  • Showing 1 - 17 results of 17
Refine Results
  1. 1
    Terminal phase of cytokinesis in D-98S cells

    Terminal phase of cytokinesis in D-98S cells by Jonathan G.L. Mullins, JJ Biesele

    Published 1977
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    Membrane topology of the Mep/Amt family of ammonium transporters

    Membrane topology of the Mep/Amt family of ammonium transporters by Gavin H. Thomas, Jonathan G.L. Mullins, Mike Merrick

    Published 2000
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    In silico drug repurposing at the cytoplasmic surface of human aquaporin 1

    In silico drug repurposing at the cytoplasmic surface of human aquaporin 1 by Aled Lloyd, Karl Austin‐Muttitt, Jonathan G.L. Mullins

    Published 2025
    Get full text
    Artigo
    Save to List
    Saved in:
  4. 4
    TMCompare: transmembrane region sequence and structure

    TMCompare: transmembrane region sequence and structure by Roberto Coiti Togawa, J. F. Antoniw, Jonathan G.L. Mullins

    Published 2001
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Resistance to antifungals that target CYP51

    Resistance to antifungals that target CYP51 by Josie E. Parker, Andrew G. S. Warrilow, Claire Price, Jonathan G.L. Mullins, Diane Kelly, Steven L. Kelly

    Published 2014
    Get full text
    Revisão
    Save to List
    Saved in:
  6. 6
    The First Virally Encoded Cytochrome P450

    The First Virally Encoded Cytochrome P450 by David C. Lamb, Li Lei, Andrew G. S. Warrilow, Galina I. Lepesheva, Jonathan G.L. Mullins, Michael R. Waterman, Steven L. Kelly

    Published 2009
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay

    Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay by Rhys H. Thomas, Seo‐Kyung Chung, S. E. Wood, Thomas D. Cushion, Cheney Drew, Chrissy L. Hammond, Jean-François Vanbellinghen, Jonathan G.L. Mullins, Mark I. Rees

    Published 2013
    Get full text
    Artigo
    Save to List
    Saved in:
  8. 8
    A Short Regulatory Domain Restricts Glycerol Transport through Yeast Fps1p

    A Short Regulatory Domain Restricts Glycerol Transport through Yeast Fps1p by Markus J. Tamás, Sara Karlgren, Roslyn M. Bill, Kristina Hedfalk, Laura Allegri, Marie Céleste Jesus De Ferreira, Johan M. Thevelein, Jan Rydström, Jonathan G.L. Mullins, Stefan Hohmann

    Published 2003
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    Claudin Association with CD81 Defines Hepatitis C Virus Entry

    Claudin Association with CD81 Defines Hepatitis C Virus Entry by Helen J. Harris, Christopher Davis, Jonathan G.L. Mullins, Ke Hu, Margaret Goodall, Michelle J. Farquhar, Christopher Mee, Kathleen McCaffrey, Stephen P. Young, Heidi E. Drummer, Peter Balfe, Jane A. McKeating

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    The glycinergic system in human startle disease: a genetic screening approach

    The glycinergic system in human startle disease: a genetic screening approach by Jeffrey S. Davies, Seo‐Kyung Chung, Rhys H. Thomas, Angela K. Robinson, Carrie L. Hammond, Jonathan G.L. Mullins, Eloisa Carta, Brian R. Pearce, Kirsten Harvey, Victoria L. Harvey, Mark I. Rees, Mark I. Rees

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  11. 11
    De Novo Mutations in the Beta-Tubulin Gene TUBB2A Cause Simplified Gyral Patterning and Infantile-Onset Epilepsy

    De Novo Mutations in the Beta-Tubulin Gene TUBB2A Cause Simplified Gyral Patterning and Infantile-Onset Epilepsy by Thomas D. Cushion, Alex R. Paciorkowski, Daniela T. Pilz, Jonathan G.L. Mullins, Laurie E. Seltzer, Robert W. Marion, Emily Tuttle, Dalia Ghoneim, Susan L. Christian, Seo‐Kyung Chung, Mark I. Rees, William B. Dobyns

    Published 2014
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  12. 12
    Overlapping cortical malformations and mutations in TUBB2B and TUBA1A

    Overlapping cortical malformations and mutations in TUBB2B and TUBA1A by Thomas D. Cushion, William B. Dobyns, Jonathan G.L. Mullins, Neil Stoodley, Seo‐Kyung Chung, Andrew E. Fry, Ute Hehr, Roxana Gunny, Arthur S. Aylsworth, Prab Prabhakar, Gökhan Uyanık, Julia Rankin, Mark I. Rees, Daniela T. Pilz

    Published 2013
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  13. 13
    Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition

    Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition by Alexander McGirr, Tatiana V. Lipina, Ho-Suk Mun, John Georgiou, Ahmed H. Al-Amri, Enoch Ng, Dongxu Zhai, Christina Elliott, Ryan T. Cameron, Jonathan G.L. Mullins, Fang Liu, George S. Baillie, Steven J. Clapcote, John Roder

    Published 2015
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  14. 14
    Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes

    Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes by Renske Oegema, Thomas D. Cushion, Ian G. Phelps, Seo‐Kyung Chung, Jennifer C. Dempsey, Sarah Collins, Jonathan G.L. Mullins, Tracy Dudding, Harinder Gill, Andrew Green, William B. Dobyns, Gisele E. Ishak, Mark I. Rees, Dan Doherty

    Published 2015
    Get full text
    Artigo
    Save to List
    Saved in:
  15. 15
    Pathophysiological Mechanisms of Dominant and Recessive GLRA1 Mutations in Hyperekplexia

    Pathophysiological Mechanisms of Dominant and Recessive GLRA1 Mutations in Hyperekplexia by Seo‐Kyung Chung, Jean-François Vanbellinghen, Jonathan G.L. Mullins, Angela K. Robinson, Janina Hantke, Chrissy L. Hammond, Daniel F. Gilbert, Michael Freilinger, Monique M. Ryan, Michael C. Kruer, Amira Masri, Candan Gürses, C D Ferrie, Kirsten Harvey, Rita Shiang, John Christodoulou, Frédérick Andermann, E. Andermann, Rhys H. Thomas, Victoria L. Harvey, Joseph W. Lynch, Mark I. Rees

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  16. 16
    GLRB is the third major gene of effect in hyperekplexia

    GLRB is the third major gene of effect in hyperekplexia by Seo‐Kyung Chung, Anna Bode, Thomas D. Cushion, Rhys H. Thomas, Charlotte Hunt, S. E. Wood, William Owen Pickrell, Cheney Drew, Sumimasa Yamashita, Rita Shiang, Steffen Leiz, Ann-Carolyn Longhardt, Vera Raile, Bernhard Weschke, Ratna Dua Puri, I. C. Verma, Victoria L. Harvey, Didi D. Ratnasinghe, Michael Parker, Chris Rittey, Amira Masri, Lokesh Lingappa, Owain W. Howell, Jean-François Vanbellinghen, Jonathan G.L. Mullins, Joseph W. Lynch, Mark I. Rees

    Published 2012
    Get full text
    Artigo
    Save to List
    Saved in:
  17. 17
    De novo mutations in GRIN1 cause extensive bilateral polymicrogyria

    De novo mutations in GRIN1 cause extensive bilateral polymicrogyria by Andrew E. Fry, Katherine A. Fawcett, Nathanel Zelnik, Hongjie Yuan, Belinda A.N. Thompson, Lilach Shemer-Meiri, Thomas D. Cushion, Hood Mugalaasi, David Sims, Neil Stoodley, Seo‐Kyung Chung, Mark I. Rees, Chirag Patel, Louise Brueton, Valérie Layet, Fabienne Giuliano, Michael Kerr, Ehud Banne, Vardiella Meiner, Tally Lerman‐Sagie, Katherine L. Helbig, Laura H. Kofman, Kristin Knight, Wenjuan Chen, Varun Kannan, Chun Hu, Hirofumi Kusumoto, Jin Zhang, Sharon A. Swanger, Gil Shaulsky, Ghayda Mirzaa, Alison M. Muir, Heather C. Mefford, William B. Dobyns, Amanda B. Mackenzie, Jonathan G.L. Mullins, Johannes R. Lemke, Nadia Bahi‐Buisson, Stephen F. Traynelis, Heledd F Iago, Daniela T. Pilz

    Published 2017
    Get full text Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: