Canlyniadau Chwilio - Helen Stewart

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  1. 1
    Fatal myocardial infarction in the Scottish adjuvant tamoxifen trial. The Scottish Breast Cancer Committee.

    Fatal myocardial infarction in the Scottish adjuvant tamoxifen trial. The Scottish Breast Cancer Committee. gan C. McDonald, Helen Stewart

    Cyhoeddwyd 1991
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  2. 2
    <scp>BRD</scp>4 associates with p53 in <scp>DNMT</scp>3A‐mutated leukemia cells and is implicated in apoptosis by the bromodomain inhibitor <scp>JQ</scp>1

    <scp>BRD</scp>4 associates with p53 in <scp>DNMT</scp>3A‐mutated leukemia cells and is implicated in apoptosis by the bromodomain inhibitor <scp>JQ</scp>1 gan Helen Stewart, Gillian A. Horne, Sarah Bastow, Timothy Chevassut

    Cyhoeddwyd 2013
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  3. 3
    Scottish Adjuvant Tamoxifen Trial: a Randomized Study Updated to 15 Years

    Scottish Adjuvant Tamoxifen Trial: a Randomized Study Updated to 15 Years gan Helen Stewart, R. J. Prescott, A P M Forrest

    Cyhoeddwyd 2001
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  4. 4
    Nanog Requires BRD4 to Maintain Murine Embryonic Stem Cell Pluripotency and Is Suppressed by Bromodomain Inhibitor JQ1 Together with Lefty1

    Nanog Requires BRD4 to Maintain Murine Embryonic Stem Cell Pluripotency and Is Suppressed by Bromodomain Inhibitor JQ1 Together with Lefty1 gan Gillian A. Horne, Helen Stewart, Jacqueline Dickson, Stefan Knapp, Bernard Ramsahoye, Timothy Chevassut

    Cyhoeddwyd 2014
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  5. 5
    GAP-43 is expressed by nonmyelin-forming Schwann cells of the peripheral nervous system.

    GAP-43 is expressed by nonmyelin-forming Schwann cells of the peripheral nervous system. gan Rory Curtis, Helen Stewart, S M Hall, Graham P. Wilkin, Rhona Mirsky, KR Jessen

    Cyhoeddwyd 1992
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  6. 6
    Identification of circulating microRNAs as diagnostic biomarkers for use in multiple myeloma

    Identification of circulating microRNAs as diagnostic biomarkers for use in multiple myeloma gan Christopher I. Jones, Maria V. Zabolotskaya, A. J. King, Helen Stewart, Gillian A. Horne, Timothy Chevassut, Sarah F. Newbury

    Cyhoeddwyd 2012
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  7. 7
    Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu–Cheney syndrome

    Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu–Cheney syndrome gan Mary Jane Gray, Chong Ae Kim, Débora Romeo Bertola, Paula Ricci Arantes, Helen Stewart, Michael A. Simpson, Melita Irving, Stephen P. Robertson

    Cyhoeddwyd 2011
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  8. 8
    Lack of galectin‐1 results in defects in myoblast fusion and muscle regeneration

    Lack of galectin‐1 results in defects in myoblast fusion and muscle regeneration gan Vassilis Georgiadis, Helen Stewart, Hilary J. Pollard, Yasemin Tavsanoglu, Rathi Prasad, Julia Horwood, Louise Deltour, Kirstin Goldring, Françoise Poirier, Diana J. Lawrence‐Watt

    Cyhoeddwyd 2007
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  9. 9
    Mutants of <i>Escherichia coli</i> Heat-Labile Toxin Act as Effective Mucosal Adjuvants for Nasal Delivery of an Acellular Pertussis Vaccine: Differential Effects of the Nontoxic AB Complex and Enzyme Activity on Th1 and Th2 Cells

    Mutants of <i>Escherichia coli</i> Heat-Labile Toxin Act as Effective Mucosal Adjuvants for Nasal Delivery of an Acellular Pertussis Vaccine: Differential Effects of the Nontoxic A... gan Elizabeth J. Ryan, Edel A. McNeela, Geraldine A. Murphy, Helen Stewart, Derek T. O’Hagan, Mariagrazia Pizza, Rino Rappuoli, Kingston H. G. Mills

    Cyhoeddwyd 1999
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  10. 10
    Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology

    Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology gan Louise Tee, Derek Lim, Renuka Dias, Marie-Odile Baudement, A Slater, Gail Kirby, Tom Hancocks, Helen Stewart, Carol Hardy, Fiona MacDonald, Eamonn R. Maher

    Cyhoeddwyd 2013
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  11. 11
    Galectin‐1 Induces Skeletal Muscle Differentiation in Human Fetal Mesenchymal Stem Cells and Increases Muscle Regeneration

    Galectin‐1 Induces Skeletal Muscle Differentiation in Human Fetal Mesenchymal Stem Cells and Increases Muscle Regeneration gan Jerry Kok Yen Chan, Keelin O’Donoghue, Manuela Gavina, Yvan Torrente, Nigel Kennea, Huseyin Mehmet, Helen Stewart, Diana J. Watt, Jennifer E. Morgan, Nicholas M. Fisk

    Cyhoeddwyd 2006
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  12. 12
    Genetic professionals' reports of nondisclosure of genetic risk information within families

    Genetic professionals' reports of nondisclosure of genetic risk information within families gan Angus Clarke, Martin Richards, L Kerzin-Storrar, Jane Halliday, Mary Young, Sheila A Simpson, Katie Featherstone, Karen Forrest, Anneke Lucassen, Patrick J. Morrison, Oliver Quarrell, Helen Stewart

    Cyhoeddwyd 2005
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  13. 13
    A<i>de novo</i>frameshift in<i>HNRNPK</i>causing a Kabuki-like syndrome with nodular heterotopia

    A<i>de novo</i>frameshift in<i>HNRNPK</i>causing a Kabuki-like syndrome with nodular heterotopia gan Leslie A. Lange, A. T. Pagnamenta, Stefano Lise, Steven Clasper, Helen Stewart, Elham Sadighi Akha, Gerardine Quaghebeur, Samantha J.L. Knight, David A. Keays, Jenny C. Taylor, Usha Kini

    Cyhoeddwyd 2016
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  14. 14
    A Transgenic Rat Model of Charcot-Marie-Tooth Disease

    A Transgenic Rat Model of Charcot-Marie-Tooth Disease gan Michael W. Sereda, Ian R. Griffiths, Anja Pühlhofer, Helen Stewart, Moritz J. Rossner, Frank Zimmermann, Josef P. Magyar, Armin Schneider, Ernst Hund, H.-M. Meinck, Ueli Suter, Klaus‐Armin Nave

    Cyhoeddwyd 1996
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  15. 15
    Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies

    Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies gan Alistair T. Pagnamenta, Stefano Lise, Victoria Harrison, Helen Stewart, Sandeep Jayawant, Gerardine Quaghebeur, Alexander T. Deng, V. Murphy, Elham Sadighi Akha, Andy Rimmer, Iain Mathieson, Samantha J.L. Knight, Usha Kini, Jenny C. Taylor, David A. Keays

    Cyhoeddwyd 2011
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  16. 16
    Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators

    Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators gan Gaia Gestri, Robert J. Osborne, Alexander W. Wyatt, Dianne Gerrelli, Susan Gribble, Helen Stewart, Alan Fryer, David J. Bunyan, Katrina Prescott, J. R. O. Collin, Tomas Fitzgerald, David Robinson, Nigel P. Carter, Stephen W. Wilson, Nicola Ragge

    Cyhoeddwyd 2009
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  17. 17
    Analysis of Transcription Factors Key for Mouse Pancreatic Development Establishes NKX2-2 and MNX1 Mutations as Causes of Neonatal Diabetes in Man

    Analysis of Transcription Factors Key for Mouse Pancreatic Development Establishes NKX2-2 and MNX1 Mutations as Causes of Neonatal Diabetes in Man gan Sarah E. Flanagan, Elisa De Franco, Hana Lango Allen, Michele Zerah, Majedah Abdul-Rasoul, Julie Edge, Helen Stewart, Elham Alamiri, Khalid Hussain, S Wallis, Liat de Vries, Oscar Rubio‐Cabezas, Jayne Houghton, Emma L. Edghill, Ann‐Marie Patch, Sian Ellard, Andrew T. Hattersley

    Cyhoeddwyd 2014
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  18. 18
    Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

    Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant gan Femke Hannes, Andrew J. Sharp, Heather C. Mefford, Thomy de Ravel, Claudia Ruivenkamp, M.H. Breuning, JP Fryns, Koenraad Devriendt, Griet Van Buggenhout, Annick Vogels, Helen Stewart, Raoul C. M. Hennekam, Gregory M. Cooper, Regina Regan, Samantha J.L. Knight, Evan E. Eichler, Joris Vermeesch

    Cyhoeddwyd 2008
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  19. 19
    Synthesis and Biological Investigation of (+)-JD1, an Organometallic BET Bromodomain Inhibitor

    Synthesis and Biological Investigation of (+)-JD1, an Organometallic BET Bromodomain Inhibitor gan Storm Hassell‐Hart, Andrew C. Runcie, T. Krojer, Jordan Doyle, Ella Lineham, Cory A. Ocasio, Brenno A. D. Neto, Oleg Fedorov, Graham P. Marsh, Hannah J. Maple, Robert Felix, Rebecca Banks, Alessio Ciulli, S. Picaud, P. Filippakopoulos, F. von Delft, Paul E. Brennan, Helen Stewart, Timothy Chevassut, Martin Walker, Carol Austin, Simon Morley, John Spencer

    Cyhoeddwyd 2019
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  20. 20
    Leukoencephalopathy with Calcifications and Cysts: A Purely Neurological Disorder Distinct from Coats Plus

    Leukoencephalopathy with Calcifications and Cysts: A Purely Neurological Disorder Distinct from Coats Plus gan Joséphine Mayer, Emma M. Jenkinson, Paul R. Kasher, Stavros Stivaros, Andrea Berger, Duccio Maria Cordelli, Patrick Ferreira, Rosalind J Jefferson, G Kutschke, Staffan Lundberg, Katrin Õunap, Prab Prabhakar, Calvin Soh, Helen Stewart, Jon Stone, Marjo S. van der Knaap, Hilde Van Esch, Christine Van Mol, Emma Wakeling, Andrea Whitney, Gillian Rice, Yanick J. Crow, John H. Livingston

    Cyhoeddwyd 2014
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