Resultados de procura - Colin Miles

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  1. 1
    Characterization of the First Definitive Hematopoietic Stem Cells in the AGM and Liver of the Mouse Embryo

    Characterization of the First Definitive Hematopoietic Stem Cells in the AGM and Liver of the Mouse Embryo por María José Sánchez, A. Holmes, Colin Miles, Elaine Dzierzak

    Publicado 1996
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  2. 2
    Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia

    Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia por Ralf Kist, Michelle Watson, Xiaomeng Wang, Paul Cairns, Colin Miles, Donald J. Reid, Heiko Peters

    Publicado 2005
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  3. 3
    Complete sequencing of the <i>Fugu</i> WAGR region from WT1 to PAX6: Dramatic compaction and conservation of synteny with human chromosome 11p13

    Complete sequencing of the <i>Fugu</i> WAGR region from WT1 to PAX6: Dramatic compaction and conservation of synteny with human chromosome 11p13 por Colin Miles, Greg Elgar, Edward G. Coles, Dirk‐Jan Kleinjan, Veronica van Heyningen, Nicholas D. Hastie

    Publicado 1998
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  4. 4
    Defining a therapeutic window for the novel <scp>TGF</scp>‐β inhibitor <scp>LY</scp>2157299 monohydrate based on a pharmacokinetic/pharmacodynamic model

    Defining a therapeutic window for the novel <scp>TGF</scp>‐β inhibitor <scp>LY</scp>2157299 monohydrate based on a pharmacokinetic/pharmacodynamic model por Ivelina Gueorguieva, Ann Cleverly, Anja J. Stauber, Nischalan Pillay, Jordi Rodón, Colin Miles, Jonathan M. Yingling, Michael Lahn

    Publicado 2013
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  5. 5
    A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies

    A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies por Shalabh Srivastava, Simon A. Ramsbottom, Elisa Molinari, Sumaya Alkanderi, Andrew Filby, Kathryn White, C. Henry, Sophie Saunier, Colin Miles, John A. Sayer

    Publicado 2017
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  6. 6
    Wt1 and retinoic acid signaling are essential for stellate cell development and liver morphogenesis

    Wt1 and retinoic acid signaling are essential for stellate cell development and liver morphogenesis por Annemieke IJpenberg, José M. Pérez‐Pomares, Juan Antonio Guadix, Rita Carmona, Victor Portillo-Sánchez, David Macías, Peter Hohenstein, Colin Miles, Nicholas D. Hastie, Ramón Muñoz‐Chápuli

    Publicado 2007
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  7. 7
    Targeted exon skipping of a <i>CEP290</i> mutation rescues Joubert syndrome phenotypes in vitro and in a murine model

    Targeted exon skipping of a <i>CEP290</i> mutation rescues Joubert syndrome phenotypes in vitro and in a murine model por Simon A. Ramsbottom, Elisa Molinari, Shalabh Srivastava, Flora Silberman, C. Henry, Sumaya Alkanderi, Laura A. Devlin, Kathryn White, David Steel, Sophie Saunier, Colin Miles, John A. Sayer

    Publicado 2018
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  8. 8
    A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys–Drash syndrome

    A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys–Drash syndrome por C.E. Patek, Melissa H. Little, Stewart Fleming, Colin Miles, Jean-Paul Charlieu, Alan R. Clarke, Kiyoshi Miyagawa, Sheila Christie, Jennifer Doig, David J. Harrison, David J. Porteous, Anthony J. Brookes, Martin Hooper, Nicholas D. Hastie

    Publicado 1999
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  9. 9
    Murine Joubert syndrome reveals Hedgehog signaling defects as a potential therapeutic target for nephronophthisis

    Murine Joubert syndrome reveals Hedgehog signaling defects as a potential therapeutic target for nephronophthisis por Ann Marie Hynes, Rachel H. Giles, Shalabh Srivastava, Lorraine Eley, Jennifer L. Whitehead, Marina Danilenko, Shreya Raman, Gisela G. Slaats, John G. Colville, Henry Ajzenberg, Hester Y. Kroes, Peter E. Thelwall, Nicholas L. Simmons, Colin Miles, John A. Sayer

    Publicado 2014
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  10. 10
    DNA replication stress underlies renal phenotypes in CEP290-associated Joubert syndrome

    DNA replication stress underlies renal phenotypes in CEP290-associated Joubert syndrome por Gisela G. Slaats, Joshua C. Saldivar, Julien Bacal, Michelle K. Zeman, Andrew C. Kile, Ann Marie Hynes, Shalabh Srivastava, Katia Nazmutdinova, Krista den Ouden, Miriam S. Zagers, Veronica Foletto, Marianne C. Verhaar, Colin Miles, John A. Sayer, Karlene A. Cimprich, Rachel H. Giles

    Publicado 2015
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  11. 11
    A Phase II randomized study of galunisertib monotherapy or galunisertib plus lomustine compared with lomustine monotherapy in patients with recurrent glioblastoma

    A Phase II randomized study of galunisertib monotherapy or galunisertib plus lomustine compared with lomustine monotherapy in patients with recurrent glioblastoma por Alba A. Brandes, Alain Carpentier, Santosh Kesari, Juan Manuel Sepúlveda-Sánchez, Helen Wheeler, Olivier Chinot, Lawrence Cher, Joachim P. Steinbach, David Capper, Pol Specenier, Jordi Rodón, Ann Cleverly, Claire Smith, Ivelina Gueorguieva, Colin Miles, Susan C. Guba, D. Desaiah, Michael Lahn, Wolfgang Wick

    Publicado 2016
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  12. 12
    ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition

    ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition por Sumaya Alkanderi, Elisa Molinari, Ranad Shaheen, Yasmin ElMaghloob, Louise A. Stephen, Veronica Sammut, Simon A. Ramsbottom, Shalabh Srivastava, George Cairns, Noel Edwards, Sarah J. Rice, Nour Ewida, Amal Alhashem, Kathryn White, Colin Miles, David Steel, Fowzan S. Alkuraya, Shehab Ismail, John A. Sayer

    Publicado 2018
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  13. 13
    An ultra-conserved poison exon in the Tra2b gene encoding a splicing activator is essential for male fertility and meiotic cell division

    An ultra-conserved poison exon in the Tra2b gene encoding a splicing activator is essential for male fertility and meiotic cell division por Caroline Dalgliesh, Saad Aldalaqan, Christian Atallah, Andrew Best, Emma Scott, Ingrid Ehrmann, George Merces, Jonathan Mannion, Barbora Badurova, Raveen Sandher, Ylva Illing, Brunhilde Wirth, Sara Wells, Gemma Codner, Lydia Teboul, Graham R. Smith, A J Hedley, Mary Herbert, Dirk G. de Rooij, Colin Miles, Louise N. Reynard, David J. Elliott

    Publicado 2025
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  14. 14
    Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations

    Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations por John Devane, Elisabeth Ott, Eric Olinger, Daniel Epting, Eva L. Decker, Anja Friedrich, Nadine Bachmann, Gina Renschler, Tobias Eisenberger, Andrea Briem‐Richter, Enke Grabhorn, Laura Powell, Ian Wilson, Sarah J. Rice, Colin Miles, Katrina Wood, Palak Trivedi, Gideon M. Hirschfield, Andrea Pietrobattista, Elizabeth Wohler, Anya Mezina, Nara Sobreira, Emanuele Agolini, Giuseppe Maggiore, Mareike Dahmer‐Heath, Ali Yılmaz, Melanie Boerries, Patrick Metzger, Christoph Schell, Inga Grünewald, Martin Konrad, Jens König, Bernhard Schlevogt, John A. Sayer, Carsten Bergmann

    Publicado 2022
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