Որոնման արդյունքները - Colin Miles
- Ցուցադրվում են 1 - 14 արդյունքները 14
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Complete sequencing of the <i>Fugu</i> WAGR region from WT1 to PAX6: Dramatic compaction and conservation of synteny with human chromosome 11p13 Colin Miles, Greg Elgar, Edward G. Coles, Dirk‐Jan Kleinjan, Veronica van Heyningen, Nicholas D. Hastie
Հրապարակվել է 1998Artigo -
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Defining a therapeutic window for the novel <scp>TGF</scp>‐β inhibitor <scp>LY</scp>2157299 monohydrate based on a pharmacokinetic/pharmacodynamic model Ivelina Gueorguieva, Ann Cleverly, Anja J. Stauber, Nischalan Pillay, Jordi Rodón, Colin Miles, Jonathan M. Yingling, Michael Lahn
Հրապարակվել է 2013Artigo -
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A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies Shalabh Srivastava, Simon A. Ramsbottom, Elisa Molinari, Sumaya Alkanderi, Andrew Filby, Kathryn White, C. Henry, Sophie Saunier, Colin Miles, John A. Sayer
Հրապարակվել է 2017Artigo -
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Wt1 and retinoic acid signaling are essential for stellate cell development and liver morphogenesis 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
Հրապարակվել է 2007Artigo -
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Targeted exon skipping of a <i>CEP290</i> mutation rescues Joubert syndrome phenotypes in vitro and in a murine model 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
Հրապարակվել է 2018Artigo -
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A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys–Drash syndrome 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
Հրապարակվել է 1999Artigo -
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Murine Joubert syndrome reveals Hedgehog signaling defects as a potential therapeutic target for nephronophthisis 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
Հրապարակվել է 2014Artigo -
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DNA replication stress underlies renal phenotypes in CEP290-associated Joubert syndrome 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
Հրապարակվել է 2015Artigo -
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A Phase II randomized study of galunisertib monotherapy or galunisertib plus lomustine compared with lomustine monotherapy in patients with recurrent glioblastoma 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
Հրապարակվել է 2016Artigo -
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ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition 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
Հրապարակվել է 2018Artigo -
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An ultra-conserved poison exon in the Tra2b gene encoding a splicing activator is essential for male fertility and meiotic cell division 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
Հրապարակվել է 2025Artigo -
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Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations 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
Հրապարակվել է 2022Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Cell biology
Phenotype
Medicine
Cilium
Joubert syndrome
Cancer research
Ciliopathies
Ciliopathy
Exon
Mutation
Pathology
Population
Allele
Biochemistry
Cancer
Environmental health
Immunology
Internal medicine
Nephronophthisis
Paleontology
Signal transduction
Stem cell
Activator (genetics)
Alternative medicine
Alternative splicing
Andrology
Bioinformatics