نتائج البحث - Lydia Teboul
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p27<sup>kip1</sup> independently promotes neuronal differentiation and migration in the cerebral cortex حسب Laurent Nguyen, Arnaud Besson, Julian Ik‐Tsen Heng, Carol Schuurmans, Lydia Teboul, Carlos Parras, Anna Philpott, James M. Roberts, François Guillemot
منشور في 2006Artigo -
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Uncoupling Antisense-Mediated Silencing and DNA Methylation in the Imprinted Gnas Cluster حسب Christine M. Williamson, Simon Ball, Claire Dawson, Stuti Mehta, C.V. Beechey, Martin Fray, Lydia Teboul, T. Neil Dear, Gavin Kelsey, Jo Peters
منشور في 2011Artigo -
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TPC1 Has Two Variant Isoforms, and Their Removal Has Different Effects on Endo-Lysosomal Functions Compared to Loss of TPC2 حسب Margarida Ruas, Kai‐Ting Chuang, Lianne C. Davis, Areej Al-Douri, Patricia W. Tynan, Ruth Tunn, Lydia Teboul, Antony Galione, John Parrington
منشور في 2014Artigo -
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Loss of O-GlcNAcase catalytic activity leads to defects in mouse embryogenesis حسب Villő Muha, Florence Authier, Zsombor Szoke-Kovacs, Sara Johnson, Jennifer Gallagher, Alison D. McNeilly, Rory J. McCrimmon, Lydia Teboul, Daan M. F. van Aalten
منشور في 2021Artigo -
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Evaluation of off-target and on-target scoring algorithms and integration into the guide RNA selection tool CRISPOR حسب Maximilian Haeussler, Kai Schönig, Hélène Eckert, Alexis Eschstruth, Joffrey Mianné, Jean-Baptiste Renaud, Sylvie Schneider‐Maunoury, Alena Shkumatava, Lydia Teboul, Jim Kent, Jean‐Stéphane Joly, Jean‐Paul Concordet
منشور في 2016Artigo -
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Microhomologies are prevalent at Cas9-induced larger deletions حسب Dominic D. G. Owens, Adam Caulder, Vincent Frontera, Joe Harman, Alasdair Allan, Akin Bucakci, Lucas Greder, Gemma Codner, Philip Hublitz, Peter J. McHugh, Lydia Teboul, Marella de Bruijn
منشور في 2019Artigo -
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Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair حسب Joffrey Mianné, Lauren Chessum, Saumya Kumar, Carlos Aguilar, Gemma Codner, Marie Hutchison, Andrew Parker, Ann‐Marie Mallon, Sara Wells, Michelle M. Simon, Lydia Teboul, Steve D. M. Brown, Michael R. Bowl
منشور في 2016Artigo -
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Adult Onset Global Loss of the Fto Gene Alters Body Composition and Metabolism in the Mouse حسب Fiona McMurray, Chris D. Church, Rachel Larder, George Nicholson, Sara Wells, Lydia Teboul, Y.C. Loraine Tung, Debra Rimmington, Fátima Bosch, Verónica Jiménez, Giles S.H. Yeo, Stephen O’Rahilly, Frances M. Ashcroft, Anthony P. Coll, Roger Cox
منشور في 2013Artigo -
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NAADP mobilizes calcium from acidic organelles through two-pore channels حسب Peter Calcraft, Margarida Ruas, Zui Pan, Xiaotong Cheng, Abdelilah Arredouani, Xue‐Mei Hao, Jisen Tang, Katja Rietdorf, Lydia Teboul, Kai-Ting Chuang, Pei‐Hui Lin, Rui Xiao, Chunbo Wang, Yingmin Zhu, Yakang Lin, Christopher N. Wyatt, John Parrington, Jianjie Ma, Allan M. Evans, Antony Galione, Michael X. Zhu
منشور في 2009Artigo -
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Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants حسب Gemma Codner, Joffrey Mianné, Adam Caulder, Jorik Loeffler, Rachel Fell, Ruairidh King, Alasdair Allan, Matthew Mackenzie, Fran J. Pike, Christopher V. McCabe, Skevoulla Christou, Sam Joynson, Marie Hutchison, Michelle Stewart, Saumya Kumar, Michelle M. Simon, Loranne Agius, Quentin M. Anstee, Kirill E. Volynski, Dimitri M. Kullmann, Sara Wells, Lydia Teboul
منشور في 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 حسب 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
منشور في 2025Artigo -
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Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) and Endolysosomal Two-pore Channels Modulate Membrane Excitability and Stimulus-Secretion Coupling in Mouse Pancreatic β Cells... حسب Abdelilah Arredouani, Margarida Ruas, Stephan C. Collins, Raman Parkesh, Frederick Clough, Toby Pillinger, George Coltart, Katja Rietdorf, J. Andrew Royle, Paul Johnson, Matthias Braun, Quan Zhang, William R. Sones, Kenju Shimomura, Anthony J. Morgan, Alexander M. Lewis, Kai‐Ting Chuang, Ruth Tunn, J. Gadea, Lydia Teboul, Paula Maria Heister, Patricia W. Tynan, Elisa A. Bellomo, Guy A. Rutter, Patrik Rorsman, Grant C. Churchill, John Parrington, Antony Galione
منشور في 2015Artigo -
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Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project حسب Abdel Ayadi, Marie‐Christine Birling, Joanna Bottomley, James Bussell, Helmut Fuchs, Martin Fray, Valérie Gailus‐Durner, Simon Greenaway, Richard Houghton, Natasha A. Karp, Sophie Leblanc, Christoph Lengger, Holger Maier, Ann‐Marie Mallon, Susan Marschall, David Melvin, Hugh W. Morgan, Guillaume Pavlovic, Edward J. Ryder, William C. Skarnes, Mohammed Selloum, Ramiro Ramírez‐Solis, Tania Sorg, Lydia Teboul, Laurent Vasseur, Alison Walling, Tom Weaver, Sara Wells, Jacqui White, Allan Bradley, David J. Adams, Karen P. Steel, Martin Hrabě de Angelis, Steve D. M. Brown, Yann Hérault
منشور في 2012Revisão -
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Mice with endogenous <scp>TDP</scp> ‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis حسب Pietro Fratta, Prasanth Sivakumar, Jack Humphrey, Kitty Lo, Thomas C. Ricketts, Hugo M. De Oliveira, José Miguel Brito Armas, Bernadett Kalmár, Agnieszka M Ule, Yichao Yu, Nicol Birsa, Cristian Bodo, Toby Collins, Alexander E. Conicella, Alan Mejia Maza, Alessandro Marrero‐Gagliardi, Michelle Stewart, Joffrey Mianné, Silvia Corrochano, Warren Emmett, Gemma Codner, Michael J. Groves, Ryutaro Fukumura, Yoichi Gondo, Mark F. Lythgoe, Erwin Pauws, Emma Peskett, Philip Stanier, Lydia Teboul, Martina Hallegger, Andrea Calvo, Adriano Chió, Adrian M. Isaacs, Nicolas L. Fawzi, Eric T. Wang, David E. Housman, Francisco E. Baralle, Linda Greensmith, Emanuele Buratti, Vincent Plagnol, Elizabeth Fisher, Abraham Acevedo‐Arozena
منشور في 2018Artigo -
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Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features حسب Teresa Santiago‐Sim, Lindsay C. Burrage, Frédéric Ebstein, Mari Tokita, Marcus J. Miller, Weimin Bi, Alicia Braxton, Jill A. Rosenfeld, Maher Shahrour, Andrea Lehmann, Benjamin Cogné, Sébastien Küry, Thomas Besnard, Bertrand Isidor, Stéphane Bézieau, Isabelle Hazart, Honey Nagakura, LaDonna Immken, Rebecca O. Littlejohn, Elizabeth Roeder, Bülent Kara, Katia Hardies, Sarah Weckhuysen, Patrick May, Johannes R. Lemke, Orly Elpeleg, Bassam Abu‐Libdeh, Kiely N. James, Jennifer L. Silhavy, Mahmoud Y. Issa, Maha S. Zaki, Joseph G. Gleeson, John R. Seavitt, Mary E. Dickinson, M. Cecilia Ljungberg, Sara Wells, Sara Johnson, Lydia Teboul, Christine M. Eng, Yaping Yang, Peter‐Michael Kloetzel, Jason D. Heaney, Magdalena Walkiewicz, Zaid Afawi, Rudi Balling, Nina Barišić, Stéphanie Baulac, Dana Craiu, Peter De Jonghe, Rosa Guerrero, Renzo Guerrini, Ingo Helbig, Helle Hjalgrim, Johanna Jähn, Karl Martin Klein, Eric LeGuern, Holger Lerche, Carla Marini, Hiltrud Muhle, Felix Rosenow, José M. Serratosa, Katalin Štěrbová, Arvid Suls, Rikke S. Møller, Pasquale Striano, Yvonne G. Weber, Federico Zara
منشور في 2017Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Gene
Computational biology
Cell biology
Medicine
Genome
Biochemistry
Genome editing
Phenotype
CRISPR
Cas9
Chemistry
Computer science
Genotype
Internal medicine
Mutant
Allele
Disease
Endocrinology
Knockout mouse
Mutation
Psychology
RNA
Single-nucleotide polymorphism
Cell
Cellular differentiation
Endoplasmic reticulum
Enzyme
Evolutionary biology