Výsledky vyhledávání - Susana Caetano
- Zobrazuji výsledky 1 - 4 z 4
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1
High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation Autor Lucie Abeler‐Dörner, Adam G. Laing, Anna Lorenc, Dmitry S. Ushakov, Simon Clare, Anneliese O. Speak, María A. Duque-Correa, Jacqueline K. White, Ramiro Ramírez‐Solis, Namita Saran, Katherine R. Bull, Belén Morón, Jua Iwasaki, P. Barton, Susana Caetano, Keng I. Hng, Emma L. Cambridge, Simon P. Forman, Tanya L. Crockford, Mark Griffiths, Leanne Kane, Katherine Harcourt, Cordelia Brandt, George Notley, Kola Babalola, Jonathan Warren, Jeremy Mason, Amrutha Meeniga, Natasha A. Karp, David Melvin, Eleanor Cawthorne, Brian Weinrick, Albina Rahim, Sibyl Drissler, Justin Meskas, Alice Yue, Markus Lux, George X. Song‐Zhao, Anna Chan, Carmen Ballesteros Reviriego, Johannes Abeler, Heather Wilson, Agnieszka Przemska-Kosicka, Matthew Edmans, Natasha Strevens, Markus Pasztorek, Terrence F. Meehan, Fiona Powrie, Ryan R. Brinkman, Gordon Dougan, William R. Jacobs, Clare M. Lloyd, Richard J. Cornall, Kevin J. Maloy, Richard K. Grencis, Gillian M. Griffiths, David J. Adams, Adrian Hayday
Vydáno 2019Artigo -
2
WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy Autor Meghna Kannan, Efil Bayam, Christel Wagner, Bruno Rinaldi, Perrine F. Kretz, Peggy Tilly, Marna Roos, L. McGillewie, Séverine Bär, Shilpi Minocha, Claire Chevalier, Chrystelle Po, Jamel Chelly, Jean‐Louis Mandel, Renato Borgatti, Amélie Piton, Craig Kinnear, Ben Loos, David J. Adams, Yann Hérault, Stephan C. Collins, Sylvie Friant, Juliette D. Godin, Binnaz Yalcin, Valerie E. Vancollie, Lauren F. E. Anthony, Simon A. Maguire, David Lafont, Selina Pearson, Amy S. Gates, Mark Sanderson, Carl Shannon, Maksymilian T. Sumowski, Robbie S. B. McLaren-Jones, Agnieszka Świątkowska, Christopher Isherwood, Emma L. Cambridge, Heather Wilson, Susana Caetano, Anna Karin B. Maguire, Antonella Galli, Anneliese O. Speak, Joshua Dench, Elizabeth Tuck, Jeanne Estabel, Angela Green, Catherine Tudor, Emma Siragher, Monika Dabrowska, Cecilia Mazzeo, Yvette Hooks, Fiona Kussy, Mark Griffiths, David Gannon, Brendan Doe, Katharina Boroviak, Hannah Wardle‐Jones, Nicola Griggs, Joanna Bottomley, Edward J. Ryder, Diane Gleeson, Jacqueline K. White, Ramiro Ramírez‐Solis, Christopher J. Lelliott
Vydáno 2017Artigo -
3
Targeting of NAT10 enhances healthspan in a mouse model of human accelerated aging syndrome Autor Gabriel Balmus, Delphine Larrieu, Ana C. Barros, Casey Collins, Monica Abrudan, Mehmet Demir, Nicola J. Geisler, Christopher J. Lelliott, Jacqueline K. White, Natasha A. Karp, James Atkinson, Andrea Kirton, Matt Jacobsen, Dean Clift, Raphaël Rodriguez, Carl Shannon, Mark Sanderson, Amy Gates, Joshua Dench, Valerie E. Vancollie, Catherine McCarthy, Selina Pearson, Emma L. Cambridge, Christopher Isherwood, Heather Wilson, Evelyn Grau, Antonella Galli, Yvette Hooks, Catherine Tudor, Angela L. Green, Fiona Kussy, Elizabeth Tuck, Emma Siragher, Robbie S. B. McLaren, Agnieszka Świątkowska, Susana Caetano, Cecilia Mazzeo, Monika Dabrowska, Simon A. Maguire, David Lafont, Lauren F. E. Anthony, Maksymilian T. Sumowski, James Bussell, Caroline Sinclair, Ellen Brown, Brendan Doe, Hannah Wardle‐Jones, Nicola Griggs, Mike Woods, Harun Kundi, George McConnell, Joanne Doran, Mark Griffiths, Christian Kipp, S. Holroyd, David J. Gannon, Rafael Alcántara, Ramiro Ramírez‐Solis, Joanna Bottomley, Catherine Ingle, Victoria Ross, Daniel M. Barrett, Debarati Sethi, Diane Gleeson, Jonathan Burvill, Radka Platte, Edward Ryder, Elodie Sins, Evelina Miklejewska, Dominique Von Schiller, Graham Duddy, Jana Urbanová, Katharina Boroviak, Maria Imran, Shalini Kamu Reddy, David J. Adams, Stephen P. Jackson
Vydáno 2018Artigo -
4
Identification of genetic elements in metabolism by high-throughput mouse phenotyping Autor Jan Rozman, Birgit Rathkolb, Manuela A. Oestereicher, Christine Schütt, Aakash Chavan Ravindranath, Stefanie Leuchtenberger, Sapna Sharma, Martin Kistler, Monja Willershäuser, Robert Brommage, Terrence F. Meehan, Jeremy Mason, Hamed Haselimashhadi, Juan Antonio Aguilar‐Pimentel, Lore Becker, Irina Treise, Kristin Moreth, Lillian Garrett, Sabine M. Hölter, Annemarie Zimprich, Susan Marschall, Oana V. Amarie, Julia Calzada-Wack, Frauke Neff, Laura Brachthäuser, Christoph Lengger, Claudia Stoeger, Lilly Zapf, Yi‐Li Cho, Patricia da Silva‐Buttkus, Markus Kraiger, Philipp Mayer‐Kuckuk, Karen Kristine Gampe, Moya Wu, Nathalie Conte, Jonathan Warren, Chao-Kung Chen, Ilinca Tudose, Mike Relac, Peter Matthews, Heather Cater, Helen P. M. Natukunda, James Cleak, Lydia Teboul, Sharon Clementson-Mobbs, Zsombor Szoke-Kovacs, Alison P. Walling, Sara Johnson, Gemma Codner, Tanja Fiegel, Natalie Ring, Henrik Westerberg, Simon Greenaway, Duncan Sneddon, Hugh W. Morgan, Jorik Loeffler, Michelle Stewart, Ramiro Ramírez‐Solis, Allan Bradley, William C. Skarnes, Karen P. Steel, Simon A. Maguire, Joshua Dench, David Lafont, Valerie E. Vancollie, Selina Pearson, Amy S. Gates, Mark Sanderson, Carl Shannon, Lauren F. E. Anthony, Maksymilian T. Sumowski, Robbie S. B. McLaren, Brendan Doe, Hannah Wardle‐Jones, Mark Griffiths, Antonella Galli, Agnieszka Świątkowska, Christopher Isherwood, Anneliese O. Speak, Emma L. Cambridge, Heather Wilson, Susana Caetano, Anna Karin B. Maguire, David J. Adams, Joanna Bottomley, Edward J. Ryder, Diane Gleeson, Laurent Pouilly, Stéphane Rousseau, Aurélie Auburtin, Patrick T. Reilly, Abdel Ayadi, Mohammed Selloum, Joshua A. Wood, Dave Clary, Peter J. Havel, Todd Tolentino, Heather Tolentino, Mike Schuchbauer, Sheryl Pedroia
Vydáno 2018Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Cell biology
Computational biology
Gene
Apoptosis
Autophagy
Botany
Computer science
Flow cytometry
Gene knockout
Genetic association
Genetic variation
Genome-wide association study
Genotype
Identification (biology)
Immune system
Immunocompetence
Immunophenotyping
Lissencephaly
Medicine
Microcephaly
Microtubule
Microtubule-associated protein
Neural development
Neural stem cell
Neurogenesis
Neuroscience
Phenotype
Single-nucleotide polymorphism