Resultados da busca - Leonardo Almeida‐Souza
- Mostrando 1 - 9 resultados de 9
-
1
Acute injury in the peripheral nervous system triggers an alternative macrophage response por Elke Ydens, Anje Cauwels, Bob Asselbergh, Sofie Goethals, Lieve Peeraer, Guillaume Lornet, Leonardo Almeida‐Souza, Jo A. Van Ginderachter, Vincent Timmerman, Sophie Janssens
Publicado em 2012Artigo -
2
A Flat BAR Protein Promotes Actin Polymerization at the Base of Clathrin-Coated Pits por Leonardo Almeida‐Souza, René Frank, Javier García‐Nafría, Adeline Colussi, Nushan Gunawardana, Christopher M. Johnson, Minmin Yu, Gillian Howard, Byron Andrews, Yvonne Vallis, Harvey T. McMahon
Publicado em 2018Artigo -
3
Increased Monomerization of Mutant HSPB1 Leads to Protein Hyperactivity in Charcot-Marie-Tooth Neuropathy por Leonardo Almeida‐Souza, Sofie Goethals, Vicky De Winter, Ines Dierick, Rodrigo Gallardo, Joost Van Durme, Joy Irobi, Jan Gettemans, Frédéric Rousseau, Joost Schymkowitz, Vincent Timmerman, Sophie Janssens
Publicado em 2010Artigo -
4
HSPB1 facilitates ERK-mediated phosphorylation and degradation of BIM to attenuate endoplasmic reticulum stress-induced apoptosis por Donna Kennedy, Katarzyna Mnich, Deepu Oommen, Reka Chakravarthy, Leonardo Almeida‐Souza, Michiel Krols, Svetlana Saveljeva, Karen Doyle, Sanjeev Gupta, Vincent Timmerman, Sophie Janssens, Adrienne M. Gorman, Afshin Samali
Publicado em 2017Artigo -
5
Mutant HSPB8 causes motor neuron-specific neurite degeneration por Joy Irobi, Leonardo Almeida‐Souza, Bob Asselbergh, Vicky De Winter, Sofie Goethals, Ines Dierick, Jyothsna Krishnan, Jean‐Pierre Timmermans, Wim Robberecht, Peter De Jonghe, Ludo Van Den Bosch, Sophie Janssens, Vincent Timmerman
Publicado em 2010Artigo -
6
Molecular Defects in the Motor Adaptor BICD2 Cause Proximal Spinal Muscular Atrophy with Autosomal-Dominant Inheritance por Koen Peeters, Ivan Litvinenko, Bob Asselbergh, Leonardo Almeida‐Souza, Teodora Chamova, Thomas Geuens, Elke Ydens, M. Zimoń, Joy Irobi, Els De Vriendt, Vicky De Winter, Tinne Ooms, Vincent Timmerman, Ivailo Tournev, Albena Jordanova
Publicado em 2013Artigo -
7
Focal adhesions contain three specialized actin nanoscale layers por Reena Kumari, Katharina Ven, Megan R. Chastney, Shrikant Babanrao Kokate, Johan Peränen, Jesse Aaron, Konstantin Kogan, Leonardo Almeida‐Souza, Elena Kremneva, Renaud Poincloux, Teng‐Leong Chew, Peter W. Gunning, Johanna Ivaska, Pekka Lappalainen
Publicado em 2024Artigo -
8
Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I por Annelies Rotthier, Michaela Auer‐Grumbach, Katrien Janssens, Jonathan Baets, Anke Penno, Leonardo Almeida‐Souza, Kim van Hoof, An Jacobs, Els De Vriendt, Beate Schlotter‐Weigel, Wolfgang N. Löscher, Petr Vondráček, Pavel Seeman, Peter De Jonghe, Patrick Van Dijck, Albena Jordanova, Thorsten Hornemann, Vincent Timmerman
Publicado em 2010Artigo -
9
Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy por Marina Kennerson, Garth A. Nicholson, Stephen G. Kaler, Bartosz Kowalski, Julian F. B. Mercer, Jingrong Tang, Roxana M. Llanos, Shannon Chu, Reinaldo Issao Takata, Carlos E. Speck‐Martins, Jonathan Baets, Leonardo Almeida‐Souza, Dirk Fischer, Vincent Timmerman, Philip Taylor, Steven S. Scherer, Toby A. Ferguson, Thomas D. Bird, Peter De Jonghe, Shawna Feely, Michael E. Shy, James Garbern
Publicado em 2010Artigo
Ferramentas de busca:
Assuntos relacionados
Biology
Biochemistry
Cell biology
Gene
Chemistry
Genetics
Medicine
Missense mutation
Phenotype
Actin
Actin cytoskeleton
Cell
Cytoskeleton
In vitro
Mutant
Mutation
Neuroscience
Organic chemistry
ATP7A
Actin remodeling
Actin-binding protein
Adhesion
Allele
Anatomy
Apoptosis
Biophysics
CCL18
Cell adhesion
Cell migration
Central nervous system