Výsledky vyhledávání - Vincent Timmerman
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Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene Autor Mathias Bähr, Fernando Andrés, Vincent Timmerman, Mar Nelis, Christine Van Broeckhoven, Johannes Dichgans
Vydáno 1999Artigo -
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Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group. Autor Peter Raeymaekers, Vincent Timmerman, Eva Nelis, Wim Van Hul, Peter De Jonghe, Jean‐Jacques Martin, Christine Van Broeckhoven
Vydáno 1992Artigo -
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BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes Autor Elias Adriaenssens, B. Tedesco, Laura Mediani, Bob Asselbergh, V. Crippa, Francesco Antoniani, Serena Carra, Angelo Poletti, Vincent Timmerman
Vydáno 2020Artigo -
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Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies Autor Mansour Haidar, Bob Asselbergh, Elias Adriaenssens, Vicky De Winter, Jean‐Pierre Timmermans, Michaela Auer‐Grumbach, Manisha Juneja, Vincent Timmerman
Vydáno 2019Artigo -
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Acute injury in the peripheral nervous system triggers an alternative macrophage response Autor Elke Ydens, Anje Cauwels, Bob Asselbergh, Sofie Goethals, Lieve Peeraer, Guillaume Lornet, Leonardo Almeida‐Souza, Jo A. Van Ginderachter, Vincent Timmerman, Sophie Janssens
Vydáno 2012Artigo -
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Increased Monomerization of Mutant HSPB1 Leads to Protein Hyperactivity in Charcot-Marie-Tooth Neuropathy Autor 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
Vydáno 2010Artigo -
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Screening for mutations in the peripheral myelin genesPMP22,MPZ andCx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients Autor Irina Mersiyanova, Sookhrat M. Ismailov, Alexandr V. Polyakov, Е. Л. Дадали, В. П. Федотов, Eva Nelis, Ann L�fgren, Vincent Timmerman, Christine Van Broeckhoven, Oleg V. Evgrafov
Vydáno 2000Artigo -
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The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotype Autor Peter De Jonghe, Vincent Timmerman, C. Ceuterick, Eva Nelis, Els De Vriendt, A. Löfgren, Anina Vercruyssen, Christine Verellen, Lionel Van Maldergem, J. J. Martin, Christine Van Broeckhoven
Vydáno 1999Artigo -
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HSPB1 facilitates ERK-mediated phosphorylation and degradation of BIM to attenuate endoplasmic reticulum stress-induced apoptosis Autor 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
Vydáno 2017Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Cell biology
Mutation
Pathology
Neuroscience
Phenotype
Disease
Biochemistry
Missense mutation
Mutant
Heat shock protein
Bioinformatics
Apoptosis
Immunology
Anatomy
Central nervous system
Chaperone (clinical)
Computational biology
Genetic heterogeneity
Autophagy
Cell
Chemistry
Endocrinology
Hsp70
In vitro
Internal medicine
Protein aggregation